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完整大鼠和肾上腺去髓质大鼠对κ阿片受体激动剂的心血管反应。

Cardiovascular responses to kappa opioid agonists in intact and adrenal demedullated rats.

作者信息

Gulati A, Bhargava H N

机构信息

Department of Pharmacodynamics, University of Illinois, Chicago 60612.

出版信息

Eur J Pharmacol. 1988 Nov 1;156(2):247-57. doi: 10.1016/0014-2999(88)90328-7.

Abstract

The effects of three kappa opioid agonists namely, bremazocine, tifluadom and U-50,488H were studied on blood pressure and heart rate in urethane-anesthetized normal and bilateral adrenal demedullated rats. Bremazocine (0.2, 0.4 and 0.6 mg/kg i.v.) produced a dose-dependent decrease in heart rate, while only 0.4 mg/kg bremazocine produced marked hypotension. The effect appeared to be long lasting because even at 60 min following drug administration the decreases in both heart rate and blood pressure continued. Bilateral adrenal demedullation did not change bremazocine-induced fall in blood pressure but the bradycardia was partially blocked. Tifluadom (0.1-0.4 mg/kg i.v.) produced an initial arrest of heart beat followed by bradycardia which recovered in about 60 min. Except for a very transient fall soon after drug administration no significant effect was observed on blood pressure. In adrenal demedullated rats, tifluadom induced initial arrest of heart was not affected but the subsequent bradycardia was blocked. U-50,488H (0.2, 0.4 and 0.6 mg/kg i.v.) produced dose-dependent bradycardia and hypotension both of which were blocked following bilateral adrenal demedullation. Naltrexone methylbromide (MRZ 2663 BR), a quaternary opioid antagonist, injected 5 min prior to U-50,488H, blocked its cardiovascular effects. The results suggest that kappa opioid agonists given i.v. depress cardiovascular system and these effects are mediated through the adrenal medulla and peripheral opioid receptors. The differential effects of kappa opioid agonists on blood pressure and heart rate suggest that either the three kappa agents interact differentially at the kappa opioid receptors or the subtypes of receptors for the kappa opioid exist.

摘要

研究了三种κ阿片受体激动剂,即布瑞马佐辛、替氟杜姆和U-50,488H,对氨基甲酸乙酯麻醉的正常大鼠和双侧肾上腺髓质切除大鼠的血压和心率的影响。布瑞马佐辛(静脉注射0.2、0.4和0.6mg/kg)可使心率呈剂量依赖性下降,而只有0.4mg/kg布瑞马佐辛可产生明显的低血压。这种作用似乎持续时间较长,因为即使在给药后60分钟,心率和血压仍持续下降。双侧肾上腺髓质切除并未改变布瑞马佐辛引起的血压下降,但心动过缓被部分阻断。替氟杜姆(静脉注射0.1-0.4mg/kg)最初会导致心跳骤停,随后出现心动过缓,约60分钟后恢复。除给药后不久出现非常短暂的下降外,未观察到对血压有显著影响。在肾上腺髓质切除的大鼠中,替氟杜姆引起的最初心跳骤停未受影响,但随后的心动过缓被阻断。U-50,488H(静脉注射0.2、0.4和0.6mg/kg)可产生剂量依赖性心动过缓和低血压,双侧肾上腺髓质切除后两者均被阻断。在U-50,488H给药前5分钟注射季铵类阿片受体拮抗剂纳曲酮甲基溴(MRZ 2663 BR),可阻断其心血管效应。结果表明,静脉注射κ阿片受体激动剂会抑制心血管系统,这些作用是通过肾上腺髓质和外周阿片受体介导的。κ阿片受体激动剂对血压和心率的不同作用表明,这三种κ药物在κ阿片受体上的相互作用不同,或者存在κ阿片受体的亚型。

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