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余甘子提取物通过减轻帕金森病小鼠模型中的线粒体功能障碍和炎症来发挥多巴胺能神经保护作用。

Garcinia morella extract confers dopaminergic neuroprotection by mitigating mitochondrial dysfunctions and inflammation in mouse model of Parkinson's disease.

机构信息

Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, Assam, India.

Department of Zoology, Pandit Deendayal Upadhyaya Adarsha Mahavidyalaya (PDUAM), Behali, Biswanath, Assam, India.

出版信息

Metab Brain Dis. 2022 Aug;37(6):1887-1900. doi: 10.1007/s11011-022-01001-9. Epub 2022 May 27.

Abstract

Dopaminergic neuroprotection is the main interest in designing novel therapeutics against Parkinson's disease (PD). In the process of dopaminergic degeneration, mitochondrial dysfunctions and inflammation are significant. While the existing drugs provide symptomatic relief against PD, a therapy conferring total neuroprotection by targeting multiple degenerative pathways is still lacking. Garcinia morella is a common constituent of Ayurvedic medication and has been used for the treatment of inflammatory disorders. The present study investigates whether administration of G. morella fruit extract (GME) in MPTP mouse model of PD protects against dopaminergic neurodegeneration, including the underlying pathophysiologies, and reverses the motor behavioural abnormalities. Administration of GME prevented the loss of dopaminergic cell bodies in the substantia nigra and its terminals in the corpus striatum of PD mice. Subsequently, reversal of parkinsonian behavioural abnormalities, viz. akinesia, catalepsy, and rearing, was observed along with the recovery of striatal dopamine and its metabolites in the experimental model. Furthermore, reduced activity of the mitochondrial complex II in the nigrostriatal pathway of brain of the mice was restored after the administration of GME. Also, MPTP-induced enhanced activation of Glial fibrillary acidic protein (GFAP) and neuronal nitric oxide synthase (nNOS) in the nigrostriatal pathway, which are the markers of inflammatory stress, were found to be ameliorated on GME treatment. Thus, our study presented a novel mode of dopaminergic neuroprotection by G. morella in PD by targeting the mitochondrial dysfunctions and neuroinflammation, which are considered to be intricately associated with the loss of dopaminergic neurons.

摘要

设计治疗帕金森病(PD)的新疗法主要关注多巴胺能神经保护。在多巴胺能变性过程中,线粒体功能障碍和炎症很重要。虽然现有的药物提供了针对 PD 的对症缓解,但仍然缺乏一种通过靶向多种退行性途径提供全面神经保护的疗法。藤黄果是阿育吠陀药物的常见成分,已用于治疗炎症性疾病。本研究调查了在 MPTP 诱导的 PD 小鼠模型中给予藤黄果提取物(GME)是否可以防止多巴胺能神经退行性变,包括潜在的病理生理学,并逆转运动行为异常。GME 的给予防止了 PD 小鼠黑质中多巴胺能细胞体及其纹状体末端的丢失。随后,观察到帕金森病行为异常(运动不能、僵住和站立)的逆转,以及实验模型中纹状体多巴胺及其代谢物的恢复。此外,GME 给药后恢复了脑黑质纹状体通路中线粒体复合物 II 的活性。此外,MPTP 诱导的神经胶质纤维酸性蛋白(GFAP)和神经元型一氧化氮合酶(nNOS)在黑质纹状体通路中的活性增强,这是炎症应激的标志物,在 GME 治疗后发现得到了改善。因此,我们的研究提出了一种通过 G. morella 靶向线粒体功能障碍和神经炎症来保护多巴胺能神经元的新型 PD 多巴胺能神经保护模式,这些被认为与多巴胺能神经元的丧失密切相关。

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