Potential applications of mitochondrial therapy with a focus on Parkinson's disease and mitochondrial transplantation

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Pranay Wal, Ankita Wal, Himangi Vig, Danish Mahmood, Mohd Masih Uzzaman Khan
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Abstract

Purpose: Both aging and neurodegenerative illnesses are thought to be influenced by mitochondrial malfunction and free radical formation. Deformities of the energy metabolism, mitochondrial genome polymorphisms, nuclear DNA genetic abnormalities associated with mitochondria, modifications of mitochondrial fusion or fission, variations in shape and size, variations in transit, modified mobility of mitochondria, transcription defects, and the emergence of misfolded proteins associated with mitochondria are all linked to Parkinson's disease. Method: This review is a condensed compilation of data from research that have been published between the years of 2014 and 2022, using search engines like Google Scholar, PubMed, and Scopus. Result: Mitochondrial transplantation is a one-of-a-kind treatment for mitochondrial diseases and deficits in mitochondrial biogenesis. The replacement of malfunctioning mitochondria with transplanted viable mitochondria using innovative methodologies has shown promising outcomes as a cure for Parkinson's, involving tissue sparing coupled with enhanced energy generation and lower oxidative damage. Numerous mitochondria-targeted therapies, including mitochondrial gene therapy, redox therapy, and others, have been investigated for their effectiveness and potency. Conclusion: The development of innovative therapeutics for mitochondria-directed treatments in Parkinson's disease may be aided by optimising mitochondrial dynamics. Many neurological diseases have been studied in animal and cellular models, and it has been found that mitochondrial maintenance can slow the death of neuronal cells. It has been hypothesised that drug therapies for neurodegenerative diseases that focus on mitochondrial dysfunction will help to delay the onset of neuronal dysfunction.
线粒体治疗的潜在应用,重点是帕金森病和线粒体移植
目的:衰老和神经退行性疾病都被认为是受线粒体功能障碍和自由基形成的影响。能量代谢畸形、线粒体基因组多态性、与线粒体相关的核DNA遗传异常、线粒体融合或裂变的改变、形状和大小的变化、转运的变化、线粒体迁移能力的改变、转录缺陷以及与线粒体相关的错误折叠蛋白质的出现都与帕金森病有关。方法:本综述使用Google Scholar、PubMed和Scopus等搜索引擎,对2014年至2022年间发表的研究数据进行了浓缩汇编。结果:线粒体移植是一种独一无二的治疗线粒体疾病和线粒体生物发生缺陷的方法。使用创新的方法,用移植的活线粒体替代功能失调的线粒体,作为治疗帕金森病的一种有希望的结果,包括组织保留,增强能量产生和降低氧化损伤。许多线粒体靶向治疗,包括线粒体基因治疗、氧化还原治疗等,已经对其有效性和效力进行了研究。结论:优化线粒体动力学可能有助于开发线粒体定向治疗帕金森病的创新疗法。许多神经系统疾病已经在动物和细胞模型中进行了研究,发现线粒体维持可以减缓神经元细胞的死亡。据推测,针对线粒体功能障碍的神经退行性疾病的药物治疗将有助于延缓神经元功能障碍的发生。
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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