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对羟基酪胺和对羟基章鱼胺在大鼠输精管前列腺部的突触前和突触后效应。

Pre- and postsynaptic effects of p-tyramine and p-octopamine in the prostatic portion of the rat vas deferens.

作者信息

Celuch S M, Juorio A V

机构信息

Neuropsychiatric Research Unit, University of Saskatchewan, Saskatoon, Canada.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 Jul;338(1):39-46. doi: 10.1007/BF00168810.

Abstract

The effect of p-tyramine and p-octopamine on the twitch responses of the prostatic portion of the rat vas deferens to electrical stimulation (0.025 Hz) were compared with the effects of noradrenaline. In tissues with normal monoamine oxidase (MAO) activity, the three amines increased the height and duration of the twitch contractions. When MAO activity was inhibited by pargyline (10 mumol/l), p-tyramine and p-octopamine had mixed excitatory-inhibitory effects on the twitches, while noradrenaline had mostly excitatory effects along the whole range of concentrations assayed (0.158-15.8 mumol/l). Selective blockade of alpha 1- and alpha 2-adrenoceptors, by corynanthine and yohimbine, respectively, showed that the excitatory effect of the amines depended on the activation of alpha 1-adrenoceptor and that the inhibitory action was related to the activation of alpha 2-adrenoceptors. Pretreatment with reserpine (5 mg/kg, 24 h; 2.5 mg/kg, 2 h before the experiment) largely prevented the effects of p-tyramine and p-octopamine, but the amines still modified the twitch responses to field stimulation. The addition of corynanthine and yohimbine to the bathing fluid revealed a considerable activation of alpha 1-excitatory and alpha 2-inhibitory adrenoceptors. Cocaine (10 mumol/l) did not antagonize, but rather enhanced the inhibitory effects of p-tyramine and p-octopamine in tissues with normal contents of noradrenaline. Moreover, cocaine did not antagonize the inhibition caused by p-tyramine, and enhanced the inhibition induced by p-octopamine in the prostatic portion of the vasa deferentia from reserpine-pretreated animals. These results suggest that in this tissue, at least when MAO activity is inhibited, p-tyramine and p-octopamine behave similarly.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

将对羟基酪胺和对章鱼胺对大鼠输精管前列腺部对电刺激(0.025赫兹)的抽搐反应的影响与去甲肾上腺素的影响进行了比较。在单胺氧化酶(MAO)活性正常的组织中,这三种胺类增加了抽搐收缩的高度和持续时间。当MAO活性被帕吉林(10微摩尔/升)抑制时,对羟基酪胺和对章鱼胺对抽搐有兴奋 - 抑制混合作用,而去甲肾上腺素在整个测定浓度范围(0.158 - 15.8微摩尔/升)大多具有兴奋作用。分别用育亨宾和柯楠碱选择性阻断α1和α2肾上腺素能受体表明,胺类的兴奋作用取决于α1肾上腺素能受体的激活,而抑制作用与α2肾上腺素能受体的激活有关。用利血平(5毫克/千克,24小时;实验前2小时2.5毫克/千克)预处理在很大程度上阻止了对羟基酪胺和对章鱼胺的作用,但这些胺类仍改变了对场刺激的抽搐反应。向浴液中添加柯楠碱和育亨宾显示α1兴奋和α2抑制性肾上腺素能受体有相当大的激活。可卡因(10微摩尔/升)并未拮抗,而是增强了对羟基酪胺和对章鱼胺在去甲肾上腺素含量正常的组织中的抑制作用。此外,可卡因并未拮抗对羟基酪胺引起的抑制作用,并且增强了利血平预处理动物输精管前列腺部中对章鱼胺诱导的抑制作用。这些结果表明,在该组织中,至少当MAO活性被抑制时,对羟基酪胺和对章鱼胺的行为相似。(摘要截短于250字)

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