Shen Yan-Qin, Hebert Guillaum, Lin Ling-Yun, Luo Yan-Ling, Moze Elizabeth, Li Kang-Sheng, Neveu Pierre J
Department of Microbiology and Immunology, Shantou University Medical College, 12 Raoping Road, Shantou, Guangdong 515031, P.R. China.
J Neuroimmunol. 2005 Jan;158(1-2):14-25. doi: 10.1016/j.jneuroim.2004.06.011.
MPTP (N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) induces diminution of the dopamine in nigrostriatal pathway and cognitive deficits in mice. MPTP treatment also increases pro-inflammatory cytokine production in substantia nigra and striatum. Since, pro-inflammatory cytokines influence striatal dopamine content and provoke cognitive impairments, the cognitive defects induced by MPTP may be partly due to brain cytokine induction in other structures than nigrostriatal pathway. Furthermore, behavioral lateralization, as assessed by paw preference, influences cytokine production at the periphery and in the central nervous system. Behavioral lateralization may thus influence brain cytokine levels after MPTP. In order to address these issues, mice selected for paw preference were injected with 25 mg/kg MPTP i.p. for five consecutive days after which striatal dopamine and DOPAC contents were measured by HPLC and IL-1beta and IL-6 quantified by ELISA in the striatum, cerebral cortex, hippocampus and hypothalamus. The results showed that MPTP treatment induced dramatic loss of DA in striatum, simultaneously, IL-6 levels decreased in the striatum and increased in hippocampus and hypothalamus, while IL-1beta levels decreased in the striatum, cerebral cortex and hippocampus. Interestingly, striatal dopamine turnover under basal conditions as well as striatal IL-1beta and IL-6 levels under basal conditions and after MPTP depended on behavioral lateralization. Left pawed mice showed a higher decrease in dopamine turnover and lower cytokine levels as compared to right pawed animals. Behavioral lateralization also influenced IL-6 hippocampal levels under basal conditions and IL-1beta cortical levels after MPTP. From these results, it can be concluded that MPTP-induced cognitive defects are accompanied by an alteration of pro-inflammatory cytokine levels in brain structures other than those involved in the nigrostriatal pathway. In addition, MPTP-induced dopamine decrease is influenced by behavioral lateralization, possibly through an effect on brain cytokine levels.
MPTP(N-甲基-4-苯基-1,2,3,6-四氢吡啶)可导致小鼠黑质纹状体通路中的多巴胺减少以及认知缺陷。MPTP处理还会增加黑质和纹状体中促炎细胞因子的产生。由于促炎细胞因子会影响纹状体多巴胺含量并引发认知障碍,MPTP诱导的认知缺陷可能部分归因于黑质纹状体通路以外其他脑区的细胞因子诱导。此外,通过爪偏好评估的行为偏侧化会影响外周和中枢神经系统中的细胞因子产生。因此,行为偏侧化可能会影响MPTP处理后的脑内细胞因子水平。为了解决这些问题,选择具有爪偏好的小鼠腹腔注射25mg/kg MPTP,连续五天,之后通过高效液相色谱法测量纹状体多巴胺和3,4-二羟基苯乙酸(DOPAC)含量,并通过酶联免疫吸附测定法(ELISA)对纹状体、大脑皮层、海马体和下丘脑的白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)进行定量。结果表明,MPTP处理导致纹状体中多巴胺显著减少,同时,纹状体中IL-6水平降低,海马体和下丘脑中IL-6水平升高,而纹状体、大脑皮层和海马体中IL-1β水平降低。有趣的是,基础条件下的纹状体多巴胺周转率以及基础条件下和MPTP处理后的纹状体IL-1β和IL-6水平取决于行为偏侧化。与右爪小鼠相比,左爪小鼠的多巴胺周转率下降幅度更大,细胞因子水平更低。行为偏侧化还影响基础条件下海马体中IL-6水平以及MPTP处理后大脑皮层中IL-1β水平。从这些结果可以得出结论,MPTP诱导的认知缺陷伴随着黑质纹状体通路以外脑区促炎细胞因子水平的改变。此外,MPTP诱导的多巴胺减少受行为偏侧化影响,可能是通过对脑内细胞因子水平的作用。