Faculté de pharmacie, Université Laval, Québec, Québec, Canada; Axe Neurosciences, Centre de recherche du CHU de Québec - Université Laval, Québec, Québec, Canada; Institut sur la Nutrition et les Aliments Fonctionnels, Québec, Québec, Canada.
Faculté de pharmacie, Université Laval, Québec, Québec, Canada; Axe Neurosciences, Centre de recherche du CHU de Québec - Université Laval, Québec, Québec, Canada.
Ageing Res Rev. 2021 Dec;72:101462. doi: 10.1016/j.arr.2021.101462. Epub 2021 Sep 15.
Alzheimer's disease (AD) is a complex age-related neurodegenerative disease, associated with central and peripheral metabolic anomalies, such as impaired glucose utilization and insulin resistance. These observations led to a considerable interest not only in lifestyle-related interventions, but also in repurposing insulin and other anti-diabetic drugs to prevent or treat dementia. Body temperature is the oldest known metabolic readout and mechanisms underlying its maintenance fail in the elderly, when the incidence of AD rises. This raises the possibility that an age-associated thermoregulatory deficit contributes to energy failure underlying AD pathogenesis. Brown adipose tissue (BAT) plays a central role in thermogenesis and maintenance of body temperature. In recent years, the modulation of BAT activity has been increasingly demonstrated to regulate energy expenditure, insulin sensitivity and glucose utilization, which could also provide benefits for AD. Here, we review the evidence linking thermoregulation, BAT and insulin-related metabolic defects with AD, and we propose mechanisms through which correcting thermoregulatory impairments could slow the progression and delay the onset of AD.
阿尔茨海默病(AD)是一种与年龄相关的复杂神经退行性疾病,与中枢和外周代谢异常有关,如葡萄糖利用受损和胰岛素抵抗。这些观察结果不仅引起了人们对与生活方式相关的干预措施的极大兴趣,也引起了人们对重新利用胰岛素和其他抗糖尿病药物以预防或治疗痴呆症的兴趣。体温是已知的最古老的代谢指标,当 AD 发病率上升时,老年人维持体温的机制就会失效。这就提出了一种可能性,即与年龄相关的体温调节缺陷可能导致 AD 发病机制中的能量衰竭。棕色脂肪组织(BAT)在产热和维持体温方面发挥着核心作用。近年来,越来越多的证据表明调节 BAT 活性可以调节能量消耗、胰岛素敏感性和葡萄糖利用,这也可能对 AD 有益。在这里,我们回顾了将体温调节、BAT 和与胰岛素相关的代谢缺陷与 AD 联系起来的证据,并提出了通过纠正体温调节障碍可能减缓 AD 进展和延迟发病的机制。