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5-羟色胺3型和5-羟色胺4型受体在豚鼠小肠环形肌的升、降反射中的作用研究。

Investigation of the role of 5-HT3 and 5-HT4 receptors in ascending and descending reflexes to the circular muscle of guinea-pig small intestine.

作者信息

Yuan S Y, Bornstein J C, Furness J B

机构信息

Department of Physiology, University of Melbourne, Parkville, Vic., Australia.

出版信息

Br J Pharmacol. 1994 Aug;112(4):1095-100. doi: 10.1111/j.1476-5381.1994.tb13196.x.

Abstract
  1. The present study was undertaken to ascertain whether 5-hydroxytryptamine (5-HT) acting at either 5-HT3 or 5-HT4 receptors plays a significant role in motility reflexes in the guinea-pig small intestine. 2. An isolated segment of small intestine was opened along its mesenteric border and pinned, mucosa uppermost, in a three chambered organ bath so that the oral, middle and anal regions of a single preparation could be separately superfused. 3. Conventional intracellular recording methods were used to monitor the responses of the circular muscle in the oral or the anal end chambers when distension was applied in either of the other two chambers or the mucosal villi were compressed in the middle chamber. Drugs were added to the middle chamber. 4. 5-HT3 receptor antagonists (tropisetron, 0.1-10 microM; granisetron, 1 microM and BRL 46470, 1 microM) depressed the ascending excitatory reflex evoked by these stimuli but had no effect on the descending inhibitory reflex. The depression of the excitatory reflex was observed whether the reflex was evoked from the chamber containing the drug or was simply conducted, via interneurones, through this chamber. 5. The 5-HT4 receptor antagonist, SDZ 205-557 (1 microM), had no significant effect on either the ascending or descending reflex pathways. However, 5-HT4 receptors were present as cisapride (0.1 microM) significantly enhanced the ascending excitation without affecting the descending inhibition. This effect of cisapride was converted to a significant depression of the ascending reflex by SDZ 205-557. 6. The results suggest that 5-HT3, but not 5-HT4, receptors play an important role in the ascending excitatory reflex and that these receptors may be on interneurones in the reflex pathway.
摘要
  1. 本研究旨在确定作用于5-羟色胺(5-HT)3型或5-HT4型受体的5-羟色胺在豚鼠小肠运动反射中是否起重要作用。2. 将一段分离的小肠沿肠系膜缘打开并固定,黏膜面朝上,置于三室器官浴槽中,以便对单个标本的口腔、中间和肛门区域分别进行灌流。3. 采用传统的细胞内记录方法,当在另外两个腔室中的任何一个施加扩张刺激或在中间腔室压缩黏膜绒毛时,监测口腔或肛门端腔室中环行肌的反应。药物添加到中间腔室。4. 5-HT3型受体拮抗剂(托烷司琼,0.1 - 10微摩尔;格拉司琼,1微摩尔;BRL 46470,1微摩尔)可抑制由这些刺激诱发的上行兴奋性反射,但对下行抑制性反射无影响。无论该反射是在含有药物的腔室诱发还是仅通过中间神经元传导通过该腔室,均观察到兴奋性反射受到抑制。5. 5-HT4型受体拮抗剂SDZ 205 - 557(1微摩尔)对上行或下行反射通路均无显著影响。然而,5-HT4型受体存在,因为西沙必利(0.1微摩尔)可显著增强上行兴奋性而不影响下行抑制性。西沙必利的这种作用被SDZ 205 - 557转变为对上行反射的显著抑制。6. 结果表明,5-HT3型而非5-HT4型受体在上行兴奋性反射中起重要作用,且这些受体可能位于反射通路中的中间神经元上。

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