Mets B, Jamdar S, Diaz J
Department of Anesthesiology, College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.
J Pharm Pharmacol. 1999 Jun;51(6):679-84. doi: 10.1211/0022357991772970.
The purpose of this study was to determine whether a catecholamine infusion administered to simulate a stress state could alter the pharmacokinetics of administered cocaine and effect the formation of benzoylecgonine, its major metabolite, in the rat. In a previous investigation we determined that catecholamine infusion enhanced the toxicity of continuous cocaine infusion by reducing the time before the onset of convulsions and respiratory arrest. We postulated that this enhanced toxicity was an effect of catecholamines on the pharmacokinetics of cocaine. To test this hypothesis we studied plasma cocaine and benzoylecgonine disposition after intravenous bolus administration of cocaine (5 mg kg(-1)) to 19 male Sprague-Dawley rats and to 10 rats which received an initial loading-dose cocaine infusion of 1 mg kg(-1) min(-1) (for 5 min) followed by continuous infusion of 100 microg kg(-1) min(-1). Rats in both studies randomly received either continuous catecholamine infusion comprising adrenaline (7.25 microg mL(-1)), noradrenaline (4.4 microg mL(-1)) and dopamine (8.0 microg mL(-1)) or saline, administered at a similar rate. Bolus dose cocaine administration, simultaneously with catecholamine infusion, resulted in significantly higher Cmax levels for cocaine (3.8 compared with 2.5 microg mL(-1)) and lower distribution half-lives (3.3 compared with 5.9 min) and central compartment volumes of distribution (1.5 compared with 2.1 L kg(-1)) compared with saline infusion. Benzoylecgonine formation was significantly reduced in rats receiving catecholamines whereas the elimination half-lives (26.3 compared with 25.0 min) and systemic clearances (146 compared with 146 mL kg(-1) min(-1)) were not different. Continuous cocaine infusion (after an initial loading infusion) resulted in the doubling of plasma cocaine levels in rats receiving catecholamines compared with the control group. These data indicate that elevated plasma catecholamines have significant effects on cocaine pharmacokinetics. This might serve to explain the enhanced toxicity from concomitant cocaine and catecholamine infusion demonstrated in previous experiments.
本研究的目的是确定给予儿茶酚胺以模拟应激状态是否会改变给予大鼠的可卡因的药代动力学,并影响其主要代谢产物苯甲酰爱康宁的形成。在先前的一项研究中,我们确定儿茶酚胺输注通过缩短惊厥发作和呼吸停止前的时间来增强连续输注可卡因的毒性。我们推测这种增强的毒性是儿茶酚胺对可卡因药代动力学的影响。为了验证这一假设,我们研究了19只雄性Sprague-Dawley大鼠和10只大鼠静脉推注可卡因(5mg kg(-1))后血浆可卡因和苯甲酰爱康宁的处置情况,这10只大鼠先接受1mg kg(-1) min(-1)(持续5分钟)的可卡因负荷剂量输注,然后持续输注100μg kg(-1) min(-1)。两项研究中的大鼠随机接受以相似速率给予的包含肾上腺素(7.25μg mL(-1))、去甲肾上腺素(4.4μg mL(-1))和多巴胺(8.0μg mL(-1))的连续儿茶酚胺输注或生理盐水。与生理盐水输注相比,在给予儿茶酚胺输注的同时静脉推注可卡因剂量,可卡因的Cmax水平显著更高(分别为3.8与2.5μg mL(-1)),分布半衰期更低(分别为3.3与5.9分钟),中央室分布容积更低(分别为1.5与2.1L kg(-1))。接受儿茶酚胺的大鼠中苯甲酰爱康宁的形成显著减少,而消除半衰期(分别为26.3与25.0分钟)和全身清除率(分别为146与146mL kg(-1) min(-1))没有差异。与对照组相比,接受儿茶酚胺的大鼠在初始负荷输注后连续输注可卡因导致血浆可卡因水平加倍。这些数据表明血浆儿茶酚胺水平升高对可卡因药代动力学有显著影响。这可能有助于解释先前实验中显示的可卡因和儿茶酚胺联合输注增强的毒性。