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格拉司琼和昂丹司琼:对大鼠回肠制动机制的影响。

Granisetron and ondansetron: effects on the ileal brake mechanism in the rat.

作者信息

Brown N J, Horton A, Rumsey R D, Read N W

机构信息

Department of Biomedical Science, The University, Sheffield, UK.

出版信息

J Pharm Pharmacol. 1993 Jun;45(6):521-4. doi: 10.1111/j.2042-7158.1993.tb05591.x.

Abstract

Studies were carried out on 20 male adult rats to investigate how the action of the selective 5-HT3-receptor antagonists, granisetron and ondansetron, influence gastrointestinal transit under control conditions and when stomach-to-caecum transit was delayed by ileal infusion of lipid. Stomach-to-caecum transit time (SCTT) was measured using environmental hydrogen analysis. Subcutaneous administration of granisetron (BRL 43694, 40, 80 or 150 micrograms kg-1) significantly delayed the passage of the head of the baked bean meal through the stomach and the small intestine under control conditions (P < 0.05). Similarly, subcutaneous administration of ondansetron (GR 38032F, 80 or 150 micrograms kg-1) delayed control SCTT of the head of the meal but this did not reach statistical significance. In contrast, granisetron significantly reversed the delay in SCTT induced by ileal infusion of lipid at 40 (P < 0.001), 80 (P < 0.01) and 150 micrograms kg-1 (P < 0.05). Ondansetron also reversed the lipid-induced delay at 40 (P < 0.01), 80 (P < 0.001) and 150 micrograms kg-1 (P < 0.001). These apparently conflicting results may be rationalized by postulating the presence of 5-HT3 receptors on afferent nerves which, when inhibited by the specific antagonists, initiate reflexes that both accelerate and delay transit.

摘要

对20只成年雄性大鼠进行了研究,以探讨选择性5-羟色胺3(5-HT3)受体拮抗剂格拉司琼和昂丹司琼在对照条件下以及回肠注入脂质导致胃至盲肠转运延迟时,其作用如何影响胃肠转运。采用环境氢气分析法测量胃至盲肠转运时间(SCTT)。在对照条件下,皮下注射格拉司琼(BRL 43694,40、80或150微克/千克)显著延迟了烘豆粕头部通过胃和小肠的时间(P<0.05)。同样,皮下注射昂丹司琼(GR 38032F,80或150微克/千克)延迟了对照条件下豆粕头部的SCTT,但未达到统计学显著性。相比之下,格拉司琼在剂量为40微克/千克(P<0.001)、80微克/千克(P<0.01)和150微克/千克(P<0.05)时,能显著逆转回肠注入脂质引起的SCTT延迟。昂丹司琼在剂量为40微克/千克(P<0.01)、80微克/千克(P<0.001)和150微克/千克(P<0.001)时也能逆转脂质引起的延迟。通过假设传入神经上存在5-HT3受体,这些明显相互矛盾的结果可能会得到合理的解释,即当被特异性拮抗剂抑制时,这些受体会引发加速和延迟转运的反射。

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