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Mech Ageing Dev ; 132(11-12): 588-91, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22015485

RESUMO

Mitochondrial DNA mutations and associated defects in cytochrome c oxidase (COX) are proposed to play an important role in human ageing; however there have been limited studies on the frequency of these defects in normal mouse ageing. Here we compare COX-deficiency in two epithelial tissues; the colon and the ciliary epithelium, from human and mouse. The pattern of accumulation of COX-deficiency is similar in both tissues in the two species; however the frequency of colonic crypts with COX-deficiency in aged humans is significantly higher than in aged mice, whereas the levels of COX-deficiency in the ciliary epithelium are higher in the mouse than in humans. This suggests the impact of mitochondrial defects on normal ageing may differ significantly between species.


Assuntos
Envelhecimento/genética , Envelhecimento/metabolismo , Deficiência de Citocromo-c Oxidase/genética , DNA Mitocondrial/genética , Animais , Colo/enzimologia , Humanos , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Mutação , Epitélio Pigmentado Ocular/enzimologia , Especificidade da Espécie
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