Improvement of metabolic parameters and vascular function by metformin in obese non-diabetic rats


Autoria(s): Lobato, N. S.; Filgueira, Fernando Paranaiba; Hagihara, Graziela Neves; Akamine, Eliana Hiromi; Pariz, J. R.; Passaglia, Rita de Cassia Aleixo Tostes; Carvalho, Maria Helena Catelli de; Fortes, Zuleica Bruno
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

31/10/2013

31/10/2013

02/08/2013

Resumo

Aims: Metformin is an insulin sensitizing agent with beneficial effects in diabetic patients on glycemic levels and in the cardiovascular system. We examined whether the metabolic changes and the vascular dysfunction in monosodium glutamate-induced obese non-diabetic (MSG) rats might be improved by metformin. Main methods: 16 week-old MSG rats were treated with metformin for 15 days and compared with age-matched untreated MSG and non-obese non-diabetic rats (control). Blood pressure, insulin sensitivity, vascular reactivity and prostanoid release in the perfused mesenteric arteriolar bed as well as nitric oxide production and reactive oxygen species generation in isolated mesenteric arteries were analyzed. Key findings: 18-week-old MSG rats displayed higher Lee index, fat accumulation, dyslipidemia, insulin resistance and hyperinsulinemia. Metformin treatment improved these alterations. The norepinephrine-induced response, increased in the mesenteric arteriolar bed from MSG rats, was corrected by metformin. Indomethacin corrected the enhanced contractile response in MSG rats but did not affect metformin effects. The sensitivity to acetylcholine, reduced in MSG rats, was also corrected by metformin. Indomethacin corrected the reduced sensitivity to acetylcholine in MSG rats but did not affect metformin effects. The sensitivity to sodium nitroprusside was increased in preparations from metformin-treated rats. Metformin treatment restored both the reduced PGI2/TXA2 ratio and the increased reactive oxygen species generation in preparations from MSG rats. Significance: Metformin improved the vascular function in MSG rats through reduction in reactive oxygen species generation, modulation of membrane hyperpolarization. correction of the unbalanced prostanoids release and increase in the sensitivity of the smooth muscle to nitric oxide. (c) 2011 Elsevier Inc. All rights reserved.

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

Fundacao de Amparo a Pesquisa doEstado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

INCT Obesity and Diabetes/CNPq, Brazil

INCT Obesity and Diabetes/CNPq, Brazil

Identificador

LIFE SCIENCES, OXFORD, v. 90, n. 41430, supl. 1, Part 3, pp. 228-235, 10959, 2012

0024-3205

http://www.producao.usp.br/handle/BDPI/37032

10.1016/j.lfs.2011.11.005

http://dx.doi.org/10.1016/j.lfs.2011.11.005

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

OXFORD

Relação

LIFE SCIENCES

Direitos

closedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #OBESITY #METFORMIN #MONOSODIUM GLUTAMATE #VASCULAR DYSFUNCTION #NITRIC-OXIDE SYNTHASE #ENDOTHELIAL-CELLS #CARDIOVASCULAR-DISEASE #INTRACELLULAR PRODUCTION #LIPOPROTEIN CHOLESTEROL #OVERWEIGHT PATIENTS #INSULIN #PROSTANOIDS #WEIGHT #COMPLICATIONS #MEDICINE, RESEARCH & EXPERIMENTAL #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion