Kamis, 26 Maret 2009

2. A Clinical Approach to the Human Brain

9.22J / HST.422J A Clinical Approach to the Human Brain

Fall 2006



Image of the brain with key areas highlighted.

Activity in the highlighted areas in the prefrontal cortex may affect the level of dopamine in the mid-brain, in a finding that has implications for schizophrenia. (Image courtesy of the National Institutes of Mental Health.)

Course Highlights

This course features summaries of each class in the lecture notes section, as well as an extensive set of readings.

Course Description

This course is designed to provide an understanding of how the human brain works in health and disease, and is intended for both the Brain and Cognitive Sciences major and the non-Brain and Cognitive Sciences major. Knowledge of how the human brain works is important for all citizens, and the lessons to be learned have enormous implications for public policy makers and educators.

The course will cover the regional anatomy of the brain and provide an introduction to the cellular function of neurons, synapses and neurotransmitters. Commonly used drugs that alter brain function can be understood through a knowledge of neurotransmitters. Along similar lines, common diseases that illustrate normal brain function will be discussed. Experimental animal studies that reveal how the brain works will be reviewed.

Throughout the seminar we will discuss clinical cases from Dr. Byrne's experience that illustrate brain function; in addition, articles from the scientific literature will be discussed in each class.

Syllabus

Goals and Overview of Course

Taught by a neurologist, the course is designed to provide an understanding of how the human brain works in health and disease, and is intended for both the Brain and Cognitive Sciences major and the non-Brain and Cognitive Sciences major. Knowledge of how the human brain works is important for all citizens, and the lessons to be learned have enormous implications for public policy makers and educators.

Many new technologies allow us to map brain function. For example, functional magnetic resonance imaging (fMRI) shows brain regions that are active when we see, move a finger, read, experience emotion or perform mental arithmetic. The course will explore how fMRI reveals that visual and spatial information, such as pictures, are stored on the right side of the brain and words are stored on the left. We will study how fMRI is being used in dyslexia and other brain disorders to assess organization of the brain in disease and its reorganization following treatment.

During "critical periods" in development, appropriate activity is required for the acquisition of mature brain circuitry and function. For example, a child born with a "lazy," or strabismic, eye must be forced to use that eye, either by surgical correction of the eye position or by patching the good eye, before about 8 years of age or the strabismic eye will never develop normal vision. Along similar lines, to speak a language with a native accent, the language must be learned before puberty. These examples of how the brain "wires" itself during critical periods of "activity-dependent" development will be discussed as outlined in the syllabus.

Of course, beyond childhood we can still learn new information and skills. The course will review imaging studies that reveal how the organization of the brain is modified by training and rehearsal. For example, we will discuss experiments showing that the area of brain that controls finger movements and sensations is reorganized in musicians who rehearse intensively. Interestingly, even mental rehearsing of keyboard instruments can lead to the reorganization of brain circuits in the premotor area of the brain, which is the site where planning of motor activities are maintained. Such mental rehearsing is routinely done by musicians (and athletes alike) because it can give rise to an improvement in performance.

The course will cover the regional anatomy of the brain and provide an introduction to the cellular function of neurons, synapses and neurotransmitters. Commonly used drugs that alter brain function can be understood through a knowledge of neurotransmitters. Along similar lines, common diseases that illustrate normal brain function will be discussed. Experimental animal studies that reveal how the brain works will be reviewed.

The primary text for the course will be Neuroscience, edited by Dale Purves, et al. Throughout the seminar we will discuss clinical cases from Dr. Byrne's experience that illustrate brain function; in addition, articles from the scientific literature will be discussed in each class.

Course Requirements

Each student is required to present at least one paper to the class. The papers will be selected from the asterisked articles in the lectures.

Grading


ACTIVITIES PERCENTAGES
Two Exams 60%
Final Exam 30%
Class Participation 10%

The class participation portion will be derived as follows: half (5% of final grade) will be determined by the presentation and half (5% of final grade) will be determined by participation in class discussions throughout the term.

Lecture Notes

SES # TOPICS LECTURE SUMMARIES
1 Brain Anatomy and Imaging

Brain as seat of consciousness: Historical introduction - Greeks, Descartes, 19th Century phrenology; British neurologist Hughlings Jackson and the modern era.

Overview of the regional anatomy of the brain and spinal cord:

  • * The regions of the human brain that serve motor and sensory functions, vision, hearing, smell, coordination, language, memory and emotion
  • * Cerebral cortex and white matter
  • * Brain stem and cerebellum
  • * Thalamus and Hypothalamus
  • * Basal ganglia
  • * Ventricles
  • * Cranial nerves

A quick tour of the regional anatomy of the brain is introduced using figures, computerized axial tomography (CT) images, and magnetic resonance images (MRI) from normal subjects and individuals with strokes and other diseases to illustrate brain function.

2 Cells and Brain Imaging
3 Synaptic Potentials

A general knowledge of the cellular basis of brain function is essential to understanding how drugs such as antidepressants, memory enhancing drugs, or stimulants such as Ritalin work. We will review:

  • * Neurons and supporting glia
  • * Axons: How neurons carry information from one part of the nervous system to another
  • * Axons and their surrounding insulation: The myelin sheath
  • * Synapses: How neurons communicate with one another
  • * Resting membrane potential: How neuronal membranes maintain a charge with the outside positive relative to the inside
  • * Action potential: How depolarization of the resting membrane potential results in a reversal in the charge of the membrane with the exterior becoming negative relative to the interior. How the action potential is propagated along the axon and how information is communicated along the axon up to 2 meters in length. How does synaptic transmission occur?

The following will be discussed:

  • * Excitatory and inhibitory synapse
  • * Release of neurotransmitters and neuromodulators from presynaptic neurons
  • * Re-uptake of neurotransmitters
  • * The neuromuscular junction
  • * Classes of neurotransmitters and neuromodulators:
  • * Acetylcholine, amino acids, monoamines and peptides


Clinical Correlation

Have you wondered what happens when you hit your "funny bone" or why your leg gets numb from crossing your legs? A common cause of fish poisoning in the tropics is due to a neurotoxin: Ciguatera poisoning from fish consumption. Seizures are caused by abnormally excitable nerve cell membranes. Some anti-seizure medications block membrane sodium channels and stabilize membranes. Seizures may cause involuntary movements or experiences e.g., olfactory and auditory hallucinations, deja vu, and other complex behaviors. See: Singing Seizure Video Neurotransmitters are chemicals which are released by one neuron, the presynaptic neuron, and pass across the synaptic cleft to stimulate the post-synaptic neuron. The post-synaptic neuron can be stimulated (depolarized) or inhibited (hyperpolarized) by the neurotransmitter. Increasing or decreasing the concentration of the neurotransmitter, therefore, can increase or decrease its effect on the post-synaptic neuron.

Some diseases have a deficiency of a specific neurotransmitter. For example, in Parkinson's disease there is a deficiency of dopamine in a specific pathway in the brain. In Alzheimer's disease there is a deficiency of acetylcholine. In these two cases drugs are administered to patients to increase the concentration of these deficient neurotransmitters. In the case of depression, there is a deficiency of serotonin and norepinephrine. Antidepressants have been developed which will increase the concentration of these neurotransmitters. Early antidepressants, such as tricyclic antidepressants, increase the concentration of both of these neurotransmitters. In the past decade serotonin reuptake inhibitors (SSRI) such as Prozac have dominated the antidepressant market. As the article from the WSJ above indicates there is again a debate over the relative importance of these two neurotransmitters in depression.

Readings from Oliver Sacks illustrate "how we know our bodies in space" and how we compensate when we lose one or more of our senses. In order to have an image of "where we are in space" our brain integrates information from our visual system, vestibular system (labyrinth of inner ear), and position sense of musculoskeletal system (proprioception). Information from each of these is integrated which leads to a "map of space" and where our bodies are in that space. Aberration of one of these inputs creates a disorienting experience. For example, alcohol impairs the vestibular system causing incoordination, staggering and falling. In diseases of the eyes, inner ear or nervous system there may be impairment of one of these inputs which leads to spatial disorientation. Some of Dr. Sacks's cases illustrate how brain plasticity permits one to overcome loss of function of one of these sensory inputs.

4

fMRI of the Human Brain

Prof. John Gabrieli, MIT


5 Seeing and Reading Others The capacity to "read" another person's emotional status, predict what they will do next or recognize what they think that you are thinking represent among the most important talents of the human brain. In a society where human interaction often determines success such abilities are highly valued. How does the human brain recognize the facial emotions of others or the sarcasm of a voice? It turns out that the neural systems responsible for recognizing facial and aural emotional content relies on the right cerebral hemisphere to a greater extent than the left where grammar and semantic meaning of words are stored.
6 Cognitive Enhancement through Neuropharmacology

Clinical Correlation

The brains of patients with Alzheimer's disease have a reduced amount of neurotransmitter acetylcholine. With our understanding of synaptic transmission, scientists have been able to develop drugs which increase the amount of acetylcholine available and modestly improve memory in Alzheimer's patients. A recent study has shown that such drugs also work in normal individuals (Yesavage). Additionally, a race among several biotechnology companies now exists to develop memory enhancement drugs to improve normal human cognition (See "Quest for a Smart Pill"). It has been said that other drugs such as methylphenidate (Ritalin), which is prescribed for attention deficit disorder, have been used without a prescription as memory enhancing drugs. Such uses in normal individuals have unknown long term medical consequences and create ethical issues as do the use of steroids in athletes. (Possible final paper topic).

Other clinical examples of drugs which affect neurotransmitter function are serotonin reuptake inhibitors (e.g. Prozac) which increases serotonin and alleviates depression but also may act by inducing neurogenesis. Antidepressants are widely accepted and improve memory in depressed patients since impaired memory is a common feature of depression. Does the role that antidepressants play in the modification of the brain affect the debate in regard to the use of memory enhancing drugs?

7 Oxytocin and Trust, Antidepressants and Neurogenesis
8 Neurogenesis: Teaching Old Dogs New Tricks A surprising discovery in the last few years in neurobiology has been that neurons are born, neurogenesis, in the adult mammalian brain. Initially, this had been shown in animals and, more recently, in the humans hippocampus, the site of declarative memory formation. (See Greenough). Furthermore, the rate of neurogenesis in animals has been enhanced by experience, both physical activity and living in enriched environments (See Scientific American article by Gage). Provocative clinical human studies suggest that memory loss (dementia) can be forestalled by rich cognitive activities e.g. board games, crossword puzzles. These animal and clinical studies may lead to a strategy for preventing dementia in humans.
9 Test 1
10 Critical Periods: Implications for Education

The nervous system has a structural organization which is genetically determined to some degree but in order for the brain to develop normally, it requires experience. This is called experience-dependent brain development. An example is the child born with a cataract. If the cataract is not removed at an early age the person will never develop normal vision in the affected eye even if it is removed later. Alternatively, a person who acquires a cataract as an adult can have the cataract removed many years later and have normal vision after it is removed. The difference in outcome is due to the "critical period" of the visual system development in childhood. Neurobiological studies have shown that opportunities exist for brain development in childhood and that once the window of opportunity closes, it never reopens. The mechanism of this is being elucidated at a molecular level and is a major area of research. The implications for childhood development, public policy and educational programs are enormous; because, as outlined in subsequent classes, for many skills we seem to have an opportunity to learn at a young age which then closes later. For example, in the case of learning a foreign language with a native accent the window of opportunity closes at about puberty in most individuals.

The articles by Christakis and Penn and Schatz demonstrate that the consequences of early experience have long-lasting behavioral and structural consequences. Throughout early childhood a much larger number of synapses form than ultimately exist in the adult. This is because those synapses which are 'used' in childhood survive and are strengthened at the expense of unused synapses which are pruned and die back during later childhood and adolescence; The 'used', and retained, synapses follow the rule first enunciated by Hebb, "neurons that fire together wire together."

Critical periods of brain development provide opportunities to permanently alter the brain wiring. Furthermore, knowledge of brain development provides a basis upon which to define educational programs. For example, the acquisition of a second language before puberty generally results in a native accent, whereas, learning a foreign language after puberty usually results in a foreign accent. The article by Kim demonstrates that when a second language is learned during early childhood the same region in Broca's area (left frontal lobe) is used for both native and second language; alternatively, when the second language is learned later in life, the second language is located in a region adjacent but not superimposed to the native language. Accent may be one of the phenotypic expressions of this difference in localization.

11 Neuroplasticity in the Adult

Primary motor cortex in the frontal lobe is organized in such a way that the left side of the brain controls the right body and that the foot neurons are near the crown of the head and the hand is midway between the crown and the ear and the mouth is just above the ear (Homunculus). These neurons control individual movements according to this motor map of the cerebral cortex. The map was first discovered by Dr. Wilder Penfield a neurosurgeon who stimulated the brain in awake patients undergoing epilepsy surgery. He was able to map different parts of the brain to different motor and sensory functions. The premotor cortex lies in front (anterior) to the motor cortex and its role is to plan voluntary movements. It is activated in mental rehearsing of a movement such as piano playing or pole vaulting before the actual execution.

Several studies have shown that even in adulthood the motor map of the brain can be modified. Studies in animals have shown that increased finger use enlarges the area of the "brain real estate" devoted to those fingers. In humans, Elbert has shown in string players that the size of the brain cortex, on the right side of the brain, devoted to the left hand is enlarged. Alternatively, if a finger or limb is amputated the adjacent functional areas "invade" the unused area and make use of it; another example of competition between neurons and the adage "use it or lose it". Recent studies using a technique called constraint behavior therapy actually limits the use of a good limb to increase the function of the impaired limb such as in cases of cerebral palsy with promising results. This is an example of basic science leading to important clinical discoveries and benefits to patients.

12 Language, Dyslexia and Universal Grammar

Language which includes both oral and written forms of communication is lateralized to the left cerebral hemisphere in nearly all right-handed individuals and in most left-handed individuals. Disturbance of language function is called aphasia. When reading alone is disturbed it is termed dyslexia. Recent fMRI studies show that in dyslexia both cerebral hemispheres are activated (Simos). When children undergo successful treatment, activation is normalized to the left cerebral hemisphere.

Functional imaging of the brain (fMRI) has permitted linguists to study the structure of language. Universal grammar has been proposed as an underlying structure of all languages. Recent studies have shown that if one learns a new foreign language with native grammar, Broca's area, the region of the brain needed to use grammar, is engaged. However, if the new foreign language is learned with an artificial grammar, Broca's area is not engaged to speak the new language; rather other areas of brain are used and the subjects have difficulty learning the new language. The findings of this study have been used as evidence to support the argument of universal grammar.

13 Visual System I

The visual system is the most studied system in the cerebral hemispheres and information learned here is often used as a model for understanding other systems such as auditory, olfaction, limbic, motor, and sensory. Visual information is relayed from the retina to the primary visual cortex of the occipital lobe. However, visual images achieve meaning when they are then analyzed in the adjacent parietal and temporal lobes. Because it is in these areas that remembered patterns, engrams, are stored from prior experience. For example the left temporal lobe is the site of recognizing letter symbols as words in reading; the right temporal and parietal lobes "contain the maps" and injury to this area can lead to topographic agnosia, such as the inability to find one's way in one's own house; injury to the undersurface of the temporal lobe can lead to inability to recognize faces, prosopagnosia. While we were able to localize these functional regions of the brain because patients with injuries to certain areas would manifest specific deficits (see Bisiach and Luzzatti above), we can now use functional imaging to study normal brain physiology in healthy individuals.

Injury to the right side of the brain can result in neglect of the left side of the body or the entire left side of internal and external space. The case of the man who mistook his wife for a hat, which illustrates this phenomenon, will be discussed.

14 Visual Neglect and Prosopagnosia

The left temporal lobe is the site of recognizing letter symbols as words in reading; the right temporal and parietal lobes "contain the maps" and injury to this area can lead to topographic agnosia, such as the inability to find one's way in one's own house; injury to the undersurface of the temporal lobe can lead to inability to recognize faces, prosopagnosia. While we were able to localize these functional regions of the brain because patients with injuries to certain areas would manifest specific deficits (see Bisiach and Luzzatti above), we can now use functional imaging to study normal brain physiology in healthy individuals.

Injury to the right side of the brain can result in neglect of the left side of the body or the entire left side of internal and external space. The case of the man who mistook his wife for a hat, which illustrates this phenomenon, will be discussed.

15 Rembrandt, Leonardo, Monet: How we See Them

The most sophisticated image processor imaginable, the brain uses several techniques to see. Among those that have been best studied, the visual system can sharpen borders and localize objects in space. We are beginning to understand some of these mechanisms. For example, an on-off (on-center and off-surround) organization of neurons from the retina to the primary visual cortex causes light objects bordered by dark objects to appear brighter than when they are not bordered by dark objects. An illustration would be a Rembrandt etching where a window is surrounded by darkness appears whiter or brighter than the paper it is printed on. In this case, the center-surround organization of the retinal cells and the visual cortex cause the light-stimulated neurons to actually have more activity (action potentials) when the surrounding cells are inactive than when the surrounding cells are stimulated.

In the example of the "where pathway" in the parietal lobe, contrast in luminance (value in art parlance) is used to identify the location of things (Livingstone). When the contrast in luminosity of adjacent colors is low, the parietal lobe has difficulty in identifying where something is in relation to its surroundings. When the contrast in luminosity is high the parietal lobe can readily localize objects in relation to one another. Renaissance artists used high contrast in luminosity to create the appearance of mass and volume. In fact, Leonardo wrote about the importance in using paint with high contrast in order to create the appearance of volume. Michaelangelo used extreme contrasts in luminance to create massive figures. Alternatively, Impressionists such as Monet attempt to paint light and movement and avoid mass. They use subtle variation in luminance in order to achieve this effect. Modern artists use this knowledge to create visual illusions and "tricks." By studying different paintings we shall explore how differences in luminance are interpreted by the brain and thus how the brain works. (See Livingstone for discussion)

16 Sensory System and Pain

Sensations from different regions of the body travel to different regions of the brain. This brain map is called a homunculus since the cartoon of the cerebral cortex illustrating different body regions looks like a person; foot at the crown, hand in the middle and face at the bottom of the parietal lobe. The homunculus can be modified based upon experience in both the child and the adult. Practicing piano changes the homunculus hand region in the brain. Cortical mapping studies of the homunculus in humans with syndactyly (fused fingers at birth) and experimental cortical mapping studies in monkeys will be discussed. Phantom limb syndromes (sensations experienced in amputated limbs) demonstrate the effect of amputation on the cortical map. These studies demonstrate that the homunculus is "plastic" or modifiable and have profound implications for teaching us how the brain learns. These studies also reveal the opportunities to improve function in the healthy and the brain injured.

The sensation of pain includes both the sensory component as well as the emotional or suffering component. The sensory component is found in the thalamus and the parietal cortex, the somatosensory cortex. The emotional or suffering element of the experience has been reported to be in the anterior cingulate cortex, a region of brain within the limbic system. The limbic system is phylogenetically an old part of our brain and is concerned with emotions and feelings. Individuals who feel pain but do not experience the suffering or affective component of pain have been shown to have diminished activity in the anterior cingulate gyrus.

17 Placebo, Empathy, and Theory of Mind

Placebos are inert substances which have physiological consequences. It has been reported that the placebo response to pain remedies accounts for about 30% of the responses. Recent functional imaging studies have demonstrated that the placebo response is mediated by the frontal lobe which anticipates a pain stimulus; this activates the endogenous opiate pathway in the midbrain, the periaqueductal grey, which is known to send fibers to the spinal cord blocking (gate) the entrance of pain impulses into the spinal cord. This new imaging data explains why opiate antagonists block the placebo response. Thus the placebo response and the expectancy of pain response rests on a physiological mechanism. (Wager)

Empathy is the feeling we experience when we share in the feelings of others. fMRI studies show the regions of brain which are activated during the experience of empathy. In the study by Singer, women were put in an fMRI scanner and were studied when they or their significant others were administered a painful stimulus. When they realized that their friend was being stimulated they showed activation of the affective region, the limbic system but not the sensory region of their own brains.

18 Test 2
19 Emotions and Feelings: Romantic and Maternal Love

Emotion-triggering sites of the brain are the limbic system - the amygdala, prefrontal cortex and the cingulate. Activation of these sites leads to activation of the hypothalamus which, in turn, causes visceral and musculoskeletal changes such as palpitations, goose bumps, sweaty palms, etc. Joy and sadness are associated with activation of different regions of the limbic system on fMRI. Painful stimuli also lead to activation of the limbic system. Placebos, pharmacologically inert substances, can alleviate pain in many individuals, which has been claimed to mean that the pain was imaginary. However, the placebo response is blocked by opiate antagonists revealing that the pain is not imagined. As discussed in the pain class, activation of the periaqueductal grey matter by placebos can block (gate) the entry of pain impulses in the spinal cord.

Bartels et al. report that they have found the regions of brain activated during the experience of recently realized romantic love. As discussed in a later class, this is different from the region of brain activated in maternal love.

20 Neuroscience and Marketing: Hitting the "Sweet Spot"

Why are emotionally charged experiences remembered so well? Why does one sometimes get an unconscious feeling that someone is staring? The answer may be that the amygdala which sits near the hippocampus is activated when we are confronted with frightening experiences such as threatening facial expressions. In addition, if threatening expressions are visually presented to us for a few milliseconds which is too short to consciously see the image, the amygdala is activated as well. There is a visual pathway to the amygdala from the thalamus which does not pass through the visual cortex and thus the image does not reach consciousness. Advertisers and other marketers can use this to influence people's emotions when presenting other information i.e., associating a product with the feeling of fear or joy at an unconscious level. Alternatively, the prefrontal cortex is reported to be the site stimulated when one feels the need to have an object. Advertisers are taking notice and a field of "neuroadvertising" is developing; see Thompson, NYT magazine.

Emotionally-charged experiences are remembered more readily than others; consider 9/11. These memories are stored through both the hippocampus and limbic system. Drugs such as adrenergic blockers and benzodiazepines can block this effect. Some have tried to "unmake" emotionally charged memories through the use of drugs that block neurotransmitters in the limbic system. See Unmaking memories.

Why we sleep is unknown. But according to a report in Nature this year, it may pay to "sleep on it." Wagner et al. report that subjects who were presented a problem and then slept did better in solving the problem than if they did not sleep afterwards.

21 Learning and Memory: The Case of HM Memory has been classified as explicit and implicit. Explicit memory is that for facts, dates, locations and the like. Examples of implicit memory are procedures and priming. Explicit memory requires the hippocampus for encoding new information. A tragic incident involving a man known as HM occurred when both his hippocampi were removed over 50 years ago in an effort to treat his epilepsy. It was not known that he would lose the ability to encode new memories. He thus can recall events in detail from before the surgery such as World War II but cannot recall people he has met repeatedly for the past 50 years. We shall discuss his findings including his MRI.
22 Structure and Function of Brains with Superior Memory

Explicit memories are stored in multiple locations distributed throughout the cerebral cortex. For example, spatial memories localize to the right cerebrum. Furthermore, experienced taxi drivers are reported to have larger right hippocampi than controls (Maguire). Recall of words activates the left hippocampus (Maguire). Individuals with superior memories often use a technique known for over 2500 years as the "Method of Loci" whereupon facts are related to locations. When these superior memorizers demonstrate their skill and undergo fMRI studies, the right cerebral hemisphere which is associated with spatial localization is activated, thereby corroborating the technique they report that they use.

The hippocampus is needed to acquire new explicit memories, as shown with HM. Alzheimer's Disease affects the hippocampus early in the disease process and not unexpectedly, memory loss for recent events is a dominant symptom. Although treatment with drugs which increase the neurotransmitter acetylcholine provide modest symptom relief, there is no cure or way of stemming the disease progression. There are, however, new imaging techniques which claim to diagnose the disease through reduced metabolism in certain brain regions, parietal lobes, or showing progressive atrophy of the hippocampi. Currently Medicare will not pay for these procedures. These tests have a high incidence of false positive results as well as false negative results. We will discuss specificity, false positive rate, and sensitivity, false negative rate; an inherent problem in all diagnostic tests in medicine. The question "Should Medicare pay for imaging to diagnose Alzheimer's disease?" is a possible final paper topic.

23 How Emotion and Antidepressants Affect Memory As common experience reveals, our recall for emotionally salient events is far superior to that of emotionally neutral experiences. The article by van Stegeren reveals that as in the case of blindsight the limbic system (amygdala in particular) is actively engaged in encoding emotionally charged experiences with both positive and negative valence. In addition, norepinephrine appears to be a major neurotransmitter necessary for this to occur. Administration of beta antagonists have been reported to mitigate the enhanced recall of emotionally charged experiences and are being investigated as a treatment to prevent post traumatic stress disorder. van stegeren and colleagues show through fMRI studies that activation of the amygdala occurs when emotionally charged material is presented to subjects. Moreover, the amygdala is attenuated with the administration of beta antagonists and the enhanced recall is diminished. Several corollary questions arise from these observations. Could memory be enhanced by stimulation of the norepinephrine system? It is known that tricyclic antidepressants which inhibit the reuptake of norepinephrine improve memory in depressed patients. Is this accomplished through this pathway or another pathway? Could other beta agonists be used in normal individuals as memory enhancing drugs? This article and the references cited emphasize the intimate interaction of the "rational" and "emotional" brain discussed in the neuroeconomics paper in the first classes.
24 Depression, Anxiety and Psychosis

Neuropsychiatric disorders such as anxiety and depression affect millions of Americans. Tens of billions of dollars are spent on the treatment of these disorders annually. Historically, psychoanalysis and behavioral therapies dominated the treatment milieu. In the past three decades, based upon our increased understanding of neurotransmitters, pharmacologic treatment has emerged as the dominant intervention in the medical community. However, pharmacologic and cognitive behavioral treatments are debated as to their relative efficacy. New imaging studies in the treatment of depression reveal that pharmacologic and cognitive behavioral therapies may work in different ways and have different durations of benefit. The study in Arch Psych 2004 above indicates that cognitive behavioral therapy has a more durable response. The debate is not showing any signs of resolution.

A case report by Bejjani of a patient undergoing brain surgery with deep brain stimulation resulted in a depressive manifestations and feelings reported by the awake patient. It is an interesting article because it demonstrates that electrical activity in the brain is the cause of depressive manifestations and not the effect.

Psychosis such as schizophrenia has been postulated in some cases to be due to an excess of monoamine neurotransmitters in selected pathways in the brain. This is based upon the observation that monoamines, such as dopamine, and drugs which cause an increase in monamines, such as LSD, cause psychosis. Alternatively, antidopaminergic drugs can effectively treat psychosis. Another example is in patients given the precursor to dopamine, L-DOPA, who can develop psychosis as seen in the movie, Awakenings, by Dr. Oliver Sacks.

25 Vision, Memory and Feelings: Binding them Together When viewing a facial expression in a painting or a person, we often share a complex array of feelings and emotions. This is sometimes called "emotional contagion." While empathy for pain activates the cingulate gyrus, fMRI studies now show us that the perception of facial expression of disgust activates the insula, the site of disgust activation when we personally experience it. In addition, the amygdala, a portion of the limbic system anterior to the hippocampus in the temporal lobe, is activated when viewing fearful and happy faces although the two patterns are different. Finally, the overwhelming love that a mother feels when she is viewing a photo of her newborn baby has been found to be associated with activation of the orbitofrontal cortex. Of interest, this is a different activation region from that seen in couples who are recently romantically involved; which provides a basis for the argument that there are different forms of love.
26 Music, Math and the Brain Musicians with perfect pitch show unique activation of the brain. We will see how fMRI has revealed how the organization of the brain is modified by training and rehearsal. For example, we will see that the area of brain which allows our fingers to move and feel is reorganized in musicians who rehearse intensively (Schlaug). Indeed even mental rehearsing has been shown to cause the brain circuits to reorganize while at the same time improving performance (Pascual-Leone). Math prodigies show unique activation of the brain when performing calculations (Presenti).

Additional Topic: Consciousness / Neuroeconomics

Consciousness, The Permanent Vegetative State, and Public Policy

The "What if" and the "Governor Bush" articles (cited above) raise issues about consciousness and when patients should be allowed to die. Unlike brain death, the permanent vegetative state can last for years. The vegetative state has been a clinical diagnosis based upon the neurological examination (See Practice Parameter). However, functional imaging has suggested that there are "islands" of the cerebral cortex that are functioning at more than 50% of normal. However, 'binding' of multiple areas of brain (not just isolated islands) appears to be necessary for there to be consciousness. Nonetheless, these findings are generating a debate as to whether these patients should be permitted to die and whether there is more hope that they are conscious than had been thought. In addition, there is now a new diagnosis which has been proposed, "the minimally conscious state." These complex medical issues have enormous personal, ethical, societal and legal implications as we grapple with patient management decisions.

Neuroeconomics

The brain provides the means by which we have thoughts, memories, reason, feelings, emotions, motor and sensory skills and social interaction. Many fields are emerging which undertake the study of the brain in order to better understand their own discipline. Examples of these fields have been termed neuro-esthetics, neuro-linguistics, neuro-ethics and neuro-economics. Neuro-economics is a fascinating field because it endeavors to understand both the rational and emotional components of social interactions (economics) which take place among people through study of the brain. I have chosen to select a paper on neuro-economics in order to introduce the concept that the human brain has both rational and emotional components which affect one another. Through functional imaging of normal subjects and patients with specific brain lesions we can learn how the brain works as illustrated by economic or social consequences. The brain contains about 100 billion neurons (nerve cells). These neurons are connected to one another at microscopic sites called synapses to form circuits. Neurons work in groups so that many neurons and synapses will function together in a circuit when the brain is undertaking a certain task. In order for neurons to function a large amount of energy requiring oxygen and glucose is necessary to maintain electrical gradients across their membranes.

The brain is organized in such a way that different regions serve different functions. For example, there is a visual area that is used to see and a motor area which is used when executing a movement. There is even an area that plans the movement before it is actually executed. In the visual system there are associated areas which relate the visual information to previously learned information. When new information matches previous information it is recognized and recalled; sometimes with an emotional component, as when we see a loved one, which arises from a different part of the brain, the limbic system. Since this process requires abundant energy, there is an increase in blood flow, to carry oxygen and glucose, to the regions of brain that are doing the additional work. Since MRI can measure blood flow, we can map blood flow and thereby map the function of different regions of the brain when the subject is performing specific tasks. The technique called functional MRI (fMRI) has emerged in the past decade and has provided an enormous amount of new information about the functioning of the normal brain. Prior to this neurologists and other neuroscientists were dependent upon damage to the brain to determine its functional organization. Other techniques such as PET can be used to measure blood flow but require the administration of a radioactive isotope. However, one advantage of PET is that we can also measure transmitter function at synapses through the use of radio-isotopes. Another technique, magnetoencephalography (MEG) measures brain electrical activity directly and has also been used. Throughout the course we will read articles which use these new technologies to study how the brain is activated in several behaviors, both simple as well as complex. For example as subsequent class syllabi indicate we will look at learning and memory; language, both native and foreign; dyslexia; grammar; romantic love and maternal love; fear; empathy; the organization of musicians' brains, among others.


Additional Topic: Can Thinking Prevent Dementia? There is considerable hope, and some limited evidence, that dementia can be avoided or delayed by engaging in cognitively stimulating activities (eg. crossword puzzles). This hope relies upon the 'mutability' or plasticity of the adult brain. If such a benefit occurs it may be based upon neurogenesis or plasticity of synapses. The clinical evidence is limited and based upon observational studies (See Verghese and Wilson) for the most part. The one prospective randomized trial (Ball) showed that engaging in cognitively stimulating activities improves testing results but does not change the performance of activities of daily living. The editorial by Coyle reviews the evidence. The major limitation of these studies is the question of whether it is the cognitive activities themselves which prevent dementia or whether individuals who at baseline perform more cognitive leisure activities do so because they have more cognitive reserves and, therefore, have a reduced risk of dementia. An oft-quoted retrospective study of nuns looked at the complexity of language structure which young nun novitiates had used to determine if it predicted later dementia; the authors found that those nuns which had used complex language structure had a lower late-life risk of dementia. The implication being that the ability to use complex language structure at a young age reflected increased cognitive reserves which somehow is associated with a reduced risk of late life dementia. Other studies have reported that there is a lower frequency of dementia in those with a higher level of education. Again, the mechanism of this is unknown but it is another incentive to study. For the athletes in the class, there may be an alternative; exercise has also been found in some animal studies to enhance neurogenesis. Recall that neurogenesis, which occurs in the hippocampus, may be associated with enhanced memory function. We will focus on the abstracts and the baseline characteristics of the clinical studies, including their limitations, and discuss the Coyle editorial. This clinical topic along with the animal studies from the neurogenesis literature is another suggestion for a final paper.

Rabu, 07 Januari 2009

Musculoskeletal Pathophysiology

HST.021 Musculoskeletal Pathophysiology

January (IAP) 2006

Dramatization of Gout as a devil attacking a foot

The Gout. James Gillray, 1799. From the Philadelphia Museum of Art.

Staff

Instructors:
Dr. Dwight R. Robinson

Guest Lecturers:
Dr. Paul Joseph Anderson
Dr. Robert Horatio Brown, Jr.
Dr. Marie Demay
Dr. Stephen Martin Krane
Dr. Young-Jo Kim
Dr. Henry Jay Mankin
Dr. Bjorn Reino Olsen
Dr. John Thomas Potts
Dr. Alan Lewis Schiller
Dr. Brian Dale Snyder

Course Meeting Times

Lectures:
Three sessions / week for 4 weeks
2 hours / session

Level

Graduate

Course Highlights

This course features a selection of downloadable lecture notes. This course is offered during the Independent Activities Period (IAP), which is a special 4-week term at MIT that runs from the first week of January until the end of the month.

Course Description

This course covers the growth, development and structure of normal bone and joints, the biomechanics of bone connective tissues, and their response to stress, calcium and phosphate homeostasis. Additional topics include regulation by parathyroid hormone and vitamin D, the pathogenesis of metabolic bone diseases and diseases of connective tissues, joints and muscle with consideration of possible mechanisms and underlying metabolic derangements.


Syllabus

Overview

This lecture based course covers the growth, development and structure of normal bone and joints, the biomechanics of bone connective tissues, and their response to stress, calcium and phosphate homeostasis. Additional topics include regulation by parathyroid hormone and vitamin D, the pathogenesis of metabolic bone diseases and diseases of connective tissues, joints and muscle with consideration of possible mechanisms and underlying metabolic derangements.

Assignments

There is one problem set and a final exam for this course.

Grading

Activities Percentages
Problem Set 10%
Final Exam 90%


Lecture Notes

Below is a selection of lecture notes courtesy of Prof. Dwight Robinson.
SES # TOPICS LECTURE NOTES
1 Bone Growth and Development (1 hr.) - Dr. Schiller

Bone Growth; Fracture Healing (1 hr.) - Dr. Schiller

2 Infections of Bone/Metabolic Bone Disease (1 hr.) - Dr. Schiller

Histology of Bone; Microscopic Lab (1 hr.) - Dr. Schiller

3 Disorders of Growth Plate (1 hr.) - Dr. Olsen

Heritable Disorders of Connective Tissues (1 hr.) - Dr. Krane

4 Basic Skeletal Biomechanics (1 hr.) - Dr. Snyder

Biomechanics of Fracture Healing (1 hr.) - Dr. Snyder

5 Cartilage Biology and Biomechanics (1 hr.) - Dr. Kim

Biomechanics in Pathogenesis of Osteoarthritis (1 hr.) - Dr. Kim

6 Rheumatic Diseases (I) (1 hr.) - Dr. Robinson

Rheumatic Diseases (II), SLE, Scleroderma (1 hr.) - Dr. Robinson
(PDF - 1.2 MB)
7 Pathogenesis of Rheumatoid Arthritis (1 hr.) - Dr. Anderson

Rheumatic Diseases (III), Vasculitis, Gout (1 hr.) - Dr. Robinson

(PDF)

8 Biomechanics Review Session (1 hr.)
9 Muscular Dystrophies/ Inflammatory Myopathies (1 hr.) - Dr. Brown

Mitochondrial Myopathies (1 hr.) - Dr. Johns

Mineral Ion Homeostasis (2 hrs.) - Dr. Potts

10 Osteoporosis; Osteomalacia (1 hr.) - Dr. DeMay

Cartilage; Structure Osteoarthritis (1 hr.) - Dr. Mankin

Demonstration: Joint Dissection (30 min.) - Dr. Mankin


Final Examination (2.5 hrs.)

Exams

Final Exam (PDF)

Solution to Final Exam (PDF)

8(^_^)8

Sabtu, 27 Desember 2008

1. Projects in Microsclae Engineering for the Life Sciences

Projects in Microscale Engineering for the Life Sciences

Spring 2007

Staff

Instructors:
Prof. Alexander Aranyosi
Prof. Dennis Freeman
Prof. Martha Gray

Course Meeting Times

Lectures:
Two sessions / week
3 hours / session

Level

Undergraduate


People in cleanroom suits view magnified wafer pattern on screen.
Members of the class inspect one of the wafers they created in lab. (Image by A. Aranyosi.)

Course Description

This course is a project-based introduction to manipulating and characterizing cells and biological molecules using microfabricated tools. It is designed for first year undergraduate students. In the first half of the term, students perform laboratory exercises designed to introduce
(1) the design, manufacture, and use of microfluidic channels,
(2) techniques for sorting and manipulating cells and biomolecules, and
(3) making quantitative measurements using optical detection and fluorescent labeling. In the second half of the term, students work in small groups to design and test a microfluidic device to solve a real-world problem of their choosing. Includes exercises in written and oral communication and team building.

Special Features

Technical Requirements

Special software is required to use some of the files in this course: .m.


Syllabus

Contents - Engineering Systems at the Scale of Cells and Biomolecules

  • How do you build tools that can manipulate cells?
    • Lithography: Shrinking patterns to the micro-scale
    • Soft lithography: Making bio-compatible fluid reservoirs
    • Rapid prototyping: Using existing microscale structures to test new ideas
  • How do you measure properties of individual cells?
    • Optical imaging
    • Electrical signals
    • Cell sorting
    • Averaging

Teaching/Learning Activities

  • Two lectures each week to introduce new material.
  • Two lab sessions each week to provide hands-on experience.
  • One project to help students learn to pose testable hypotheses, to conduct research, and to communicate results.
  • Weekly homework assignments to encourage students to actively assimilate the course material.

Homework

Weekly homework assignments provide an opportunity to develop intuition for new concepts by actively applying the new concepts to solve problems and answer questions. The process of actively struggling with the use of new ideas until you understand them is an effective and rewarding form of education.

Weekly homework assignments will be distributed in class on Thursdays and will be due the following Thursday at the start of lecture. Late homework will not be accepted. Homework assignments will be corrected, graded, and returned the week after they are due. The solution to each homework assignment will generally be made available to the class a few days after the homework due date. Paper copies of homework assignments and solutions will not be distributed.

Homework problems will be chosen for their educational value. Reading someone's solution to a problem is not educationally equivalent to generating your own solution. If you skip the process of personally struggling with the use of new concepts, you will have destroyed your most important educational experience.

Collaboration Policy

We encourage students to discuss the homework with other students and with the teaching staff to better understand the concepts. However, we expect that you wrote the solutions that you submit under your name. Students should not use solutions of other students (from this year or from previous years) in preparing their own solutions. Students should not take credit for computer code or electronic plots generated by other students. Students should not share their solutions with other students. Any student caught plagiarizing will receive a grade of zero on the assignment. All incidents of plagiarism will be reported to the Committee on Discipline (COD). More information about what constitutes plagiarism can be found at MIT Academic Integrity.

Projects

This subject includes one project. In this project, students are asked to improve on an existing microfluidic design or technique. Students will be expected to demonstrate the improvement with a working prototype. The project provides an opportunity to learn about, planning R&D and experiments, acquiring, processing, and interpreting data, communicating the results to others. The project requires a written proposal, which includes a well-defined hypothesis and procedures to test the hypothesis. Students are encouraged to work in pairs for the project. Partners are encouraged to submit a joint proposal and to cooperate in design, in collecting and processing data, in discussing interpretations, and in preparing their reports. Partners are also encouraged to submit a joint report. We strongly believe that students learn more by working with other students than by working in isolation. The final report will be presented in the form of a short talk to the class. It should be 12 minutes in length and should be delivered during the next to last week of the semester. The report has a firm due date, which is listed on the subject calendar. There are severe lateness penalties for missing the due date.

Communications Intensive

This subject is communications intensive. We feel that communications skills are essential for professional engineers and scientists. We also feel that the process of creating written manuscripts and oral presentations can help clarify thinking and can be an effective way to learn technical material. Homework assignments will often ask you to explain something or to define something that you have been taught. In addition the project is communications intensive. For the project, you and your partner must submit a written proposal and revise the proposal until it is approved by the staff. You and your partner must prepare a formal report that is structured as a scientific oral presentation. First drafts of the report are due approximately one week before the final draft, and will be reviewed by the technical staff, staff from the Writing Program, and by student peers. You and your partner will be assigned to prepare a written critique of a first draft from a different team. The critiques will be discussed during a special session held between the first draft and final draft deadlines. Students can satisfy their freshman year communications requirement by taking this subject.

Grade

Because of the project-oriented nature of this subject, grades will depend strongly on the final project. It should be noted that this project grade itself has several components which will be graded separately (e.g., proposal, first draft, written critique, etc.). In addition, your final presentation will be graded on several metrics (technical content, effective use of slides, clarity of presentation, etc.). More detail on grading is provided in the assignments section of this site. The weighting factors for determining letter grades are:


ACTIVITIES PERCENTAGES
Homework 50%
Lab project 50%

For students near grade boundaries, other factors may be taken into account, including participation in class, laboratory performance not evidenced in the laboratory grade, etc. The grades are determined by the staff.

Text

The course has no required text. Supplementary materials will be distributed over the course of the semester.

Calendar


LEC # TOPICS KEY DATES
Introductory exercises
1 Microfluidics
2 Microfabrication
3 Cells and membranes
4 Cells and membranes (cont.) Homework 1 due after five days
5 Models of diffusion and cell experiment
6 Laminar flow Homework 2 due
7 Data analysis using MATLAB®
8 Research applications Homework 3 due
9 Research paper discussion
10 Visit research lab Homework 4 due
11 Cell traps
12 Cell traps (cont.)
13 Project brainstorming
Projects
14-18 Projects

Homework 5 due Lec #15

Project propsal due Lec #16

19 Device fabrication
20-23 Projects
24

Project presentation

Dry runs


25 Projects
26 Project presentations

Kamis, 11 Desember 2008

Training Programs


In addition to the specialized training programs designed as tracks within the Medical Engineering Medical Physics Doctoral Program, described above, HST offers three training programs in specific areas.

Biomedical Informatics Program

Biomedical informatics is concerned with the cognitive, information-processing, and communication tasks of medical practice, education, and research. It includes the information sciences and technology needed to support those tasks. The field is intrinsically interdisciplinary, drawing together all traditional medical disciplines, the science and technology of computing, biostatistics, epidemiology, decision sciences, and health care policy and management. In addition to a focus on clinical practice, additional areas of emphasis are in bioinformatics, and in informatics related to health services research.

HST's predoctoral and postdoctoral training program in biomedical informatics offers fellowships to qualified US citizens or permanent residents. Several training options are offered: the Master of Science in Biomedical Informatics from HST; the PhD in Computer Science from MIT's Department of Electrical Engineering and Computer Science; the PhD in Health Decision Science in the Department of Health Policy and Management at the Harvard School of Public Health; and research fellowship training at biomedical informatics laboratories in Boston-area hospitals carried out in conjunction with the HST Biomedical Informatics Master's Program. The master's program is available only to HST-enrolled medical students or to individuals who already have advanced training in the health sciences (e.g., a doctoral degree in medicine, dentistry, nursing, veterinary medicine, clinical psychology, or a PhD in a medical relevant field such as physiology).

The combined training program offers several opportunities for education, research, and interaction among the various training sites. Course offerings at MIT and Harvard, as well as a variety of seminars, journal clubs, and other opportunities to exchange information, provide all trainees with opportunities to learn about the work at various laboratories and affiliated institutions, as well as the broader field of biomedical and health informatics.

Predoctoral fellowship applicants must concurrently apply for admission to MIT or a Harvard doctoral degree program. Postdoctoral applicants typically have at least one year and preferably three years of clinical residency before beginning their fellowship. For more information about the Biomedical Informatics Training Program, visit http://www.mi-boston.org/Boston-Informatics/index.html or contact Dr. Lucila Ohno-Machado, Decision Systems Group, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, machado@dsg.harvard.edu.

Clinical Investigator Training Program

The Clinical Investigator Training Program (CITP) trains postdoctoral physicians from various clinical disciplines in the techniques and processes used in patient-oriented research. Trainees develop expertise in clinical investigation while participating in an extensive educational program. The two-year program is a cooperative effort between HST, Beth Israel Deaconess Medical Center, and Pfizer, Inc. The curriculum allows trainees to develop direct experience in performing clinical investigation while, simultaneously through didactic course work, providing a strong foundation in computational and statistical sciences, biomedical ethics, the principles of clinical pharmacology, in vitro and in vivo measurement techniques, and various aspects of the drug development process.

The fellowship program consists of a primary project and core curriculum, plus an elective curriculum and a project elective. Although not required, fellows may choose to pursue a Master of Medical Sciences degree from Harvard Medical School in conjunction with CITP. The degree is awarded at the end of the two-year period upon successful completion of didactic coursework, a research project, a thesis or thesis equivalent, and a qualifying examination. CITP is open to physicians who have completed the clinical requirements for Board eligibility in their chosen specialty or subspecialty. For more information or to obtain an application, visit http://www.bidmc.harvard.edu/citp/ or contact the CITP administrative manager, Linda Bard, Beth Israel Deaconess Medical Center, 330 Brookline Ave, GZ 811, Boston, MA 02215, lbard@bidmc.harvard.edu.

Graduate Education in Medical Sciences Certificate Program

The MIT Graduate Education in Medical Sciences (GEMS) Training Program is a part-time certificate program that can be taken concurrently with doctoral studies and research by students in the Schools of Engineering and Science to gain exposure to biomedical and clinical sciences, including translational medicine. This educational experience for PhD graduate students in the sciences and engineering fields addresses a national need articulated by the Howard Hughes Medical Institute: the growing gap between advances in basic biology and the translation of those advances into medically relevant therapies and tools for the improvement of human health.

The GEMS training program aims to integrate medical knowledge into graduate education at MIT by training a select group of PhD students to bridge the widening chasm between concept and functional execution with a supplementary curriculum that entails: (1) a human pathology course, including molecular and cellular mechanisms of disease, (2) a medical pathophysiology course, a kaleidoscope of HST's pathophysiology curriculum, (3) a student-individualized clinical experience, working with experienced mentors who move seamlessly between clinical medicine and basic biological research, (4) a seminar showcasing examples of translation, and (5) HST's Graduate Seminar—attended by all HST PhD candidates—focusing on professional skills needed to succeed in interdisciplinary research (ethics, responsible conduct of research, communication, etc.). GEMS participants will gain an understanding of the elements of translation, appreciate the science and art of medicine in a way that cannot be conveyed by textbooks, and develop relationships with students and faculty in the broad biomedical community.

Inquiries

Additional information on degree programs, admissions, and financial aid can be obtained from HST's Academic Office, Room E25-518, 617-492-4091.

Minggu, 07 Desember 2008

Speech and Hearing Bioscience and Technology

HST's doctoral program in Speech and Hearing Bioscience and Technology (SHBT), formerly Speech and Hearing Sciences, prepares students with an undergraduate background in science or engineering to have a broad acquaintance with the field of speech and hearing, and to develop specialized knowledge that focuses on a particular approach in research.

The only program of its type in the country—and the only doctoral training program funded in this area by the National Institutes of Health—SHBT is designed to develop research scientists who can apply the concepts and methods of the physical and biological sciences to basic and clinical problems in speech and hearing using innovative research.

No other research training program provides the multidisciplinary depth and breadth offered by SHBT. The five-to-seven–year program leads to a PhD in speech and hearing bioscience and technology from MIT. SHBT's more than 50 participating faculty members represent 10 academic departments from Harvard and MIT, with research facilities at MIT, Harvard University, Harvard Medical School and affiliated teaching hospitals, and the Massachusetts Eye and Ear Infirmary (MEEI).

The small class size of this unique program (seven to eight students per class year) ensures personalized and high-quality training by a diverse and dedicated faculty from the two institutions.

SHBT's curriculum provides an effective method of training researchers by introducing the physical and biological bases of speech and hearing mechanisms involved in the communications process. While SHBT seeks to develop research scientists rather than clinical practitioners, there is a strong emphasis on providing students with exposure to clinical problems, approaches, and techniques. Graduates are thoroughly prepared for successful careers in basic and applied research in industry, universities, or government laboratories involved with biological and synthetic communication systems.

Typically, a student's first two years in the program are devoted to coursework, which is supplemented by significant exposure to various research projects. Courses in the first year assume familiarity with calculus and differential equations, college-level physics, probability and statistics, and biology. The core curriculum covers the anatomical, acoustical, physiological, perceptual, and cognitive basics, as well as the clinical approaches to speech and hearing problems.

The early introduction of important concepts in acoustics, anatomy, and physiology provides a solid base from which to pursue individual research interests. Early in the curriculum, students are introduced to various research laboratories that use different approaches to solving speech and hearing problems. 

This involvement in research provides an immediate application of classroom subjects. Students work with research advisors to develop a thorough understanding of basic concepts and tools in their fields of concentration. Later, students participate in subjects that require them to apply basic concepts to clinical problems and scientific research.

Throughout the curriculum, special attention is devoted to developing personal integrity, scientific values, and scholarly practice. With faculty guidance, each student plans a concentration tailored to the student's particular interest.

By the end of their second year, students identify an area of professional interest and choose a research project that forms the basis for their doctoral thesis. SHBT research in the speech and hearing sciences focuses on the biological and physical mechanisms underlying human communication by spoken language. 

The processes addressed by these sciences include the physical acoustics of sound and the perceptual neurophysiological bases of hearing, as well as the linguistic, cognitive, and motor levels of processing by talkers and listeners.

Applicants to the program should have a bachelor's degree in physical science, biology, psychology, linguistics, communication sciences and disorders, engineering, computer science, or a related field. Superior analytical skills are strongly recommended for all applicants. Additional information may be obtained at http://web.mit.edu/shbt/ or by contacting Dr. M. Christian Brown, Massachusetts Eye and Ear Infirmary, 243 Charles Street, Boston, MA 02114, 617-573-9635, mcb@epl.meei.harvard.edu.

Sumber:

Harvard-MIT Division of Health Sciences and Technology

Senin, 01 Desember 2008

Harvard-MIT Division of Health Sciences and Technology

Doctoral Programs

Medical Engineering and Medical Physics

The Medical Engineering and Medical Physics (MEMP) Program is a five-to-seven–year program that leads to the PhD in Medical Engineering and Medical Physics awarded by MIT or by the Harvard Faculty of Arts and Sciences. The program trains students as engineers or physical scientists who also have extensive knowledge of the medical sciences. By understanding engineering and physical science applications, as well as their clinical implications, graduates of this program are well positioned to define new questions and formulate novel approaches in biomedical research.

The MEMP program is founded on a philosophy of openness and collaboration, characteristics that encourage innovative and independent thinking and creativity. This philosophy is fostered by the unique environment in which MEMP students study. While each MEMP student has depth in one classical discipline of engineering or physical science, the collective community has students in all disciplines. MEMP students also have peers with diverse career paths in medicine, science, engineering, business, and government. This community promotes an open exchange of ideas and exposes students to different perspectives on the health sciences.

Moreover, MEMP students have access to research opportunities in labs at Harvard, MIT, and the Harvard teaching hospitals. Students can do research with faculty at any of these institutions and have many opportunities through classes, events, and projects to interact with faculty from all of these institutions. 

The program's academic curriculum includes three phases that prepare students to be medical innovators who will advance human health. First, HST provides MEMP students with a thorough graduate education in a classical discipline of engineering or physical science. Each student selects a concentration area, such as mechanical engineering, chemistry and chemical engineering, materials science, electrical engineering, computer science, physics, aeronautics and astronautics, or nuclear engineering, and completes substantial coursework in this discipline.

Students then become conversant in the biological sciences through preclinical coursework followed by a series of clinical experiences. They acquire a hands-on understanding of clinical care, medical decision-making, and the role of technology in medical practice both in the classroom and in patient care. Because the interface of technology and clinical medicine represents a continuum that extends from the molecular to the whole-organism levels, MEMP offers two distinct but related curricular sequences in the biomedical sciences: the cellular and molecular medicine sequence and the systems physiology and medicine sequence.

Finally, MEMP students investigate important problems at the interfaces of science, technology, and clinical medicine through individualized research projects that prepare them to undertake independent research. MEMP students have the opportunity to perform thesis research in laboratories at MIT, Harvard, and the Harvard affiliated teaching hospitals.

Bioinformatics and integrative genomics (BIG), neuroimaging and bioastronautics are areas of specialization within MEMP for which HST offers specially designed training programs. MEMP candidates may choose to apply through MIT, Harvard, or both. Those applying to MEMP through MIT should submit a single application. Those applying to MEMP through Harvard must also apply to the School of Engineering and Applied Sciences or the Biophysics Program. Additional information about applying to MEMP is available at http://hst.mit.edu/public/admissions/.

Medical Sciences

HST's Medical Sciences Program leads to the MD degree from Harvard Medical School. It is oriented toward students with a strong interest and background in quantitative science, especially in the biological, physical, engineering, and chemical sciences. The subjects in human biology developed for this curriculum represent the joint efforts of life scientists, physicians, physical scientists, and engineers from the faculties of Harvard and MIT.

The programs of study are designed to meet the interests and needs of the individual student. The student is encouraged to pursue advanced study in areas of interest that may complement the subjects offered in the division. Such study may be undertaken as part of the MD degree requirements or may be pursued in a program that combines the MD with a master's or doctoral degree. HST students join the students of the regular Harvard Medical School curriculum in the clinical clerkships.

Because HST is committed to educating physicians who have a deep understanding of the scientific basis of medicine and who are well equipped for an interdisciplinary research career, HST encourages students in the MD curriculum to devote time to research and requires a thesis for completion of the degree. 

Many MD students desire even more research training than is possible during the standard four-year MD curriculum. For such students, one option is to pursue a formal PhD program in addition to an MD program. Another option expands the MD program to five or more years in order to include a major research training component. This option may lead to a master's degree in health sciences and technology in addition to the MD degree.

The general requirements for a master's degree at MIT are given under Graduate Education in Part 1. The subject requirements must be in addition to the minimum number of units required for the MD degree. Subjects may be chosen in scientific, technical, or clinical areas relevant to the student's research area. Thesis research may be conducted at MIT, Harvard, or at Harvard-affiliated teaching hospitals. The completed thesis must be approved by the thesis supervisor and submitted to HST's Graduate Committee. The master's thesis simultaneously fulfills the thesis requirement for HST's MD degree. The two degrees are not formally linked; the MD degree is not a prerequisite for the master's degree.

Further details on the Medical Sciences Program and application forms may be obtained from the Office of Admissions, Harvard Medical School, 25 Shattuck Street, Boston, Massachusetts 02115. Applications must be submitted by October 15 of the year before desired matriculation. For further information, candidates can contact HST's Medical Sciences Admissions Coordinator at hst-md-admissions@mit.edu.

Radiological Sciences Joint Program

The Radiological Sciences Joint Program (RSJP) offers a unique integration of engineering and physical sciences education with research opportunities in a broad spectrum of biomedical research laboratories. The RSJP doctoral program is administered in collaboration with MIT's Nuclear Science and Engineering Department and Boston-area teaching hospitals. Students complete a doctoral program in nuclear science and engineering in addition to a focused clinical experience that includes basic biomedical courses and a clinical practicum. 

Training is provided in ionizing and non-ionizing radiation systems engineering and applications to biological and biomedical issues. This is accomplished through an academic core of nuclear physics and radiation engineering supplemented by biomedical subjects and a focused clinical experience. Student research topics typically involve radiation therapy or imaging, such as magnetic resonance imaging (MRI), computer-aided tomography (CT), positron emission tomography (PET), or single-photon emission tomography (SPECT). Recent innovations in the areas of particle radiation therapy and medical imaging have made this area one of the most exciting in the field of applied nuclear and radiation science.

The core curriculum includes topics in nuclear and radiation physics, radiation biology, medical imaging, and the biomedical application of radiation. These subjects form the basis of the departmental doctoral examination taken by most students two years after entering the program. After successful completion of the exam, full-time thesis research is pursued in specialty areas of radiation therapy, medical imaging, radiation biology, and biophysics, or image processing and computer applications. 

To supplement the program's academic training, a one-month clinical practicum in one of the affiliated Boston-area hospitals is also required. Students submit a doctoral thesis and defend it before a committee of MIT faculty, including members from HST and the Department of Nuclear Science and Engineering, in accordance with the interdisciplinary nature of the program.

Admission to the RSJP program is decided jointly by HST and MIT's Department of Nuclear Science and Engineering. In addition to a strong background in the physical and engineering sciences, applicants should have completed two undergraduate subjects in biology or biochemistry before entering RSJP. Additional information may be obtained by contacting Clare Egan, Room 24-102, 617-253-3814, cegan@mit.edu.

Sumber:

Harvard-MIT Division of Health Sciences and Technology 

Jumat, 28 November 2008

Harvard-MIT Division of Health Sciences and Technology



Faculty and Staff

Faculty and Teaching Staff

Martha L. Gray, PhD
Edward Hood Taplin Professor of Medical and Electrical Engineering, MIT
Director
David E. Cohen, MD, PhD
Associate Professor of Medicine and Health Sciences and Technology, HMS, BWH
Director
Lee Gehrke, PhD
Hermann von Helmholtz Professor of Health Sciences and Technology, MIT, HMS
Professor of Microbiology and Molecular Genetics, HMS
Associate Director for Faculty
Richard N. Mitchell, MD, PhD
Associate Professor of Pathology and Health Sciences and Technology, HMS, BWH
Associate Master for MD Program

Professors

R. Rox Anderson, MD
Professor of Dermatology and Health Sciences and Technology, HMS, MGH
George B. Benedek, PhD
Alfred H. Caspary Professor of Physics and Biological Physics and Health Sciences and Technology, MIT
Sangeeta N. Bhatia, MD, PhD
Professor of Health Sciences and Technology and of Electrical Engineering and Computer Science, MIT
Howard Hughes Medical Investigator
Joseph V. Bonventre, MD, PhD
Robert H. Ebert Professor of Medicine and Health Sciences and Technology, HMS, BWH
Louis D. Braida, PhD
Henry Ellis Warren Professor of Electrical Engineering and Health Sciences and Technology, MIT
Emery N. Brown, MD, PhD
Professor of Health Sciences and Technology and of Computational Neuroscience, MIT
Thomas N. Byrne, MD
Clinical Professor of Neurology and Health Sciences and Technology, HMS, MGH
Richard J. Cohen, MD, PhD
Whitaker Professor in Biomedical Engineering, MIT
Ernest G. Cravalho, PhD
Professor of Mechanical Engineering and Health Sciences and Technology, MIT
Elazer R. Edelman, MD, PhD
Thomas D. and Virginia W. Cabot Professor of Health Sciences and Technology, MIT
Dennis M. Freeman, PhD
Professor of Electrical Engineering, MIT
John D. E. Gabrieli, PhD
Grover Hermann Professor of Health Sciences and Technology and Professor of Brain and Cognitive Sciences, MIT
David E. Housman, PhD
Ludwig Professor of Biology, MIT
Robert D. Howe, PhD
Gordon McKay Professor of Engineering, Harvard University
Isaac S. Kohane, MD, PhD
Lawrence J. Henderson Professor of Pediatrics and Health Sciences and Technology, HMS, CHB
Robert S. Langer Jr., ScD
Kenneth J. Germeshausen Professor of Chemical and Biomedical Engineering and Health Sciences and Technology, MIT
Institute Professor
M. Charles Liberman, PhD
Professor of Otology and Laryngology and Health Sciences and Technology, HMS, MEEI
Roger G. Mark, MD, PhD
Distinguished Professor in Health Sciences and Technology and Electrical Engineering and Computer Science, MIT
Bruce R. Rosen, MD, PhD
Professor of Radiology and Health Sciences and Technology, HMS, MGH
John J. Rosowski, PhD
Professor of Otology and Laryngology and Health Sciences and Technology, HMS, MEEI
Robert H. Rubin, MD
Gordon and Marjorie Osborne Professor of Health Sciences and Technology, HMS, HST
Professor of Medicine, HMS, BWH
Ram Sasisekharan, PhD
Professor of Biological Engineering and Health Sciences and Technology, MIT
Frederick J. Schoen, MD, PhD
Professor of Pathology and Health Sciences and Technology, HMS, BWH
Brian Seed, PhD
Professor of Genetics and Health Sciences and Technology, HMS, MGH
Daniel C. Shannon, MD
Professor of Pediatrics and Health Sciences and Technology, HMS, MGH
Anthony J. Sinskey, ScD
Professor of Biology and Health Sciences and Technology, MIT
Peter Szolovits, PhD
Professor of Computer Science and Engineering and Health Sciences and Technology, MIT
Mehmet Toner, PhD
Professor of Surgery and Health Sciences and Technology, HMS, MGH
Richard J. Wurtman, MD
Cecil H. Green Distinguished Professor of Neuropharmacology and Health Sciences and Technology, MIT
Martin L. Yarmush, MD, PhD
Helen Andrus Benedict Professor of Surgery (Biological Chemistry and Molecular Pharmacology), HMS, MGH
Laurence R. Young, ScD
Apollo Program Professor of Astronautics and Health Sciences and Technology, MIT

Associate Professors

Elfar Adalsteinsson, PhD
Associate Professor of Health Sciences and Technology and of Electrical Engineering and Computer Science, MIT
Brett Bouma, PhD
Associate Professor of Dermatology and Health Sciences and Technology, HMS, MGH
M. Christian Brown, PhD
Associate Professor of Otology and Laryngology, HMS, MEEI
Martha Bulyk, PhD
Associate Professor of Medicine and Health Sciences and Technology, HMS, BWH
Deborah Burstein, PhD
Associate Professor of Radiology and Health Sciences and Technology, HMS, BIDMC
W. H. Churchill Jr., MD
Associate Professor of Medicine and Health Sciences and Technology, HMS, BWH
Bertrand Delgutte, PhD
Associate Professor of Otology and Laryngology and Health Sciences and Technology, HMS, MEEI
Donald K. Eddington, PhD
Associate Professor of Otology and Laryngology and Health Sciences and Technology, HMS, MEEI
John J. Guinan, Jr., PhD
Associate Professor of Otology and Laryngology, HMS, MEEI
Hugh M. Herr, PhD
Associate Professor in Media Arts and Sciences, and Health Sciences and Technology, MIT
Robert E. Hillman, PhD
Associate Professor of Surgery and Health Sciences and Technology, HMS, MGH
Leonid A. Mirny, PhD
Samuel A. Goldblith Career Development Associate Professor of Health Sciences and Technology and Physics, MIT
Lucila Ohno-Machado, MD, PhD
Associate Professor of Radiology and Health Sciences and Technology, HMS, BWH
Lee H. Schwamm, MD
Associate Professor of Neurology, HMS, MGH
Christopher A. Shera, PhD
Associate Professor of Otology and Laryngology and Health Sciences and Technology, HMS, MEEI
A. G. Sorensen, MD
Associate Professor of Radiology and Health Sciences and Technology, HMS, MGH
Collin M. Stultz, MD, PhD
Associate Professor of Health Sciences and Technology and of Electrical Engineering and Computer Science, MIT

Assistant Professors

Kamran Badizadegan, MD
Assistant Professor of Pathology and Health Sciences and Technology, HMS, MGH
Utkan Demirci, PhD
Assistant Professor of Medicine and Health Sciences and Technology, HMS, BWH
Alireza Khademhosseini, PhD
Assistant Professor in Medicine and Health Sciences and Technology, HMS, BWH
Jennifer R. Melcher, PhD
Assistant Professor of Otology and Laryngology and Health Sciences and Technology, HMS, MEEI
Shiladitya Sengupta , PhD
Assistant Professor in Medicine and Health Sciences and Technology, HMS, BWH
Jagesh V. Shah, PhD
Assistant Professor of Systems Biology, Medicine, and Health Sciences and Technology, HMS, BWH
Shamil R. Sunyaev, PhD
Assistant Professor of Medicine and Health Sciences and Technology, HMS, BWH

Faculty Teaching Staff

Jeffrey M. Karp, PhD
Instructor in Medicine and Health Sciences and Technology, HMS, BWH

Senior Lecturers

Stephen K. Burns, PhD
Teodoro F. Dagi, MD
Howard L. Golub, MD, PhD
Stanley N. Lapidus

Lecturers

Laurence I. Alpert, MD
Jeffrey S. Behrens, MS, MBA
Carl M. Berke, PhD
Jeffrey Blander, ScD
Jonathan P. Gertler, MD
Linda C. Hemphill, MD
Jacob Joseph, MD
Susanne Klingenstein, PhD
J. Christian Kryder, MD
Steven M. Lulich, PhD
Robert P. Marini, DVM
Timothy A. Wagner, PhD

Research Staff

Senior Research Scientist

Stan N. Finkelstein, MD
James C. Weaver, PhD

Principal Research Scientists

Jane-Jane Chen, PhD
Gari D. Clifford, PhD
Lisa E. Freed, MD, PhD
Julie E. Greenberg, PhD
Chi-Sang Poon, PhD
Simona Socrate, PhD

Research Scientists

Mercedes Balcells-Camps, PhD
T. R. Gowrishankar, PhD
Kichang Lee, PhD
Glover W. Martin, PhD
Gang Song, PhD
Gregory H. Underhill, PhD

Research Engineers

Michelle L. Farley
Li-Wei H. Lehman, PhD
George B. Moody

Research Associate

Ann M. Lees, MD

Research Fellows

Gil Alterovitz, PhD
David A. Harmon, MD
Michael Jernigan, MD
Ronilda C. Lacson, MD
Elizabeth L. Scheufele, MD

Postdoctoral Associates

Amit Agrawal, PhD
Natalie Artzi, PhD
Edwin Pak-Nin Chan, PhD
Aaron M. Dollar, PhD
Paula L. Feinberg-Zadek, PhD
Shmuel Hess, PhD
Elliot E. Hui, PhD
Salman R. Khetani, PhD
Vijaya B. Kolachalama, PhD
Li Yuan Mi, PhD
Neetu Singh, PhD
Evgeny Ter-Ovanesyan, PhD
A. Rami Tzafriri, PhD
Piia K. Valonen, PhD
David K. Wood, PhD
Brett G. Zani, PhD

Postdoctoral Fellows

Jeremy Slade Abramson, MD
Rajendra D. Badgaiyan, MD
Aaron B. Baker, PhD
Stephan B. Danik, MD
George C. Engelmayr, PhD
Elizabeth A. Hoge, MD
Steven Jay Isakoff, MD, PhD
Sandra March-Riera, PhD
Jason W. Nichol, PhD
N. V. S. Rajasekhar Suragani, PhD

Technical Assistants

Stephen M. Katz, BA
Emma-Kate Loveday, BS
Michele P. Miele, BS
Wanting Zhao, BA

Visiting Engineer

Mauricio C. Villarroel Montoya

Visiting Scientists

Robert G. Dennis, PhD
Yingle Fan, PhD
Pedro E. Huertas, MD, PhD
Luismar Marques Porto, PhD
Andrew T. Reisner, MD
Igor B. Rozenvald, MD
Viswanathan Sasisekharan, PhD
Rajesh V. Swaminathan, MD
Gordana V. Vunjak-Novakovic, PhD
Sang Hoon Yi, PhD
Stephen E. Zale, PhD

Visiting Scholars

Iram Amjad, MSc
Dina Uzri, BS

Professors Emeriti

Walter H. Abelmann, MD
Professor of Medicine, Emeritus, HMS
Director, Alumni Affairs
Robert S. Lees, MD
Professor of Health Sciences and Technology, Emeritus, MIT
Irving M. London, MD
Professor of Medicine, Emeritus, HMS
Professor of Biology, Emeritus, MIT
Kenneth N. Stevens, ScD
Clarence J. Lebel Professor of Electrical Engineering and Health Sciences and Technology, Emeritus, MIT

Rabu, 26 November 2008

Harvard-MIT Division of Health Sciences and Technology

Harvard-MIT Division of Health Sciences and Technology



 http://hst.mit.edu/

Founded more than 35 years ago, the Harvard-MIT Division of Health Sciences and Technology (HST) is one of the oldest and largest biomedical engineering and physician-scientist training programs in the United States and the longest-standing collaboration between Harvard and MIT.

HST's unique interdisciplinary educational program brings engineering as well as the physical and biological sciences from the scientist's bench to the patient's bedside. Conversely, it brings clinical insight from the patient's bedside to the laboratory bench.

In this way, HST students are trained to have deep understanding of engineering, physical sciences, and the biological sciences, complemented with hands-on experience in the clinic or in industry; and they become conversant with the underlying quantitative and molecular aspects of medicine and biomedical science.

Within the division, more than 400 graduate students work with eminent faculty and affiliated faculty members from throughout the MIT and Harvard communities.

In addition to its outstanding record of accomplishment for research in human health care, HST educational programs are distinguished by three key elements:
  • A strong quantitative orientation
  • Required hands-on experience in a clinical or industry setting
  • A focused interdisciplinary research project
HST offers nine multidisciplinary options for graduate study:
  1. Medical Sciences MD Program
  2. Medical Engineering and Medical Physics Doctoral Program
  3. Speech and Hearing Bioscience and Technology Doctoral Program
  4. Radiological Sciences Joint Program
  5. Biomedical Enterprise Master's Program
  6. Biomedical Informatics Training Program
  7. Clinical Investigator Training Program
  8. Master of Engineering in Biomedical Engineering
  9. Graduate Education in Medical Sciences Certificate Program

Master's Programs

Biomedical Enterprise Program



Launched in 2002 as a collaboration with the MIT Sloan School of Management, HST's Biomedical Enterprise Program (BEP) is designed for individuals with business experience and a strong foundation in science and engineering. BEP prepares students for leadership roles in the transfer of new technologies from concept through product development to clinical adoption in the context of existing companies or newly established ventures.

Acknowledging that medical innovations in laboratory research and clinical care benefit society only when they become commercial products and services, BEP offers a unique curriculum that leverages the strengths of HST, MIT Sloan, Harvard Medical School (HMS), and the affiliated hospitals.

BEP students take preclinical and engineering courses alongside HST's MD and PhD students, and business courses with other MIT Sloan students. They participate in unique integrative courses designed to address the specific needs of starting, growing, and managing a biomedical enterprise.

These courses were developed and are taught by a team of HST and Sloan faculty, including several local entrepreneurs. Also included in the curriculum is a hands-on hospital-based clinical experience that pairs students with physician-scientists and provides insight into the hospital environment and patient care.

BEP offers two dual-degree options for individuals who need training in both management and science, and a one-year degree option for business executives who already have a graduate degree in management. The dual-degree option leads to an MBA or SM degree from MIT Sloan and an SM degree from HST. The single-degree option leads to the SM degree from HST. Further information is available at http://bep.mit.edu/ or by contacting bep@mit.edu.

Master of Engineering in Biomedical Engineering


The Master of Engineering (MEng) in Biomedical Engineering aims to educate students at the interface between engineering and biology or medicine, preparing them for leadership positions in the medical products, pharmaceutical, and biotechnology industries.

The five-year program leads to a bachelor's degree in a science or engineering discipline and a Master of Engineering in Biomedical Engineering. The program emphasizes engineering applications in systems physiology and clinical medicine; it is of particular value to students interested in applying biomedical engineering to the basic understanding of disease processes in the post-genomic era, and is designed for individuals desiring a medical and clinical focus in their careers.

Students take subjects that enable them to apply engineering expertise to problems in the medical and clinical sciences. Admission to HST's MEng program is open only to current MIT undergraduate students and requires candidates to demonstrate adequate quantitative and engineering credentials through coursework as part of their undergraduate degree program. Students interested in applying should submit a standard MIT graduate application by the end of their junior year.



In addition to satisfying the undergraduate requirements of their departmental program, candidates also are expected to complete subjects in differential equations (18.03); organic chemistry (5.12); biochemistry (7.05 or 5.07); and one engineering transport or systems subject (e.g., 2.005, 3.185, 6.002, 10.310).

More detailed program objectives and the requirements can be found on the HST website, http://hst.mit.edu/.

 

Master of Health Sciences and Technology


HST offers a general master's degree program that can be coupled to other degree programs, such as the MD degree described below. To accommodate a wide range of student interests, the curriculum for the Master of Health Sciences and Technology degree is determined by agreement between the student and his or her advisor.

There are no specific requirements other than the Institute requirement for 66 subject units and a thesis. In each case, the Institute requirement for the master's degree must be satisfied. Further information can be obtained from HST's Academic Office, Room E25-518, 617-258-7084.

Sumber:

Harvard-MIT Division of Health Sciences and Technology

Minggu, 26 Oktober 2008

Subjects Taught

Subjects Taught HST Website

Harvard-MIT Division of Health Sciences and Technology

HST Home

left arrow | HST.00-HST.599 | HST.600-HST.999 plus UROP and Thesis | right arrow


IMPORTANT NOTES regarding preclinical subjects (HST.011-HST.185 and HST.191):

-Students not enrolled in an HST degree program may take preclinical subjects if space is available. Non-HST students are limited to one HST preclinical course and must provide justification for enrolling in this course. They must obtain permission from the course director and the Associate Master of HST at HMS.

-These subjects are scheduled according to the Harvard Medical School academic calendar, which differs from the MIT calendar. Students whose graduation depends upon completing one or more of
these subjects should take particular care regarding the schedule.

Rabu, 01 Oktober 2008

Strategi Membangun Sekolah Super

1. Menjaring dan mencari pelajar-pelajar terbaik dari seluruh negeri

2. Mengoptimalkan peran Sekolah Bertaraf Internasional di Indonesia

3. Memperkuat proses pendidikan Dasar di Indonesia