Harnessing Metabolism to Combat Neurodegeneration: Strategies for Reversing Age-Related Cognitive Decline

IF 3.7 Q1 CHEMISTRY, MEDICINAL
Smita Jain*, Reetuparna Acharya, Lavkush Verma and Aparna Chauhan, 
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引用次数: 0

Abstract

Age-related cognitive decline, a hallmark of neurodegenerative disorders such as Alzheimer’s disease, has been increasingly associated with metabolic dysregulation. Targeting metabolic pathways to enhance brain function and slow neurodegeneration presents a novel therapeutic approach. This review discusses key metabolic interventions that may reverse or delay cognitive decline. Mitochondrial dysfunction, oxidative stress, and impaired energy metabolism are central to neurodegenerative progression. Therapies aimed at boosting mitochondrial biogenesis, such as nicotinamide adenine dinucleotide (NAD+) precursors, adenosine monophosphate-activated protein kinase (AMPK) activators, and peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) modulators, have shown promise in improving neuronal energy balance and reducing oxidative damage. Metabolic interventions like caloric restriction, intermittent fasting, and ketogenic diets have demonstrated neuroprotective effects by enhancing insulin sensitivity, promoting autophagy, and shifting the brain’s energy reliance toward ketone bodies, which improves cognitive function. These strategies also mitigate neuroinflammation, a key driver of neuronal damage, by modulating immune responses and reducing the accumulation of toxic protein aggregates. Lipid metabolism also plays a crucial role in maintaining neuronal integrity. Enhancing lipid turnover, optimizing fatty acid profiles, and regulating cholesterol homeostasis may improve synaptic plasticity and reduce neuroinflammation, offering additional therapeutic avenues. By integrating current insights into metabolic regulation, this review underscores the potential of metabolic therapies to reverse or mitigate the cognitive decline associated with aging. Advancing our understanding of the intricate relationship between metabolism and neurodegeneration may pave the way for novel treatments targeting age-related cognitive impairment.

Abstract Image

利用新陈代谢对抗神经退化:逆转与年龄相关的认知衰退的策略
与年龄相关的认知能力下降是阿尔茨海默病等神经退行性疾病的标志,与代谢失调的关系日益密切。靶向代谢途径增强脑功能和减缓神经变性提出了一种新的治疗方法。这篇综述讨论了可能逆转或延缓认知衰退的关键代谢干预措施。线粒体功能障碍、氧化应激和能量代谢受损是神经退行性进展的核心。旨在促进线粒体生物发生的疗法,如烟酰胺腺嘌呤二核苷酸(NAD+)前体、腺苷单磷酸活化蛋白激酶(AMPK)激活剂和过氧化物酶体增殖体激活受体-γ共激活因子-1α (PGC-1α)调节剂,已显示出改善神经元能量平衡和减少氧化损伤的希望。代谢干预,如热量限制、间歇性禁食和生酮饮食,通过增强胰岛素敏感性、促进自噬、将大脑的能量依赖转向酮体,从而改善认知功能,已经证明了神经保护作用。这些策略还通过调节免疫反应和减少有毒蛋白聚集体的积累来减轻神经炎症,这是神经元损伤的关键驱动因素。脂质代谢在维持神经元完整性方面也起着至关重要的作用。增强脂质转换,优化脂肪酸谱,调节胆固醇稳态可能改善突触可塑性,减少神经炎症,提供额外的治疗途径。通过整合目前对代谢调节的见解,本综述强调了代谢疗法逆转或减轻与衰老相关的认知能力下降的潜力。推进我们对新陈代谢和神经退行性变之间复杂关系的理解,可能为针对年龄相关认知障碍的新治疗铺平道路。
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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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