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vol.40 suppl.1Psycho-education, the Lithium of Psycho-therapies. Some Considerations Regarding its efficiency and Implementation in Daily PracticeFunctional Magnetic Resonance Imaging in euthymic Adult Patients with Bipolar Disorder Type I: Neuropsychological and Neurofunctional Aspects author indexsubject indexarticles search
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Revista Colombiana de Psiquiatría

Print version ISSN 0034-7450

Abstract

MINUZZI, Luciano; BEHR, MSC, Guilherme Antônio; FONSECA MOREIRA, José Cláudio  and  FREY, Benicio N.. Mitochondrial Dysfunction in Bipolar Disorder: Lessons from Brain Imaging and Molecular Markers. rev.colomb.psiquiatr. [online]. 2011, vol.40, suppl.1, pp.166-182. ISSN 0034-7450.

Bipolar disorder (BD) is a chronic major mental illness characterized by extreme mood episodes, cognitive impairment, and high rates of disability. Several lines of evidence suggest that BD may be associated with abnormalities in mitochondrial function. Here we critically review findings from brain imaging and from preclinical studies that investigated markers of energy metabolism in BD. Research with postmortem brain and peripheral tissue revealed changes in size and distribution of mitochondria, as well as decreased mitochondrial electron transport chain function, increased oxidative stress, and increased lipid and protein damage. PET imaging studies revealed decreased glucose metabolism in sub-areas of the prefrontal cortex, amygdala, and hippocampus structures in BD. On the other hand, increased lactate levels in BD have been found in cerebrospinal fluid and in gray matter by magnetic resonance spectroscopy, which suggest that distinct pathophysiological processes may be region-specific. Resting state fMRI studies have demonstrated decreased functional connectivity between fronto-limbic circuits. In conclusion, these results support the hypothesis of mitochondrial dysfunction in BD and suggest that BD is associated with decreased energy production and a shift towards anaerobic glycolysis. Such changes in energy metabolism can potentially decrease cell plasticity and ultimately disrupt brain circuits associated with mood and cognitive control.

Keywords : Mitochondrial dysfunction; bipolar disorder; PET; biomarkers.

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