Regulators of mitochondrial complex I activity: A review of literature and evaluation in postmortem prefrontal cortex from patients with bipolar disorder

Duong A., Che Y., Ceylan D., Pinguelo A., Andreazza A. C., Young L. T., ...More

PSYCHIATRY RESEARCH, vol.236, pp.148-157, 2016 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 236
  • Publication Date: 2016
  • Doi Number: 10.1016/j.psychres.2015.12.015
  • Journal Name: PSYCHIATRY RESEARCH
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Social Sciences Citation Index (SSCI), Scopus
  • Page Numbers: pp.148-157
  • Keywords: Bipolar disorder, Mitochondrial complex I, Mitochondrial regulators, Gene expression, Microarray, DJ-1, ARACHIDONIC-ACID CASCADE, PARKINSONS-DISEASE, NITRIC-OXIDE, GLUTATHIONE DEPLETION, OXIDATIVE STRESS, ALPHA-SYNUCLEIN, CELL-DEATH, NEUROPSYCHIATRIC DISORDERS, DOPAMINERGIC-NEURONS, HYDROGEN-PEROXIDE
  • Dokuz Eylül University Affiliated: No

Abstract

Phenomenologically, bipolar disorder (BD) is characterized by biphasic increases and decreases in energy. As this is a state-related phenomenon, identifying regulators responsible for this phasic dysregulation has the potential to uncover key elements in the pathophysiology of BD. Given the evidence suggesting mitochondrial complex I dysfunction in BD, we aimed to identify the main regulators of complex I in BD by reviewing the literature and using the published microarray data to examine their gene expression profiles. We also validated protein expression levels of the main complex I regulators by immunohistochemistry. Upon reviewing the literature, we found PARK-7, STAT-3, SIRT-3 and IMP-2 play an important role in regulating complex I activity. Published microarray studies however revealed no significant direction of regulation of STAT-3, SIRT-3, and IMP-2, but a trend towards downregulation of PARK 7 was observed in BD. Immunocontent of DJ-1 (PARK-7-encoded protein) were not elevated in post mortem prefrontal cortex from patients with BD. We also found a trend towards upregulation of DJ-1 expression with age. Our results suggest that DJ-1 is not significantly altered in BD subjects, however further studies are needed to examine DJ-1 expression levels in a cohort of older patients with BD. (C) 2015 Elsevier Ireland Ltd. All rights reserved.