The clinical pharmacology of L-arginine

被引:226
作者
Böger, RH
Bode-Böger, SM
机构
[1] Hannover Med Sch, Inst Clin Pharmacol, D-30623 Hannover, Germany
[2] Univ Clin Eppendorf, Inst Expt & Clin Pharmacol & Toxicol, D-20246 Hamburg, Germany
关键词
endothelium; nitric oxide; cardiovascular disease; pharmacokinetics; side effects;
D O I
10.1146/annurev.pharmtox.41.1.79
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
L-Arginine (2-amino-5-guanidinovaleric acid) is the precursor of nitric oxide, an endogenous messenger molecule involved in a variety of endothelium-mediated physiological effects in the vascular system. Acute and chronic administration of L-arginine has been shown to improve endothelial function in animal models of hypercholesterolemia and atherosclerosis. L-Arginine also improves endothelium-dependent vasodilation in humans with hypercholesterolemia and atherosclerosis. The responsiveness to L-arginine depends on the specific cardiovascular disease studied, the vessel segment, and morphology of the artery. The pharmacokinetics of L-arginine have recently been investigated. Side effects are rare and mostly mild and dose dependent. The mechanism of action of L-arginine may involve nitric oxide synthase substrate provision. especially in patients with elevated levels of the endogenous NO synthase inhibitor asymmetric dimethylarginine. Endocrine effects and unspecific reactions may contribute to L-arginine-induced vasodilation after higher doses. Several long-term studies have been performed that show that chronic oral administration of L-arginine or intermittent infusion therapy with L-arginine can improve clinical symptoms of cardiovascular disease in man.
引用
收藏
页码:79 / 99
页数:21
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