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首页> 外文期刊>Hormone and Metabolic Research >Asymmetric dimethylarginine (ADMA) and other endogenous nitric oxide synthase (NOS) inhibitors as an important cause of vascular insulin resistance.
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Asymmetric dimethylarginine (ADMA) and other endogenous nitric oxide synthase (NOS) inhibitors as an important cause of vascular insulin resistance.

机译:不对称二甲基碱(ADMA)和其他内源一氧化氮合酶(NOS)抑制剂作为血管胰岛素抗性的重要原因。

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摘要

Asymmetric dimethylarginine (ADMA) and NG-monomethyl- L-arginine ( L-NMMA) are important endogenous endothelial nitric oxide synthase (eNOS) inhibitors. Studies have shown that patients with insulin resistance have elevated plasma levels of ADMA. Moreover, ADMA levels have a prognostic value on long-term outcome of patients with coronary artery disease. Insulin resistance, a disorder associated to inadequate biological responsiveness to the actions of exogenous or endogenous insulin, is a metabolic condition, which exists in patients with cardiovascular diseases. This disorder affects the functional balance of vascular endothelium via changes of nitric oxide (NO) metabolism. Nitric oxide is produced in endothelial cells from the substrate L-arginine via eNOS. Elevated ADMA levels cause eNOS uncoupling, a mechanism which leads to decreased NO bioavailability and increased production of hydrogen peroxide. According to clinical studies, the administration of L-arginine to patients with high ADMA levels improves NO synthesis by antagonizing the deleterious effect of ADMA on eNOS function, although in specific populations such as diabetes mellitus, this might even been harmful. More studies are required in order to certify the role of NOS inhibitors in insulin resistance and endothelial dysfunction. It is still difficult to say whether increased ADMA levels in certain populations is only a reason or the result of the molecular alterations, which take place in vascular disease states.
机译:不对称二甲基尿苷(ADMA)和Ng-单甲基-1-精氨酸(L-NMMA)是重要的内源内皮一氧化氮合酶(ENOS)抑制剂。研究表明,胰岛素抵抗患者血浆水平升高。此外,ADMA水平对冠状动脉疾病患者的长期结果具有预后价值。胰岛素抵抗,与外源性或内源性胰岛素的动作不充分的生物反应性相关的疾病是一种代谢条件,其存在于心血管疾病的患者中。该疾病通过一氧化氮(NO)代谢的变化影响血管内皮的功能平衡。通过eNOS从基质L-精氨酸的内皮细胞中产生一氧化氮。升高的ADMA水平导致ENOS uncoping,一种导致无生物利用度降低和增加过氧化氢产量的机制。根据临床研究,L-精氨酸向高分症水平的患者给予患者通过拮抗ADMA对eNOS功能的有害效果来提高合成,尽管在糖尿病如糖尿病等特定群体中,这甚至可能是有害的。需要进行更多的研究,以证明NoS抑制剂在胰岛素抵抗和内皮功能障碍中的作用。仍然很难说某些群体中的adma水平是否只是一个原因或分子改变的结果,其在血管疾病状态中发生。

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