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恒河猴中d,l-青藤碱1.5-磷酸盐滥用潜力的实验研究。

Experimental studies of the abuse potential of d, l-glaucine. 1.5-phosphate in rhesus monkeys.

作者信息

Schuster C R, Aigner T, Johanson C E, Gieske T H

出版信息

Pharmacol Biochem Behav. 1982 May;16(5):851-4. doi: 10.1016/0091-3057(82)90248-9.

Abstract

d-Glaucine is an alkaloid derived from Glaucium flavum, which is as effective as codeine as an antitussive. d, l-Glaucine. 1.5 phosphate is a synthetic compound related to d-glaucine. The ability of d, l-glaucine.1.5 phosphate to maintain responding in rhesus monkeys was assessed in 2 procedures. In the first responding was maintained under a fixed-ratio 10 schedule of codeine delivery during daily 3-hr sessions. When d, l-glaucine.1.5 phosphate (0.05-0.4 mg/kg) was substituted for codeine, responding was not maintained. In the second procedure, monkeys given 23-hr/day access to 0.5-1.0 mg/kg under a fixed-ratio schedule did not self-administer d,l-glaucine.1.5 phosphate above saline levels even after a 21-day period of programmed injections. Following the period of programmed injections, there were not signs of opiate withdrawal following the administration of naloxone. These results indicate that the abuse potential of d,l-glaucine.1.5 phosphate is low relative to codeine.

摘要

d-青藤碱是一种从黄罂粟中提取的生物碱,其镇咳效果与可待因相当。d, l-青藤碱1.5磷酸盐是一种与d-青藤碱相关的合成化合物。通过两种程序评估了d, l-青藤碱1.5磷酸盐在恒河猴中维持反应的能力。在第一个程序中,在每天3小时的实验时段内,反应在可待因给药的固定比例10的时间表下维持。当用d, l-青藤碱1.5磷酸盐(0.05 - 0.4毫克/千克)替代可待因时,反应无法维持。在第二个程序中,即使经过21天的程序化注射,按固定比例时间表每天有23小时可获取0.5 - 1.0毫克/千克的猴子,其自行给药的d, l-青藤碱1.5磷酸盐量也未超过生理盐水水平。在程序化注射期之后,注射纳洛酮后没有出现阿片类药物戒断的迹象。这些结果表明,相对于可待因,d, l-青藤碱1.5磷酸盐的滥用可能性较低。

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