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用于大鼠肠道吸收和分泌实验的麻醉剂选择。

Choice of anesthetic for intestinal absorption and secretion experiments using rats.

作者信息

Coupar I M

出版信息

J Pharmacol Methods. 1985 Jul;13(4):331-8. doi: 10.1016/0160-5402(85)90015-4.

Abstract

The net rates of glucose and water absorption from, and secretion of water into, the lumen of the rat small intestine were compared using alpha-chloralose, halothane, pentobarbitone, and urethane as anesthetics. Water and glucose transport were determined by recirculation of perfusion fluid through the lumen of the jejunum. Net fluid secretion was stimulated by intraarterial (i.a.) infusion of prostaglandin E1 (PGE1) and vasoactive intestinal peptide (VIP). The results show that the anesthetics used exert only minimal influence on the physiological rates of glucose and water absorption and there is no correlation between the small differences in glucose and water absorption among the anesthetics. However, when the fluid secretory mechanism of the mucosa is stimulated with either PGE1 or VIP, pentobarbitone allows the greatest rates of secretion, but halothane prevents secretion. It is suggested that of the anesthetics used, pentobarbitone is the most appropriate for intestinal secretion experiments.

摘要

使用α-氯醛糖、氟烷、戊巴比妥和氨基甲酸乙酯作为麻醉剂,比较了大鼠小肠肠腔中葡萄糖和水的净吸收速率以及水向肠腔的分泌速率。通过使灌注液在空肠肠腔内循环来测定水和葡萄糖的转运。通过动脉内(i.a.)输注前列腺素E1(PGE1)和血管活性肠肽(VIP)刺激净液体分泌。结果表明,所用麻醉剂对葡萄糖和水的生理吸收速率仅产生极小的影响,且麻醉剂之间葡萄糖和水吸收的微小差异之间不存在相关性。然而,当用PGE1或VIP刺激黏膜的液体分泌机制时,戊巴比妥允许最大的分泌速率,但氟烷可阻止分泌。建议在所使用的麻醉剂中,戊巴比妥最适合用于肠道分泌实验。

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