Protective effects of the antioxidant sulforaphane on behavioral changes and neurotoxicity in mice after the administration of methamphetamine

被引:40
|
作者
Chen, Hongxian [1 ,2 ]
Wu, Jin [1 ]
Zhang, Jichun [1 ]
Fujita, Yuko [1 ]
Ishima, Tamaki [1 ]
Iyo, Masaomi [3 ]
Hashimoto, Kenji [1 ]
机构
[1] Chiba Univ, Ctr Forens Mental Hlth, Div Clin Neurosci, Chiba 2608670, Japan
[2] Cent South Univ, Xiangya Hosp 2, WHO Collaborating Ctr Drug Abuse & Hlth, Mental Hlth Inst, Changsha 410011, Hunan, Peoples R China
[3] Chiba Univ, Grad Sch Med, Dept Psychiat, Chiba 2608670, Japan
关键词
Sulforaphane; Dopamine; Methamphetamine; Microglia; Neurotoxicity; Sensitization; INDUCED DOPAMINERGIC NEUROTOXICITY; ACETYL-L-CYSTEINE; OXIDATIVE STRESS; MOLECULAR-MECHANISM; AMPHETAMINE; SENSITIZATION; BRAIN; TRANSPORTERS; ACTIVATION; REDUCTION;
D O I
10.1007/s00213-011-2619-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Methamphetamine (METH) is a powerfully addictive stimulant associated with serious health conditions. Accumulating evidence suggests a role of oxidative stress in METH-induced behavioral abnormalities. Sulforaphane (SFN), found in cruciferous vegetables, is a potent antioxidant. It is of interest to determine whether SFN can attenuate behavioral and neuropathological changes associated with METH exposure. This study was undertaken to examine the effects of SFN on behavioral changes and dopaminergic neurotoxicity in mice exposed to METH. The effects of SFN on acute hyperlocomotion and the development of behavioral sensitization induced by the administration of METH were examined. Levels of dopamine (DA) and its major metabolite 3,4-dihydroxyphenyl acetic acid (DOPAC) in the striatum were measured. In addition, DA transporter (DAT) immunoreactivity was also performed. Pretreatment with SFN at 1, 3, and 10 mg/kg elicited a dose-dependent attenuation of acute hyperlocomotion in mice, after a single administration of METH (3 mg/kg). The development of behavioral sensitization after repeated administrations of METH (3 mg/kg/day, once daily for 5 days) was significantly reduced by pretreatment with SFN (10 mg/kg). In addition, the lowering of DA levels and DOPAC as well as DAT immunoreactivity in the striatum, usually seen after repeated administration of METH, was significantly attenuated by both pretreatment and the subsequent administration of SFN. Furthermore, SFN significantly reduced microglial activation in the striatum after repeated exposure to METH. It is therefore likely that SFN can be a useful drug for the treatment of signs associated with METH abuse in humans.
引用
收藏
页码:37 / 45
页数:9
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