Impaired L-arginine transport and endothelial function in hypertensive and genetically predisposed normotensive subjects
Autor: | Tanneale Marshall, Wei-Zheng Zhang, Samara Finch, Melinda M. Parnell, Markus P. Schlaich, David M. Kaye, Belinda A. Ahlers |
---|---|
Rok vydání: | 2004 |
Předmět: |
Adult
Male Nitroprusside medicine.medical_specialty Endothelium Arginine Adolescent Nitric Oxide Synthase Type III Vasodilation In Vitro Techniques Essential hypertension Nitric Oxide Peripheral blood mononuclear cell Physiology (medical) Internal medicine medicine Humans Genetic Predisposition to Disease Nitric Oxide Donors RNA Messenger Cationic Amino Acid Transporter 1 business.industry Cell Membrane Biological Transport medicine.disease Acetylcholine Forearm medicine.anatomical_structure Endocrinology Blood pressure Pathophysiology of hypertension Hypertension Sodium nitroprusside Endothelium Vascular Nitric Oxide Synthase Cardiology and Cardiovascular Medicine business medicine.drug |
Zdroj: | Circulation. 110(24) |
ISSN: | 1524-4539 |
Popis: | Background— Impaired endothelium-dependent NO-mediated vasodilation is a key feature of essential hypertension and may precede the increase in blood pressure. We investigated whether transport of the NO precursor l -arginine is related to decreased endothelial function. Methods and Results— Radiotracer kinetics ([ 3 H] l -arginine) were used to measure forearm and peripheral blood mononuclear cell arginine uptake in hypertensive subjects (n=12) and in 2 groups of healthy volunteers with (n=15) and without (n=15) a family history of hypertension. In conjunction, forearm blood flow responses to acetylcholine and sodium nitroprusside were measured before and after a supplemental intra-arterial infusion of l -arginine. In vivo and in vitro measures of l -arginine transport were substantially reduced in the essential hypertension and positive family history groups compared with the negative family history group; however, no difference was detected in peripheral blood mononuclear cell mRNA or protein expression levels for the cationic amino acid transporter CAT-1. Plasma concentrations of l -arginine and N G , N G′ -dimethylarginine (ADMA) did not differ between groups. l -Arginine supplementation improved the response to acetylcholine only in subjects with essential hypertension and positive family history. Conclusions— Similar to their hypertensive counterparts, normotensive individuals at high risk for the development of hypertension are characterized by impaired l -arginine transport, which may represent the link between a defective l -arginine/NO pathway and the onset of essential hypertension. The observed transport defect is not due to apparent alterations in CAT-1 expression or elevated endogenous ADMA. |
Databáze: | OpenAIRE |
Externí odkaz: |