The pathophysiology of erectile dysfunction related to endothelial dysfunction and mediators of vascular function

被引:170
作者
Maas, R [1 ]
Schwedhelm, E [1 ]
Albsmeier, J [1 ]
Böger, RH [1 ]
机构
[1] Univ Hamburg, Hosp Eppendorf, Inst Expt & Klin Pharmakol & Toxikol, D-20246 Hamburg, Germany
关键词
asymmetrical dimethylarginine; endothelial dysfunction; endothelin; erectile dysfunction; nitric oxide; nitric oxide synthase; oxidative stress; prostaglandin;
D O I
10.1191/1358863x02vm429ra
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The incidence of erectile dysfunction increases with diabetes, hypertension, hypercholesterolaemia, cardiovascular disease and renal failure. All these conditions are associated with endothelial dysfunction. This review addresses the pathophysiology of erectile dysfunction with a special focus on new insights into nitric oxide (NO)-mediated pathways, oxidative stress and parallels to endothelial dysfunction. NO appears to be the key mediator promoting endothelium-derived vasodilation and penile erection. The possibility is discussed that elevated plasma concentrations of asymmetrical dimethylarginine (ADMA), an endogenous NO synthase inhibitor, may provide an additional pathomechanism for various forms of erectile dysfunction associated with cardiovascular risk factors and disease. Likewise, the role of endothelium-derived factors mediating NO-independent pathways is evaluated.
引用
收藏
页码:213 / 225
页数:13
相关论文
共 232 条
[41]   NITRIC-OXIDE - A PHYSIOLOGICAL MEDIATOR OF PENILE ERECTION [J].
BURNETT, AL ;
LOWENSTEIN, CJ ;
BREDT, DS ;
CHANG, TSK ;
SNYDER, SH .
SCIENCE, 1992, 257 (5068) :401-403
[42]   BIOSYNTHESIS OF NITRIC-OXIDE AND CITRULLINE FROM L-ARGININE BY CONSTITUTIVE NITRIC-OXIDE SYNTHASE PRESENT IN RABBIT CORPUS CAVERNOSUM [J].
BUSH, PA ;
GONZALEZ, NE ;
IGNARRO, LJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (01) :308-314
[43]   NITRIC-OXIDE IS A POTENT RELAXANT OF HUMAN AND RABBIT CORPUS CAVERNOSUM [J].
BUSH, PA ;
ARONSON, WJ ;
BUGA, GM ;
RAJFER, J ;
IGNARRO, LJ .
JOURNAL OF UROLOGY, 1992, 147 (06) :1650-1655
[44]   Endothelial dysfunction in cardiovascular diseases - The role of oxidant stress [J].
Cai, H ;
Harrison, DG .
CIRCULATION RESEARCH, 2000, 87 (10) :840-844
[45]   Endothelin-1-induced enhancement of coronary smooth muscle contraction via MAPK-dependent and MAPK-independent [Ca2+]i sensitization pathways [J].
Cain, AE ;
Tanner, DM ;
Khalil, RA .
HYPERTENSION, 2002, 39 (02) :543-549
[46]  
CALVER A, 1993, J HUM HYPERTENS, V7, P193
[47]   Rate of vasoconstrictor prostanoids released by endothelial cells depends on cyclooxygenase-2 expression and prostaglandin I synthase activity [J].
Camacho, M ;
Löpez-Belmonte, J ;
Vila, L .
CIRCULATION RESEARCH, 1998, 83 (04) :353-365
[48]   Impairment of corpus cavernosal smooth muscle relaxation by glycosylated human haemoglobin [J].
Cartledge, JJ ;
Eardley, I ;
Morrison, JFB .
BJU INTERNATIONAL, 2000, 85 (06) :735-741
[49]   Roles of cyclooxygenase (COX)-1 and COX-2 in prostanoid production by human endothelial cells: Selective up-regulation of prostacyclin synthesis by COX-2 [J].
Caughey, GE ;
Cleland, LG ;
Penglis, PS ;
Gamble, JR ;
James, MJ .
JOURNAL OF IMMUNOLOGY, 2001, 167 (05) :2831-2838
[50]   Passive smoking and impaired endothelium-dependent arterial dilatation in healthy young adults [J].
Celermajer, DS ;
Adams, MR ;
Clarkson, P ;
Robinson, J ;
McCredie, R ;
Donald, A ;
Deanfield, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (03) :150-154