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高丽红参提取物可减轻 3-硝基丙酸诱导的亨廷顿病样症状。

Korean Red Ginseng Extract Attenuates 3-Nitropropionic Acid-Induced Huntington's-Like Symptoms.

机构信息

Department of Anatomy, College of Korean Medicine and Institute of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2013;2013:237207. doi: 10.1155/2013/237207. Epub 2013 Jan 27.

Abstract

Korean red ginseng (KRG) possesses neuroprotective activity. However, the potential neuroprotective value of KRG for the striatal toxicity is largely unknown. We investigated whether KRG extract (KRGE) could have a neuroprotective effect in a 3-nitropropionic acid- (3-NP) induced (i.p.) Huntington's disease (HD) model. KRGE (50, 100, and 250 mg/kg/day, p.o.) was administrated 10 days before 3-NP injection (pre-administration), from the same time with 3-NP injection (co-administration), or from the peak point of neurological impairment by 3-NP injection (post-administration). Pre-administration of KRGE produced the greatest neuroprotective effect in this model. Pre-administration of KRGE significantly decreased 3-NP-induced neurological impairment, lethality, lesion area, and neuronal loss in the 3-NP-injected striatum. KRGE attenuated microglial activation and phosphorylation of mitogen-activated protein kinases (MAPKs) and nuclear factor-kappa B (NF-κB) signal pathway. KRGE also reduced the level of mRNA expression of tumor necrosis factor-alpha, interleukin- (IL-) 1β, IL-6, inducible nitric oxide synthase, and OX-42. Interestingly, the intrathecal administration of SB203580 (a p38 inhibitor) or PD98059 (an inhibitor of MAPK Kinase, MEK) increased the survival rate in the 3-NP-induced HD model. Pre-administration of KRGE may effectively inhibit 3-NP-induced striatal toxicity via the inhibition of the phosphorylation of MAPKs and NF-κB pathways, indicating its therapeutic potential for suppressing Huntington's-like symptoms.

摘要

高丽红参具有神经保护活性。然而,高丽红参提取物(KRGE)对纹状体毒性的潜在神经保护价值在很大程度上尚不清楚。我们研究了 KRGE 是否对 3-硝基丙酸(3-NP)诱导的(腹腔内)亨廷顿病(HD)模型具有神经保护作用。KRGE(50、100 和 250mg/kg/天,口服)在 3-NP 注射前 10 天(预处理)、与 3-NP 注射同时(共处理)或从 3-NP 注射引起的神经损伤高峰点开始(后处理)给予。预处理 KRGE 在该模型中产生了最大的神经保护作用。预处理 KRGE 显著降低了 3-NP 诱导的神经损伤、死亡率、纹状体损伤面积和神经元丢失。KRGE 减弱了小胶质细胞的激活和丝裂原活化蛋白激酶(MAPKs)和核因子-κB(NF-κB)信号通路的磷酸化。KRGE 还降低了肿瘤坏死因子-α、白细胞介素-(IL-)1β、IL-6、诱导型一氧化氮合酶和 OX-42 的 mRNA 表达水平。有趣的是,鞘内给予 SB203580(p38 抑制剂)或 PD98059(MAPK 激酶抑制剂,MEK)可提高 3-NP 诱导的 HD 模型中的存活率。预处理 KRGE 可能通过抑制 MAPKs 和 NF-κB 途径的磷酸化有效抑制 3-NP 诱导的纹状体毒性,表明其具有抑制亨廷顿样症状的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d0b/3568869/4238e33b1300/ECAM2013-237207.001.jpg

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