Wang Yixuan, Hu Hao, Liu Xinyu, Guo Xiangyu
Dongfang Hospital of Beijing University of Chinese Medicine, Beijing, China.
Front Pharmacol. 2023 Feb 23;14:1138499. doi: 10.3389/fphar.2023.1138499. eCollection 2023.
Alzheimer's Disease (AD) is a global chronic disease in adults with beta-amyloid (Aβ) deposits and hyperphosphorylated tau protein as the pathologic characteristics. Although the exact etiology of AD is still not fully elucidated, aberrant metabolism including insulin signaling and mitochondria dysfunction plays an important role in the development of AD. Binding to insulin receptor substrates, insulin can transport through the blood-brain barrier (BBB), thus mediating insulin signaling pathways to regulate physiological functions. Impaired insulin signaling pathways, including PI3K/Akt/GSK3β and MAPK pathways, could cause damage to the brain in the pathogenesis of AD. Mitochondrial dysfunction and overexpression of TXNIP could also be causative links between AD and DM. Some antidiabetic medicines may have benefits in the treatment of AD. Metformin can be beneficial for cognition improvement in AD patients, although results from clinical trials were inconsistent. Exendin-4 may affect AD in animal models but there is a lack of clinical trials. Liraglutide and dulaglutide could also benefit AD patients in adequate clinical studies but not semaglutide. Dipeptidyl peptidase IV inhibitors (DPP4is) such as saxagliptin, vildagliptin, linagliptin, and sitagliptin could boost cognitive function in animal models. And SGLT2 inhibitors such as empagliflozin and dapagliflozin were also considerably protective against new-onset dementia in T2DM patients. Insulin therapy is a promising therapy but some studies indicated that it may increase the risk of AD. Herbal medicines are helpful for cognitive function and neuroprotection in the brain. For example, polyphenols, alkaloids, glycosides, and flavonoids have protective benefits in cognition function and glucose metabolism. Focusing on glucose metabolism, we summarized the pharmacological mechanism of hypoglycemic drugs and herbal medicines. New treatment approaches including antidiabetic synthesized drugs and herbal medicines would be provided to patients with AD. More clinical trials are needed to produce definite evidence for the effectiveness of hypoglycemic medications.
阿尔茨海默病(AD)是一种发生于成年人的全球性慢性疾病,其病理特征为β淀粉样蛋白(Aβ)沉积和tau蛋白过度磷酸化。尽管AD的确切病因仍未完全阐明,但包括胰岛素信号传导和线粒体功能障碍在内的异常代谢在AD的发展过程中起着重要作用。胰岛素与胰岛素受体底物结合后,可穿过血脑屏障(BBB),从而介导胰岛素信号通路来调节生理功能。受损的胰岛素信号通路,包括PI3K/Akt/GSK3β和MAPK通路,在AD发病机制中可导致脑损伤。线粒体功能障碍和TXNIP的过表达也可能是AD与糖尿病(DM)之间的因果联系。一些抗糖尿病药物可能对AD治疗有益。二甲双胍对AD患者的认知改善可能有益,尽管临床试验结果并不一致。艾塞那肽-4可能在动物模型中影响AD,但缺乏临床试验。在充分的临床研究中,利拉鲁肽和度拉糖肽也可能使AD患者受益,但司美格鲁肽则不然。二肽基肽酶IV抑制剂(DPP4is),如沙格列汀、维格列汀、利格列汀和西格列汀,可在动物模型中增强认知功能。而钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂,如恩格列净和达格列净,对2型糖尿病(T2DM)患者新发痴呆也有相当的保护作用。胰岛素治疗是一种有前景的治疗方法,但一些研究表明它可能会增加AD的风险。草药对大脑的认知功能和神经保护有益。例如,多酚、生物碱、糖苷和黄酮类化合物对认知功能和葡萄糖代谢具有保护作用。围绕葡萄糖代谢,我们总结了降糖药物和草药的药理机制。将为AD患者提供包括抗糖尿病合成药物和草药在内的新治疗方法。需要更多的临床试验来为降糖药物的有效性提供确凿证据。