Mann Amandeep, Miksys Sharon, Lee Anna, Mash Deborah C, Tyndale Rachel F
Centre for Addiction and Mental Health, University of Toronto, Canada M5S 1A8.
Neuropharmacology. 2008 Dec;55(7):1147-55. doi: 10.1016/j.neuropharm.2008.07.017. Epub 2008 Jul 19.
Cytochrome P450 (CYP) 2D6, an enzyme found in the liver and the brain, is involved in the metabolism of numerous centrally acting drugs (e.g. antidepressants, neuroleptics, opiates), endogenous neurochemicals (e.g. catecholamines) and in the inactivation of neurotoxins (e.g. pesticides, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)). Although CYP2D6 is essentially an uninducible enzyme in the liver, we show that smokers have higher CYP2D6 in the brain, especially in the basal ganglia. In order to determine whether nicotine, a component of cigarette smoke, could increase brain CYP2D, African Green monkeys were treated chronically with nicotine (0.05 mg/kg for 2 days, then 0.15 mg/kg for 2 days followed by 0.3 mg/kg for 18 days s.c., b.i.d.). Monkeys treated with nicotine showed significant induction of CYP2D in brain when compared to saline-treated animals as detected by western blotting and immunocytochemistry. No changes in liver CYP2D were observed in nicotine-treated monkeys. Induction was observed in various brain regions including those affected in Parkinson's disease (PD) such as substantia nigra (3-fold, p = 0.01), putamen (2.1-fold, p = 0.001) and brainstem (2.4-fold, p = 0.001), with the caudate nucleus approaching significance (1.6-fold, p = 0.07). Immunocytochemistry revealed that the expression of CYP2D in both saline- and nicotine-treated monkeys is cell-specific particularly in the cerebellum, frontal cortex and hippocampus. These results suggest that monkey brain expresses CYP2D, which is induced in specific cells and brain regions upon chronic nicotine treatment. Smokers, or those using nicotine treatment, may have higher levels of brain CYP2D6 that may result in altered localized CNS drug metabolism and inactivation of neurotoxins.
细胞色素P450(CYP)2D6是一种存在于肝脏和大脑中的酶,参与多种中枢作用药物(如抗抑郁药、抗精神病药、阿片类药物)、内源性神经化学物质(如儿茶酚胺)的代谢以及神经毒素(如杀虫剂、1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP))的失活。尽管CYP2D6在肝脏中本质上是一种不可诱导的酶,但我们发现吸烟者大脑中的CYP2D6水平更高,尤其是在基底神经节。为了确定香烟烟雾中的成分尼古丁是否会增加大脑中的CYP2D,对非洲绿猴进行了尼古丁长期治疗(0.05mg/kg,持续2天,然后0.15mg/kg,持续2天,随后0.3mg/kg,皮下注射,每日两次,持续18天)。与生理盐水处理的动物相比,经尼古丁处理的猴子通过蛋白质免疫印迹法和免疫细胞化学检测显示大脑中CYP2D有显著诱导。在经尼古丁处理的猴子中未观察到肝脏CYP2D的变化。在包括帕金森病(PD)受累区域(如黑质(增加3倍,p = 0.01)、壳核(增加2.1倍,p = 0.001)和脑干(增加2.4倍,p = 0.001))在内的各个脑区均观察到诱导,尾状核接近显著水平(增加1.6倍,p = 0.07)。免疫细胞化学显示,生理盐水处理和尼古丁处理的猴子中CYP2D的表达均具有细胞特异性,特别是在小脑、额叶皮质和海马体中。这些结果表明,猴脑表达CYP2D,在长期尼古丁处理后,特定细胞和脑区中该酶会被诱导。吸烟者或使用尼古丁治疗的人,其大脑中CYP2D6水平可能更高,这可能导致局部中枢神经系统药物代谢改变以及神经毒素失活。