Cellular and Molecular Signaling, New York, NY 10022, USA.
Biomolecules. 2023 May 11;13(5):816. doi: 10.3390/biom13050816.
It is estimated that, at minimum, 500 million individuals suffer from cellular metabolic dysfunction, such as diabetes mellitus (DM), throughout the world. Even more concerning is the knowledge that metabolic disease is intimately tied to neurodegenerative disorders, affecting both the central and peripheral nervous systems as well as leading to dementia, the seventh leading cause of death. New and innovative therapeutic strategies that address cellular metabolism, apoptosis, autophagy, and pyroptosis, the mechanistic target of rapamycin (mTOR), AMP activated protein kinase (AMPK), growth factor signaling with erythropoietin (EPO), and risk factors such as the apolipoprotein E (APOE-ε4) gene and coronavirus disease 2019 (COVID-19) can offer valuable insights for the clinical care and treatment of neurodegenerative disorders impacted by cellular metabolic disease. Critical insight into and modulation of these complex pathways are required since mTOR signaling pathways, such as AMPK activation, can improve memory retention in Alzheimer's disease (AD) and DM, promote healthy aging, facilitate clearance of β-amyloid (Aß) and tau in the brain, and control inflammation, but also may lead to cognitive loss and long-COVID syndrome through mechanisms that can include oxidative stress, mitochondrial dysfunction, cytokine release, and APOE-ε4 if pathways such as autophagy and other mechanisms of programmed cell death are left unchecked.
据估计,全球至少有 5 亿人患有细胞代谢功能障碍,如糖尿病(DM)。更令人担忧的是,代谢疾病与神经退行性疾病密切相关,影响中枢和周围神经系统,导致痴呆,这是第七大死亡原因。针对细胞代谢、细胞凋亡、自噬和细胞焦亡、雷帕霉素(mTOR)的机制靶点、AMP 激活蛋白激酶(AMPK)、红细胞生成素(EPO)的生长因子信号以及载脂蛋白 E (APOE-ε4) 基因和 2019 年冠状病毒病 (COVID-19) 等危险因素的新的和创新的治疗策略,可以为受细胞代谢疾病影响的神经退行性疾病的临床护理和治疗提供有价值的见解。由于 mTOR 信号通路,如 AMPK 激活,可以改善阿尔茨海默病(AD)和 DM 中的记忆保留,促进健康衰老,促进大脑中β-淀粉样蛋白(Aß)和 tau 的清除,并控制炎症,但也可能导致认知丧失和长 COVID 综合征通过机制,包括氧化应激、线粒体功能障碍、细胞因子释放和 APOE-ε4,如果自噬和其他程序性细胞死亡机制不受控制。