fedotozine对人远端结肠的影响。

M Adami, G Bertaccini, L Roncoroni, F Cobianchi
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引用次数: 0

摘要

从患有不同结肠疾病的患者手术中取出的结肠条中含有Fedotozine;并与吗啡和选择性阿片激动剂U-69593进行了比较。Fedotozine不影响人结肠条带的自发运动,除非使用非常高的浓度。Fedotozine (10(-6)-3 x 10(-4) M)诱导了场刺激引起的兴奋效应的浓度依赖性降低,这一作用部分被化合物U-69593和吗啡所模拟,但不被纳洛酮所抑制。fedotozine (3 × 10(-4) M)抑制了外源性乙酰胆碱的累积剂量-反应曲线,而吗啡在3 × 10(-4) M以下没有作用。在与[3H]-胆碱孵育的结肠条中,fedotozine (10(-5)-10(-4) M)诱导电刺激引起的乙酰胆碱释放不稳定下降。在我们的实验模型中,fedotozine的抑制作用似乎与阿片受体的激活无关。
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Effect of fedotozine on human distal colon.

Fedotozine was rested in colonic strips removed during surgery from patients suffering from different diseases of the colon; the effects were compared to those of morphine and of the selective opiate agonist U-69593. Fedotozine did not affect the spontaneous motility of human colonic strips, unless very high concentrations were used. Fedotozine (10(-6)-3 x 10(-4) M) induced a concentration-dependent reduction of the excitatory effect induced by field stimulation, an effect which was partially mimicked by compound U-69593 and by morphine but not inhibited by naloxone. The cumulative dose-response curve to exogenous acetylcholine was inhibited by fedotozine (3 x 10(-4) M), whereas morphine had no effect up to 3 x 10(-4) M. In colonic strips incubated with [3H]-choline, fedotozine (10(-5)-10(-4) M) induced an erratic decrease of acetylcholine-release induced by electric stimulation. In our experimental model, the inhibitory effect of fedotozine does not seem to be related to opioid receptor activation.

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