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注意代谢间隙:通过大脑胰岛素抵抗弥合偏头痛和阿尔茨海默病。

Mind the Metabolic Gap: Bridging Migraine and Alzheimer's disease through Brain Insulin Resistance.

机构信息

Personalized Medicine, Asthma and Allergy, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.

出版信息

Aging Dis. 2024 Jun 16;15(6):2526-2553. doi: 10.14336/AD.2024.0351.

Abstract

Brain insulin resistance has recently been described as a metabolic abnormality of brain glucose homeostasis that has been proven to downregulate insulin receptors, both in astrocytes and neurons, triggering a reduction in glucose uptake and glycogen synthesis. This condition may generate a mismatch between brain's energy reserve and expenditure, ??mainly during high metabolic demand, which could be involved in the chronification of migraine and, in the long run, at least in certain subsets of patients, in the prodromic phase of Alzheimer's disease, along a putative metabolic physiopathological continuum. Indeed, the persistent disruption of glucose homeostasis and energy supply to neurons may eventually impair protein folding, an energy-requiring process, promoting pathological changes in Alzheimer's disease, such as amyloid-β deposition and tau hyperphosphorylation. Hopefully, the "neuroenergetic hypothesis" presented herein will provide further insight on there being a conceivable metabolic bridge between chronic migraine and Alzheimer's disease, elucidating novel potential targets for the prophylactic treatment of both diseases.

摘要

脑胰岛素抵抗最近被描述为脑葡萄糖稳态的代谢异常,已被证明可下调星形胶质细胞和神经元中的胰岛素受体,从而导致葡萄糖摄取和糖原合成减少。这种情况可能导致大脑的能量储备和消耗之间不匹配,主要是在高代谢需求期间,这可能与偏头痛的慢性化有关,从长远来看,至少在某些患者亚组中,与阿尔茨海默病的前驱期有关,沿着一个假定的代谢生理病理连续体。事实上,葡萄糖稳态和神经元能量供应的持续破坏最终可能会损害蛋白质折叠这一耗能过程,从而促进阿尔茨海默病的病理变化,如淀粉样β沉积和tau 过度磷酸化。希望本文提出的“神经能量假说”将为慢性偏头痛和阿尔茨海默病之间存在一种可以想象的代谢桥梁提供进一步的见解,为这两种疾病的预防性治疗确定新的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb71/11567252/f3da40e99d9e/AD-15-6-2526-g1.jpg

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