Kaschube M, Brasch H
Department of Pharmacology, Medical University Lübeck, F.R.G.
Eur J Pharmacol. 1990 Mar 20;178(2):151-9. doi: 10.1016/0014-2999(90)90470-q.
The influence of N-ethylmaleimide (NEM) on contractions due to exogenously applied noradrenaline and bethanechol and on the inhibitory effects of clonidine, of the enkephalin derivative, FK 33-824, and 2-chloroadenosine (2-CLA) on field stimulation-response curves and [3H]noradrenaline [( 3H]NA) release was studied in the isolated mouse vas deferens. Exposure to NEM (60 microM: 10 min) caused a 30% reduction of the maximal contraction due to NA but nearly abolished the response to bethanechol. NEM partially reversed the depression of the pulse width-response curves by clonidine and FK 33-824 but was without effect with 2-CLA. The contractions evoked by stimulation frequencies above 20 Hz were depressed by NEM both in presence and absence of the agonists. NEM diminished the inhibition of the stimulation-evoked release of [3H]NA by the three agonists. The prejunctional effect of NEM was markedly influenced by the stimulation parameters. These findings support the suggestion that the inhibition mediated by alpha 2-adrenoceptors, mu- and P1-receptors in the mouse vas deferens is NEM-sensitive and possibly transmitted by a pertussis toxin-sensitive G-protein.
在离体小鼠输精管中,研究了N - 乙基马来酰亚胺(NEM)对外源性应用去甲肾上腺素和氨甲酰甲胆碱引起的收缩以及可乐定、脑啡肽衍生物FK 33 - 824和2 - 氯腺苷(2 - CLA)对场刺激 - 反应曲线和[3H]去甲肾上腺素([3H]NA)释放的抑制作用的影响。暴露于NEM(60 microM,10分钟)导致NA引起的最大收缩降低30%,但几乎消除了对氨甲酰甲胆碱的反应。NEM部分逆转了可乐定和FK 33 - 824对脉冲宽度 - 反应曲线的抑制作用,但对2 - CLA无效。在有和没有激动剂的情况下,NEM均抑制了高于20 Hz刺激频率引起的收缩。NEM减弱了三种激动剂对刺激诱发的[3H]NA释放的抑制作用。NEM的突触前效应受刺激参数的显著影响。这些发现支持以下观点,即小鼠输精管中由α2 - 肾上腺素能受体、μ - 和P1 - 受体介导的抑制作用对NEM敏感,并且可能由百日咳毒素敏感的G蛋白传递。