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Am J Pathol ; 177(2): 575-85, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20566748

RESUMO

Postmortem, genetic, brain imaging, and peripheral cell studies all support decreased mitochondrial activity as a factor in the manifestation of Bipolar Disorder (BD). Because abnormal mitochondrial morphology is often linked to altered energy metabolism, we investigated whether changes in mitochondrial structure were present in brain and peripheral cells of patients with BD. Mitochondria from patients with BD exhibited size and distributional abnormalities compared with psychiatrically-healthy age-matched controls. Specifically, in brain, individual mitochondria profiles had significantly smaller areas, on average, in BD samples (P = 0.03). In peripheral cells, mitochondria in BD samples were concentrated proportionately more within the perinuclear region than in distal processes (P = 0.0008). These mitochondrial changes did not appear to be correlated with exposure to lithium. Also, these abnormalities in brain and peripheral cells were independent of substantial changes in the actin or tubulin cytoskeleton with which mitochondria interact. The observed changes in mitochondrial size and distribution may be linked to energy deficits and, therefore, may have consequences for cell plasticity, resilience, and survival in patients with BD, especially in brain, which has a high-energy requirement. The findings may have implications for diagnosis, if they are specific to BD, and for treatment, if they provide clues as to the underlying pathophysiology of BD.


Assuntos
Transtorno Bipolar/patologia , Mitocôndrias/patologia , Córtex Pré-Frontal , Trifosfato de Adenosina/metabolismo , Adulto , Idoso , Idoso de 80 Anos ou mais , Antidepressivos/farmacologia , Linhagem Celular , Citocromos c/metabolismo , Citoesqueleto/ultraestrutura , Metabolismo Energético , Feminino , Fibroblastos/efeitos dos fármacos , Fibroblastos/ultraestrutura , Humanos , Carbonato de Lítio/farmacologia , Masculino , Pessoa de Meia-Idade , Mitocôndrias/ultraestrutura , Córtex Pré-Frontal/citologia , Córtex Pré-Frontal/metabolismo , Adulto Jovem
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