CNC-Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, Portugal; IIIUC-Institute of Interdisciplinary Research, University of Coimbra, Coimbra, Portugal.
CNC-Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, Portugal; Laboratory of Physiology-Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Int Rev Neurobiol. 2020;155:37-64. doi: 10.1016/bs.irn.2020.02.010. Epub 2020 Aug 11.
Medical and scientific communities have been striving to disentangle the complexity of neurodegenerative diseases, particularly Alzheimer's disease (AD) and Parkinson's disease (PD), in order to develop a cure or effective treatment for these diseases. Along this journey, it has become important to identify the early events occurring in the prodromal phases of these diseases and the disorders that increase the risk of neurodegeneration highlighting common pathological features. This strategy has led to a wealth of evidence identifying diabetes, mainly type 2 diabetes mellitus (T2DM) as a main risk factor for the onset and progression of AD and PD. Impaired glucose metabolism, insulin resistance, and mitochondrial dysfunction are features common to both type 2 diabetes mellitus (T2DM), and AD and PD, and they appear before clinical diagnosis of the two neurodegenerative diseases. These could represent the strategic nodes of therapeutic intervention. Following this line of thought, a conceivable approach is to repurpose antidiabetic drugs as valuable agents that may prevent or reduce the risk of cognitive decline and neurodegeneration. This review summarizes the past and current findings that link AD and PD with T2DM, emphasizing the common pathological mechanisms. The efficacy of antidiabetic drugs, namely intranasal insulin, metformin, and thiazolidinediones, in the prevention and/or treatment of AD and PD is also discussed.
医学和科学界一直在努力理清神经退行性疾病(尤其是阿尔茨海默病(AD)和帕金森病(PD))的复杂性,以便为这些疾病开发出治愈方法或有效治疗方法。在这个过程中,识别这些疾病前驱期发生的早期事件以及增加神经退行性风险的疾病变得非常重要,这突出了共同的病理特征。这一策略带来了大量证据,表明糖尿病(主要是 2 型糖尿病(T2DM))是 AD 和 PD 发病和进展的主要危险因素。葡萄糖代谢受损、胰岛素抵抗和线粒体功能障碍是 2 型糖尿病(T2DM)和 AD 及 PD 的共同特征,它们出现在两种神经退行性疾病的临床诊断之前。这些可能代表着治疗干预的战略节点。基于这一思路,可以想象将抗糖尿病药物重新用于预防或降低认知能力下降和神经退行性风险的有价值的药物。本综述总结了将 AD 和 PD 与 T2DM 联系起来的过去和当前发现,强调了共同的病理机制。还讨论了抗糖尿病药物(即鼻内胰岛素、二甲双胍和噻唑烷二酮类药物)在预防和/或治疗 AD 和 PD 中的疗效。