Cooperation between insulin and leptin in the modulation of vascular tone
- PMID: 12835332
- DOI: 10.1161/01.HYP.0000082806.73530.68
Cooperation between insulin and leptin in the modulation of vascular tone
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.
Comment in
-
Insulin, leptin, and membrane microviscosity in blood pressure regulation.Hypertension. 2004 Apr;43(4):e15-6; author reply e15-6. doi: 10.1161/01.HYP.0000118363.35532.73. Epub 2004 Feb 9. Hypertension. 2004. PMID: 14769807 No abstract available.
Similar articles
-
Leptin effect on endothelial nitric oxide is mediated through Akt-endothelial nitric oxide synthase phosphorylation pathway.Diabetes. 2002 Jan;51(1):168-73. doi: 10.2337/diabetes.51.1.168. Diabetes. 2002. PMID: 11756337
-
AKT participates in endothelial dysfunction in hypertension.Circulation. 2004 Jun 1;109(21):2587-93. doi: 10.1161/01.CIR.0000129768.35536.FA. Epub 2004 May 10. Circulation. 2004. PMID: 15136501
-
G972R IRS-1 variant impairs insulin regulation of endothelial nitric oxide synthase in cultured human endothelial cells.Circulation. 2004 Jan 27;109(3):399-405. doi: 10.1161/01.CIR.0000109498.77895.6F. Epub 2004 Jan 5. Circulation. 2004. PMID: 14707024
-
Estrogen induced changes in Akt-dependent activation of endothelial nitric oxide synthase and vasodilation.Steroids. 2004 Sep;69(10):637-45. doi: 10.1016/j.steroids.2004.05.016. Steroids. 2004. PMID: 15465108
-
HDL induces NO-dependent vasorelaxation via the lysophospholipid receptor S1P3.J Clin Invest. 2004 Feb;113(4):569-81. doi: 10.1172/JCI18004. J Clin Invest. 2004. PMID: 14966566 Free PMC article.
Cited by
-
Endothelial dysfunction in (pre)diabetes: characteristics, causative mechanisms and pathogenic role in type 2 diabetes.Rev Endocr Metab Disord. 2013 Mar;14(1):39-48. doi: 10.1007/s11154-013-9239-7. Rev Endocr Metab Disord. 2013. PMID: 23417760 Review.
-
Perivascular adipose tissue and its role in type 2 diabetes and cardiovascular disease.Curr Diab Rep. 2011 Jun;11(3):211-7. doi: 10.1007/s11892-011-0186-y. Curr Diab Rep. 2011. PMID: 21461998 Free PMC article. Review.
-
High-Fat Diet-Induced Obesity Model Does Not Promote Endothelial Dysfunction via Increasing Leptin/Akt/eNOS Signaling.Front Physiol. 2019 Mar 20;10:268. doi: 10.3389/fphys.2019.00268. eCollection 2019. Front Physiol. 2019. PMID: 30949067 Free PMC article.
-
Leptin augments cerebral hemodynamic reserve after three-vessel occlusion: distinct effects on cerebrovascular tone and proliferation in a nonlethal model of hypoperfused rat brain.J Cereb Blood Flow Metab. 2011 Apr;31(4):1085-92. doi: 10.1038/jcbfm.2010.192. Epub 2010 Oct 27. J Cereb Blood Flow Metab. 2011. PMID: 20978518 Free PMC article.
-
Adipocytokines in atherothrombosis: focus on platelets and vascular smooth muscle cells.Mediators Inflamm. 2010;2010:174341. doi: 10.1155/2010/174341. Epub 2010 Jun 28. Mediators Inflamm. 2010. PMID: 20652043 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases
Miscellaneous