Gulati O D, Hemavathi K G, Joshi D P
J Auton Pharmacol. 1985 Mar;5(1):19-23. doi: 10.1111/j.1474-8673.1985.tb00561.x.
The effects of levamisole on responses to various agonists were studied in guinea-pig vas deferens. Levamisole did not itself exhibit any contractile or relaxant effect on guinea-pig vas deferens but in the presence of levamisole the concentration-response curve of noradrenaline (NA) was shifted to the left and the maximal response was increased. Responses to field-stimulation at 5 and 10 Hz were potentiated by levamisole. Cocaine and denervation caused potentiation of NA responses and these enhanced responses remained unchanged in the presence of levamisole. Acetylcholine (ACh) responses were potentiated by levamisole whereas responses to histamine, KCl and methoxamine remained unaltered. These results suggest that levamisole does not have any action at postsynaptic alpha-adrenoreceptors. The increased responses to NA and ACh in the presence of levamisole may be due to its uptake1, blocking and anticholinesterase activities respectively.
在豚鼠输精管中研究了左旋咪唑对各种激动剂反应的影响。左旋咪唑本身对豚鼠输精管未表现出任何收缩或舒张作用,但在有左旋咪唑存在时,去甲肾上腺素(NA)的浓度-反应曲线向左移动,最大反应增强。左旋咪唑增强了5Hz和10Hz场刺激的反应。可卡因和去神经支配使NA反应增强,且在左旋咪唑存在时这些增强的反应保持不变。左旋咪唑增强了乙酰胆碱(ACh)的反应,而对组胺、氯化钾和甲氧明的反应保持不变。这些结果表明,左旋咪唑在突触后α-肾上腺素受体处没有任何作用。在左旋咪唑存在下对NA和ACh反应的增强可能分别归因于其摄取1、阻断和抗胆碱酯酶活性。