Pharmacological responses by different portions of guinea pig vas deferens circular muscle preparation.

E Minker, C Bartha
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引用次数: 0

Abstract

The different segments of the guinea pig vas deferens circular muscle exhibit differential response patterns upon pharmacological stimulation. Namely, apart from barium chloride, the affinity and intrinsic activity of certain agonists and the strength of maximum contractions they induce appear to decrease along the path from the epididymis toward the prostate. If one subdivides the vas deferens into 3 parts of equal length such as epididymal, medial and prostatic portions, then adrenaline, acetylcholine, acetyl-beta-methylcholine, dopamine, histamine and bradykinin induce contractions on each of the 3 parts; whereas tyramine, ephedrine elicit responses in the epididymal and medial portions; amphetamine, DMPP, serotonin and PGF2 alpha in turn provoking contractions exclusively on the epididymal portion. The effects of adrenaline and noradrenaline are blocked by phentolamine and tolazoline; the responses to acetylcholine, acetyl-beta-methylcholine and carbamyl-beta-methylcholine are antagonized by atropine over a specific concentration range. The effects of tyramine, ephedrine and amphetamine are inhibited by phentolamine in an remarkably low dose range (pA2 = 13.51 +/- 0.09; 14.54 +/- 0.31; 14.35 +/- 0.12). The situation was the same when tyramine-dibenamine and tyramine-phenoxybenzamine combinations were tested (pD'2 = 14.03 +/- 0.37; 13.26 +/- 0.03). Based on these findings the presence of a peculiar alpha adrenergic receptor is suggested on the sympathetic postganglionic fibres. In addition to the already identified alpha adrenergic, muscarinic cholinergic and histamine H1 receptors, we could show the presence of dopaminergic receptors too in the vas deferens circular muscle.

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豚鼠输精管环形肌制剂不同部位的药理作用。
豚鼠输精管环形肌的不同节段在药物刺激下表现出不同的反应模式。也就是说,除了氯化钡外,某些激动剂的亲和力和内在活性以及它们诱导的最大收缩强度似乎沿着从附睾到前列腺的路径下降。如果将输精管细分为附睾、内侧和前列腺等长度的3个部分,则肾上腺素、乙酰胆碱、乙酰- β -甲基胆碱、多巴胺、组胺和缓激肽分别在这3个部分引起收缩;而酪胺、麻黄碱在附睾和内侧部分引起反应;安非他明,DMPP, 5 -羟色胺和PGF2 α反过来只在附睾部分引起收缩。肾上腺素和去甲肾上腺素的作用被酚妥拉明和托唑啉阻断;对乙酰胆碱、乙酰- β -甲基胆碱和氨基甲酰- β -甲基胆碱的反应在一定浓度范围内被阿托品拮抗。苯妥拉明在极低剂量范围内抑制酪胺、麻黄碱和安非他明的作用(pA2 = 13.51 +/- 0.09;14.54 +/- 0.31;14.35 +/- 0.12)。酪胺-二苯胺和酪胺-苯氧苄胺联合用药的pD′2 = 14.03 +/- 0.37;13.26 +/- 0.03)。基于这些发现,在交感神经节后纤维上存在一种特殊的α肾上腺素能受体。除了已经确定的α肾上腺素能、毒蕈碱胆碱能和组胺H1受体外,我们还可以在输精管环状肌中发现多巴胺能受体的存在。
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