Dipeptidyl peptidase IV in the hypothalamus and hippocampus of monosodium glutamate obese and food-deprived rats


Autoria(s): ALPONTI, Rafaela Fadoni; FREZZATTI, Rodrigo; BARONE, Juliana Marton; ALEGRE, Valter de Sousa; SILVEIRA, Paulo Flavio
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Proline-specific dipeptidyl peptidases are emerging as a protease family with important roles in the regulation of signaling by peptide hormones related to energy balance. The treatment of neonatal rats with monosodium glutamate (MSG) is known to produce a selective damage on the arcuate nucleus with development of obesity. This study investigates the relationship among dipeptidyl peptidase IV (DPPIV) hydrolyzing activity, CD26 protein, fasting, and MSG model of obesity in 2 areas of the central nervous system. Dipeptidyl peptidase IV and CD26 were, respectively, evaluated by fluorometry, and enzyme-linked immunosorbent assay and reverse transcriptase polymerase chain reaction in soluble (SF) and membrane-bound (MF) fractions from the hypothalamus and hippocampus of MSG-treated and normal rats, submitted or not to food deprivation (FD). Dipeptidyl peptidase IV in both areas was distinguished kinetically as insensitive (DI) and sensitive (DS) to diprotin A. Compared with the controls, MSG and/or FD decreased the activity of DPPIV-DI in the SF and MF from the hypothalamus, as well as the activity of DPPIV-DS in the SF from the hypothalamus and in the MF from the hippocampus. Monosodium glutamate and/or FD increased the activity of DPPIV-DI in the MF from the hippocampus. The monoclonal protein expression of membrane CD26 by enzyme-linked immunosorbent assay decreased in the hypothalamus and increased in the hippocampus of MSG and/or FD relative to the controls. The existence of DPPIV-like activity with different sensitivities to diprotin A and the identity of insensitive with CD26 were demonstrated for the first time in the central nervous system. Data also demonstrated the involvement of DPPIV-DI/CD26 hydrolyzing activity in the energy balance probably through the regulation of neuropeptide Y and beta-endorphin levels in the hypothalamus and hippocampus. (C) 2011 Elsevier Inc. All rights reserved.

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

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Brazil)[05/04699-2]

CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazil)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

METABOLISM-CLINICAL AND EXPERIMENTAL, v.60, n.2, p.234-242, 2011

0026-0495

http://producao.usp.br/handle/BDPI/27742

10.1016/j.metabol.2009.12.031

http://dx.doi.org/10.1016/j.metabol.2009.12.031

Idioma(s)

eng

Publicador

W B SAUNDERS CO-ELSEVIER INC

Relação

Metabolism-clinical and Experimental

Direitos

restrictedAccess

Copyright W B SAUNDERS CO-ELSEVIER INC

Palavras-Chave #INDUCED DIABETIC-RATS #AMINOPEPTIDASE ACTIVITIES #ADENOSINE-DEAMINASE #GENE-EXPRESSION #TRANSGENIC MICE #TREATED-RATS #BODY-WEIGHT #FEMALE RATS #BRAIN #RECEPTOR #Endocrinology & Metabolism
Tipo

article

original article

publishedVersion