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5-羟色胺3和5-羟色胺4受体激动剂对绵羊皱胃的运动调节特性

Motor-modifying properties of 5-HT3 and 5-HT4 receptor agonists on ovine abomasum.

作者信息

Brikas P

机构信息

Laboratory of Physiology, Veterinary Faculty, Aristotelian University, Thessaloniki, Greece.

出版信息

Zentralbl Veterinarmed A. 1994 Mar;41(2):150-8. doi: 10.1111/j.1439-0442.1994.tb00078.x.

Abstract

The effects and sites of action of 5-HT3 and 5-HT4 receptor agonists and antagonists on the abomasal myoelectric activity were examined in conscious sheep, chronically fitted with intravenous (i.v.) and intracerebroventricular (ICV) cannulas and intraparietal electrodes on the gastric body and antrum. The 5-HT3 receptor agonist 2-methylserotonin, injected either i.v. (150 micrograms/kg) or ICV (5 micrograms/kg), induced an inhibition of the spiking activity in both the gastric body and antrum. This inhibition was abolished when the 5-HT3 antagonist granisetron was preinjected either i.v. (150 micrograms/kg) or ICV (15 micrograms/kg). The i.v. injection of 5-HT4 agonist 5-methoxytryptamine (200 micrograms/kg) initially provoked stimulation and thereafter inhibition of abomasal activity, while its ICV administration (10 micrograms/kg) resulted in only inhibition of the gastric body activity. BIMU 1, another 5-HT4 agonistic substance, injected i.v. (300-1000 micrograms/kg), mimicked only the stimulatory actions of 5-methoxytryptamine, while its ICV administration (10-50 micrograms/kg) had no effect on the abomasal activity. The i.v. (2000 micrograms/kg), but not the ICV (100 micrograms/kg), pre-injection of the 5-HT4 antagonist DAU 6285 blocked the stimulation of the abomasal spiking activity resulting from the i.v. injection of either 5-methoxytryptamine or BIMU 1. These results suggest that, in sheep, inhibitory 5-HT3 and excitatory 5-HT4 receptors, located at brain and peripheral levels respectively, participate in the control of the abomasal contractions.

摘要

在清醒的绵羊身上,研究了5-羟色胺3(5-HT3)和5-羟色胺4(5-HT4)受体激动剂及拮抗剂对皱胃肌电活动的影响和作用部位。这些绵羊长期植入静脉(i.v.)和脑室内(ICV)插管,并在胃体和胃窦处植入壁内电极。静脉注射(150微克/千克)或脑室内注射(5微克/千克)5-HT3受体激动剂2-甲基5-羟色胺,均可抑制胃体和胃窦的锋电位活动。预先静脉注射(150微克/千克)或脑室内注射(15微克/千克)5-HT3拮抗剂格拉司琼后,这种抑制作用消失。静脉注射5-HT4激动剂5-甲氧基色胺(200微克/千克)最初可刺激皱胃活动,随后抑制其活动,而脑室内注射(10微克/千克)则仅抑制胃体活动。另一种5-HT4激动剂BIMU 1静脉注射(300 - 1000微克/千克)时,仅模拟5-甲氧基色胺的刺激作用,而脑室内注射(10 - 50微克/千克)对皱胃活动无影响。静脉注射(2000微克/千克)而非脑室内注射(100微克/千克)5-HT4拮抗剂DAU 6285,可阻断静脉注射5-甲氧基色胺或BIMU 1所引起的皱胃锋电位活动的刺激。这些结果表明,在绵羊中,分别位于脑和外周水平的抑制性5-HT3受体和兴奋性5-HT4受体参与了皱胃收缩的控制。

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