INHIBITION OF NITRIC-OXIDE SYNTHESIS INCREASES BLOOD-PRESSURE IN HEALTHY HUMANS

被引:284
作者
HAYNES, WG
NOON, JP
WALKER, BR
WEBB, DJ
机构
[1] Department of Medicine, University of Edinburgh, Western General Hospital, Edinburgh
关键词
N-G-MONOMETHYL-L-ARGININE; CARDIAC FUNCTION; SODIUM; KIDNEY; VASCULAR RESISTANCE; HUMAN;
D O I
10.1097/00004872-199312000-00009
中图分类号
R6 [外科学];
学科分类号
1002 [临床医学]; 100210 [外科学];
摘要
Objective: To examine whether endogenous production of the endothelium-derived vasodilator nitric oxide influences blood pressure in healthy humans. Methods: After preliminary pilot dose-ranging studies, 3 mg/kg N-G-monomethyl-L-arginine (L-NMMA), an inhibitor of nitric oxide synthase, and saline placebo were infused intravenously over 5 min to eight healthy subjects in a two-phase, randomized, single-blind crossover study. Blood pressure and cardiac and renal function were measured. Results: Compared with placebo, L-NMMA increased mean arterial pressure by 10%, decreased heart rate by 19%, decreased cardiac index by 25% and increased calculated total peripheral resistance by 46%. Effects were maximal 10-15 min after starting L-NMMA infusion. Urinary sodium and fractional sodium excretions were increased by L-NMMA, but creatinine clearance was unchanged. Conclusions: Basal generation of nitric oxide influences total peripheral resistance and blood pressure in healthy humans. The natriuresis induced by L-NMMA may be related to the increase in blood pressure, or arise from inhibition of the intrarenal actions of nitric oxide. Any decrease in nitric oxide generation, as has been postulated to occur in essential hypertension, could have substantial effects on blood pressure and tissue blood flow.
引用
收藏
页码:1375 / 1380
页数:6
相关论文
共 23 条
[1]
NITRIC-OXIDE ATTENUATES CARDIAC MYOCYTE CONTRACTION [J].
BRADY, AJB ;
WARREN, JB ;
POOLEWILSON, PA ;
WILLIAMS, TJ ;
HARDING, SE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (01) :H176-H182
[2]
N(G)-NITRO L-ARGININE METHYL-ESTER AND OTHER ALKYL ESTERS OF ARGININE ARE MUSCARINIC RECEPTOR ANTAGONISTS [J].
BUXTON, ILO ;
CHEEK, DJ ;
ECKMAN, D ;
WESTFALL, DP ;
SANDERS, KM ;
KEEF, KD .
CIRCULATION RESEARCH, 1993, 72 (02) :387-395
[3]
INHIBITION AND STIMULATION OF NITRIC-OXIDE SYNTHESIS IN THE HUMAN FOREARM ARTERIAL BED OF PATIENTS WITH INSULIN-DEPENDENT DIABETES [J].
CALVER, A ;
COLLIER, J ;
VALLANCE, P .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2548-2554
[4]
CALVER A, 1992, J HYPERTENS, V10, P1025
[5]
EVANS CE, 1989, J HYPERTENS, V7, P133
[6]
THE ENDOTHELIN FAMILY OF PEPTIDES - LOCAL HORMONES WITH DIVERSE ROLES IN HEALTH AND DISEASE [J].
HAYNES, WG ;
WEBB, DJ .
CLINICAL SCIENCE, 1993, 84 (05) :485-500
[7]
ENDOTHELIUM-DEPENDENT VASODILATION IS ATTENUATED IN PATIENTS WITH HEART-FAILURE [J].
KUBO, SH ;
RECTOR, TS ;
BANK, AJ ;
WILLIAMS, RE ;
HEIFETZ, SM .
CIRCULATION, 1991, 84 (04) :1589-1596
[8]
INDIRECT EVIDENCE FOR RELEASE OF ENDOTHELIUM-DERIVED RELAXING FACTOR IN HUMAN FOREARM CIRCULATION INVIVO - BLUNTED RESPONSE IN ESSENTIAL-HYPERTENSION [J].
LINDER, L ;
KIOWSKI, W ;
BUHLER, FR ;
LUSCHER, TF .
CIRCULATION, 1990, 81 (06) :1762-1767
[9]
NITRIC-OXIDE IN LIVER-FAILURE [J].
MIDGLEY, S ;
GRANT, IS ;
HAYNES, WG ;
WEBB, DJ .
LANCET, 1991, 338 (8782-3) :1590-1590
[10]
MONCADA S, 1991, PHARMACOL REV, V43, P109