EFFECT OF N-G-MONOMETHYL-L-ARGININE ON KININ-INDUCED VASODILATION IN THE HUMAN FOREARM

被引:55
作者
COCKCROFT, JR
CHOWIENCZYK, PJ
BRETT, SE
RITTER, JM
机构
[1] Department of Clinical Pharmacology, United Medical School, Guy's Hospital, London
关键词
ENDOTHELIUM; NITRIC OXIDE; N-G-MONOMETHYL-L-ARGININE; BRADYKININ; SUBSTANCE P; HUMAN FOREARM VASCULATURE;
D O I
10.1111/j.1365-2125.1994.tb04358.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 We compared effects of N-G-monomethyl-L-arginine (L-NMMA), an NO synthase inhibitor, on vasodilator responses to intra-arterial infusion of bradykinin and substance P in the human forearm. 2 Bradykinin (100 pmol min(-1)) increased forearm blood flow when infused into the brachial artery of eight healthy male volunteers, from 2.8 +/- 0.2 (mean +/- s.e. mean) to 9.3 +/- 1.0 ml min(-1) per 100 ml forearm volume. 3 Co-infusion of L-NMMA (2 mu mol min(-1) and 4 mu mol min(-1)) with bradykinin (100 pmol min(-1)) for 6 min produced respectively a 9 +/- 14% and 42 +/- 14% inhibition (compared with L-NMMA vehicle) in the response to bradykinin. 4 Substance P (1 pmol min(-1)) when infused into the brachial artery of a further eight male subjects increased forearm blood flow from 3.4 +/- 0.2 to 6.3 +/- 0.7 ml min(-1) 100 ml(-1). 5 Co-infusion of L-NMMA (2 mu mol min(-1) and 4 mu mol min(-1)) with substance P (1 pmol min(-1)) for 6 min produced respectively a 27 +/- 8% and 70 +/- 13% inhibition (compared with L-NMMA vehicle) in the response to substance P. 6 These results demonstrate that vasodilator responses to both bradykinin and substance P are mediated in part via the L-arginine/NO pathway. Bradykinin and substance P may be useful agonists with which to study endothelial function in this vascular bed.
引用
收藏
页码:307 / 310
页数:4
相关论文
共 28 条
[1]   LOCAL INHIBITION OF CONVERTING ENZYME AND VASCULAR-RESPONSES TO ANGIOTENSIN AND BRADYKININ IN THE HUMAN FOREARM [J].
BENJAMIN, N ;
COCKCROFT, JR ;
COLLIER, JG ;
DOLLERY, CT ;
RITTER, JM ;
WEBB, DJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1989, 412 :543-555
[2]  
BHOOLA KD, 1992, PHARMACOL REV, V44, P1
[3]   ROLE OF ENDOTHELIAL-CELLS IN RELAXATION OF ISOLATED ARTERIES BY BRADYKININ [J].
CHERRY, PD ;
FURCHGOTT, RF ;
ZAWADZKI, JV ;
JOTHIANANDAN, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (06) :2106-2110
[4]   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
[5]   SUBSTANCE-P DILATES EPICARDIAL CORONARY-ARTERIES AND INCREASES CORONARY BLOOD-FLOW IN HUMANS [J].
CROSSMAN, DC ;
LARKIN, SW ;
FULLER, RW ;
DAVIES, GJ ;
MASERI, A .
CIRCULATION, 1989, 80 (03) :475-484
[6]   EFFECTS OF PEPTIDES AND NON-PEPTIDES ON ISOLATED ARTERIAL SMOOTH MUSCLES - ROLE OF ENDOTHELIUM [J].
DORLEANSJUSTE, P ;
DION, S ;
MIZRAHI, J ;
REGOLI, D .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 114 (01) :9-21
[7]   INHIBITION OF NITRIC-OXIDE SYNTHESIS IN FOREARM VASCULATURE OF INSULIN-DEPENDENT DIABETIC-PATIENTS - BLUNTED VASOCONSTRICTION IN PATIENTS WITH MICROALBUMINURIA [J].
ELLIOTT, TG ;
COCKCROFT, JR ;
GROOP, PH ;
VIBERTI, GC ;
RITTER, JM .
CLINICAL SCIENCE, 1993, 85 (06) :687-693
[8]   ATHEROSCLEROSIS OR LIPOPROTEIN-INDUCED ENDOTHELIAL DYSFUNCTION - POTENTIAL MECHANISMS UNDERLYING REDUCTION IN EDRF/NITRIC OXIDE ACTIVITY [J].
FLAVAHAN, NA .
CIRCULATION, 1992, 85 (05) :1927-1938
[9]   EFFECT OF SUBSTANCE-P ON CARDIOVASCULAR AND RESPIRATORY-FUNCTION IN SUBJECTS [J].
FULLER, RW ;
MAXWELL, DL ;
DIXON, CMS ;
MCGREGOR, GP ;
BARNES, VF ;
BLOOM, SR ;
BARNES, PJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1987, 62 (04) :1473-1479
[10]   ROLE OF ENDOTHELIUM IN RESPONSES OF VASCULAR SMOOTH-MUSCLE [J].
FURCHGOTT, RF .
CIRCULATION RESEARCH, 1983, 53 (05) :557-573