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育亨宾碱具有抑制作用,而咪唑克生具有增强作用,二者对哇巴因的心脏毒性作用存在影响。

Corynanthine inhibits, while idazoxan potentiates, cardiotoxic effects of ouabain.

作者信息

Thomas G P

机构信息

Department of Pharmacology, IDPL Research Centre, Hyderabad, India.

出版信息

J Auton Pharmacol. 1995 Apr;15(2):85-91. doi: 10.1111/j.1474-8673.1995.tb00294.x.

Abstract
  1. Ouabain, infused intravenously to anaesthetized guinea-pigs induced ventricular premature beats, ventricular tachyarrhythmias and lethality. 2. Corynanthine (1, 2 and 4 mg kg-1), an alpha 1-adrenoceptor antagonist and idazoxan (100, 200 and 400 micrograms kg-1), an alpha 2-adrenoceptor antagonist were administered 10 min prior to ouabain. Corynanthine (2 and 4 micrograms kg-1) showed significant increase in the amount of ouabain required to cause arrhythmia and lethality, whereas idazoxan (200 and 400 micrograms kg-1) decreased it. 3. Corynanthine inhibited the ouabain-induced pressor response while idazoxan potentiated it. 4. Effects of these agents on the sympathetic nervous system appear to have played a significant role in its anti- and proarrhythmic actions.
摘要
  1. 向麻醉的豚鼠静脉注射哇巴因可诱发室性早搏、室性心律失常和致死性。2. 在注射哇巴因前10分钟给予α1肾上腺素能受体拮抗剂育亨宾(1、2和4毫克/千克)和α2肾上腺素能受体拮抗剂咪唑克生(100、200和400微克/千克)。育亨宾(2和4微克/千克)显示导致心律失常和致死所需的哇巴因量显著增加,而咪唑克生(200和400微克/千克)则使其减少。3. 育亨宾抑制哇巴因诱导的升压反应,而咪唑克生则增强该反应。4. 这些药物对交感神经系统的作用似乎在其抗心律失常和促心律失常作用中起了重要作用。

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