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吗啡持续治疗可增加小鼠大脑中地西泮结合抑制剂的信使核糖核酸。

Continuous treatment with morphine increases diazepam binding inhibitor mRNA in mouse brain.

作者信息

Katsura M, Hara A, Higo A, Tarumi C, Hibino Y, Ohkuma S

机构信息

Department of Pharmacology, Kawasaki Medical School, Matsushima, Kurashiki, Japan.

出版信息

J Neurochem. 1998 Dec;71(6):2638-41. doi: 10.1046/j.1471-4159.1998.71062638.x.

Abstract

Effects of acute and chronic morphine treatment on the expression of diazepam binding inhibitor (DBI) mRNA in the mouse brain were examined. Cerebral DBI mRNA expression significantly increased in morphine-dependent mice, and this increase is more remarkable in morphine-withdrawn mice, whereas a single administration of morphine (50 mg/kg) produced no changes in the expression. Simultaneous administration of naloxone (3 mg/kg) with morphine completely abolished the increase in cerebral DBI mRNA expression observed in morphine-dependent and -withdrawn mice. These results indicate that a chronic functional interaction between morphine and opioid receptors has a critical role in increases in DBI mRNA expression.

摘要

研究了急性和慢性吗啡处理对小鼠脑中地西泮结合抑制剂(DBI)mRNA表达的影响。吗啡依赖小鼠脑内DBI mRNA表达显著增加,且这种增加在吗啡戒断小鼠中更明显,而单次给予吗啡(50 mg/kg)对表达无影响。纳洛酮(3 mg/kg)与吗啡同时给药完全消除了在吗啡依赖和戒断小鼠中观察到的脑内DBI mRNA表达增加。这些结果表明,吗啡与阿片受体之间的慢性功能相互作用在DBI mRNA表达增加中起关键作用。

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