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维拉帕米和普萘洛尔对氨茶碱中毒犬的抗心律失常作用。

The antiarrhythmic effects of verapamil and propranolol in aminophylline toxic dogs.

作者信息

Friesen R M, Bonet J F

出版信息

Can Anaesth Soc J. 1983 Mar;30(2):124-31. doi: 10.1007/BF03009340.

Abstract

The antiarrhythmic effects of the calcium blocker verapamil and the beta adrenoreceptor blocker propranolol were examined in aminophylline toxic dogs. Eighteen dogs were intubated and ventilated after induction of anaesthesia (pentobarbitone 30 mg/kg and paccuronium 0.1 mg/kg). All animals were rendered toxic by aminophylline infusion; an initial dose of 50 mg/kg over five minutes with subsequent doses of 10 mg/kg over 30 seconds. Twenty minutes after each aminophylline infusion, the dog was challenged with phenylephrine (10 to 20 micrograms/kg). This resulted in short duration hypertension and reproducible emergence of ventricular arrhythmias. The dogs were divided into three groups of six animals each. Group I (control) received no antiarrhythmics whereas Group II received verapamil 0.2 mg/kg and Group III received propranolol 0.1 mg/kg for the treatment of persistent ventricular arrhythmias. Both verapamil and propranolol exerted an antiarrhythmic effect in aminophylline induced ventricular arrhythmias. The efficacy of verapamil was independent of the accompanying reduction in blood pressure and systemic vascular resistance as subsequent phenylephrine induced hypertension could not reinstitute these arrhythmias. Propranolol appeared less effective since it did not completely suppress the arrhythmias in three dogs and could not prevent emergence of PVC's in four following repeat phenylephrine challenge. Further development of this animal model may be useful for the better understanding of ventricular arrhythmias.

摘要

在氨茶碱中毒的犬中研究了钙通道阻滞剂维拉帕米和β肾上腺素能受体阻滞剂普萘洛尔的抗心律失常作用。18只犬在麻醉诱导(戊巴比妥30mg/kg和泮库溴铵0.1mg/kg)后进行气管插管和通气。所有动物通过输注氨茶碱使其中毒;初始剂量为50mg/kg,5分钟内输注完毕,随后剂量为10mg/kg,30秒内输注完毕。每次输注氨茶碱20分钟后,用去氧肾上腺素(10至20μg/kg)对犬进行激发试验。这导致了短暂的高血压和可重复出现的室性心律失常。将犬分为三组,每组6只动物。第一组(对照组)未接受抗心律失常药物,而第二组接受维拉帕米0.2mg/kg,第三组接受普萘洛尔0.1mg/kg用于治疗持续性室性心律失常。维拉帕米和普萘洛尔在氨茶碱诱导的室性心律失常中均发挥了抗心律失常作用。维拉帕米的疗效与伴随的血压和全身血管阻力降低无关,因为随后去氧肾上腺素诱导的高血压并不能再次引发这些心律失常。普萘洛尔似乎效果较差,因为它没有完全抑制三只犬的心律失常,并且在重复去氧肾上腺素激发试验后,无法预防四只犬出现室性早搏。进一步开发这种动物模型可能有助于更好地理解室性心律失常。

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