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埃托啡对大鼠的心血管作用。

Cardiovascular effects of etorphine in rats.

作者信息

Roquebert J, Delgoulet C

机构信息

UER de Pharmacie, Université de Bordeaux, France.

出版信息

J Auton Pharmacol. 1988 Mar;8(1):39-43. doi: 10.1111/j.1474-8673.1988.tb00167.x.

Abstract
  1. Cardiovascular effects of intravenously administered etorphine were investigated in mechanically ventilated normotensive rats under pentobarbitone anaesthesia. 2. Etorphine (0.1-2 micrograms kg-1) induced a dose-related bradycardia and hypotension which was prevented by pretreatment with naloxone (0.1 mg kg-1). 3. After bilateral vagotomy etorphine (1 microgram kg-1) produced a pressor effect which was prevented by prazosin (0.5 mg kg-1), but unaltered by adrenalectomy. 4. The bradycardia due to etorphine was abolished by bilateral vagotomy, but only partially reduced by atropine (1 mg kg-1) and still evident after propranolol (1.5 mg kg-1). 5. Etorphine was without effect on blood pressure in the pithed rat, although there was a small bradycardia which was not seen after naloxone. 6. The data presented indicate that etorphine produces an opioid receptor-mediated stimulation of both vagal (partially cholinergic) and sympathetic outflow and a direct cardiodepressant effect.
摘要
  1. 在戊巴比妥麻醉下,对机械通气的正常血压大鼠静脉注射埃托啡的心血管效应进行了研究。2. 埃托啡(0.1 - 2微克/千克)引起剂量相关的心动过缓和低血压,预先给予纳洛酮(0.1毫克/千克)可预防。3. 双侧迷走神经切断后,埃托啡(1微克/千克)产生升压效应,哌唑嗪(0.5毫克/千克)可预防,但肾上腺切除后无变化。4. 埃托啡引起的心动过缓经双侧迷走神经切断后消除,但阿托品(1毫克/千克)仅部分减轻,普萘洛尔(1.5毫克/千克)后仍明显。5. 埃托啡对脊髓切断的大鼠血压无影响,尽管有轻微心动过缓,纳洛酮后未见此现象。6. 所呈现的数据表明,埃托啡产生阿片受体介导的迷走神经(部分为胆碱能)和交感神经传出刺激以及直接的心脏抑制作用。

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