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α,β-亚甲基三磷酸腺苷、去甲肾上腺素对大鼠输精管收缩的差异阻断及电诱发收缩

Differential blockade of alpha,beta-methylene-ATP, noradrenaline and electrically evoked contractions of the rat vas deferens.

作者信息

Boselli C, Grana E

机构信息

Istituto di Farmacologia, Facoltà di Farmacia, Università di Pavia, Italy.

出版信息

J Auton Pharmacol. 1999 Aug;19(4):249-56. doi: 10.1046/j.1365-2680.1999.00143.x.

DOI:10.1046/j.1365-2680.1999.00143.x
PMID:10589976
Abstract

The present study was carried out compare the effects of nifedipine, verapamil, papaverine and chloroethylclonidine (CEC) on the electrically-induced contractions and on the contractions produced by exogenous noradrenaline and alpha, beta methylene-ATP in the epidydimal portion of rat vas deferens. Nifedipine inhibited in a concentration-dependent fashion the purinergic component (phase I) of the electrically evoked response. Verapamil (10(-7) M-10(-5) M) did not inhibit significantly or even potentiated phase I of the contractile response to single-pulse field stimulation but inhibited the response to alpha,beta methylene-ATP. Papaverine left unaffected phase I but depressed the response to alpha,beta methylene-ATP. CEC significantly potentiated the purinergic component of the electrically-evoked response and the response induced by alpha,beta methylene-ATP. Nifedipine was devoid of any inhibitory action on the noradrenergic component (phase II) of the response to single shock. Verapamil at the highest concentration used (10(-5) M) was able to partially inhibit phase II. Papaverine abolished in a concentration-dependent manner the noradrenergic component of the response to single shock. CEC abolished the phase II of single shock while was devoid of any inhibitory action on exogenous noradrenaline. The implications of these differences among the compounds studied in the present work are discussed in relation to roles of calcium channels.

摘要

本研究旨在比较硝苯地平、维拉帕米、罂粟碱和氯乙可乐定(CEC)对大鼠输精管附睾部电诱发收缩以及对外源性去甲肾上腺素和α,β-亚甲基三磷酸腺苷(α,β-methylene-ATP)所产生收缩的影响。硝苯地平以浓度依赖性方式抑制电诱发反应的嘌呤能成分(I期)。维拉帕米(10⁻⁷M - 10⁻⁵M)对单脉冲场刺激的收缩反应I期无显著抑制作用,甚至有增强作用,但抑制对α,β-亚甲基三磷酸腺苷的反应。罂粟碱对I期无影响,但抑制对α,β-亚甲基三磷酸腺苷的反应。CEC显著增强电诱发反应的嘌呤能成分以及α,β-亚甲基三磷酸腺苷诱导的反应。硝苯地平对单次电击反应的去甲肾上腺素能成分(II期)无任何抑制作用。所用最高浓度(10⁻⁵M)的维拉帕米能够部分抑制II期。罂粟碱以浓度依赖性方式消除单次电击反应的去甲肾上腺素能成分。CEC消除单次电击的II期,但对外源性去甲肾上腺素无任何抑制作用。结合钙通道的作用,讨论了本研究中所研究化合物之间这些差异的意义。

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