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重复给予吗啡处理后再撤药的小鼠脑内儿茶酚胺耗竭以及对吗啡增强去甲肾上腺素耗竭作用产生耐受性的发展过程。

Cerebral catecholamine depletion in mice withdrawn from repeated morphine treatment and development of tolerance to the enhancing effect of morphine on noradrenaline depletion.

作者信息

Etemadzadeh E

机构信息

Department of Pharmacy, University of Helsinki, Finland.

出版信息

J Pharmacol Exp Ther. 1993 Aug;266(2):749-55.

PMID:8355206
Abstract

The effect of repeated morphine administration on the alpha-methyl-rho-tyrosine (alpha M rho T)-induced depletion of catecholamines was investigated in various brain areas of mice withdrawn for 1, 2, 3 and 7 days from 5-day morphine treatment. In addition, to clarify the development of tolerance, the effect of acute morphine administration on alpha M rho T-induced depletion of catecholamines was studied in these selected brain areas of mice withdrawn from repeated morphine treatment. Dopamine depletion was significantly (P < .01) retarded in the striatum and "rest of forebrain + midbrain" of mice withdrawn for 1 day from morphine treatment. Withdrawal from morphine treatment did not alter alpha M rho T-induced noradrenaline depletion in the lower brain stem, rest of forebrain + midbrain or hypothalamus. The 10-mg/kg test dose of morphine significantly enhanced alpha M rho T-induced dopamine depletion in the rest of forebrain + midbrain of control mice withdrawn for 2 days, but did not clearly enhance it in mice withdrawn from morphine. The test dose significantly enhanced noradrenaline depletion in all selected brain areas of control mice withdrawn for 1 to 3 days from saline, but tolerance to the test dose developed in morphine-withdrawn mice. These results suggest that dopamine depletion is retarded in the striatum and rest of forebrain + midbrain of mice withdrawn for 1 day from repeated morphine treatment. However, noradrenaline depletion remains unchanged in all selected brain areas of mice withdrawn from morphine, and tolerance develops to the enhancing effect of morphine on the depletion of noradrenaline in mice withdrawn for 1 to 2 days from morphine.

摘要

在从5天吗啡治疗中撤药1、2、3和7天的小鼠的各个脑区,研究了重复给予吗啡对α-甲基-ρ-酪氨酸(αMρT)诱导的儿茶酚胺耗竭的影响。此外,为了阐明耐受性的发展,在从重复吗啡治疗中撤药的小鼠的这些选定脑区,研究了急性给予吗啡对αMρT诱导的儿茶酚胺耗竭的影响。从吗啡治疗撤药1天的小鼠,其纹状体以及“前脑其余部分+中脑”中的多巴胺耗竭显著延迟(P<0.01)。从吗啡治疗撤药并未改变αMρT诱导的低位脑干、前脑其余部分+中脑或下丘脑的去甲肾上腺素耗竭。10mg/kg的吗啡测试剂量显著增强了撤药2天的对照小鼠前脑其余部分+中脑中αMρT诱导的多巴胺耗竭,但在从吗啡撤药的小鼠中并未明显增强。该测试剂量显著增强了撤药1至3天的对照小鼠所有选定脑区的去甲肾上腺素耗竭,但从吗啡撤药的小鼠对该测试剂量产生了耐受性。这些结果表明,从重复吗啡治疗撤药1天的小鼠,其纹状体以及前脑其余部分+中脑中的多巴胺耗竭延迟。然而,从吗啡撤药的小鼠所有选定脑区的去甲肾上腺素耗竭保持不变,并且从吗啡撤药1至2天的小鼠对吗啡增强去甲肾上腺素耗竭的作用产生了耐受性。

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