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在帕金森病大鼠模型中,生酮饮食通过上调谷胱甘肽来保护多巴胺能神经元免受6-羟基多巴胺的神经毒性。

Ketogenic diet protects dopaminergic neurons against 6-OHDA neurotoxicity via up-regulating glutathione in a rat model of Parkinson's disease.

作者信息

Cheng Baohua, Yang Xinxin, An Liangxiang, Gao Bo, Liu Xia, Liu Shuwei

机构信息

Jining Medical College, Jining, China.

出版信息

Brain Res. 2009 Aug 25;1286:25-31. doi: 10.1016/j.brainres.2009.06.060. Epub 2009 Jun 25.

Abstract

The high-fat ketogenic diet (KD) leads to an increase of blood ketone bodies (KB) level and has been used to treat refractory childhood seizures for over 80 years. Recent reports show that KD, KB and their components (d-beta-hydroxybutyrate, acetoacetate and acetone) have neuroprotective for acute and chronic neurological disorders. In our present work, we examined whether KD protected dopaminergic neurons of substantia nigra (SN) against 6-hydroxydopamine (6-OHDA) neurotoxicity in a rat model of Parkinson's disease (PD) using Nissl staining and tyrosine hydroxylase (TH) immunohistochemistry. At the same time we measured dopamine (DA) and its metabolites dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) in the striatum. To elucidate the mechanism, we also measured the level of glutathione (GSH) of striatum. Our data showed that Nissl and TH-positive neurons increased in rats fed with KD compared to rats with normal diet (ND) after intrastriatal 6-OHDA injection, so did DA and its metabolite DOPAC. While HVA had not changed significantly. The change of GSH was significantly similar to DA. We concluded that KD had neuroprotective against 6-OHDA neurotoxicity and in this period GSH played an important role.

摘要

高脂肪生酮饮食(KD)会导致血液中酮体(KB)水平升高,并且已经用于治疗难治性儿童癫痫超过80年。最近的报告显示,KD、KB及其成分(d-β-羟基丁酸、乙酰乙酸和丙酮)对急性和慢性神经疾病具有神经保护作用。在我们目前的研究中,我们使用尼氏染色和酪氨酸羟化酶(TH)免疫组织化学,在帕金森病(PD)大鼠模型中研究了KD是否能保护黑质(SN)中的多巴胺能神经元免受6-羟基多巴胺(6-OHDA)的神经毒性。同时,我们测量了纹状体中多巴胺(DA)及其代谢产物二羟基苯乙酸(DOPAC)和高香草酸(HVA)的含量。为了阐明其机制,我们还测量了纹状体中谷胱甘肽(GSH)的水平。我们的数据显示,与正常饮食(ND)的大鼠相比,纹状体内注射6-OHDA后,喂食KD的大鼠中尼氏和TH阳性神经元增加,DA及其代谢产物DOPAC也增加。而HVA没有显著变化。GSH的变化与DA显著相似。我们得出结论,KD对6-OHDA神经毒性具有神经保护作用,在此过程中GSH发挥了重要作用。

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