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兔和大鼠输精管对场刺激收缩反应双相性质的药理学研究。

A pharmacological investigation of the biphasic nature of the contractile response of rabbit and rat vas deferens to field stimulation.

作者信息

Sneddon P, Westfall D P, Colby J, Fedan J S

出版信息

Life Sci. 1984 Nov 5;35(19):1903-12. doi: 10.1016/0024-3205(84)90470-3.

Abstract

It has been demonstrated previously with the vas deferens of the guinea-pig that the first and second phases of the contractile response to motor nerve stimulation are preferentially antagonized by the P2-purinoceptor antagonist arylazido aminopropionyl ATP (ANAPP3), and the alpha 1-adrenoceptor antagonist prazosin, respectively. We have now investigated the effect of the two antagonists on the biphasic contraction in the vas deferens of two other species; rabbit and rat. ANAPP3, in a concentration which antagonized responses to exogenously applied ATP but not those to exogenous norepinephrine, preferentially reduced the initial phasic response of the rabbit vas deferens to motor nerve stimulation without significantly reducing the secondary, tonic phase of the response. Prazosin had the opposite effect; antagonizing the response to norepinephrine but not to ATP and reducing the tonic response to motor nerve stimulation without significantly reducing the initial phasic response. Results obtained with the rat vas deferens were similar. The present results combined with previous findings suggest that ATP and norepinephrine act as cotransmitters in the vas deferens of several species.

摘要

先前在豚鼠输精管实验中已证实,对运动神经刺激的收缩反应的第一和第二阶段,分别优先被P2嘌呤受体拮抗剂芳基叠氮氨基丙酰ATP(ANAPP3)和α1肾上腺素能受体拮抗剂哌唑嗪所拮抗。我们现在研究了这两种拮抗剂对另外两个物种(兔和大鼠)输精管双相收缩的影响。ANAPP3在拮抗对外源性ATP的反应但不拮抗对外源性去甲肾上腺素的反应的浓度下,优先降低兔输精管对运动神经刺激的初始相反应,而不显著降低反应的继发性强直相。哌唑嗪则有相反的作用;拮抗对去甲肾上腺素的反应但不拮抗对ATP的反应,并降低对运动神经刺激的强直反应,而不显著降低初始相反应。大鼠输精管的实验结果相似。目前的结果与先前的发现相结合表明,ATP和去甲肾上腺素在几种物种的输精管中作为共同递质起作用。

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