Long-term intermittent feeding, but not caloric restriction, leads to redox imbalance, insulin receptor nitration, and glucose intolerance


Autoria(s): CERQUEIRA, Fernanda M.; CUNHA, Fernanda M. da; SILVA, Camille C. Caldeira da; CHAUSSE, Bruno; ROMANO, Renato L.; GARCIA, Camila C. M.; COLEPICOLO, Pio; MEDEIROS, Marisa H. G.; KOWALTOWSKI, Alicia J.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Calorie restriction is a dietary intervention known to improve redox state, glucose tolerance, and animal life span. Other interventions have been adopted as study models for caloric restriction, including nonsupplemented food restriction and intermittent, every-other-day feedings. We compared the short- and long-term effects of these interventions to ad libitum protocols and found that, although all restricted diets decrease body weight, intermittent feeding did not decrease intra-abdominal adiposity. Short-term calorie restriction and intermittent feeding presented similar results relative to glucose tolerance. Surprisingly, long-term intermittent feeding promoted glucose intolerance, without a loss in insulin receptor phosphorylation. Intermittent feeding substantially increased insulin receptor nitration in both intra-abdominal adipose tissue and muscle, a modification associated with receptor inactivation. All restricted diets enhanced nitric oxide synthase levels in the insulin-responsive adipose tissue and skeletal muscle. However, whereas calorie restriction improved tissue redox state, food restriction and intermittent feedings did not. In fact, long-term intermittent feeding resulted in largely enhanced tissue release of oxidants. Overall, our results show that restricted diets are significantly different in their effects on glucose tolerance and redox state when adopted long-term. Furthermore, we show that intermittent feeding can lead to oxidative insulin receptor inactivation and glucose intolerance. (C) 2011 Elsevier Inc. All rights reserved.

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Instituto Nacional de Ciencia e Tecnologia de Processos Redox em Biomedicina (INCT)

Instituto Nacional de Ciencia e Tecnologia de Processos Redox em Biomedicina (INCT)

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CAPES Coordenacao de Aperfeicoamento do Pessoal de Nivel Superior

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

John Simon Guggenheim Memorial Foundation

John Simon Guggenheim Memorial Foundation

Identificador

FREE RADICAL BIOLOGY AND MEDICINE, v.51, n.7, p.1454-1460, 2011

0891-5849

http://producao.usp.br/handle/BDPI/30933

10.1016/j.freeradbiomed.2011.07.006

http://dx.doi.org/10.1016/j.freeradbiomed.2011.07.006

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Free Radical Biology and Medicine

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #Calorie restriction #Free radicals #Insulin receptor #Glucose tolerance #Nitration #Nitric oxide synthase #DIETARY RESTRICTION #OXIDATIVE STRESS #NITRIC-OXIDE #LIFE-SPAN #MITOCHONDRIAL-FUNCTION #TYROSINE NITRATION #MICE #RESISTANCE #RATS #AGE #Biochemistry & Molecular Biology #Endocrinology & Metabolism
Tipo

article

original article

publishedVersion