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大鼠体内3,4-亚甲基二氧甲基苯丙胺代谢物的鉴定

Identification of metabolites of 3,4-methylenedioxymethamphetamine in rats.

作者信息

Yousif M Y, Fitzgerald R L, Narasimhachari N, Rosecrans J A, Blanke R V, Glennon R A

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298.

出版信息

Drug Alcohol Depend. 1990 Oct;26(2):127-35. doi: 10.1016/0376-8716(90)90119-y.

Abstract

Liquid chromatography with electrochemical detection (LC/ECD) and gas chromatography/mass spectrometry (GC/MS) were used to identify metabolites of N-methyl-3,4-methylenedioxyamphetamine (MDMA) in samples of rat plasma and urine. Several potential metabolites, based on what is known about the metabolism of the desmethyl analog (i.e., MDA), were synthesized as standards to aid in the identification of the MDMA metabolites. MDA and N-methyl-1-(4-hydroxy-3-methoxy-phenyl)-2-aminopropane (3b) were identified in urine by HPLC and confirmed by GC/MS. 1-(4-Hydroxy-3-methyoxyphenyl)2-aminopropane, (3a), N-methyl-1-(3-hydroxy-4-methoxyphenyl)-2-aminopropane (2b) and 1-(3,4-dihydroxyphenyl)-2-aminopropane (4a) were tentatively identified by LC/ECD but insufficient sample size precluded confirmation by mass spectrometry. MDA was also identified in brain and plasma extracts. Because MDA is a metabolite of MDMA in humans, and because it has been speculated that the neurotoxic effects of MDA and MDMA may be due to a metabolite, the results of the present study may ultimately aid our understanding of the neurotoxic mechanism of these drugs of abuse.

摘要

采用液相色谱 - 电化学检测法(LC/ECD)和气相色谱/质谱联用法(GC/MS)对大鼠血浆和尿液样本中N - 甲基 - 3,4 - 亚甲基二氧基苯丙胺(MDMA)的代谢产物进行鉴定。基于对去甲基类似物(即MDA)代谢情况的了解,合成了几种潜在的代谢产物作为标准品,以协助鉴定MDMA的代谢产物。通过高效液相色谱法(HPLC)在尿液中鉴定出MDA和N - 甲基 - 1 -(4 - 羟基 - 3 - 甲氧基苯基)- 2 - 氨基丙烷(3b),并通过气相色谱/质谱联用法(GC/MS)进行了确认。通过LC/ECD初步鉴定出1 -(4 - 羟基 - 3 - 甲氧基苯基)- 2 - 氨基丙烷(3a)、N - 甲基 - 1 -(3 - 羟基 - 4 - 甲氧基苯基)- 2 - 氨基丙烷(2b)和1 -(3,4 - 二羟基苯基)- 2 - 氨基丙烷(4a),但样本量不足无法通过质谱法进行确认。在脑和血浆提取物中也鉴定出了MDA。由于MDA是人类MDMA的代谢产物,并且据推测MDA和MDMA的神经毒性作用可能归因于一种代谢产物,因此本研究结果最终可能有助于我们理解这些滥用药物的神经毒性机制。

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