5-(4-Hydroxy-3-dimethoxybenzylidene)-thiazolidinone improves motor functions and exerts antioxidant potential in hemiparkinsonian rats.

IF 1.6 4区 心理学 Q3 BEHAVIORAL SCIENCES Behavioural Pharmacology Pub Date : 2023-02-01 DOI:10.1097/FBP.0000000000000712
Zhili Ren, Hui Ding, Ming Zhou, Nan Yang, Yanyong Liu, Piu Chan
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引用次数: 1

Abstract

Our previous study demonstrated that 5-(4-hydroxy-3-dimethoxybenzylidene)-thiazolidinone (RD-1), one of rhodamine derivatives, significantly improves motor function in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mice model and could minimize mitochondrial impairment, which is a potential therapeutic target to slow down the dopaminergic neurodegeneration in Parkinson's disease. To further evaluate its therapeutic and antioxidative potential in Parkinson's disease, the current study was designed to explore the effect of RD-1 on hemiparkinsonian rats following unilateral 6-hydroxydopamine lesions. Motor functional behavioral tests, including apomorphine-induced rotational analysis and beam walking tests, were assessed. Our results showed that oral RD-1 administration for 2 weeks alleviated beam walking disability, but not the rotational behavior. Furthermore, compared to the sham group, tyrosine hydroxylase- (TH-) positive neurons in the substantia nigra pars compacta and fibers in the striatum were significantly preserved in the RD-1 treatment group. The abnormal activities of superoxide dismutase, catalase, and glutathione peroxidase and contents of MDA were evidently ameliorated by RD-1, at least partly. We conclude that RD-1 could improve motor functions and alleviate the loss of dopaminergic expression in the nigrostriatal pathway of Parkinson's disease rats, and the protective mechanism of RD-1 against neurodegeneration was possibly via its modulation of antioxidation.

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5-(4-羟基-3-二甲氧基苄基)-噻唑烷酮改善半帕金森大鼠运动功能并发挥抗氧化潜能。
我们前期的研究表明罗丹明衍生物之一的5-(4-羟基-3-二甲氧基苄基)-噻唑烷酮(RD-1)能显著改善1-甲基-4-苯基-1,2,3,6-四氢吡啶小鼠模型的运动功能,并能最大限度地减少线粒体损伤,是减缓帕金森病多巴胺能神经退行性变的潜在治疗靶点。为了进一步评估其在帕金森病中的治疗和抗氧化潜力,本研究旨在探讨RD-1对单侧6-羟多巴胺损伤后的半帕金森大鼠的影响。运动功能行为测试,包括阿吗啡诱导的旋转分析和梁行走测试进行评估。我们的研究结果显示,口服RD-1 2周可以减轻步行障碍,但不能减轻旋转行为。此外,与假手术组相比,RD-1治疗组黑质致密部和纹状体纤维中酪氨酸羟化酶- (TH-)阳性神经元明显保留。RD-1能明显改善小鼠超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性及MDA含量。我们认为,RD-1可以改善帕金森病大鼠的运动功能,减轻黑质纹状体通路多巴胺能表达的缺失,其抗氧化作用可能与RD-1对神经退行性变的保护作用有关。
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来源期刊
Behavioural Pharmacology
Behavioural Pharmacology 医学-行为科学
CiteScore
3.40
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Behavioural Pharmacology accepts original full and short research reports in diverse areas ranging from ethopharmacology to the pharmacology of schedule-controlled operant behaviour, provided that their primary focus is behavioural. Suitable topics include drug, chemical and hormonal effects on behaviour, the neurochemical mechanisms under-lying behaviour, and behavioural methods for the study of drug action. Both animal and human studies are welcome; however, studies reporting neurochemical data should have a predominantly behavioural focus, and human studies should not consist exclusively of clinical trials or case reports. Preference is given to studies that demonstrate and develop the potential of behavioural methods, and to papers reporting findings of direct relevance to clinical problems. Papers making a significant theoretical contribution are particularly welcome and, where possible and merited, space is made available for authors to explore fully the theoretical implications of their findings. Reviews of an area of the literature or at an appropriate stage in the development of an author’s own work are welcome. Commentaries in areas of current interest are also considered for publication, as are Reviews and Commentaries in areas outside behavioural pharmacology, but of importance and interest to behavioural pharmacologists. Behavioural Pharmacology publishes frequent Special Issues on current hot topics. The editors welcome correspondence about whether a paper in preparation might be suitable for inclusion in a Special Issue.
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