Kinin B1 Receptor in Adipocytes Regulates Glucose Tolerance and Predisposition to Obesity


Autoria(s): Mori, Marcelo Alves da Silva; Sales, Vicencia Micheline; Motta, Fabiana Louise; Fonseca, Raphael Gomes; Alenina, Natalia; Guadagnini, Dioze; Schadock, Ines; Silva, Elton Dias; Torres, Hugo Arruda de Moura; dos Santos, Edson Lucas; Castro, Charlles Heldan; D'Almeida, Vania; Sertie, Sandra Andreotti; Campana, Amanda Baron; Sertié, Rogério Antonio Laurato; Saad, Mario Jose Abdalla; Lima, Fabio Bessa; Bader, Michael; Pesquero, João Bosco
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

25/10/2013

25/10/2013

2012

Resumo

Background: Kinins participate in the pathophysiology of obesity and type 2 diabetes by mechanisms which are not fully understood. Kinin B-1 receptor knockout mice (B-1(-/-)) are leaner and exhibit improved insulin sensitivity. Methodology/Principal Findings: Here we show that kinin B-1 receptors in adipocytes play a role in controlling whole body insulin action and glucose homeostasis. Adipocytes isolated from mouse white adipose tissue (WAT) constitutively express kinin B-1 receptors. In these cells, treatment with the B-1 receptor agonist des-Arg(9)-bradykinin improved insulin signaling, GLUT4 translocation, and glucose uptake. Adipocytes from B-1(-/-) mice showed reduced GLUT4 expression and impaired glucose uptake at both basal and insulin-stimulated states. To investigate the consequences of these phenomena to whole body metabolism, we generated mice where the expression of the kinin B-1 receptor was limited to cells of the adipose tissue (aP2-B-1/B-1(-/-)). Similarly to B-1(-/-) mice, aP2-B-1/B-1(-/-) mice were leaner than wild type controls. However, exclusive expression of the kinin B1 receptor in adipose tissue completely rescued the improved systemic insulin sensitivity phenotype of B-1(-/-) mice. Adipose tissue gene expression analysis also revealed that genes involved in insulin signaling were significantly affected by the presence of the kinin B-1 receptor in adipose tissue. In agreement, GLUT4 expression and glucose uptake were increased in fat tissue of aP2-B-1/B-1(-/-) when compared to B-1(-/-) mice. When subjected to high fat diet, aP2-B-1/B-1(-/-) mice gained more weight than B-1(-/-) littermates, becoming as obese as the wild types. Conclusions/Significance: Thus, kinin B-1 receptor participates in the modulation of insulin action in adipocytes, contributing to systemic insulin sensitivity and predisposition to obesity.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (Fapesp)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (Capes)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Deutsche Forschungsgemeinschaft

Deutsche Forschungsgemeinschaft [BA1374/16-1]

German Ministry of Education and Science

German Ministry of Education and Science [BRA09/014]

Identificador

PLOS ONE, SAN FRANCISCO, v. 7, n. 9, supl. 4, Part 1-2, pp. 39-47, SEP 14, 2012

1932-6203

http://www.producao.usp.br/handle/BDPI/36057

10.1371/journal.pone.0044782

http://dx.doi.org/10.1371/journal.pone.0044782

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS ONE

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #SYSTEMIC INSULIN-RESISTANCE #ADIPOSE-TISSUE #GLUT4 TRANSLOCATION #B-2 RECEPTOR #BRADYKININ #MUSCLE #ADIPONECTIN #METABOLISM #INHIBITION #EXPRESSION #MULTIDISCIPLINARY SCIENCES
Tipo

article

original article

publishedVersion