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多巴胺对大鼠输精管神经传递的抑制作用。

Inhibition by dopamine of the neurotransmission in the rat vas deferens.

作者信息

Dopico A M, Fiszman M L, Stefano F J

出版信息

Acta Physiol Pharmacol Latinoam. 1986;36(3):257-64.

PMID:3033993
Abstract

The effects of alpha-adrenoceptor and dopaminoceptor agonists and antagonists were investigated on presynaptic receptors in the prostatic portion of rat vas deferens. The variable studied was the early component (250 msec) of the motor response elicited by field stimulation (single pulses). All the experiments were carried out in the presence of cocaine 30 mumol/l and hydrocortisone 28 mumol/l so as to block the sites of amines loss and 1-propranolol 0.3 mumol/l to block beta-adrenoceptors. Clonidine, noradrenaline (NA) and dopamine (DA) inhibited the motor response in a concentration-dependent manner. DA was 10 and 10(4) times less potent than NA and clonidine respectively. The selective D2 agonist, LY 141865, failed to inhibit the motor response even at a high concentration (30 mumol/l). Yohimbine (0.1, 0.3 and 1 mumol/l) antagonized competitively the effect of clonidine, NA and DA showing similar - log KB values (7.57; 7.68 and 7.09 respectively). Likewise, idaxozan (0.03 mumol/l) blocked the inhibitory effect of DA in the same order of potency (- log KB = 7.81). On the other hand, pimozide 0.21 mumol/l and Schering 23390 3 mumol/l antagonized the inhibitory effect of DA, showing a lower potency than the other antagonists. Taken together, these findings do not support the hypothesis that DA activates a specific population of prejunctional dopaminoceptors to inhibit the motor response elicited by field stimulation in the presence of cocaine, hydrocortisone and 1-propranolol in the prostatic portion of the rat vas deferens. Instead, the population of prejunctional alpha 2-adrenoceptor may be involved.

摘要

研究了α-肾上腺素能受体和多巴胺受体激动剂及拮抗剂对大鼠输精管前列腺部突触前受体的作用。所研究的变量是场刺激(单脉冲)引发的运动反应的早期成分(250毫秒)。所有实验均在30μmol/L可卡因和28μmol/L氢化可的松存在的情况下进行,以阻断胺类丢失位点,并在0.3μmol/L 1-普萘洛尔存在的情况下进行,以阻断β-肾上腺素能受体。可乐定、去甲肾上腺素(NA)和多巴胺(DA)以浓度依赖性方式抑制运动反应。DA的效力分别比NA和可乐定低10倍和10⁴倍。选择性D₂激动剂LY 141865即使在高浓度(30μmol/L)下也未能抑制运动反应。育亨宾(0.1、0.3和1μmol/L)竞争性拮抗可乐定、NA和DA的作用,显示出相似的-log KB值(分别为7.57;7.68和7.09)。同样,伊达唑胺(0.03μmol/L)以相同的效力顺序阻断DA的抑制作用(-log KB = 7.81)。另一方面,0.21μmol/L匹莫齐特和3μmol/L先灵葆雅23390拮抗DA的抑制作用,其效力低于其他拮抗剂。综上所述,这些发现不支持以下假设:在大鼠输精管前列腺部存在可卡因、氢化可的松和1-普萘洛尔的情况下,DA激活特定群体的突触前多巴胺受体以抑制场刺激引发的运动反应。相反,突触前α₂-肾上腺素能受体群体可能参与其中。

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