氟西汀对离体大鼠小肠电场刺激反应的影响。

F Farajian-Mashhadi, R J Naylor, F A Javid
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引用次数: 1

摘要

研究了血清素再摄取抑制剂氟西汀在离体大鼠小肠中的作用。电场刺激(EFS)在1.0 ~ 10.0 μM范围内对河豚毒素和氟西汀敏感,可触发松弛和/或收缩反应。氟西汀(1.0 μM)对0.1 mM六甲基铵处理后的组织产生10.0 Hz的松弛反应,同时降低了EFS收缩反应的衰减。在PCPA预处理的大鼠空肠和回肠中,1.0 μM氟西汀诱导了更大的电场弛豫反应,并显著减弱了十二指肠的电场收缩反应(10.0 Hz)。在另一项实验中,瑞波西汀(1.0-10.0 μM)是一种去肾上腺素能再摄取抑制剂,在10.0 Hz时,在大多数区域使用瑞波西汀可以减少收缩,增加弛豫反应。在六甲铵(0.1 mM)存在的情况下,10.0 μM的瑞波西汀在10.0 Hz的频率下降低了对EFS的收缩响应,同时增强了对EFS的松弛响应。数据表明,氟西汀的作用似乎与选定的肠道区域有关,并可能有助于更好地了解与氟西汀临床使用相关的回肠活动和胃肠道不适有关的血清素能和胆碱能递质机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of fluoxetine on electrical field stimulation-induced responses in the isolated rat small intestine.

The effects of fluoxetine, a serotonin reuptake inhibitor, were studied in the isolated rat small intestine. Electrical field stimulation (EFS) triggered relaxant and/or contractile responses that were sensitive to tetrodotoxin and fluoxetine at 1.0-10.0 μM. In 0.1 mM hexamethonium-treated tissues, fluoxetine (1.0 μM) induced a relaxant response at 10.0 Hz, while it decreased the attenuation of the contractile responses to EFS. In PCPA pretreated rat jejunum and ileum, 1.0 μM of fluoxetine induced a greater relaxation response to EFS and significantly attenuated the contractile responses to EFS (10.0 Hz) in the duodenum. In a separate experiment, the application of reboxetine (1.0-10.0 μM), a noradrenergic reuptake inhibitor, reduced the contraction and increased the relaxation responses to EFS at 10.0 Hz in most regions. In the presence of hexamethonium (0.1 mM) the application of 10.0 μM reboxetine reduced contractile responses to ESF while enhancing the relaxant responses to EFS at 10.0 Hz. The data suggest that the effects of fluoxetine appear to be related to the selected region of the intestine and may contribute to a better understanding of the serotonergic and cholinergic transmitter mechanisms involved in ileal activity and the gastrointestinal discomfort associated with the clinical use of fluoxetine.

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