Kadowaki M, Wade P R, Gershon M D
Department of Anatomy and Cell Biology, College of Physicians and Surgeons, Columbia University, New York 10032, USA.
Am J Physiol. 1996 Nov;271(5 Pt 1):G849-57. doi: 10.1152/ajpgi.1996.271.5.G849.
The roles of 5-hydroxytryptamine3 (5-HT3), 5-HT4, and nicotinic receptors in the peristaltic reflex were investigated in isolated segments of guinea pig distal colon. The reflex assessed by measuring the propulsion of solid pellets, was affected neither by 5-HT3-selective antagonists (ondansetron granisetron) nor by 5-HT4-selective antagonists (SDZ-205-557, GR-113808A, SB-204070) applied individually (1.0 microM); nevertheless, the reflex was inhibited by combining these antagonists or by applying a 5-HT3/5-HT4 dual antagonist (FK-1052). Hexamethonium abolished the peristaltic reflex at 100 microM, but not at 10-32 microM. In contrast, the peristaltic reflex was inhibited when hexamethonium (32 microM was combined with either a 5-HT3- or 5-HT4-selective antagonist (1.0 microM). These observations suggest that 5-HT3, 5-HT4, and nicotinic receptors participate in the initiation and/or propagation of the peristaltic reflex. The data are consistent with the idea that these receptors are arranged in parallel in the neural pathways that mediate the peristaltic reflex in the distal colon.
在豚鼠远端结肠的离体节段中,研究了5-羟色胺3(5-HT3)、5-HT4和烟碱受体在蠕动反射中的作用。通过测量固体小球的推进来评估的反射,单独应用5-HT3选择性拮抗剂(昂丹司琼、格拉司琼)或5-HT4选择性拮抗剂(SDZ-205-557、GR-113808A、SB-204070)(1.0微摩尔)时均不受影响;然而,联合应用这些拮抗剂或应用5-HT3/5-HT4双重拮抗剂(FK-1052)可抑制该反射。六甲铵在100微摩尔时可消除蠕动反射,但在10 - 32微摩尔时则不能。相反,当六甲铵(32微摩尔)与5-HT3或5-HT4选择性拮抗剂(1.0微摩尔)联合应用时,蠕动反射受到抑制。这些观察结果表明,5-HT3、5-HT4和烟碱受体参与蠕动反射的起始和/或传播。这些数据与以下观点一致,即这些受体在介导远端结肠蠕动反射的神经通路中呈平行排列。