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

Authors :
Edson Lucas dos Santos
Kely de Picoli Souza
João Bosco Pesquero
Paola Bianchi Guimarães
Jacqueline Luz
Claudio M. Costa-Neto
Felipe C.G. Reis
Sylvia Maria Affonso Silva
Source :
International Immunopharmacology. 8:247-253
Publication Year :
2008
Publisher :
Elsevier BV, 2008.

Abstract

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 anti-hypertensive 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.

Details

ISSN :
15675769
Volume :
8
Database :
OpenAIRE
Journal :
International Immunopharmacology
Accession number :
edsair.doi.dedup.....4153ac95068186d47db1944702a8d6da
Full Text :
https://doi.org/10.1016/j.intimp.2007.07.021