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Título: Improved Lipid and glucose metabolism in transgenic rats with increased circulating angiotensin-(1-7)
Autor(es): Santos, S. H. S.
Braga, J. F.
Mario, E. G.
Pôrto, L. C. J.
Rodrigues- Machado, M. G.
Murari, A.
Botion, L. M.
Alenina, N.
Bader, M.
Santos, R. A. S.
Assunto: Angiotensin-(1-7) Mas axis
Glucose metabolism
Adipose tissue
Cholesterol
Triglycerides
Adiponectin
Publicador: American Heart Association
Data de publicação: 3-Fev-2010
Referência: SANTOS, S. H. S. et al. Improved Lipid and glucose metabolism in transgenic rats with increased circulating angiotensin-(1-7). Arteriosclerosis, Thrombosis and Vascular Biology, [S.l.], v. 30, n. 5, p. 953-961, May 2010.
Abstract: Objective—Obesity and diabetes remain among the world’s most pervasive health problems. Although the importance of angiotensin II for metabolic regulation is well documented, the role of the angiotensin-(1-7)/Mas axis in this process is poorly understood. The aim of this study was to evaluate the effect of increased angiotensin-(1-7) plasma levels in lipid and glucose metabolism using transgenic rats that express an angiotensin-(1-7)-releasing fusion protein, TGR(A1-7)3292 (TGR). Methods and Results—The increased angiotensin-(1-7) levels in TGR induced enhanced glucose tolerance, insulin sensitivity, and insulin-stimulated glucose uptake. In addition, TGR presented decreased triglycerides and cholesterol levels, as well as a significant decrease in abdominal fat mass, despite normal food intake. These alterations were accompanied by a marked decrease of angiotensinogen expression and increased Akt in adipose tissue. Furthermore, augmented plasma levels and expression in adipose tissue was observed for adiponectin. Accordingly, angiotensin-(1-7) stimulation increased adiponectin production by primary adipocyte culture, which was blocked by the Mas antagonist A779. Circulating insulin and muscle glycogen content were not altered in TGR. Conclusion—These results show that increased circulating angiotensin-(1-7) levels lead to prominent changes in glucose and lipid metabolism.
URI: http://atvb.ahajournals.org/content/30/5/953
http://repositorio.ufla.br/jspui/handle/1/9700
Idioma: en
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