Cholesterol imbalance and neurotransmission defects in neurodegeneration

IF 9.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Experimental and Molecular Medicine Pub Date : 2024-08-01 DOI:10.1038/s12276-024-01273-4
Kyung Chul Shin, Houda Yasmine Ali Moussa, Yongsoo Park
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Abstract

The brain contains the highest concentration of cholesterol in the human body, which emphasizes the importance of cholesterol in brain physiology. Cholesterol is involved in neurogenesis and synaptogenesis, and age-related reductions in cholesterol levels can lead to synaptic loss and impaired synaptic plasticity, which potentially contribute to neurodegeneration. The maintenance of cholesterol homeostasis in the neuronal plasma membrane is essential for normal brain function, and imbalances in cholesterol distribution are associated with various neurodegenerative disorders, including Alzheimer’s disease, Parkinson’s disease, and Huntington’s disease. This review aims to explore the molecular and pathological mechanisms by which cholesterol imbalance can lead to neurotransmission defects and neurodegeneration, focusing on four key mechanisms: (1) synaptic dysfunction, (2) alterations in membrane structure and protein clustering, (3) oligomers of amyloid beta (Aβ) protein, and (4) α-synuclein aggregation. Cholesterol, a substance crucial for the brain, can lead to diseases like Alzheimer’s and Parkinson’s when imbalanced. This review investigates how this imbalance causes brain cell degeneration, focusing on issues like communication breakdown and harmful protein build-up. The study combines findings from different experiments to understand cholesterol’s role in the brain. The review emphasizes the need for cholesterol balance for brain health and identifies potential treatment targets for neurodegenerative diseases. The main findings suggest that cholesterol imbalance disrupts brain cell communication and leads to harmful protein build-up, causing brain cell degeneration. The researchers conclude that focusing on cholesterol metabolism and distribution could lead to new treatments for these conditions. Future research may lead to treatments that correct cholesterol imbalances, possibly slowing or preventing neurodegenerative diseases. This summary was initially drafted using artificial intelligence, then revised and fact-checked by the author.

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胆固醇失衡与神经变性中的神经传递缺陷
人体内胆固醇含量最高的部位是大脑,这凸显了胆固醇在大脑生理学中的重要性。胆固醇参与神经发生和突触生成,与年龄相关的胆固醇水平降低会导致突触丢失和突触可塑性受损,从而可能导致神经退化。维持神经元质膜中胆固醇的平衡对大脑的正常功能至关重要,而胆固醇分布的失衡与阿尔茨海默病、帕金森病和亨廷顿病等多种神经退行性疾病有关。本综述旨在探讨胆固醇失衡导致神经传导缺陷和神经退行性病变的分子和病理机制,重点关注以下四种关键机制:(1) 突触功能障碍;(2) 膜结构和蛋白质聚类的改变;(3) 淀粉样 beta(Aβ)蛋白的寡聚体;(4) α-突触核蛋白的聚集。
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来源期刊
Experimental and Molecular Medicine
Experimental and Molecular Medicine 医学-生化与分子生物学
CiteScore
19.50
自引率
0.80%
发文量
166
审稿时长
3 months
期刊介绍: Experimental & Molecular Medicine (EMM) stands as Korea's pioneering biochemistry journal, established in 1964 and rejuvenated in 1996 as an Open Access, fully peer-reviewed international journal. Dedicated to advancing translational research and showcasing recent breakthroughs in the biomedical realm, EMM invites submissions encompassing genetic, molecular, and cellular studies of human physiology and diseases. Emphasizing the correlation between experimental and translational research and enhanced clinical benefits, the journal actively encourages contributions employing specific molecular tools. Welcoming studies that bridge basic discoveries with clinical relevance, alongside articles demonstrating clear in vivo significance and novelty, Experimental & Molecular Medicine proudly serves as an open-access, online-only repository of cutting-edge medical research.
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