Chan H C, Lui K M, Wong W S, Poon A M
Department of Physiology, The Chinese University of Hong Kong, Shatin.
Life Sci. 1998;62(23):2151-8. doi: 10.1016/s0024-3205(98)00190-8.
The effect of melatonin on human colonic T84 cells was studied using the short-circuit current (I(SC)) technique. Basolateral, as well as apical, addition of melatonin stimulated I(SC) in a concentration-dependent manner (EC50 at about 100 microM). The I(SC) response to melatonin was nearly abolished when external Cl- was removed. The increase in I(SC) was also blocked by apical addition of two Cl- channel blockers, 4,4'-diisothiocyanatostibene-2,2'-disulfonic acid (DIDS) and diphenylamine-2-carboxylic acid (DPC), indicating that melatonin stimulated Cl- secretion. The effect of different melatonin analogs was compared and the order of potency appeared to be 2-iodomelatonin > melatonin > 6-hydroxymelatonin, indicating the involvement of melatonin receptors. However, inhibitors for Gi-protein, adenylate cyclase or phospholipase C were found to be ineffective in inhibiting the melatonin-induced I(SC). Pretreatment of the cells with melatonin was also found to exert little effect on subsequent forskolin- or VIP-induced I(SC), further excluding its interaction with adenylate cyclase. Our data suggest that melatonin may play a role in regulating colonic Cl- secretion via melatonin receptors; however, the signal transduction pathway(s) involved remains to be elucidated.
采用短路电流(I(SC))技术研究了褪黑素对人结肠T84细胞的作用。从基底外侧以及顶端加入褪黑素均以浓度依赖的方式刺激I(SC)(半数有效浓度约为100微摩尔)。去除细胞外氯离子后,褪黑素引起的I(SC)反应几乎完全消失。顶端加入两种氯离子通道阻滞剂4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)和二苯胺-2-羧酸(DPC)也可阻断I(SC)的增加,这表明褪黑素刺激了氯离子分泌。比较了不同褪黑素类似物的作用效果,其效力顺序似乎为2-碘褪黑素>褪黑素>6-羟基褪黑素,提示褪黑素受体参与其中。然而,发现Gi蛋白、腺苷酸环化酶或磷脂酶C的抑制剂对抑制褪黑素诱导的I(SC)无效。还发现用褪黑素预处理细胞对随后的福斯可林或血管活性肠肽诱导的I(SC)几乎没有影响,这进一步排除了其与腺苷酸环化酶的相互作用。我们的数据表明,褪黑素可能通过褪黑素受体在调节结肠氯离子分泌中发挥作用;然而,所涉及的信号转导途径仍有待阐明。