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Mitochondrial dysfunction in bipolar disorder: Evidence, pathophysiology and translational implications

期刊

NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
卷 68, 期 -, 页码 694-713

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neubiorev.2016.06.040

关键词

Mitochondria; Bipolar disorder; Mania; Depression; Mitochondrial dysfunction; Oxidative stress; Inflammation; Apoptosis; Neurogenesis

资金

  1. Department of Psychiatry and Behavioral Sciences, The University of Texas Medical School at Houston
  2. CNPq
  3. FAPESC
  4. Instituto Cerebro e Mente
  5. UNESC
  6. NHMRC [1059660]
  7. NIH
  8. Cooperative Research Centre
  9. Simons Autism Foundation
  10. Cancer Council of Victoria
  11. Stanley Medical Research Foundation
  12. MBF
  13. Beyond Blue
  14. Rotary Health
  15. Geelong Medical Research Foundation
  16. Bristol-Myers Squibb
  17. Eli Lilly
  18. GlaxoSmithKline
  19. Meat and Livestock Board
  20. Organon
  21. Novartis
  22. Mayne Pharma
  23. Servier
  24. Woolworths

向作者/读者索取更多资源

Bipolar disorder (BD) is a chronic psychiatric illness characterized by severe and biphasic changes in mood. Several pathophysiological mechanisms have been hypothesized to underpin the neurobiology of BD, including the presence of mitochondrial dysfunction. A confluence of evidence points to an underlying dysfunction of mitochondria, including decreases in mitochondrial respiration, high-energy phosphates and pH; changes in mitochondrial morphology; increases in mitochondrial DNA polymorphisms; and downregulation of nuclear mRNA molecules and proteins involved in mitochondrial respiration. Mitochondria play a pivotal role in neuronal cell survival or death as regulators of both energy metabolism and cell survival and death pathways. Thus, in this review, we discuss the genetic and physiological components of mitochondria and the evidence for mitochondrial abnormalities in BD. The final part of this review discusses mitochondria as a potential target of therapeutic interventions in BD. (C) 2016 Elsevier Ltd. All rights reserved.

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