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5-羟色胺4受体激动剂与δ-阿片受体拮抗剂协同作用,刺激结肠推进。

5-HT4 receptor agonists and delta-opioid receptor antagonists act synergistically to stimulate colonic propulsion.

作者信息

Foxx-Orenstein A E, Jin J G, Grider J R

机构信息

Departments of Medicine and Physiology, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia 23298-0551, USA.

出版信息

Am J Physiol. 1998 Nov;275(5):G979-83. doi: 10.1152/ajpgi.1998.275.5.G979.

Abstract

Opioid neurons exert a tonic restraint on inhibitory VIP/PACAP/NOS motoneurons of the enteric nervous system. A decrease in opioid peptide release during the descending phase of the peristaltic reflex, which underlies propulsive activity, leads to an increase in vasoactive intestinal peptide (VIP), pituitary adenylate cyclase-activating polypeptide (PACAP), and nitric oxide (NO) release and circular muscle relaxation. These effects are accentuated by opioid receptor antagonists. Endogenous opioid peptides and selective opioid delta-, kappa- and mu-receptor agonists decreased the velocity of pellet propulsion in isolated segments of guinea pig colon, whereas selective antagonists increased velocity in a concentration-dependent fashion with an order of potency indicating preferential involvement of delta-receptors. 5-HT4 agonists (HTF-919 and R-093877), which also increase the velocity of propulsion, acted synergistically with the delta-receptor antagonist naltrindole; a threshold concentration of naltrindole (10 nM) shifted the concentration-response curve to HTF-919 to the left by 70-fold. A combination of 10 nM naltrindole with threshold concentrations of the 5-HT4 agonists caused significant increases in the velocity of propulsion (50 +/- 7 to 77 +/- 8%). We conclude that 5-HT4 agonists and opioid delta-receptor antagonists act synergistically to facilitate propulsive activity in isolated colonic segments.

摘要

阿片类神经元对肠神经系统中抑制性血管活性肠肽/垂体腺苷酸环化酶激活肽/一氧化氮运动神经元施加持续性抑制作用。在蠕动反射的下降期,阿片肽释放减少,这是推进活动的基础,会导致血管活性肠肽(VIP)、垂体腺苷酸环化酶激活肽(PACAP)和一氧化氮(NO)释放增加以及环形肌松弛。阿片受体拮抗剂会加剧这些效应。内源性阿片肽和选择性阿片δ、κ和μ受体激动剂降低了豚鼠结肠离体段中颗粒推进的速度,而选择性拮抗剂则以浓度依赖性方式增加速度,其效力顺序表明δ受体优先参与其中。5-HT4激动剂(HTF-919和R-093877)也会增加推进速度,它们与δ受体拮抗剂纳曲吲哚协同作用;纳曲吲哚的阈浓度(10 nM)使HTF-919的浓度-反应曲线向左移动70倍。10 nM纳曲吲哚与5-HT4激动剂的阈浓度组合导致推进速度显著增加(从50±7%增加到77±8%)。我们得出结论,5-HT4激动剂和阿片δ受体拮抗剂协同作用以促进离体结肠段的推进活动。

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