Laizure S Casey, Parker Robert B
Department of Clinical Pharmacy, University of Tennessee, Suite 308, 910 Madison Ave., Memphis, TN 38163, USA.
Drug Metab Dispos. 2009 Feb;37(2):310-4. doi: 10.1124/dmd.108.023531. Epub 2008 Nov 12.
One of the most common drug dependencies occurring with alcoholism is cocaine dependence. This combination is particularly worrisome because of the increased risk of cardiovascular events associated with their coabuse. Although it is well known that ethanol increases the cardiovascular effects of cocaine by inhibiting cocaine clearance and the formation of cocaethylene, it has also been postulated that ethanol enhances the cardiovascular effects of cocaine independent of the two latter mechanisms. In this study, we investigated the cardiovascular pharmacodynamics of the cocaine-ethanol interaction to determine whether ethanol directly enhanced the cardiovascular effects of cocaine. Dogs (n = 6) were administered cocaine alone (3 mg/kg i.v.) and in combination with ethanol (1 g/kg i.v.) on separate study days. Blood pressure, heart rate, and the electrocardiogram were monitored continuously, and blood samples were collected periodically after drug administration. Concentration-time data were fitted to a two-compartment model, and concentration-effect data were fitted to a simple E(max) model using WinNonlin software. Pharmacokinetic and pharmacodynamic parameters were compared between the two treatment phases by a paired t test. The administration of ethanol before cocaine resulted in a decrease in cocaine clearance, but there were no differences in any of the other pharmacokinetic or pharmacodynamic parameter values between the cocaine alone and cocaine plus ethanol phases. As has been demonstrated in previous animal and human studies, the clearance of cocaine was decreased by prior administration of ethanol. However, ethanol did not change the concentration-effect relationship of the cardiovascular response to cocaine administration. It is concluded from this study that ethanol does not directly enhance the cardiovascular effects of cocaine.
与酒精中毒相关的最常见药物依赖之一是可卡因依赖。这种组合尤其令人担忧,因为同时滥用这两种药物会增加心血管事件的风险。虽然众所周知,乙醇通过抑制可卡因清除和可卡因乙烯酯的形成来增强可卡因的心血管效应,但也有人推测,乙醇增强可卡因的心血管效应与后两种机制无关。在本研究中,我们研究了可卡因 - 乙醇相互作用的心血管药效学,以确定乙醇是否直接增强可卡因的心血管效应。在不同的研究日,给狗(n = 6)单独静脉注射可卡因(3 mg/kg)以及与乙醇联合静脉注射(1 g/kg)。连续监测血压、心率和心电图,并在给药后定期采集血样。使用WinNonlin软件将浓度 - 时间数据拟合为二室模型,将浓度 - 效应数据拟合为简单的E(max)模型。通过配对t检验比较两个治疗阶段的药代动力学和药效学参数。在可卡因之前给予乙醇会导致可卡因清除率降低,但单独使用可卡因阶段和可卡因加乙醇阶段之间的任何其他药代动力学或药效学参数值均无差异。正如先前在动物和人体研究中所证明的,预先给予乙醇会降低可卡因的清除率。然而,乙醇并没有改变可卡因给药后心血管反应的浓度 - 效应关系。从这项研究得出的结论是,乙醇不会直接增强可卡因的心血管效应。