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5-羟色胺受体在右芬氟拉明对胃排空及摄食行为的影响中所起的作用(跑道试验研究)

Role of 5-HT receptors in the effect of d-fenfluramine on gastric emptying and feeding behaviour as examined in the runway test.

作者信息

Samanin R, Neill J C, Grignaschi G, Padura I M, Bizzi A, Garattini S

机构信息

Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

Eur J Pharmacol. 1991 May 2;197(1):69-73. doi: 10.1016/0014-2999(91)90366-x.

Abstract

In one experiment, the effect of d-fenfluramine (DF) on gastric emptying was studied in rats treated i.p. with metergoline, a non-selective serotonin (5-HT) receptor antagonist, ritanserin, a selective 5-HT2 and 5-HT1C receptor antagonist, and xylamidine, a 5-HT antagonist which has poor access to the brain. Metergoline (1 mg/kg) but not ritanserin (0.5 mg/kg) or xylamidine (3 mg/kg) blocked the effect of 2.5 mg/kg DF studied 2 and 4 h after injection. In a second experiment, we studied the ability of metergoline to antagonise the effect of DF, administered after a meal, on runway performance, food intake and gastric emptying assessed 4 h later. Metergoline at a dose of 1 mg/kg did not antagonise the effect of DF (2.5 mg/kg) on runway performance but completely blocked the effect on gastric emptying. The data clearly show that DF delays gastric emptying by indirectly activating 5-HT1 receptors; this effect is not important for the ability of DF to reduce runway performance and food intake when the drug is injected after a pre-feeding period. While there is evidence that DF hastens the termination of the meal by a 5-HT mechanism, the data suggest that DF may prolong the satiating effect of food during the post-absorptive phase by mechanisms other than 5-HT.

摘要

在一项实验中,研究了右旋芬氟拉明(DF)对经腹腔注射以下药物的大鼠胃排空的影响:美替拉酮,一种非选择性5-羟色胺(5-HT)受体拮抗剂;利坦色林,一种选择性5-HT2和5-HT1C受体拮抗剂;以及赛拉米定,一种难以进入大脑的5-HT拮抗剂。美替拉酮(1毫克/千克)可阻断注射2小时和4小时后2.5毫克/千克DF的作用,但利坦色林(0.5毫克/千克)或赛拉米定(3毫克/千克)则不能。在第二项实验中,我们研究了美替拉酮拮抗进食后给予的DF对跑道行为、食物摄入量以及4小时后评估的胃排空的影响的能力。1毫克/千克剂量的美替拉酮不能拮抗DF(2.5毫克/千克)对跑道行为的影响,但完全阻断了对胃排空的影响。数据清楚地表明,DF通过间接激活5-HT1受体来延迟胃排空;当在进食前给药后注射该药物时,这种作用对于DF降低跑道行为和食物摄入量的能力并不重要。虽然有证据表明DF通过5-HT机制加速进食的终止,但数据表明DF可能通过5-HT以外的机制在吸收后阶段延长食物的饱腹感作用。

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