Tallarida Christopher S, Tallarida Ronald J, Rawls Scott M
Center for Substance Abuse Research, Temple University School of Medicine, Philadelphia, PA, USA; Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA, USA.
Center for Substance Abuse Research, Temple University School of Medicine, Philadelphia, PA, USA; Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA, USA.
Drug Alcohol Depend. 2015 Apr 1;149:145-50. doi: 10.1016/j.drugalcdep.2015.01.035. Epub 2015 Feb 7.
The Drug Enforcement Agency estimates that 80% of cocaine seized in the United States contains the veterinary pharmaceutical levamisole (LVM). One problem with LVM is that it is producing life-threatening neutropenia in an alarming number of cocaine abusers. The neuropharmacological profile of LVM is also suggestive of an agent with modest reinforcing and stimulant effects that could enhance cocaine's addictive effects.
We tested the hypothesis that LVM (ip) enhances the rewarding and locomotor stimulant effects of cocaine (ip) using rat conditioned place preference (CPP) and locomotor assays. Effects of LVM by itself were also tested.
LVM (0-10 mg/kg) produced CPP at 1mg/kg (P<0.05) and locomotor activation at 5mg/kg (P < 0.05). For CPP combination experiments, a statistically inactive dose of LVM (0.1 mg/kg) was administered with a low dose of cocaine (2.5 mg/kg). Neither agent produced CPP compared to saline (P > 0.05); however, the combination of LVM and cocaine produced enhanced CPP compared to saline or either drug by itself (P < 0.01). For locomotor experiments, the same inactive dose of LVM (0.1mg/kg, ip) was administered with low (10 mg/kg) and high doses (30 mg/kg) of cocaine. LVM (0.1 mg/kg) enhanced locomotor activation produced by 10mg/kg of cocaine (P < 0.05) but not by 30 mg/kg (P>0.05).
LVM can enhance rewarding and locomotor-activating effects of low doses of cocaine in rats while possessing modest activity of its own.
美国缉毒局估计,在美国查获的80%的可卡因含有兽药左旋咪唑(LVM)。LVM的一个问题是,它正在使数量惊人的可卡因滥用者出现危及生命的中性粒细胞减少症。LVM的神经药理学特征也表明它是一种具有适度强化和刺激作用的药物,可能会增强可卡因的成瘾作用。
我们使用大鼠条件性位置偏爱(CPP)和运动试验,检验了LVM(腹腔注射)增强可卡因(腹腔注射)的奖赏和运动刺激作用的假设。同时也测试了LVM单独的作用。
LVM(0 - 10毫克/千克)在1毫克/千克时产生条件性位置偏爱(P<0.05),在5毫克/千克时产生运动激活(P < 0.05)。对于CPP联合实验,将统计学上无活性剂量的LVM(0.1毫克/千克)与低剂量可卡因(2.5毫克/千克)一起给药。与生理盐水相比,两种药物单独使用时均未产生条件性位置偏爱(P > 0.05);然而,与生理盐水或单独使用任何一种药物相比,LVM和可卡因联合使用产生了增强的条件性位置偏爱(P < 0.01)。对于运动实验,将相同无活性剂量的LVM(0.1毫克/千克,腹腔注射)与低剂量(10毫克/千克)和高剂量(30毫克/千克)的可卡因一起给药。LVM(0.1毫克/千克)增强了10毫克/千克可卡因产生的运动激活(P < 0.05),但未增强30毫克/千克可卡因产生的运动激活(P>0.05)。
LVM可以增强低剂量可卡因对大鼠的奖赏和运动激活作用,同时自身具有适度活性。