L-ARGININE INDUCES RELAXATION OF HUMAN UTERINE ARTERY WITH BOTH INTACT AND DENUDED ENDOTHELIUM

被引:25
作者
JOVANOVIC, A [1 ]
GRBOVIC, L [1 ]
TULIC, I [1 ]
机构
[1] UNIV BELGRADE, FAC MED, MED CTR, OBSTET & GYNECOL CLIN, YU-11000 BELGRADE, YUGOSLAVIA
关键词
UTERINE ARTERY; L-ARGININE; RELAXATION; EDRF (ENDOTHELIUM-DERIVED RELAXING FACTOR); NITRIC OXIDE (NO); (HUMAN);
D O I
10.1016/0014-2999(94)90623-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of L-arginine on isolated human uterine artery rings was investigated. L-Arginine, but not D-arginine, induced concentration-dependent relaxation. Removal of the endothelium enhanced the relaxant effects of L-arginine. Methylene blue and dexamethasone non-competitively inhibited L-arginine-induced relaxation, while N-G-monomethyl-L-arginine competitively antagonized the response to L-arginine. Calmidazolium did not affect relaxation evoked by L-arginine. The dissociation constants obtained for L-arginine and N-G-monomethyl-L-arginine in intact rings were not significantly different from those in endothelium-denuded rings. It is concluded that the relaxation induced by L-arginine in human uterine artery is mediated by non-endothelial nitric oxide production. We suggest that the NO synthase mediating the L-arginine-induced relaxation is an inducible type.
引用
收藏
页码:103 / 107
页数:5
相关论文
共 15 条
[1]   SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J].
ARUNLAKSHANA, O ;
SCHILD, HO .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01) :48-58
[2]   FEEDBACK INHIBITION OF NITRIC-OXIDE SYNTHASE ACTIVITY BY NITRIC-OXIDE [J].
ASSREUY, J ;
CUNHA, FQ ;
LIEW, FY ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) :833-837
[3]   ENDOTHELIN AND NEUROPEPTIDE-Y ARE VASOCONSTRICTORS IN HUMAN UTERINE BLOOD-VESSELS [J].
FRIED, G ;
SAMUELSON, U .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1991, 164 (05) :1330-1336
[4]   DEPLETION OF ARTERIAL L-ARGININE CAUSES REVERSIBLE TOLERANCE TO ENDOTHELIUM-DEPENDENT RELAXATION [J].
GOLD, ME ;
BUSH, PA ;
IGNARRO, LJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 164 (02) :714-721
[5]  
KENAKIN TP, 1987, PHARM ANAL DRUG RECE
[6]  
MARCZIN N, 1992, J PHARMACOL EXP THER, V263, P170
[7]  
MARTIN W, 1985, J PHARMACOL EXP THER, V232, P708
[8]   INHIBITION OF NITRIC-OXIDE SYNTHESIS BY METHYLENE-BLUE [J].
MAYER, B ;
BRUNNER, F ;
SCHMIDT, K .
BIOCHEMICAL PHARMACOLOGY, 1993, 45 (02) :367-374
[9]   THE L-ARGININE - NITRIC-OXIDE PATHWAY [J].
MONCADA, S .
ACTA PHYSIOLOGICA SCANDINAVICA, 1992, 145 (03) :201-227
[10]   NITRIC-OXIDE SYNTHASE RESPONSIBLE FOR L-ARGININE-INDUCED RELAXATION OF RAT AORTIC RINGS INVITRO MAY BE AN INDUCIBLE TYPE [J].
MORITOKI, H ;
TAKEUCHI, S ;
HISAYAMA, T ;
KONDOH, W .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 107 (02) :361-366