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从糖尿病角度看阿尔茨海默病的治疗策略。

Therapeutic Strategies for Alzheimer's Disease in the View of Diabetes Mellitus.

机构信息

Department of Neurology and Geriatric Medicine, Graduate School of Medicine, Ehime University, Toon, Ehime, Japan.

Long-Term Care Health Facility Cosmos, Kushiro-mutsumi, Hokkaido, Japan.

出版信息

Adv Exp Med Biol. 2019;1128:227-248. doi: 10.1007/978-981-13-3540-2_11.

Abstract

Recently, Alzheimer's disease (AD) is understood as "diabetes of the brain" or "type 3 diabetes." Recent clinical trials of anti-amyloid β-protein (Aβ) therapies have not proved to be successful. Thus, glucose-insulin metabolism in the brain is thought to be an alternative therapeutic target. Various types of antidiabetic drugs such as insulin, thiazolidinediones, dipeptidyl peptidase-4 (DPP4) inhibitors, glucagon-like peptide-1 (GLP-1) agonists, biguanides, and others have been reported to be effective on cognitive impairment in animal models and patients with DM or AD. Here, recent reports are reviewed. While we identified apomorphine (APO) as a novel drug that promoted intracellular Aβ degradation and improved memory function in an AD mouse model, more recently, we have revealed that APO treatment improves neuronal insulin resistance and activates insulin-degrading enzyme (IDE), a major Aβ-degrading enzyme. In this context, recovery of impaired insulin signaling in AD neurons may be a promising therapeutic strategy for AD dementia.

摘要

最近,阿尔茨海默病(AD)被理解为“大脑的糖尿病”或“第三型糖尿病”。最近针对抗β淀粉样蛋白(Aβ)疗法的临床试验并未证明是成功的。因此,人们认为大脑中的葡萄糖-胰岛素代谢是另一种治疗靶点。各种类型的抗糖尿病药物,如胰岛素、噻唑烷二酮类、二肽基肽酶-4(DPP4)抑制剂、胰高血糖素样肽-1(GLP-1)激动剂、二甲双胍等,已被报道可有效改善动物模型和糖尿病或 AD 患者的认知障碍。在这里,我们回顾了最近的报告。虽然我们发现阿扑吗啡(APO)是一种促进细胞内 Aβ降解并改善 AD 小鼠模型记忆功能的新型药物,但最近我们发现,APO 治疗可改善神经元胰岛素抵抗并激活胰岛素降解酶(IDE),这是一种主要的 Aβ降解酶。在这种情况下,恢复 AD 神经元中受损的胰岛素信号可能是治疗 AD 痴呆症的一种有前途的治疗策略。

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