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纳洛酮及其他阿片类拮抗剂对急性乙醇中毒大鼠血液乙醇浓度的影响。

Effects of naloxone and other opiate antagonists on blood-ethanol concentration in acutely-ethanol-intoxicated rats.

作者信息

Badawy A A, Aliyu S U

出版信息

Neuropeptides. 1985 Feb;5(4-6):341-4. doi: 10.1016/0143-4179(85)90023-x.

Abstract

The effects of naloxone hydrochloride (NAL) and other opiate antagonists on blood-ethanol concentration (BEC) in acutely-ethanol-intoxicated rats were examined. Using a 1 mg/kg body wt. dose of NAL, the maximum decrease in BEC was found to occur at 30 min. At 30 min after administration of various doses of NAL, it was found that BEC was decreased maximally by a 2 mg/kg dose, whereas the first significant decrease was caused by a 10 micrograms/kg dose. BEC was also decreased by naltrexone (1 mg/kg), but not by a 4 mg/kg dose of any of four Mr compounds (Mr 1452, Mr 1453, Mr 2266 and Mr 2267). It is suggested that pharmacokinetic antagonism of acute alcohol intoxication by naloxone and naltrexone is unrelated to the property of opiate antagonism, but may involve the ability of certain such antagonists to interact with hepatic NAD+-dependent oxidative metabolism.

摘要

研究了盐酸纳洛酮(NAL)和其他阿片类拮抗剂对急性乙醇中毒大鼠血液乙醇浓度(BEC)的影响。使用1mg/kg体重剂量的NAL时,发现BEC的最大降幅出现在30分钟时。在给予不同剂量NAL后的30分钟时,发现2mg/kg剂量可使BEC最大程度降低,而首次显著降低是由10μg/kg剂量引起的。纳曲酮(1mg/kg)也可降低BEC,但四种Mr化合物(Mr 1452、Mr 1453、Mr 2266和Mr 2267)中任何一种的4mg/kg剂量均无此作用。提示纳洛酮和纳曲酮对急性酒精中毒的药代动力学拮抗作用与阿片类拮抗特性无关,但可能涉及某些此类拮抗剂与肝脏NAD+依赖性氧化代谢相互作用的能力。

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