Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSPCERQUEIRA, Fernanda M.CUNHA, Fernanda M.LAURINDO, Francisco R. M.KOWALTOWSKI, Alicia J.2013-07-302013-07-302012FREE RADICAL BIOLOGY AND MEDICINE, v.52, n.7, p.1236-1241, 20120891-5849https://observatorio.fm.usp.br/handle/OPI/1517Calorie restriction (CR) enhances animal life span and prevents age-related diseases, including neurological decline. Recent evidence suggests that a mechanism involved in CR-induced life-span extension is NO-stimulated mitochondrial biogenesis. We examine here the effects of CR on brain mitochondrial content. CR increased eNOS and nNOS and the content of mitochondria] proteins (cytochrome c oxidase, citrate synthase, and mitofusin) in the brain. Furthermore, we established an in vitro system to study the neurological effects of CR using serum extracted from animals on this diet. In cultured neurons, CR serum enhanced nNOS expression and increased levels of nitrite (a NO product). CR serum also enhanced the levels of cytochrome c oxidase and increased citrate synthase activity and respiratory rates in neurons. CR serum effects were inhibited by L-NAME and mimicked by the NO donor SNAP. Furthermore, both CR sera and SNAP were capable of improving neuronal survival. Overall, our results indicate that CR increases mitochondrial biogenesis in a NO-mediated manner, resulting in enhanced reserve respiratory capacity and improved survival in neurons.engrestrictedAccessCaloric restrictionnitric oxide synthasemitochondrial biogenesisagingendogenous nitric-oxideskeletal-muscleoxidative stresscortical-neuronss-nitrosylationcomplex-ibiogenesisglutamatebrainmicearticleCopyright ELSEVIER SCIENCE INC10.1016/j.freeradbiomed.2012.01.011Biochemistry & Molecular BiologyEndocrinology & Metabolism