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亚甲二氧基甲基苯丙胺(摇头丸)对小鼠和大鼠中枢血清素能作用的差异。

Differences in the central serotonergic effects of methylenedioxymethamphetamine (MDMA) in mice and rats.

作者信息

Stone D M, Hanson G R, Gibb J W

机构信息

Department of Pharmacology and Toxicology, University of Utah, Salt Lake City 84112.

出版信息

Neuropharmacology. 1987 Nov;26(11):1657-61. doi: 10.1016/0028-3908(87)90017-7.

Abstract

The effects of subcutaneous injection of 3,4-methylenedioxymethamphetamine (MDMA), a psychoactive amphetamine congener, on mouse central monoaminergic systems were assessed and compared to effects in rats. Whereas neostriatal concentrations of 5-hydroxytryptamine and 5-hydroxyindoleacetic acid in mouse were transiently decreased after a single moderately high dose of MDMA (15 mg/kg), mouse neostriatal or hippocampal tryptophan hydroxylase activity was not significantly affected, even after a dose of 60 mg/kg. These results are in contrast to effects in rats, in which a single 10 mg/kg dose of MDMA induced immediate and prolonged decreases in both central tryptophan hydroxylase activity and 5-hydroxyindole concentrations. Decreases in mouse central tryptophan hydroxylase activity, and prolonged decreases in mouse 5-hydroxyindole concentrations, were observed only after multiple doses of MDMA, suggesting that the duration of exposure may be an important determinant of toxic effects. These results show mice to be less susceptible than rats to MDMA-induced neurotoxicity, and are discussed in terms of possible interspecies differences in MDMA pharmacokinetics.

摘要

对精神活性苯丙胺类似物3,4-亚甲基二氧甲基苯丙胺(MDMA)皮下注射对小鼠中枢单胺能系统的影响进行了评估,并与大鼠的影响进行了比较。在单次中等高剂量的MDMA(15毫克/千克)后,小鼠新纹状体中5-羟色胺和5-羟吲哚乙酸的浓度短暂降低,而即使在60毫克/千克的剂量后,小鼠新纹状体或海马色氨酸羟化酶活性也未受到显著影响。这些结果与大鼠的情况形成对比,在大鼠中,单次10毫克/千克剂量的MDMA会立即并长期降低中枢色氨酸羟化酶活性和5-羟吲哚浓度。仅在多次注射MDMA后,才观察到小鼠中枢色氨酸羟化酶活性降低以及小鼠5-羟吲哚浓度的长期降低,这表明暴露持续时间可能是毒性作用的一个重要决定因素。这些结果表明,小鼠比大鼠对MDMA诱导的神经毒性更不敏感,并从MDMA药代动力学可能存在的种间差异方面进行了讨论。

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