Departamento de Fisiología (Fisiología Animal II), Facultad de Biología, Universidad Complutense, Calle José Antonio Nováis 2, 28040, Madrid, Spain.
J Comp Physiol B. 2009 Nov;179(8):951-9. doi: 10.1007/s00360-009-0373-1. Epub 2009 Jun 20.
The present study investigates the possible direct actions of melatonin (N-acetyl-5-methoxytryptamine) on intestinal motility in goldfish (Carassius auratus) using an in vitro system of isolated intestine in an organ bath engaged to an isometric transducer. The longitudinal strips from goldfish intestine in the organ bath showed a resting spontaneous myogenic rhythmic activity which is not altered by melatonin. The addition of acetylcholine (1 nmol l(-1)-10 mmol l(-1)) to the organ bath induces a significant contraction of the intestinal strips in a concentration-dependent manner. The addition of melatonin and its agonist, 2-iodomelatonin, induced a concentration-dependent attenuation of acetylcholine-induced contractile response. The specificity of this effect is tested by the preincubation of the intestine strips in the presence of two melatoninergic antagonists, luzindole (a non-selective MT(1)/MT(2) melatonin receptor antagonist) and 4-P-PDOT (preferred antagonist of MT2 receptor subtype), which counteracted the melatonin-induced relaxation in a concentration-dependent manner. Finally, present results demonstrate that this melatoninergic effect on intestinal strips is a process highly dependent on extracellular calcium. In conclusion, this is the first study demonstrating the role of melatonin in the control of gut motility in a non-mammalian vertebrate. The melatonin effects on isolated intestine from goldfish are mediated by melatoninergic membrane receptors, and could suggest a delay in food transit time, supporting its anorectic effect reported on in vivo studies.
本研究采用离体肠器官浴槽系统,应用等长换能器,研究褪黑素(N-乙酰-5-甲氧基色胺)对金鱼(Carassius auratus)肠道运动的可能直接作用。在器官浴槽中,金鱼肠的纵向条带显示出静止的自发性肌源性节律性活动,褪黑素不会改变这种活动。向器官浴槽中添加乙酰胆碱(1 nmol l(-1)-10 mmol l(-1))会以浓度依赖的方式引起肠条带的显著收缩。褪黑素及其激动剂 2-碘褪黑素的添加会引起乙酰胆碱诱导的收缩反应的浓度依赖性衰减。通过在肠条带存在下预先孵育两种褪黑素能拮抗剂( luzindole(非选择性 MT(1)/MT(2) 褪黑素受体拮抗剂)和 4-P-PDOT(MT2 受体亚型的首选拮抗剂),可以测试这种效应的特异性,这两种拮抗剂以浓度依赖的方式拮抗褪黑素诱导的松弛。最后,目前的结果表明,这种褪黑素对肠条带的作用是一个高度依赖细胞外钙的过程。总之,这是第一项研究表明褪黑素在非哺乳动物脊椎动物肠道运动控制中的作用。褪黑素对金鱼离体肠的作用是通过褪黑素能膜受体介导的,这可能表明食物通过时间延迟,支持其在体内研究中报道的厌食作用。