罗布达树树脂提取物对3-硝基丙酸诱导的大鼠亨廷顿病症状的影响。

IF 2.1 Q3 CHEMISTRY, MEDICINAL
Chirag Patel, Khushboo Thakur, Lalita Shagond, Sanjeev Acharya, Ketan Ranch, Sai Hs Boddu
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引用次数: 0

摘要

背景与目的:亨廷顿氏病(HD)是一种以纹状体神经元死亡为特征的神经退行性疾病。亚洲酸是一种具有神经保护作用的植物活性成分,被认为是治疗不同神经退行性疾病的可接受的候选药物。本研究以3-硝基丙酸(3-NP)诱导的HD大鼠为研究对象,研究了罗布沙树树脂提取物(SRRE)的有益药理作用。实验方法:通过测定3-NP (10 mg/kg)诱导大鼠的体重、神经系统评分、运动协调、空间记忆、抑郁样行为等行为参数、神经生化参数(γ -氨基丁酸和乙酰胆碱酯酶)以及脑内氧化应激参数,研究SRRE(285.7和666.7 mg/kg, p.o, 14 d)对大鼠的神经保护作用。并对大鼠脑组织病理学进行了研究。结果:与3- np治疗大鼠相比,SRRE治疗(285.7 mg/kg和666.7 mg/kg)显著恢复了大鼠的体重、运动协调和线粒体酶复合体I功能,并改善了记忆障碍。此外,SRRE处理显著恢复脑组织抗氧化酶活性,改善3-NP引起的组织病理改变。结论与意义:SRRE对3- np诱导的HD大鼠的神经保护作用可能是通过降低氧化应激介导的,这可能有利于Shorea robusta在HD中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of <i>Shorea robusta</i> resin extract in 3-nitropropionic acid-induced Huntington's disease symptoms in Sprague-Dawley rats.

Effect of <i>Shorea robusta</i> resin extract in 3-nitropropionic acid-induced Huntington's disease symptoms in Sprague-Dawley rats.

Effect of <i>Shorea robusta</i> resin extract in 3-nitropropionic acid-induced Huntington's disease symptoms in Sprague-Dawley rats.

Effect of Shorea robusta resin extract in 3-nitropropionic acid-induced Huntington's disease symptoms in Sprague-Dawley rats.

Background and purpose: Huntington's disease (HD) is a neurodegenerative disease characterized by neuronal death in the striatum. Asiatic acid is an active component of Shorea robusta (Dipterocarpaceae) plants with neuroprotective activity and is considered an acceptable therapeutic candidate for different neurodegenerative diseases. In the present study, the beneficial pharmacological action of Shorea robusta resin extract (SRRE) was assessed in 3-nitropropionic acid (3-NP)-induced HD in rats.

Experimental approach: The neuroprotective effect of SRRE (285.7 and 666.7 mg/kg, p.o., 14 days) was studied in 3-NP (10 mg/kg)-induced rats by measuring body weight, behavioral parameters including neurological scoring, motor coordination, spatial memory, and depression-like behavior, neuro-biochemical parameters (gamma-aminobutyric acid and acetylcholinesterase), and oxidative stress parameter in the brain. Histopathology of the rat's brain was also studied.

Findings/results: SRRE treatment (285.7 mg/kg and 666.7 mg/kg) substantially restored body weight, motor coordination, and mitochondrial enzyme complex I function and improved memory impairment as compared to 3-NP-treated rats. Furthermore, SRRE treatment significantly restored the antioxidant enzyme activity in brain tissue and ameliorated the histopathological changes induced by 3-NP.

Conclusion and implications: The neuroprotective effect of SRRE on 3-NP-induced HD in rats was mediated by a reduction in oxidative stress which may favor the usefulness of Shorea robusta in HD.

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来源期刊
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences CHEMISTRY, MEDICINAL-
CiteScore
3.60
自引率
19.00%
发文量
50
审稿时长
34 weeks
期刊介绍: Research in Pharmaceutical Sciences (RPS) is included in Thomson Reuters ESCI Web of Science (searchable at WoS master journal list), indexed with PubMed and PubMed Central and abstracted in the Elsevier Bibliographic Databases. Databases include Scopus, EMBASE, EMCare, EMBiology and Elsevier BIOBASE. It is also indexed in several specialized databases including Scientific Information Database (SID), Google Scholar, Iran Medex, Magiran, Index Copernicus (IC) and Islamic World Science Citation Center (ISC).
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