NITRIC-OXIDE AND NITROVASODILATORS - SIMILARITIES, DIFFERENCES AND POTENTIAL INTERACTIONS

被引:81
作者
ANDERSON, TJ [1 ]
MEREDITH, IT [1 ]
GANZ, P [1 ]
SELWYN, AP [1 ]
YEUNG, AC [1 ]
机构
[1] BRIGHAM & WOMENS HOSP, DIV CARDIOVASC, BOSTON, MA 02115 USA
关键词
D O I
10.1016/0735-1097(94)90316-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Many similarities exist between the exogenous nitrates and endothelium-derived relaxing factor, which is nitric oxide or a thiol derivative. Both act by way of guanylate cyclase, which increases intracellular concentrations of cyclic guanosine monophosphate, resulting in smooth muscle cell relaxation and antiplatelet effects. Thiols may be important in the biotransformation of exogenous nitrates and other intracellular processes involving nitric oxide. As such, important interactions might be expected between nitrates and endothelium-dependent processes that involve nitric oxide. This review explores the mechanisms of action, biologic effects and potential interactions between nitrates and endothelium-derived relaxing factor.
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收藏
页码:555 / 566
页数:12
相关论文
共 166 条
[1]   GLYCERYL TRINITRATE INHIBITS PHOSPHATIDYLINOSITOL HYDROLYSIS AND PROTEIN KINASE-C ACTIVITY IN BOVINE MESENTERIC-ARTERY [J].
AHLNER, J ;
AXELSSON, KL ;
KARLSSON, JOG ;
ANDERSSON, RGG .
LIFE SCIENCES, 1988, 43 (15) :1241-1248
[2]  
AHLNER J, 1991, PHARMACOL REV, V43, P351
[3]   NG-METHYLARGININE, AN INHIBITOR OF ENDOTHELIUM-DERIVED NITRIC-OXIDE SYNTHESIS, IS A POTENT PRESSOR AGENT IN THE GUINEA-PIG - DOES NITRIC-OXIDE REGULATE BLOOD-PRESSURE INVIVO [J].
AISAKA, K ;
GROSS, SS ;
GRIFFITH, OW ;
LEVI, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 160 (02) :881-886
[4]   HUMAN-ENDOTHELIAL CELLS INHIBIT PLATELET-AGGREGATION BY SEPARATELY STIMULATING PLATELET CYCLIC-AMP AND CYCLIC-GMP [J].
ALHEID, U ;
REICHWEHR, I ;
FORSTERMANN, U .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1989, 164 (01) :103-110
[5]  
AXELSSON KL, 1984, ACTA PHARMACOL TOX, V55, P203
[6]   ENDOTHELIUM-DEPENDENT INHIBITION OF PLATELET-AGGREGATION [J].
AZUMA, H ;
ISHIKAWA, M ;
SEKIZAKI, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1986, 88 (02) :411-415
[7]   NITRIC-OXIDE GENERATION FROM NITROPRUSSIDE BY VASCULAR TISSUE - EVIDENCE THAT REDUCTION OF THE NITROPRUSSIDE ANION AND CYANIDE LOSS ARE REQUIRED [J].
BATES, JN ;
BAKER, MT ;
GUERRA, R ;
HARRISON, DG .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 :S157-S165
[8]   PRIMARY SEQUENCE OF CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE ISOZYMES AND THE DESIGN OF SELECTIVE INHIBITORS [J].
BEAVO, JA ;
REIFSNYDER, DH .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1990, 11 (04) :150-155
[9]  
BIRNBAUMER L, 1990, ANNU REV PHARMACOL, V30, P675
[10]   PREVENTIVE ADMINISTRATION OF INTRAVENOUS N-ACETYLCYSTEINE AND DEVELOPMENT OF TOLERANCE TO ISOSORBIDE DINITRATE IN PATIENTS WITH ANGINA-PECTORIS [J].
BOESGAARD, S ;
ALDERSHVILE, J ;
POULSEN, HE .
CIRCULATION, 1992, 85 (01) :143-149