Effect of angiotensin converting enzyme inhibitor enalapril on body weight and composition in young rats

Autor(es)

Santos‚ E.L. ; de Picoli Souza‚ K. ; Guimarães‚ P.B. ; Reis‚ F.C.G. ; Silva‚ S.M.A. ; Costa-Neto‚ C.M. ; Luz‚ J. ; Pesquero‚ J.B.

• Tipo de documento: Artigo Científico
• Fonte: International Immunopharmacology; v. 8, n. 2, p. 247-253, 2008.

Resumo

Obesity is considered a worldwide public health problem showing an increased prevalence in developing countries, with urgent need for new and more efficient drugs and therapies. Enalapril, an angiotensin-I converting enzyme inhibitor (ACEi), is classically used in antihypertensive therapies, however, earlier publications have shown that this drug could also have significant impact on body weight in rats as well as in humans, besides reducing blood pressure. The effect of this drug in the white adipose tissue has been neglected for long time, even considering that most components of the renin-angiotensin and kallikrein-kinin system are expressed in this tissue. Furthermore, the adipose tissue is considered today as one of the most important sites for endocrine/inflammatory regulation of appetite and energy output and AngII has been linked to the metabolism in this tissue. Therefore, we analyzed the influence of chronic enalapril treatment in normotensive rats at earlier ages, evaluating body weight, energy homeostasis, lipid profile and serum levels of the hormones leptin and insulin, in the presence of a standard or a palatable hyperlipidic diet regimen for one month. Our results show that enalapril treatment is able to reduce body fat on both diets, without alteration in serum lipid profile. Furthermore, animals receiving enalapril showed reduction in food intake, leptin level and energy intake. In summary, these findings show for the first time that the ACEi enalapril reduces body fat in young normotensive rats and highlights a novel target to treat obesity and associated diseases. (c) 2007 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 02/00807-7 - Biologia molecular dos sistemas renina-angiotensina e calicreínas cininas
• Beneficiário: João Bosco Pesquero
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 04/07715-6 - Analise estrutural e funcional do receptor b1 de cininas e sua dimerizacao com o receptor at1 da angiotensina.
• Beneficiário: Edson Lucas dos Santos
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado