Takaki M, Mizutani M, Nakayama S
Department of Physiology, Okayama University Medical School, Japan.
Arch Int Pharmacodyn Ther. 1988 Jan-Feb;291:132-41.
The mechanism of the contractile action of tryptamine on the longitudinal smooth muscle with adherent myenteric plexus in the guinea-pig ileum was reexamined in view of new evidence that tryptamine releases the enteric neural serotonin (5-HT) and noradrenaline. The desensitization to 5-HT abolished the contractile response to tryptamine (5 and 10 microM). The contractile response to tryptamine (1-5 microM) was progressively decreased by repeated application. The progressive decrease by tryptamine was more pronounced than that by exogenous 5-HT. Tetrodotoxin and atropine significantly decreased the contraction upon the 2nd trial of tryptamine (5 microM) by about 40% and 45% of the control, respectively. However, guanethidine or cocaine did not change the contraction by tryptamine (5 microM). A 5-HT uptake inhibitor, zimelidine, which had been demonstrated to block the release of preloaded [3H]5-HT by tryptamine (Takaki et al., 1985), intensively reduced the contractile response to tryptamine to the same extent as atropine. These results are consistent with the previous finding that tryptamine releases the physiologically active 5-HT from myenteric neurons (Takaki et al., 1985). The 5-HT released by tryptamine, at least in part, acts on myenteric cholinergic neurons, resulting in the muscular contraction.
鉴于色胺可释放肠神经5-羟色胺(5-HT)和去甲肾上腺素这一新证据,我们重新研究了色胺对豚鼠回肠带附着肌间神经丛的纵行平滑肌的收缩作用机制。对5-HT脱敏消除了对色胺(5和10微摩尔)的收缩反应。重复应用后,对色胺(1 - 5微摩尔)的收缩反应逐渐降低。色胺引起的逐渐降低比外源性5-HT更明显。河豚毒素和阿托品分别使色胺(5微摩尔)第二次试验时的收缩幅度显著降低约40%和45%。然而,胍乙啶或可卡因并未改变色胺(5微摩尔)引起的收缩。一种5-HT摄取抑制剂齐美利定,已被证明可阻断色胺释放预加载的[3H]5-HT(高木等人,1985年),它对色胺收缩反应的降低程度与阿托品相同。这些结果与先前的发现一致,即色胺从肌间神经元释放生理活性5-HT(高木等人,1985年)。色胺释放的5-HT至少部分作用于肌间胆碱能神经元,导致肌肉收缩。