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人体滥用者的甲基苯丙胺血药浓度:在药代动力学建模中的应用。

Methamphetamine blood concentrations in human abusers: application to pharmacokinetic modeling.

作者信息

Melega William P, Cho Arthur K, Harvey Dennis, Laćan Goran

机构信息

Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Los Angeles, California 90095, USA.

出版信息

Synapse. 2007 Apr;61(4):216-20. doi: 10.1002/syn.20365.

Abstract

Characterization of methamphetamine's (METH) dose-dependent effects on brain neurochemistry may represent a critical component for better understanding the range of resultant behavioral pathologies. Most human studies, however, have assessed only the effects of long term, high dose METH abuse (e.g., greater than 1000 mg/day) in individuals meeting DSM-IV criteria for METH dependence. Yet, for the majority of METH abusers, their patterns of METH exposure that consist of lower doses remain less well-characterized. In this study, blood samples were obtained from 105 individuals detained by police for possible criminal activity and testing positive for stimulants by EMIT assay. METH blood concentrations were subsequently quantified by GC-MS and were predominantly in the low micromolar range (0.1-11.1 microM), with median and mean values of 1.3 microM (0.19 mg/l) and 2 microM (0.3 mg/l), respectively. Pharmacokinetic calculations based on these measured values were used to estimate initial METH body burdens, the median value being 52 mg. Modeling a 52 mg dose for a 4 day-METH maintenance exposure pattern of 4 doses/day at 4 h intervals showed that blood concentrations remained between 1 and 4 microM during this period. Collectively, these data present evidence for a METH exposure pattern distinct from high dose-METH abuse and provide the rationale for assessing potential brain pathology associated with such lower dose-METH exposure.

摘要

表征甲基苯丙胺(METH)对脑内神经化学的剂量依赖性效应,可能是更好地理解由此产生的一系列行为病理学的关键组成部分。然而,大多数人体研究仅评估了符合DSM-IV甲基苯丙胺依赖标准的个体中长期、高剂量甲基苯丙胺滥用(例如,大于1000毫克/天)的影响。然而,对于大多数甲基苯丙胺滥用者来说,他们较低剂量的甲基苯丙胺接触模式仍未得到充分表征。在本研究中,从105名因可能的犯罪活动被警方拘留且通过EMIT分析检测出兴奋剂呈阳性的个体中采集了血样。随后通过气相色谱-质谱联用仪(GC-MS)对甲基苯丙胺血药浓度进行定量,其主要处于低微摩尔浓度范围(0.1 - 11.1微摩尔),中位数和平均值分别为1.3微摩尔(0.19毫克/升)和2微摩尔(0.3毫克/升)。基于这些测量值的药代动力学计算用于估计甲基苯丙胺的初始体内负荷,中位数为52毫克。以4天的甲基苯丙胺维持接触模式、每天4剂、每4小时一剂的方式模拟52毫克剂量,结果显示在此期间血药浓度保持在1至4微摩尔之间。总体而言,这些数据为一种不同于高剂量甲基苯丙胺滥用的甲基苯丙胺接触模式提供了证据,并为评估与这种低剂量甲基苯丙胺接触相关的潜在脑部病理学提供了理论依据。

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