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胆囊收缩素-8对甲基苯丙胺诱导的小鼠行为改变和多巴胺能神经变性的保护作用。

Protective effects of cholecystokinin-8 on methamphetamine-induced behavioral changes and dopaminergic neurodegeneration in mice.

作者信息

Gou Hongyan, Wen Di, Ma Chunling, Li Ming, Li Yingmin, Zhang Wenfang, Liu Li, Cong Bin

机构信息

Department of Forensic Medicine, Hebei Medical University, Hebei Key Laboratory of Forensic Medicine, Shijiazhuang 050017, China.

Department of Forensic Medicine, Hebei Medical University, Hebei Key Laboratory of Forensic Medicine, Shijiazhuang 050017, China.

出版信息

Behav Brain Res. 2015 Apr 15;283:87-96. doi: 10.1016/j.bbr.2015.01.028. Epub 2015 Jan 25.

Abstract

We investigated whether pretreatment with the neuropeptide cholecystokinin-8 affected methamphetamine (METH)-induced behavioral changes and dopaminergic neurodegeneration in male C57/BL6 mice. CCK-8 pretreatment alone had no effect on locomotion and stereotypic behavior and could not induce behavioral sensitization; however, it attenuated, in a dose-dependent manner, hyperlocomotion and behavioral sensitization induced by a low dose of METH (1mg/kg). CCK-8 attenuated METH-induced stereotypic behavior at a dose of 3mg/kg but not at 10mg/kg. CCK-8 pretreatment attenuated METH (10mg/kg)-induced hyperthermia, the decrease of tyrosine hydroxylase (TH) and dopamine transporter (DAT) in the striatum, and TH in the substantia nigra. CCK-8 alone had no effect on rectal temperature, TH and DAT expression in the nigrostriatal region. In conclusion, our study demonstrated that pretreatment with CCK-8 inhibited changes typically induced by repeated exposure to METH, such as hyperlocomotion, behavioral sensitization, stereotypic behavior, and dopaminergic neurotoxicity. These findings make CCK-8 a potential therapeutic agent for the treatment of multiple symptoms associated with METH abuse.

摘要

我们研究了用神经肽胆囊收缩素-8(CCK-8)预处理是否会影响雄性C57/BL6小鼠中甲基苯丙胺(METH)诱导的行为变化和多巴胺能神经变性。单独使用CCK-8预处理对运动和刻板行为没有影响,也不能诱导行为敏化;然而,它以剂量依赖的方式减弱了低剂量METH(1mg/kg)诱导的运动亢进和行为敏化。CCK-8在3mg/kg剂量时减弱了METH诱导的刻板行为,但在10mg/kg剂量时没有。CCK-8预处理减弱了METH(10mg/kg)诱导的体温过高、纹状体中酪氨酸羟化酶(TH)和多巴胺转运体(DAT)的减少以及黑质中TH的减少。单独使用CCK-8对直肠温度、黑质纹状体区域的TH和DAT表达没有影响。总之,我们的研究表明,用CCK-8预处理可抑制反复接触METH通常诱导的变化,如运动亢进、行为敏化、刻板行为和多巴胺能神经毒性。这些发现使CCK-8成为治疗与METH滥用相关的多种症状的潜在治疗药物。

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