首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >The effects of alpha-adrenoceptor agonists and antagonists on responses of transmurally stimulated prostatic and epididymal portions of the isolated vas deferens of the rat.
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The effects of alpha-adrenoceptor agonists and antagonists on responses of transmurally stimulated prostatic and epididymal portions of the isolated vas deferens of the rat.

机译:α-肾上腺素受体激动剂和拮抗剂对大鼠离体输精管的经壁刺激的前列腺和附睾部分反应的影响。

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摘要

1 The effects of alpha-adrenoceptor agonists and antagonists on contractile responses of transmurally stimulated prostatic and epididymal portions of the rat isolated vas deferens were examined. 2 Responses to single stimuli consisted of two phases, the first predominant in the prostatic and the second in the epididymal portion. The first phase was resistant to alpha-adrenoceptor antagonists but the second was reduced in a dose-related manner in the order of potency prazosin greater than azapetine greater than phentolamine greater than labetalol greater than yohimbine. 3 Both phases of the response to a single stimulus were reduced by clonidine but only the first could be reliably restored by yohimbine. 4 Trains of transmural stimuli produced biphasic responses, an early rapid component predominant in the prostatic and a slow secondary component predominant in the epididymal portion. The effects of alpha-adrenoceptor antagonists on these responses were complex. Prazosin produced the most straightforward inhibition of responses with relative resistance of the early rapid component. Only yohimbine and phentolamine produced increases in responses which could be pre-junctional in origin. 5 The alpha-adrenoceptor agonists, oxymetazoline and clonidine, reduced while phenylephrine increased responses to trains of stimuli. 6 These results are discussed in relation to the nature of the innervation of rat vas deferens and the usefulness of the preparation in pharmacological tests for activity at alpha-adrenoceptors.
机译:1考察了α-肾上腺素受体激动剂和拮抗剂对大鼠离体输精管的经壁刺激的前列腺和附睾部分的收缩反应的影响。 2对单个刺激的反应包括两个阶段,第一阶段主要发生在前列腺,第二阶段主要发生在附睾。第一阶段对α-肾上腺素受体拮抗剂具有抗性,但第二阶段以剂量相关的方式降低,其效价为吡唑嗪大于阿扎哌丁大于苯妥拉明大于拉贝洛尔大于育亨宾。 3可乐定减少了对单个刺激的反应的两个阶段,但是育亨宾可以可靠地恢复第一个阶段。 4透壁刺激序列产生了两相反应,主要是前列腺的早期快速成分,而附睾部分则是缓慢的次级成分。 α-肾上腺素能受体拮抗剂对这些反应的作用是复杂的。吡唑嗪产生了最直接的抑制反应,且早期快速成分具有相对耐药性。仅育亨宾和酚妥拉明产生的响应可能是结前的增加。 5,α-肾上腺素受体激动剂羟甲唑啉和可乐定减少,而去氧肾上腺素增加了对一系列刺激的反应。 6讨论了这些结果,涉及大鼠输精管神经支配的性质以及该制剂在药理学试验中对α-肾上腺素受体活性的有用性。

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