Alterations of NADPH Oxidase Activity in Rat Pancreatic Islets Induced by a High-Fat Diet


Autoria(s): VALLE, Maira Mello Rezende; GRACIANO, Maria Fernanda Rodrigues; OLIVEIRA, Eduardo Rebelato Lopes de; CAMPOREZ, Joao Paulo Gabriel; AKAMINE, Eliana Hiromi; CARVALHO, Carla Roberta de Oliveira; Curi, Rui; CARPINELLI, Angelo Rafael
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Objective: The aim of this study was to evaluate the effect of a high-fat diet (HFD) on nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity in rat pancreatic islets. We investigated if changes in NADPH oxidase are connected to beta cell dysfunction reported in obese animals. Methods: Male Wistar rats were fed a HFD or control diet for 3 months. DNA fragmentation, insulin secretion, and [U-(14)C] glucose oxidation were examined in isolated pancreatic islets. The oxidative stress markers nitrotyrosine and 4-hydroxy-2-nonenal were assessed by immunohistochemistry. The protein content of gp91(phox) and p47(phox) was evaluated by Western blotting. Production of reactive oxygen species (ROS) was determined by a fluorescence assay using hydroethidine. Results: Occurrence of DNA fragmentation was reduced in pancreatic islets from HFD rats. There were no differences in oxidative stress markers between the groups. Glucose oxidation and insulin secretion were elevated due to high glucose in pancreatic islets from HFD rats. Protein concentrations of p47(phox) and gp91(phox) subunits were reduced and ROS production was diminished in pancreatic islets from HFD rats. Conclusions: The diminished content of NADPH oxidase subunits and ROS concentrations may be associated with increased glucose oxidation and insulin secretion in an attempt to compensate for the peripheral insulin resistance elicited by the HFD.

FAPESP

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

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

CAPES

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Identificador

PANCREAS, v.40, n.3, p.390-395, 2011

0885-3177

http://producao.usp.br/handle/BDPI/27960

10.1097/MPA.0b013e31820569d0

http://dx.doi.org/10.1097/MPA.0b013e31820569d0

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

Relação

Pancreas

Direitos

restrictedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #lard #pancreas #NOX2 #glucose metabolism #reactive oxygen species #insulin secretion #STIMULATED INSULIN-SECRETION #OXIDATIVE STRESS #METABOLIC SYNDROME #NAD(P)H OXIDASE #GENE-EXPRESSION #BETA-CELLS #NOX FAMILY #GLUCOSE #LANGERHANS #RESISTANCE #Gastroenterology & Hepatology
Tipo

article

original article

publishedVersion