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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.

DOI:10.1111/j.1474-8673.1988.tb00167.x
PMID:3392053
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。

相似文献

1
Cardiovascular effects of etorphine in rats.埃托啡对大鼠的心血管作用。
J Auton Pharmacol. 1988 Mar;8(1):39-43. doi: 10.1111/j.1474-8673.1988.tb00167.x.
2
Multiple sites for the cardiovascular actions of fentanyl in rats.芬太尼对大鼠心血管作用的多个部位
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[Influence of intraventricular injection of etorphine and naloxone on the vagus-pressor response in rats].[脑室内注射埃托啡和纳洛酮对大鼠迷走神经升压反应的影响]
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1986 Jun;8(3):184-7.
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Antinociception and cardiovascular responses produced by intravenous morphine: the role of vagal afferents.静脉注射吗啡产生的抗伤害感受和心血管反应:迷走神经传入纤维的作用
Brain Res. 1991 Mar 15;543(2):256-70. doi: 10.1016/0006-8993(91)90036-u.
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Cardiovascular effects in the Sprague-Dawley rat of 8-hydroxy-2(di-N-propylamino) tetralin, a selective 5-hydroxytryptamine receptor agonist.
J Pharm Pharmacol. 1985 Apr;37(4):263-5. doi: 10.1111/j.2042-7158.1985.tb05057.x.
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The use of specific opioid agonists and antagonists to delineate the vagally mediated antinociceptive and cardiovascular effects of intravenous morphine.使用特定的阿片类激动剂和拮抗剂来阐明静脉注射吗啡的迷走神经介导的抗伤害感受和心血管效应。
Brain Res. 1993 Feb 19;603(2):186-200. doi: 10.1016/0006-8993(93)91237-m.
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Cardiac slowing induced by peripheral kappa-opiate receptor stimulation in rats.外周κ-阿片受体刺激诱导的大鼠心脏减慢
Eur J Pharmacol. 1984 Jun 15;102(1):159-63. doi: 10.1016/0014-2999(84)90351-0.
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Etorphine inhibition of pancreatic exocrine secretion in rats: comparison with methadone.埃托啡对大鼠胰腺外分泌的抑制作用:与美沙酮的比较。
Eur J Pharmacol. 1986 Feb 11;121(1):73-81. doi: 10.1016/0014-2999(86)90394-8.
10
Vagally mediated bradycardiac effect of prazosin in anaesthetized rats.哌唑嗪对麻醉大鼠的迷走神经介导的心动过缓作用
Eur J Pharmacol. 1984 Oct 15;105(3-4):223-8. doi: 10.1016/0014-2999(84)90613-7.

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