Unraveling Pathophysiological Link Between Mitophagy Pathway and Vascular Dementia

IF 0.4 Q4 NEUROSCIENCES Archives of Neuroscience Pub Date : 2022-08-17 DOI:10.5812/ans-124588
M. Kumas, Ozge Altintas Kadirhan, M. Demirci
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引用次数: 0

Abstract

Context: Vascular dementia (VaD) is the second most common type of dementia after Alzheimer’s disease worldwide. Vascular dementia is a neurodegenerative disorder characterized by gradual cognitive impairment. Ischemic and hemorrhagic strokes result in VaD, markedly distributing cerebral blood flow and decreasing patients’ cognitive and memory performance. Due to their high energy demands, neurons are more sensitive to cellular architecture changes and exposed to mitochondrial stress than other cell types. Mitochondrial dysfunction and selective autophagy of mitochondria, known as mitophagy, are associated with VaD. This review aims to elucidate the association between mitophagy and VaD. Evidence Acquisition: This review was conducted independently by at least two researchers dominant in various VaD studies. We searched databases including Elsevier, Google Scholar, and PubMed using the terms ‘vascular dementia’, ‘vascular cognitive impairment’, and ‘mitophagy’. We evaluated 70 articles on the relationship between VaD and mitophagy and interpreted the results. Adobe Photoshop 2022 was used for drawing figures by researchers. Results: The autophagy process plays a protective role in experimental VaD models via preserving vascular integrity and the structure of the blood-brain barrier, upregulating occludin and claudin protein expressions, reducing oxidative stress, and decreasing cognitive dysfunction. Some studies claim that autophagy could have adverse effects in a time-dependent manner against neuronal injury. Prolonged autophagy and overexpressed autophagic proteins induce ischemic injury and cause neuronal cells to undergo apoptotic cell death. Conclusions: Although there are limited studies on the activation of mitophagy-related pathways in VaD, and the definitive role of mitophagy in neuronal healing is unclear, further research is needed to elucidate mitophagy pathways in neurons.
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线粒体自噬途径与血管性痴呆的病理生理联系
背景:血管性痴呆(VaD)是世界范围内仅次于阿尔茨海默病的第二常见痴呆类型。血管性痴呆是一种以逐渐认知障碍为特征的神经退行性疾病。缺血性和出血性中风导致VaD,显著分布脑血流量,降低患者的认知和记忆能力。由于神经元的高能量需求,与其他细胞类型相比,神经元对细胞结构变化更敏感,并暴露于线粒体应激。线粒体功能障碍和线粒体选择性自噬,即线粒体自噬,与VaD有关。本综述旨在阐明线粒体自噬与VaD之间的关系。证据获取:该综述由至少两名在各种VaD研究中占主导地位的研究人员独立进行。我们使用术语“血管性痴呆”、“血管性认知障碍”和“线粒体自噬”搜索了包括爱思唯尔、谷歌学者和PubMed在内的数据库。我们评估了70篇关于VaD与线粒体自噬之间关系的文章,并对结果进行了解释。研究人员使用Adobe Photoshop 2022绘制人物。结果:自噬过程通过保持血管完整性和血脑屏障结构、上调occludin和claudin蛋白表达、减少氧化应激和减少认知功能障碍,在实验性VaD模型中发挥保护作用。一些研究声称,自噬可能以时间依赖的方式对神经元损伤产生不利影响。长时间的自噬和过表达的自噬蛋白诱导缺血性损伤,并导致神经元细胞发生凋亡细胞死亡。结论:尽管对VaD中线粒体自噬相关通路的激活研究有限,而且线粒体自噬在神经元愈合中的确切作用尚不清楚,但仍需要进一步研究来阐明神经元中的线粒体自噬通路。
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来源期刊
Archives of Neuroscience
Archives of Neuroscience NEUROSCIENCES-
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32
期刊介绍: Archives of neuroscience is a clinical and basic journal which is informative to all practitioners like Neurosurgeons, Neurologists, Psychiatrists, Neuroscientists. It is the official journal of Brain and Spinal Injury Research Center. The Major theme of this journal is to follow the path of scientific collaboration, spontaneity, and goodwill for the future, by providing up-to-date knowledge for the readers. The journal aims at covering different fields, as the name implies, ranging from research in basic and clinical sciences to core topics such as patient care, education, procuring and correct utilization of resources and bringing to limelight the cherished goals of the institute in providing a standard care for the physically disabled patients. This quarterly journal offers a venue for our researchers and scientists to vent their innovative and constructive research works. The scope of the journal is as far wide as the universe as being declared by the name of the journal, but our aim is to pursue our sacred goals in providing a panacea for the intractable ailments, which leave a psychological element in the daily life of such patients. This authoritative clinical and basic journal was founded by Professor Madjid Samii in 2012.
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