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致幻性苯丙胺选择性地破坏脑血清素神经末梢。

Hallucinogenic amphetamine selectively destroys brain serotonin nerve terminals.

作者信息

Ricaurte G, Bryan G, Strauss L, Seiden L, Schuster C

出版信息

Science. 1985 Sep 6;229(4717):986-8. doi: 10.1126/science.4023719.

Abstract

(+/-)-3,4-Methylenedioxyamphetamine (MDA), an amphetamine analog with hallucinogenic activity, produced selective long-lasting reductions in the level of serotonin, the number of serotonin uptake sites, and the concentration of 5-hydroxyindoleacetic acid in rat brain. Morphological studies suggested that these neurochemical deficits were due to serotonin nerve terminal degeneration. These results show that MDA has toxic activity for serotonin neurons in rats and raise the question of whether exposure to MDA and related hallucinogenic amphetamines can produce serotonin neurotoxicity in the human brain.

摘要

(±)-3,4-亚甲二氧基苯丙胺(MDA)是一种具有致幻活性的苯丙胺类似物,它能使大鼠脑中血清素水平、血清素摄取位点数量以及5-羟吲哚乙酸浓度产生选择性的持久降低。形态学研究表明,这些神经化学缺陷是由于血清素神经末梢变性所致。这些结果表明,MDA对大鼠的血清素神经元具有毒性作用,并引发了一个问题,即接触MDA及相关致幻苯丙胺是否会在人脑中产生血清素神经毒性。

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