Pharmacological characterization of adrenoceptors in horse corpus cavernosum penis

被引:10
|
作者
Recio, P
Lopez, PG
Fernandez, JLG
GarciaSacristan, A
机构
[1] Departamento de Fisiología, Facultad de Veterinaria, Universidad Complutense
来源
JOURNAL OF AUTONOMIC PHARMACOLOGY | 1997年 / 17卷 / 03期
关键词
D O I
10.1046/j.1365-2680.1997.00457.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1 The presence and types of alpha and beta-adrenoceptors in the corpus cavernosum of the horse were studied in vitro by using selected ligands of adrenoceptors and isometric tension recording. 2 Noradrenaline and phenylephrine induced concentration-dependent contractions in corpus cavernosum preparations. B-HT 920 had no effect. 3 Phentolamine and prazosin produced a shift to the right of the dose-response curve of noradrenaline, while the alpha(2)-antagonist, rauwolscine had no effect on the response to noradrenaline. Phenylephrine-evoked contractions of corporal strips were significantly inhibited by the alpha(1)-adrenoceptor antagonist, prazosin. 4 Isoprenaline and salbutamol each relaxed precontracted corpus cavernosum preparations in a concentration-dependent manner; the isoprenaline effect was blocked by propranolol, practolol and butoxamine. The salbutamol effect was blocked by butoxamine. 5 These results suggest the presence of postjunctional alpha(1)-adrenoceptors in horse corpus cavernosum. There is also a heterogenous population of beta-adrenoceptors in this tissue, belonging to the beta(1) and beta(2) subtypes.
引用
收藏
页码:191 / 198
页数:8
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