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口服补充肌酸可减轻6-羟基多巴胺损伤大鼠中左旋多巴诱导的运动障碍。

Oral creatine supplementation attenuates L-DOPA-induced dyskinesia in 6-hydroxydopamine-lesioned rats.

作者信息

Valastro Barbara, Dekundy Andrzej, Danysz Wojciech, Quack Guenter

机构信息

Preclinical Research and Development, In Vitro Screening, Merz Pharmaceuticals GmbH, Altenhöferallee 3, 60438 Frankfurt am Main, Germany.

出版信息

Behav Brain Res. 2009 Jan 30;197(1):90-6. doi: 10.1016/j.bbr.2008.08.004. Epub 2008 Aug 12.

Abstract

L-DOPA-induced dyskinesia (LID) is among the motor complications that arise in Parkinson patients after a prolonged treatment with levodopa (L-DOPA). Since previous transcriptome and proteomic studies performed in the rat model of LID suggested important changes in striatal energy-related components, we hypothesize that oral creatine supplementation could prevent or attenuate the occurrence of LID. In this study, 6-hydroxydopamine-lesioned rats received a 2% creatine-supplemented diet for 1 month prior to L-DOPA therapy. During the 21 days of L-DOPA treatment, significant reductions in abnormal involuntary movements (AIMs) have been observed in the creatine-supplemented group, without any worsening of parkinsonism. In situ hybridization histochemistry and immunohistochemistry analysis of the striatum also showed a reduction in the levels of prodynorphin mRNA and FosB/DeltaFosB-immunopositive cells in creatine-supplemented diet group, an effect that was dependant on the development of AIMs. Further investigation of the bioenergetics' status of the denervated striatum revealed significant changes in the levels of creatine both after L-DOPA alone and with the supplemented diet. In conclusion, we demonstrated that combining L-DOPA therapy with a diet enriched in creatine could attenuate LID, which may represent a new way to control the motor complications associated with L-DOPA therapy.

摘要

左旋多巴诱导的运动障碍(LID)是帕金森病患者在长期接受左旋多巴(L-DOPA)治疗后出现的运动并发症之一。由于先前在LID大鼠模型中进行的转录组和蛋白质组学研究表明纹状体能量相关成分发生了重要变化,我们推测口服补充肌酸可以预防或减轻LID的发生。在本研究中,6-羟基多巴胺损伤的大鼠在接受L-DOPA治疗前1个月接受含2%肌酸的饮食。在L-DOPA治疗的21天期间,补充肌酸的组中异常不自主运动(AIMs)显著减少,且帕金森病没有任何恶化。对纹状体进行原位杂交组织化学和免疫组织化学分析还显示,补充肌酸饮食组中前强啡肽原mRNA水平和FosB/DeltaFosB免疫阳性细胞减少,这种效应取决于AIMs的发展。对去神经支配纹状体的生物能量状态的进一步研究表明,单独使用L-DOPA以及补充饮食后,肌酸水平均有显著变化。总之,我们证明将L-DOPA治疗与富含肌酸的饮食相结合可以减轻LID,这可能代表了一种控制与L-DOPA治疗相关的运动并发症的新方法。

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