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胰岛素与瘦素在调节血管张力方面的协同作用。

Cooperation between insulin and leptin in the modulation of vascular tone.

作者信息

Vecchione Carmine, Aretini Alessandra, Maffei Angelo, Marino Gennaro, Selvetella Giulio, Poulet Roberta, Trimarco Valentina, Frati Giacomo, Lembo Giuseppe

机构信息

Department of Angio-Cardio-Neurology, La Sapienza University, Rome, Italy.

出版信息

Hypertension. 2003 Aug;42(2):166-70. doi: 10.1161/01.HYP.0000082806.73530.68. Epub 2003 Jun 30.

Abstract

High levels of insulin and leptin have been reported in human hypertension, suggesting a role for these metabolic hormones in blood pressure homeostasis. These hormones interact on intermediate metabolism, but nothing is known about their interaction at the vascular level. Our data demonstrate that insulin (0.6 nmol/L) is able to enhance vasodilation induced by leptin (10(-11) to 10(-6) mol/L; percentage change in maximal vasodilation, 39+/-3% vs 26+/-2%; n=6, P<0.03) but not by acetylcholine. Moreover, we demonstrate by 4,5-diaminofluorescein (DAF)-2 that insulin potentiates leptin-induced nitric oxide (NO) release. Finally, Western blotting studies show that insulin enhances the leptin-induced phosphorylation of Akt in Ser473 and Thr308 and of endothelial NO synthase in Ser1177. In conclusion, our data demonstrate that insulin and leptin cooperate in the modulation of vascular tone through enhancement of endothelial NO release. This phenomenon could have a major impact on the regulation of the cardiovascular system, principally in those clinical conditions characterized by endothelial NO dysfunction and metabolic disorders, such as arterial hypertension.

摘要

据报道,人类高血压患者体内胰岛素和瘦素水平较高,这表明这些代谢激素在血压稳态中发挥作用。这些激素在中间代谢过程中相互作用,但它们在血管水平上的相互作用尚不清楚。我们的数据表明,胰岛素(0.6 nmol/L)能够增强瘦素(10(-11)至10(-6) mol/L)诱导的血管舒张(最大血管舒张百分比变化:39±3%对26±2%;n = 6,P<0.03),但不能增强乙酰胆碱诱导的血管舒张。此外,我们通过4,5-二氨基荧光素(DAF)-2证明胰岛素可增强瘦素诱导的一氧化氮(NO)释放。最后,蛋白质印迹研究表明,胰岛素可增强瘦素诱导的Akt在Ser473和Thr308位点以及内皮型一氧化氮合酶在Ser1177位点的磷酸化。总之,我们的数据表明,胰岛素和瘦素通过增强内皮NO释放来协同调节血管张力。这种现象可能对心血管系统的调节产生重大影响,主要见于那些以内皮NO功能障碍和代谢紊乱为特征的临床疾病,如动脉高血压。

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