Supplementation with vitamins D3 and a mitigates Parkinsonism in a haloperidol mice model

IF 2.7 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of chemical neuroanatomy Pub Date : 2024-01-01 DOI:10.1016/j.jchemneu.2023.102366
Mujittapha Umar Sirajo , John C. Oyem , Mohammed Ibrahim Badamasi
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Abstract

Background

Earlier reports suggest that vitamin D3 (Vit D3) supplementation attenuates Parkinsonism in drug-induced motor deficits. Moreover, the function of Vit D3 may be optimized by co-administration with vitamin A (Vit A). In line with the synergistic interplay between vitamins, we hypothesized that the efficacy of Vit D3 to attenuate Parkinsonism in a haloperidol-induced mouse model of motor deficits would be more potent when concomitantly administered with Vit A.

Methods

Thirty-six (36) adult male mice were randomly divided into six groups of six animals each: the control group, the PD model (haloperidol-treated only group) (-D2), and four other groups treated with haloperidol together with either one or two of the following vitamin supplementations: Vit D3, Vit A, Vit D3 +VA, or bromocriptine a known PD drug respectively. Motor functions were assessed using a battery of neurobehavioral tests in experimental animals, after which brain tissues were harvested and processed for biochemical and histomorphological analysis.

Results

We recorded a significant decline in motor activity in the PD mice model treated with haloperidol alone compared to other experimental groups that received vitamin supplementations. The significant decrease in motor activity observed in the PD mice model corresponded with marked neurodegenerative features in the cytoarchitecture of the pyramidal cells in the striatum and primary motor cortex (M1). Furthermore, the haloperidol-induced PD mice model treated with Vit D3 +Vit A showed significant improvement in motor activity and attenuation of oxidative stress levels and neurodegenerative features compared to other groups treated with Vit A, Vit D3 and bromocriptine alone.

Conclusion

Altogether, our findings suggest that concomitant administration of both Vit D3 and Vit A prevents the development of Parkinsonism features in the haloperidol mouse model of motor deficit. Thus, supplementation with Vit D3 +Vit A may be a viable option for slowing the onset and progression of motor deficits.

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补充维生素D3和A减轻氟哌啶醇小鼠模型中的帕金森病。
背景:早期的报告表明,补充维生素D3 (Vit D3)可减轻药物性运动缺陷的帕金森病。此外,维生素D3与维生素A (Vit A)共给药可能会优化其功能。根据维生素之间的协同相互作用,我们假设维生素D3与维生素A同时给药对氟哌啶醇诱导的运动缺陷小鼠模型中的帕金森病的缓解效果更强。对照组,PD模型(仅氟哌啶醇治疗组)(-D2)和其他四个组,分别使用氟哌啶醇和以下一种或两种维生素补充剂:维生素D3,维生素A,维生素D3+VA或溴硝子汀(已知的PD药物)。通过对实验动物进行一系列神经行为测试来评估运动功能,之后采集脑组织并进行生化和组织形态学分析。结果:我们记录到,与其他接受维生素补充的实验组相比,氟哌啶醇单独治疗的PD小鼠模型的运动活动明显下降。在PD小鼠模型中观察到的运动活动的显著下降与纹状体和初级运动皮层(M1)锥体细胞结构的显著神经退行性特征相一致。此外,与单独用Vit A、Vit D3和溴隐亭治疗的其他组相比,用Vit D3 +Vit A治疗的氟哌啶醇诱导的PD小鼠模型显示出运动活动、氧化应激水平和神经退行性特征的显著改善。结论:总之,我们的研究结果表明,在氟哌啶醇运动缺陷小鼠模型中,同时给予维生素D3和维生素A可以防止帕金森病特征的发展。因此,补充维生素D3+维生素A可能是减缓运动缺陷发生和进展的可行选择。
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来源期刊
Journal of chemical neuroanatomy
Journal of chemical neuroanatomy 医学-神经科学
CiteScore
4.50
自引率
3.60%
发文量
87
审稿时长
62 days
期刊介绍: The Journal of Chemical Neuroanatomy publishes scientific reports relating the functional and biochemical aspects of the nervous system with its microanatomical organization. The scope of the journal concentrates on reports which combine microanatomical, biochemical, pharmacological and behavioural approaches. Papers should offer original data correlating the morphology of the nervous system (the brain and spinal cord in particular) with its biochemistry. The Journal of Chemical Neuroanatomy is particularly interested in publishing important studies performed with up-to-date methodology utilizing sensitive chemical microassays, hybridoma technology, immunocytochemistry, in situ hybridization and receptor radioautography, to name a few examples. The Journal of Chemical Neuroanatomy is the natural vehicle for integrated studies utilizing these approaches. The articles will be selected by the editorial board and invited reviewers on the basis of their excellence and potential contribution to this field of neurosciences. Both in vivo and in vitro integrated studies in chemical neuroanatomy are appropriate subjects of interest to the journal. These studies should relate only to vertebrate species with particular emphasis on the mammalian and primate nervous systems.
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