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The therapeutic potential of metabolic hormones in the treatment of age-related cognitive decline and Alzheimer’s disease

机译:代谢激素在治疗与年龄有关的认知下降和阿尔茨海默氏病中的治疗潜力

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摘要

Aging leads to a number of physiological alterations, specifically changes in circulating hormone levels, increases in fat deposition, decreases in metabolism, changes in inflammatory responses, and reductions in growth factors. These progressive changes in physiology and metabolism are exacerbated by modern culture and Western diet and give rise to diseases such as obesity, metabolic syndrome, and type 2 (non–insulin-dependent) diabetes (T2D). These age and lifestyle-related metabolic diseases are often accompanied by insulin and leptin resistance, as well as aberrant amylin production and signaling. Many of these alterations in hormone production and signaling are directly influenced by an increase in both oxidative stress and inflammation. Importantly, changes in hormone production and signaling have direct effects on brain function and the development of age-related neurologic disorders. Therefore, this review aims to present evidence on the effects that diet and metabolic disease have on age-related cognitive decline and the development of cognitive diseases, particularly Alzheimer disease. This review will focus on the metabolic hormones insulin, leptin, and amylin and their role in cognitive decline, as well as the therapeutic potential of these hormones in treating cognitive disease. Future investigations targeting the long-term effects of insulin and leptin treatment may reveal evidence to reduce risk of cognitive decline and Alzheimer disease.
机译:衰老会导致许多生理变化,特别是循环激素水平的变化,脂肪沉积的增加,新陈代谢的下降,炎症反应的变化以及生长因子的减少。现代文化和西方饮食加剧了生理和代谢的这些不断变化,并导致了肥胖,代谢综合症和2型(非胰岛素依赖型)糖尿病(T2D)等疾病。这些与年龄和生活方式有关的代谢性疾病通常伴有胰岛素和瘦素抵抗以及异常的胰岛淀粉样多肽产生和信号传导。这些激素产生和信号转导的许多变化直接受到氧化应激和炎症增加的影响。重要的是,激素产生和信号传导的变化对脑功能和与年龄有关的神经系统疾病的发展具有直接影响。因此,本综述旨在就饮食和代谢性疾病对与年龄有关的认知能力下降和认知疾病(尤其是阿尔茨海默氏病)的发展所产生的影响提供证据。这项审查将侧重于代谢激素胰岛素,瘦素和胰岛淀粉样多肽及其在认知功能下降中的作用,以及这些激素在治疗认知疾病中的治疗潜力。针对胰岛素和瘦素治疗的长期作用的未来研究可能会发现降低认知能力下降和阿尔茨海默氏病风险的证据。

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