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通过在豚鼠空肠黏膜应用营养性氨基酸激发的局部抑制反射。

Local inhibitory reflexes excited by mucosal application of nutrient amino acids in guinea pig jejunum.

作者信息

Gwynne R M, Bornstein J C

机构信息

Dept. of Physiology, Univ. of Melbourne, Parkville, Victoria 3010, Australia.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2007 Jun;292(6):G1660-70. doi: 10.1152/ajpgi.00580.2006. Epub 2007 Mar 8.

Abstract

The motility of the gut depends on the chemicals contained in the lumen, but the stimuli that modify motility and their relationship to enteric neural pathways are unclear. This study examined local inhibitory reflexes activated by various chemical stimulants applied to the mucosa to characterize effective physiological stimuli and the pathways they excite. Segments of the jejunum were dissected to allow access to the circular muscle on one-half of the preparation while leaving the mucosa intact on the circumferentially adjacent half. Chemicals were transiently applied to the mucosa, and responses were recorded intracellularly in nearby circular muscle cells. The amino acids l-phenylalanine, l-alanine, or l-tryptophan (all 1 mM) evoked inhibitory junction potentials (IJPs; latency 150-300 ms, amplitude 3-8 mV, each n > 6) that were blocked by TTX and partially blocked by antagonists of P2X receptors and/or a combination of antagonists at 5-HT(3) and 5-HT(4) receptors. The putative mediators 5-HT (10 microM), ATP (1 mM), and CCK-8 (1-10 microM) elicited IJPs mediated via 5-HT(3), P2X, and CCK-B receptors, respectively. Responses were only partially reduced by the effective antagonists. IJPs evoked by electrically stimulating the mucosa were unaffected by antagonists that reduced chemically evoked responses. Both chemically and electrically evoked IJPs were resistant to nicotinic, NK(1), NK(3), alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid, N-methyl-d-aspartate, or CGRP receptor blockade. We conclude that mucosal stimulation by amino acids activates local neural pathways whose pharmacology depends on the nature of the stimulus. Transmitters involved at some synapses in these pathways remain to be identified.

摘要

肠道的蠕动取决于肠腔内所含的化学物质,但改变蠕动的刺激因素及其与肠神经通路的关系尚不清楚。本研究检测了应用于黏膜的各种化学刺激剂激活的局部抑制反射,以确定有效的生理刺激及其激发的通路。解剖空肠段,使制剂的一半能够接触到环行肌,而在圆周相邻的另一半保持黏膜完整。将化学物质短暂应用于黏膜,并在附近的环行肌细胞内记录反应。氨基酸L-苯丙氨酸、L-丙氨酸或L-色氨酸(均为1 mM)诱发抑制性接头电位(IJPs;潜伏期150 - 300 ms,幅度3 - 8 mV,每组n > 6),这些电位被TTX阻断,并被P2X受体拮抗剂和/或5-HT(3)和5-HT(4)受体拮抗剂组合部分阻断。推测的介质5-HT(10 μM)、ATP(1 mM)和CCK-8(1 - 10 μM)分别通过5-HT(3)、P2X和CCK-B受体诱发IJPs。有效拮抗剂仅使反应部分降低。电刺激黏膜诱发的IJPs不受降低化学诱发反应的拮抗剂影响。化学和电诱发的IJPs对烟碱、NK(1)、NK(3)、α-氨基-3-羟基-5-甲基异恶唑-4-丙酸、N-甲基-D-天冬氨酸或CGRP受体阻断均有抗性。我们得出结论,氨基酸对黏膜的刺激激活了局部神经通路,其药理学特性取决于刺激的性质。这些通路中某些突触所涉及的递质仍有待确定。

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