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转基因大鼠循环血管紧张素-(1-7)增加可改善脂代谢和糖代谢。

Improved lipid and glucose metabolism in transgenic rats with increased circulating angiotensin-(1-7).

机构信息

Laboratory of Hypertension, INCT-NanoBiofar, Minas Gerais, Brazil.

出版信息

Arterioscler Thromb Vasc Biol. 2010 May;30(5):953-61. doi: 10.1161/ATVBAHA.109.200493. Epub 2010 Mar 4.

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.

摘要

目的

肥胖和糖尿病仍然是世界上最普遍的健康问题之一。尽管血管紧张素 II 对代谢调节的重要性已有充分的文献记载,但血管紧张素-(1-7)/Mas 轴在这一过程中的作用仍知之甚少。本研究旨在评估通过表达血管紧张素-(1-7)-释放融合蛋白 TGR(A1-7)3292(TGR)的转基因大鼠来增加血管紧张素-(1-7) 血浆水平对脂质和葡萄糖代谢的影响。

方法和结果

TGR 中增加的血管紧张素-(1-7)水平可增强葡萄糖耐量、胰岛素敏感性和胰岛素刺激的葡萄糖摄取。此外,TGR 降低了甘油三酯和胆固醇水平,尽管食物摄入量正常,但腹部脂肪量也显著减少。这些变化伴随着脂肪组织中血管紧张素原表达和 Akt 的明显减少。此外,脂肪组织中血管紧张素原的表达和增加的血浆水平观察到脂联素。因此,血管紧张素-(1-7)刺激可增加原代脂肪细胞培养物中的脂联素产生,而 Mas 拮抗剂 A779 可阻断其产生。TGR 中循环胰岛素和肌肉糖原含量没有改变。

结论

这些结果表明,循环中血管紧张素-(1-7)水平的增加会导致葡萄糖和脂质代谢的显著变化。

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