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New Research on Brain Energy in Mood and Psychotic Disorders

NAMI-MA October 30, 2010. New Research on Brain Energy in Mood and Psychotic Disorders. Bruce M. Cohen, M.D., Ph.D. Director, Shervert Frazier Research Institute, McLean Hospital President and Psychiatrist in Chief Emeritus, McLean Hospital

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New Research on Brain Energy in Mood and Psychotic Disorders

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  1. NAMI-MA October 30, 2010 New Research on Brain Energy in Mood and Psychotic Disorders Bruce M. Cohen, M.D., Ph.D. Director, Shervert Frazier Research Institute, McLean Hospital President and Psychiatrist in Chief Emeritus, McLean Hospital Robertson-Steele Professor of Psychiatry, Harvard Medical School

  2. Relevant Financial Relationships: None

  3. Relevant Personal Relationships: Many

  4. List of Investigators Working on Project Suzann Babb, M.S.Jin Kim, B.A. Tom Berry, B.A. Nick Lange, Sc.D. Brian Brennan, M.D. Eve Lewandowski. Ph.D. Anne Carpenter, Ph.D. David Logan, Ph.D. Anne Cataldo, Ph.D. Jeanne Lothrop, B.S. Bruce M. Cohen, M.D., Ph.D. Julie McCarthy, B.A. Diane Damez-Werno, B.A. Donna McPhie, Ph.D. Joe DePaola, B.A. Emily Mensale, B.A. Sarah Elmiligy, B.A. Beth Murphy, M.D., Ph.D. Laura Flynn, B.A. Dost Öngür, M.D., Ph.D. Brent Forester, M.D. Caitlin Ravichandran, Ph.D. Jennifer Gelda, B.A. Laura Sargent, B.A. Linda Hassinger, M.S. Jordan Smoller, M.D., Sc.D. Hannah Irving, B.A. Nancy Ye, Ph.D.

  5. A Caveat: Bipolar disorders and other psychiatric disorders are not homogeneous or unitary by cause or pathophysiology. They are likely the consequence of the interaction of numerous factors, both inherited and environmental, which differ from person to person.

  6. Problems in energy production may be one factor contributing to the risk of developing bipolar or other brain disorders

  7. Background: Energy production and brain disorders

  8. Blood Flow and Metabolism of the Human Brain in Health and Disease Seymour S. Kety, M.D. “The blood flow of the brain represents about one-sixth of the cardiac output and its oxygen consumption nearly one quarter of that of the entire body.” Trans Stud Coll Physicians Phila. 1950 Dec;18:103-8.

  9. The brain maintains energy production within a narrow margin. Energy use of the brain changes little, even in illness, except under extreme circumstances, such as coma. Seymour S. Kety, M.D.

  10. The brain uses ten times more energy per unit weight than the rest of the body Even subtle abnormalities of energy metabolism can affect brain function Energy abnormalities have been observed in many disorders of the brain

  11. Why Is the Brain So Energy Dependent?

  12. The Brain is a High-Precision Electro-Chemical Organ The brain must not only generate, but must quite accurately control, numerous electrical and chemical signals. Each of these tasks is highly energy expensive, and the energy must be made close to where it is used.

  13. Pellerin and Magistretti, Science 2004

  14. Nearly 99% of the energy production of the brain is used to support intrinsic (resting) activity. It is energy expensive just to support the basic background state and maintenance work of the brain. Raichle & Mintun, 2006

  15. Where Does the Brain Get Its Energy?

  16. Most of the energy produced to support the work of the brain comes from oxidative phosphorylation, the complete ‘burning’ (oxidation) of glucose (sugar) to carbon dioxide and water. Oxidative phosphorylation occurs in, and only in, subcellular organelles called mitochondria.

  17. Energy Production and Bipolar Disorders

  18. A variety of early studies, including: Genetic In vivo brain imaging Post mortem gene expression Peripheral cell gene expression CSF metabolite studies All suggest abnormalities of energy metabolism in patients with bipolar disorder

  19. We looked directly at mitochondria of patients with bipolar disorders. We studied both brain and peripheral cells from public tissue banks.

  20. Mitochondrial Distribution in Brain Cells (Post Mortem-Cytochrome C Staining) CONTROL BIPOLAR DISEASE Magnification 1,000X

  21. BD Control BD Brains Have More Smaller Mitochondria Than Control Brains (p<0.03) Number of Mitochondria Area in Square Microns

  22. Mitochondrial Shape Abnormalities in Post Mortem Brain Tissue CONTROL BIPOLAR DISORDER EM Magnification 15,000X

  23. Can We See Abnormalities in Peripheral Cells?

  24. Is There an Abnormality of Mitochondrial Distribution in Peripheral Cells, as Observed in Brain, in BD?

  25. Mitochondria Look Abnormal in Fibroblasts from Patients with Bipolar Disorder Mitochondria from fibroblasts in patients with bipolar disorder show an altered morphology consisting of short, thickened profiles that are arranged in a predominantly perinuclear location compared to age-matched controls.

  26. Mitochondrial Network in Control and BD Lymphocytes Light Microscopy Magnification 1,000X

  27. Quantification of Mitochondrial Distribution in Fibroblasts

  28. Quantification of Changes in Mitochondrial Distribution BD vs Control, p<0.0008 BD vs. Control, p<0.0008

  29. Are there more or fewer mitochondria in BD?

  30. No Difference in Total Mitochondrial Area Between Bipolar Disorder and Control Fibroblasts 140,000 120,000 100,000 80,000 Square Pixels 60,000 40,000 20,000 0 Control BD

  31. Is the Difference in Distribution of Mitochondria in BD a Drug Effect? (There was a wide assortment of drugs taken by the subjects. Lithium was used by only half, and its use was not correlated with the mitochondrial abnormalities observed.)

  32. 1mM Li2+ No Treatment Lithium Does Not Make Healthy Subject’s Cells Look Sick or BD Cells Look Healthy Control BD

  33. Are There Abnormalities of Mitochondrial Shape in Peripheral Cells, as Observed in Brain, in BD?

  34. Spherical and Cup Shaped Mitochondriain BD Fibroblasts BD Magnification 1,000X EM Magnification 10,000X

  35. Quantification of Ring Shaped Mitochondria in Control and BD Fibroblasts • Ultrastructural images from thirty fibroblasts were obtained at random (magnification 10,000X by electron microscopy) from each of 4 healthy controls and 4 BD cell lines (in total, 120 controls fibroblasts and 120 BD fibroblasts). • We found that the number of ring structures was increased in cells from the BD patients compared to controls (Controls<1, BD>1, per cell, p<0.01).

  36. Is There a Functional Abnormality of Mitochondria in Peripheral Cells in Bipolar Disorder?

  37. BIPOLAR DISEASE CONTROL Mitochondrial Membrane Potential Staining (JC1) in Control and BD Fibroblasts Red = Healthy Mitochondria Green = Compromised Mitochondria with lower membrane potential

  38. Are These Abnormalities Specific to BD?

  39. Schizophrenic Patient’s Fibroblasts May Exhibit Distinct Mitochondrial Abnormalities Bipolar Disorder Schizophrenia Control Magnification 630X

  40. HOWEVER: While consistent and from multiple sources, all of the evidence for abnormalities of energy production or mitochondrial shape and location in bipolar or related disorders is subtle, preliminary and needs confirmation

  41. Future Directions: Much More To Do By computerized analyses, we are determining many features of the shape and distribution of the mitochondrial network in our samples. With electron microscopy, we have begun to look at individual mitochondria in our samples. We are studying mitochondrial function at McLean and in collaboration with local colleagues.

  42. Future Directions: Genetics The risk of psychiatric illnesses is highly determined by genetic factors. Given our findings, might some of the genes associated with bipolar disorders and schizophrenias be genes for mitochondrial form and function?

  43. Future Directions: Proteins Many diseases are associated with abnormal levels or activities of the proteins which perform cell functions.We have begun to look directly at proteins known to be involved in determining mitochondrial location, shape and activity.

  44. MITOCHONDRIAL MORPHOLOGICAL ABNORMALITIES DYSREGULATION OF MOTOR PROTEINS, WHICH MOVE MITOCHONDRIA IN THE CELL, e.g .MIRO, MISATO, MYOSIN V DYSREGULATION OF CYTOSKELETAL PROTEINS, TO WHICH MITOCHONDRIA ATTACH, e.g. ACTIN, TUBULIN DYSREGULATION OF FUSION AND FISSION PROTEINS, WHICH CONTROL MITOCHONDRIAL SHAPE, e.g. DRP1, ORA1

  45. There are no Large Scale Changes in the Actin Cytoskeleton in BD Green = Mitochondria Red = Actin Blue = Nuclei

  46. No Overall Changes are Seen in the Tubulin Cytoskeleton in BD Control BD Red/Orange = mitochondria Green = Tubulin

  47. Clinical trials: We are testing agents believed to increase mitochondrial function Brian Brennan et al - Acetyl-L-carnitine and alpha lipoic acid for bipolar depression Brent Forrester et al - Coenzyme Q10 for geriatric bipolar depression

  48. Can mitochondria be repaired or replaced?

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