Centre de Recherche du CHUL (CHUQ), Axe Neurosciences, Québec, QC, Canada.
Neurobiol Dis. 2012 Jan;45(1):529-38. doi: 10.1016/j.nbd.2011.09.009. Epub 2011 Sep 21.
The identification of modifiable nutritional risk factors is highly relevant to the development of preventive strategies for neurodegenerative disorders including Parkinson's disease (PD). In this study, adult C57BL/6 mice were fed either a control (CD-12%kcal) or a high-fat diet (HFD-60%kcal) for 8 weeks prior to MPTP exposure, a toxin which recreates a number of pathological features of PD. HFD-fed mice significantly gained weight (+41%), developed insulin resistance and a systemic immune response characterized by an increase in circulating leukocytes and plasmatic cytokines/chemokines (interleukin-1α, MCP-1, MIP-1α). As expected, the MPTP treatment produced nigral dopaminergic degeneration as evidenced by the loss of striatal dopamine and the decreased number of nigral tyrosine hydroxylase (TH)- and dopamine transporter-expressing neurons (23% and 25%, respectively). However, exposure to HFD exacerbated the effects of MPTP on striatal TH (23%) and dopamine levels (32%), indicating that diet-induced obesity is associated with a reduced capacity of nigral dopaminergic terminals to cope with MPTP-induced neurotoxicity. Since high-fat consumption is commonplace in our modern society, dietary fat intake may represent an important modifiable risk factor for PD.
鉴定可改变的营养风险因素与包括帕金森病(PD)在内的神经退行性疾病的预防策略的制定密切相关。在这项研究中,成年 C57BL/6 小鼠在接受 MPTP 暴露前,分别用对照(CD-12%kcal)或高脂肪饮食(HFD-60%kcal)喂养 8 周,MPTP 是一种可重现 PD 许多病理特征的毒素。高脂肪饮食喂养的小鼠体重显著增加(增加 41%),发展出胰岛素抵抗和全身性免疫反应,表现为循环白细胞和血浆细胞因子/趋化因子(白细胞介素-1α、MCP-1、MIP-1α)增加。正如预期的那样,MPTP 处理产生了黑质多巴胺能神经元变性,表现为纹状体多巴胺的丧失和黑质酪氨酸羟化酶(TH)和多巴胺转运蛋白表达神经元数量减少(分别为 23%和 25%)。然而,高脂肪饮食暴露加剧了 MPTP 对纹状体 TH(23%)和多巴胺水平(32%)的影响,表明饮食诱导的肥胖与黑质多巴胺能末梢应对 MPTP 诱导的神经毒性的能力降低有关。由于高脂肪摄入在我们的现代社会中很常见,因此饮食中的脂肪摄入可能是 PD 的一个重要可改变的风险因素。