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镇咳药对臭鼩(家麝鼩)呕吐反射的作用。

Action of anti-tussive drugs on the emetic reflex of Suncus murinus (house musk shrew).

作者信息

Chan Shun-Wan, Rudd John A, Lin Ge, Li Ping

机构信息

Department of Pharmacology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong.

出版信息

Eur J Pharmacol. 2007 Mar 22;559(2-3):196-201. doi: 10.1016/j.ejphar.2006.12.008. Epub 2006 Dec 29.

Abstract

The cough and emetic reflexes involve a synchronized firing of motor neurones involved in respiratory control. Tachykinin NK1 receptor antagonists and 5-HT1A receptor agonists are examples of centrally acting drugs that reduce cough and emesis. In the present studies, therefore, we examined the possibility that other classes of drugs known to reducing cough have anti-emetic properties to prevent emesis induced by diverse challenges. We examined the potential of codeine (1-10 mg/kg), baclofen (1-10 mg/kg), scopolamine (0.3-10 mg/kg), diphenhydramine (1-10 mg/kg), imperialine (1-30 mg/kg) and verticine (0.3-3 mg/kg) to inhibit emesis induced by nicotine (5 mg/kg, s.c.), copper sulphate (120 mg/kg, intragastric), and provocative motion (4 cm horizontal displacement, delivered at 1 Hz) in Suncus murinus (house musk shrew). Only codeine had broad inhibitory properties (P<0.05) to antagonize emesis induced by all challenges with ID50 values ranging from 1.2 to 2.3 mg/kg. Baclofen antagonized emesis induced by nicotine (maximum reduction was 44.9%, P<0.05) and motion (maximum reduction was 97.3%, P<0.01), but potentiated copper sulphate-induced emesis (maximum potentiation was 73.0%, P<0.05). Scopolamine antagonized copper sulphate-induced emesis (maximum reduction was 61.2%, P<0.05) and imperialine antagonized nicotine-induced emesis (maximum reduction was 30.2%, P<0.01), but verticine potentiated motion-induced emesis (maximum potentiation was 60.0%, P<0.05). Diphenhydramine did not significantly reduce emesis induced by any of the challenges (P>0.05). In conclusion, codeine has broad inhibitory anti-emetic actions but a known ability to reduce coughing does not necessarily predict broad inhibitory anti-emetic properties.

摘要

咳嗽和催吐反射涉及参与呼吸控制的运动神经元的同步放电。速激肽NK1受体拮抗剂和5-羟色胺1A受体激动剂是具有中枢作用、可减轻咳嗽和呕吐的药物实例。因此,在本研究中,我们研究了其他已知可减轻咳嗽的药物类别是否具有抗呕吐特性,以预防由多种刺激引起的呕吐。我们研究了可待因(1-10毫克/千克)、巴氯芬(1-10毫克/千克)、东莨菪碱(0.3-10毫克/千克)、苯海拉明(1-10毫克/千克)、浙贝母碱(1-30毫克/千克)和藜芦碱(0.3-3毫克/千克)抑制小家鼠(家麝鼩)中由尼古丁(5毫克/千克,皮下注射)、硫酸铜(120毫克/千克,灌胃)和刺激性运动(4厘米水平位移,以1赫兹频率施加)诱导的呕吐的潜力。只有可待因具有广泛的抑制特性(P<0.05),可拮抗所有刺激诱导的呕吐,半数有效剂量值范围为1.2至2.3毫克/千克。巴氯芬拮抗尼古丁诱导的呕吐(最大减少率为44.9%,P<0.05)和运动诱导的呕吐(最大减少率为97.3%,P<0.01),但增强了硫酸铜诱导的呕吐(最大增强率为73.0%,P<0.05)。东莨菪碱拮抗硫酸铜诱导的呕吐(最大减少率为61.2%,P<0.05),浙贝母碱拮抗尼古丁诱导的呕吐(最大减少率为30.2%,P<0.01),但藜芦碱增强了运动诱导的呕吐(最大增强率为60.0%,P<0.05)。苯海拉明对任何刺激诱导的呕吐均无显著减少作用(P>0.05)。总之,可待因具有广泛的抑制性抗呕吐作用,但已知的减轻咳嗽的能力不一定预示着广泛的抑制性抗呕吐特性。

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