Vasoconstrictor sensitivity to noradrenaline and NG-monomethyl-L-arginine in men and women

被引:30
作者
Kneale, BJ
Chowienczyk, PJ
Cockcroft, JR
Coltart, DJ
Ritter, JM
机构
[1] United Med & Dent Sch Guys & St Thomas Hosp, Dept Clin Pharmacol, London SE1 7EH, England
[2] St Thomas Hosp, Dept Cardiol, London SE1 7EH, England
[3] Univ Nottingham Hosp, Queens Med Ctr, Dept Med & Therapeut, Nottingham NG7 2UH, England
关键词
endothelium; gender; nitric oxide;
D O I
10.1042/cs0930513
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1, Nitric oxide has potential anti-atherogenic actions as well as regulating vascular tone, Animal studies suggest that there are sex differences in basal nitric oxide biosynthesis, but it is not known whether such differences exist between men and women, 2, We have investigated this question by measuring forearm blood flow responses, using venous occlusion plethysmography, to brachial artery infusion of NG-monomethyl-L-arginine (an inhibitor of NO biosynthesis) and noradrenaline in 40 healthy subjects (20 men and 20 premenopausal women), Mean arterial blood pressure was 89 +/- 10 mmHg (mean +/- SD) in men and 87 +/- 9 mmHg in women, and mean total cholesterol was 4.25 +/- 0.99 mmol/l (mean +/- SD) and 4.26 +/- 0.80 mmol/l respectively, 3, In men, vasoconstrictor responses to N-G-mono-methyl-L-arginine, 1-4 mu mol/min (15-28% mean reduction in blood flow), were consistently less than responses to noradrenaline, 60-240 pmol/min (26-37%), whereas in women, vasoconstrictor responses to NG-monomethyl-L-arginine (19-30%) were consistently greater than those to noradrenaline(11-17%). The sex difference in relative sensitivity to vasoconstrictors was significant (P < 0.001), 4, Our findings are consistent with either greater sensitivity to noradrenaline in men compared with premenopausal women, or a greater basal nitric oxide biosynthesis in premenopausal women compared with men.
引用
收藏
页码:513 / 518
页数:6
相关论文
共 53 条
[1]  
ANGUS JA, 1986, FASEB J, V45, P2355
[2]  
BOCKMAN CS, 1993, J PHARMACOL EXP THER, V267, P1126
[3]  
Bockman CS, 1996, J PHARMACOL EXP THER, V278, P1235
[4]   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
[5]  
CALVER A, 1992, J HYPERTENS, V10, P1025
[6]   FOREARM BLOOD-FLOW RESPONSES TO A NITRIC-OXIDE SYNTHASE INHIBITOR IN PATIENTS WITH TREATED ESSENTIAL-HYPERTENSION [J].
CALVER, A ;
COLLIER, J ;
VALLANCE, P .
CARDIOVASCULAR RESEARCH, 1994, 28 (11) :1720-1725
[7]   THE ROLE OF NITRIC-OXIDE IN ENDOTHELIUM-DEPENDENT VASODILATION OF HYPERCHOLESTEROLEMIC PATIENTS [J].
CASINO, PR ;
KILCOYNE, CM ;
QUYYUMI, AA ;
HOEG, JM ;
PANZA, JA .
CIRCULATION, 1993, 88 (06) :2541-2547
[8]   CHRONIC INHIBITION OF NITRIC-OXIDE PRODUCTION ACCELERATES NEOINTIMA FORMATION AND IMPAIRS ENDOTHELIAL FUNCTION IN HYPERCHOLESTEROLEMIC RABBITS [J].
CAYATTE, AJ ;
PALACINO, JJ ;
HORTEN, K ;
COHEN, RA .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (05) :753-759
[9]   DIFFERENTIAL INHIBITION BY N(G)-MONOMETHYL-L-ARGININE OF VASODILATOR EFFECTS OF ACETYLCHOLINE AND METHACHOLINE IN HUMAN FOREARM VASCULATURE [J].
CHOWIENCZYK, PJ ;
COCKCROFT, JR ;
RITTER, JM .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (02) :736-738
[10]   BLOOD FLOW RESPONSES TO INTRAARTERIAL ACETYLCHOLINE IN MAN - EFFECTS OF BASAL FLOW AND CONDUIT VESSEL LENGTH [J].
CHOWIENCZYK, PJ ;
COCKCROFT, JR ;
RITTER, JM .
CLINICAL SCIENCE, 1994, 87 (01) :45-51