胡柏对氟哌啶醇诱导的帕金森病动物模型的神经保护作用

R. Saravanan, Bavani, S. Murugesan
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引用次数: 1

摘要

神经炎症、小胶质细胞激活和相互作用增加以及氧化应激是帕金森治疗的新靶点。非甾体抗炎药和抗氧化剂的保护作用已在许多动物研究中得到证实,但流行病学报告尚无定论。广泛分布于印度的一种常见灌木——东树(Thuja orientalis, TOFE)对6-OHDA诱导的SH-SY细胞毒性具有神经保护作用。目的:评价和比较TOFE与布洛芬、维生素E对氟哌啶醇诱导的帕金森大鼠模型的神经保护作用。方法:4组成年雄性sd大鼠6只,每组口服紫花藤(500mg/kg) /布洛芬(100mg/kg)和维生素E (35mg/kg), 1 h后口服氟哌啶醇。(2mg/kg.IP) 7天。运动活动度和僵硬度分别用体温计和普通杆试验测定。也做了紧张症评分。采用单因素方差分析和Kruscal-Wallis检验后再进行Dunn多重比较检验,差异有统计学意义<0.05。结果:在第7天,所有患者的运动活动均明显减少。侧柏对运动强直有轻度保护作用,p值为0.032,对紧张症有2.5分。结论:抗氧化剂和抗炎药物在体外实验中显示的神经保护作用在我们的体内动物研究中没有显示出明显的帕金森病临床特征。这种不确定的标准和观察到的神经保护作用表明,由于存在许多差异,所有来自体外研究的临床前数据都不能有效地推断到体内动物和人体研究。建议在这方面作进一步的探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroprotective effect of Thuja orientalis in haloperidol induced animal model of Parkinsons Disease
Introduction: Neuro-inflammation, increased microglial activation & interaction and oxidative stress are the new targets for Parkinson management. Protective effect of NSAIDs and anti-oxidants has been demonstrated in many animal studies with inconclusive epidemiological reports. Thuja orientalis (TOFE) a common shrub found widely in India has shown neuro-protective effect against 6-OHDA induced toxicity on SH-SY cells. Aim & Objective: To assess and compare neuro-protective effect of TOFE with Ibuprofen and vitamin E in haloperidol induced rat models of Parkinson. Methodology: 6 adult male Sprague Dawley rats each in 4 groups were given Thuja orientalis (500mg/kg) / Ibuprofen (100mg/kg) and Vitamin E (35mg/kg) orally followed 1 hour latter by haloperidol. (2mg/kg.IP) for 7 days. Motor activity and rigidity were assessed with actophotometer and common bar test. Catatonia scoring was also done. One way ANOVA and Kruscal-Wallis tests followed by Dunn’s multiple comparison test were used for statistical significance of <0.05. Results: Significant reduction in motor activity was observed in all on 7 th day. Mild protection by thuja orientalis against motor rigidity was noted with p-value of 0.032 and against catatonia with 2.5 scoring. Conclusion: Neuroprotective effect shown in-vitro experiments by anti-oxidants and anti-inflammatory drugs did not show any significant effects in our in vivo animals study against clinical features as seen in Parkinson’s disease. This inconclusive neuroprotective effect of standards & thuja observed signifies that all preclinical data from in vitro studies cannot be effectively extrapolated to in vivo animal & human studies due to many variations. Further probe in this aspect is suggested.
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