Receptor-specific influence of endothelin-1 in the erectile response of the rat

被引:43
作者
Dai, Y
Pollock, DM
Lewis, RL
Wingard, CJ
Stopper, VS
Mills, TM [1 ]
机构
[1] Med Coll Georgia, Dept Physiol & Endocrinol, Augusta, GA 30912 USA
[2] Med Coll Georgia, Dept Surg, Urol Sect, Augusta, GA 30912 USA
[3] Med Coll Georgia, Vasc Biol Ctr, Augusta, GA 30912 USA
关键词
endothelin-A and endothelin-B receptors; penile erection; corpus cavernosum; vasoconstriction;
D O I
10.1152/ajpregu.2000.279.1.R25
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Specific receptor antagonists were used to examine the role of endothelin-1 (ET-1) in the erectile response of the rat. In these studies, intact rats were cannulated to permit the continuous recording of mean arterial pressure (MAP) and intracavernosal pressure (CCP). Erection was induced by electrical stimulation of the autonomic ganglion, which regulates blood flow to the penis. The animals were subjected to intracavernosal injection with vehicle only (Cont) or with an antagonist to the endothelin-A receptor (ETA) or to the endothelin-B receptor (ETB). Blockade of the ETA or the ETB had no effect on the erectile response (CCP/MAP) during maximal ganglionic stimulation. When ET-1 was injected into Cont rats, there was a marked vasoconstriction with a sharp rise in MAP and a decline in CCP as the cavernosal arterioles constricted and limited inflow. The injection of the ETA antagonist prevented the vasoconstriction after ET-1 injection into Cont rats, whereas blockade of the ETB had no effect on the vasoconstrictive effect to ET-1. Similar results were obtained during submaximal ganglionic stimulation. With minimal levels of ganglionic stimulation, ET-1 injection led to a moderated degree of vasodilation in the presence of the ETA antagonist. The ETB antagonist failed to alter the CCP response during minimal stimulation, but it did have a marked effect on the MAP response to ET-1 injection. The results of these studies confirm that cavernosal tissue of the rat penis is highly responsive to ET-1. However, the failure of the ET-1 antagonists to affect penile erection in response to ganglionic stimulation reflects a minimal role of ET-1 in the erectile response in the rat.
引用
收藏
页码:R25 / R30
页数:6
相关论文
共 31 条
[1]   Neurotransmission and the contraction and relaxation of penile erectile tissues [J].
Andersson, KE ;
Stief, CG .
WORLD JOURNAL OF UROLOGY, 1997, 15 (01) :14-20
[2]   Possible role for endothelins in penile erection [J].
Ari, G ;
Vardi, Y ;
Hoffman, A ;
Finberg, JPM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 307 (01) :69-74
[3]   THE DENSITY AND DISTRIBUTION OF ENDOTHELIN-1 AND ENDOTHELIN RECEPTOR SUBTYPES IN NORMAL AND DIABETIC RAT CORPUS CAVERNOSUM [J].
BELL, CRW ;
SULLIVAN, ME ;
DASHWOOD, MR ;
MUDDLE, JR ;
MORGAN, RJ .
BRITISH JOURNAL OF UROLOGY, 1995, 76 (02) :203-207
[4]   ROLE OF NITRIC BRIDE IN THE PHYSIOLOGY OF ERECTION [J].
BURNETT, AL .
BIOLOGY OF REPRODUCTION, 1995, 52 (03) :485-489
[5]   Nitrergic control of peripheral sympathetic responses in the human corpus cavernosum: A comparison with other species [J].
Cellek, S ;
Moncada, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8226-8231
[6]  
Champion HC, 1997, J ANDROL, V18, P513
[7]   ENDOTHELIN-1 AS A PUTATIVE MODULATOR OF ERECTILE DYSFUNCTION .1. CHARACTERISTICS OF CONTRACTION OF ISOLATED CORPORAL TISSUE STRIPS [J].
CHRIST, GJ ;
LERNER, SE ;
KIM, DC ;
MELMAN, A .
JOURNAL OF UROLOGY, 1995, 153 (06) :1998-2003
[8]   ENDOTHELIN BINDING TO CULTURED CALF ADRENAL ZONA GLOMERULOSA CELLS AND STIMULATION OF ALDOSTERONE SECRETION [J].
COZZA, EN ;
GOMEZSANCHEZ, CE ;
FOECKING, MF ;
CHIOU, S .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :1032-1035
[9]   ENDOTHELIN - LOCALIZATION, SYNTHESIS, ACTIVITY, AND RECEPTOR TYPES IN HUMAN PENILE CORPUS CAVERNOSUM [J].
DETEJADA, IS ;
CARSON, MP ;
DELASMORENAS, A ;
GOLDSTEIN, I ;
TRAISH, AM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (04) :H1078-H1085
[10]   Drugs for the treatment of impotence [J].
GarciaReboll, L ;
Mulhall, JP ;
Goldstein, I .
DRUGS & AGING, 1997, 11 (02) :140-151