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Serotonin and cholecystokinin activate different populations of rat mesenteric vagal afferents.

机译:5-羟色胺和胆囊收缩素激活大鼠肠系膜迷走神经传入的不同群体。

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摘要

This electrophysiological study was performed to elucidate the interactions of serotonin (5-hydroxytryptamine, 5-HT) and cholecystokinin (CCK) on mesenteric afferents supplying the rat jejunum. 5-HT and CCK produced characteristic responses in multi-unit recordings of mesenteric afferents. Waveform analysis to extract single units from the whole nerve recording identified populations of single afferents that were sensitive to either 5-HT or CCK, but not both. Furthermore, devazepide (0.5 mg/kg) completely abolished the response to CCK without altering the response to 5-HT while granisetron (0.5 mg/kg) abolished the response to 5-HT with no effect on the response to CCK. These results suggest that there are discrete, noninteractive populations of jejunal afferents that possess either 5-HT3 or CCK-A receptors but not both.
机译:进行这项电生理研究是为了阐明5-羟色胺(5-羟色胺,5-HT)和胆囊收缩素(CCK)在供应大鼠空肠的肠系膜传入细胞上的相互作用。 5-HT和CCK在肠系膜传入的多单位记录中产生了特征响应。从整个神经记录中提取单个单位的波形分析确定了对5-HT或CCK敏感但对两者都不敏感的单个传入群体。此外,devazepide(0.5 mg / kg)完全消除了对CCK的响应,而没有改变对5-HT的响应,而granisetron(0.5 mg / kg)消除了对5-HT的响应,对CCK的响应没有影响。这些结果表明存在离散的,非交互性的空肠传入群体,它们具有5-HT3或CCK-A受体,但不能同时具有两者。

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