THE ROLE OF NITRIC-OXIDE AND OTHER ENDOTHELIUM-DERIVED VASOACTIVE SUBSTANCES IN VASCULAR-DISEASE

被引:244
作者
COHEN, RA [1 ]
机构
[1] UNIV BOSTON HOSP, MED CTR, ROBERT DAWSON EVANS DEPT CLIN RES, PERIPHERAL VASC MED SECT, BOSTON, MA 02118 USA
关键词
D O I
10.1016/S0033-0620(05)80002-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alteration in the release and action of endothelium-derived vasoactive factors is responsible for changes in vascular reactivity early in the course of vascular disease. These factors include nitric oxide, eicosanoids, endothelium-derived hyperpolarizing factor, endothelin, and angiotensin II. Because endothelial dysfunction occurs at early stages of disease, it may reflect physiological changes that, if allowed to become chronic, are responsible for changes in vascular structure and growth and adhesivity to platelets and leukocytes, ultimately leading to atherosclerosis and thrombosis. Each of the major risk factors predisposing to vascular disease are associated with endothelial cell dysfunction, suggesting a direct etiologic link between the effects of the risk factors on the endothelium and their propensity to accelerate vascular disease. Restoration or replacement of endothelium-derived factors such as nitric oxide and prostacyclin, which impede the progression of vascular disease, or preventing the action of mediators such as vasoconstrictor eicosanoids, angiotensin II, or endothelin, which accelerate the progression of vascular disease, has become a useful paradigm in the treatment and prevention of vascular disease. Thus, understanding the physiology of endothelium-derived vasoactive factors is a necessary part of every physician's education. © 1995 W.B. Saunders Company. All rights reserved.
引用
收藏
页码:105 / 128
页数:24
相关论文
共 291 条
[1]  
ABIRU T, 1990, RES COMMUN CHEM PATH, V68, P13
[2]   VASCULAR BOUND RECOMBINANT EXTRACELLULAR SUPEROXIDE-DISMUTASE TYPE-C PROTECTS AGAINST THE DETRIMENTAL EFFECTS OF SUPEROXIDE RADICALS ON ENDOTHELIUM-DEPENDENT ARTERIAL RELAXATION [J].
ABRAHAMSSON, T ;
BRANDT, U ;
MARKLUND, SL ;
SJOQVIST, PO .
CIRCULATION RESEARCH, 1992, 70 (02) :264-271
[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]   LOW-DENSITY LIPOPROTEINS INHIBIT ENDOTHELIUM-DEPENDENT RELAXATION IN RABBIT AORTA [J].
ANDREWS, HE ;
BRUCKDORFER, KR ;
DUNN, RC ;
JACOBS, M .
NATURE, 1987, 327 (6119) :237-239
[5]   AGGREGATING PLATELETS INCREASE INTRACELLULAR CALCIUM IN ENDOTHELIAL-CELLS THROUGH RELEASE OF ADENINE-NUCLEOTIDES [J].
ASHMORE, RC ;
OBRIEN, RF ;
STELZNER, TJ ;
DAUBER, IM ;
HORWITZ, LD ;
MCMURTRY, IF ;
VANBENTHUYSEN, KM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 166 (02) :909-915
[6]   ENDOTHELIUM-DERIVED CONTRACTING FACTOR RELEASED BY SEROTONIN IN THE AORTA OF THE SPONTANEOUSLY HYPERTENSIVE RAT [J].
AUCHSCHWELK, W ;
VANHOUTTE, PM .
AMERICAN JOURNAL OF HYPERTENSION, 1991, 4 (09) :769-772
[7]  
BAR RS, 1992, ENDOTHELIAL CELL DYS, P363
[8]   NITRIC-OXIDE AND PROSTACYCLIN - DIVERGENCE OF INHIBITORY EFFECTS ON MONOCYTE CHEMOTAXIS AND ADHESION TO ENDOTHELIUM INVITRO [J].
BATH, PMW ;
HASSALL, DG ;
GLADWIN, AM ;
PALMER, RMJ ;
MARTIN, JF .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (02) :254-260
[9]   PRESERVATION OF ENDOTHELIAL FUNCTION BY RAMIPRIL IN RABBITS ON A LONG-TERM ATHEROGENIC DIET [J].
BECKER, RHA ;
WIEMER, G ;
LINZ, W .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 18 :S110-S115
[10]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624