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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >The cardiovascular and subjective effects of methamphetamine combined with gamma-vinyl-gamma-aminobutyric acid (GVG) in non-treatment seeking methamphetamine-dependent volunteers.
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The cardiovascular and subjective effects of methamphetamine combined with gamma-vinyl-gamma-aminobutyric acid (GVG) in non-treatment seeking methamphetamine-dependent volunteers.

机译:甲基苯丙胺与γ-乙烯基-γ-氨基丁酸(GVG)联合在非治疗中寻求甲基苯丙胺依赖性志愿者的心血管和主观影响。

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Gamma-vinyl-gamma-aminobutyric acid (GVG) elevates central nervous system gamma-aminobutyric acid (GABA) levels by irreversibly inhibiting GABA transaminase. An open-label clinical trial in humans suggested that GVG may reduce cocaine and methamphetamine use. To test safety and to obtain preliminary data on efficacy of GVG for treating methamphetamine dependence, we conducted a double-blind, placebo-controlled, parallel group study of GVG interaction with the cardiovascular and subjective effects produced by methamphetamine. Non-treatment seeking methamphetamine-dependent volunteers received either GVG (N=8) or placebo (N=9) by random assignment. GVG treatment was initiated at 1 g/day and increased to 5 g/day. After reaching the target dose of 5 g/day, participants received methamphetamine (15+30 mg, IV), and cardiovascular and subjective effects were assessed. No serious adverse events were noted, and the total number of adverse events was similar between the treatment groups. Considering the full time course and peak effects independently, no significant differences were detected between the groups for systolic or diastolic blood pressures, or heart rate, following methamphetamine exposure. Some methamphetamine-induced cardiovascular changes approached significance (p<0.10) and may warrant attention in future trials. Methamphetamine-induced subjective effects ("any drug effect", "high", "crave methamphetamine") were statistically similar between GVG and placebo treatment groups. Pharmacokinetic data indicate that GVG treatment did not alter methamphetamine or amphetamine plasma levels, and there was no association between methamphetamine or amphetamine plasma levels and peak cardiovascular effects. Taken together, the data indicate that GVG treatment is generally well tolerated but not efficacious in attenuating the positive subjective effects of methamphetamine in the laboratory.
机译:γ-乙烯基-γ-氨基丁酸(GVG)通过不可逆转地抑制GABA转氨酶来升高中枢神经系统γ-氨基丁酸(GABA)的水平。一项针对人体的开放标签临床试验表明,GVG可以减少可卡因和甲基苯丙胺的使用。为了测试安全性并获得有关GVG治疗甲基苯丙胺依赖性的功效的初步数据,我们进行了GVG相互作用与甲基苯丙胺产生的心血管和主观作用的双盲,安慰剂对照,平行组研究。非治疗寻求甲基苯丙胺依赖的志愿者通过随机分配接受GVG(N = 8)或安慰剂(N = 9)。 GVG治疗开始于1克/天,并增加到5克/天。在达到每天5克的目标剂量后,参与者接受了甲基苯丙胺(15 + 30毫克,静脉注射),并评估了其心血管和主观效果。没有观察到严重的不良事件,并且治疗组之间的不良事件总数相似。考虑到全时程和峰值效应,在甲基苯丙胺暴露后,两组之间的收缩压或舒张压或心率均无显着差异。一些由甲基苯丙胺引起的心血管变化已接近显着性(p <0.10),可能需要在以后的试验中予以关注。甲基苯丙胺引起的主观效果(“任何药物作用”,“高”,“渴望甲基苯丙胺”)在GVG和安慰剂治疗组之间在统计学上相似。药代动力学数据表明,GVG治疗不会改变甲基苯丙胺或苯丙胺血浆水平,并且甲基苯丙胺或苯丙胺血浆水平与峰值心血管效应之间没有关联。总体而言,数据表明,GVG治疗在实验室中通常具有良好的耐受性,但在减弱甲基苯丙胺的积极主观效果方面无效。

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