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Bridging Type 2 Diabetes and Alzheimer's Disease: Assembling the Puzzle Pieces in the Quest for the Molecules With Therapeutic and Preventive Potential

机译:桥接2型糖尿病和阿尔茨海默病:在寻求具有治疗和预防潜力的分子中组装拼图件

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Abstract Type 2 diabetes (T2D) and Alzheimer's disease (AD) are two age‐related amyloid diseases that affect millions of people worldwide. Broadly supported by epidemiological data, the higher incidence of AD among type 2 diabetic patients led to the recognition of T2D as a tangible risk factor for the development of AD. Indeed, there is now growing evidence on brain structural and functional abnormalities arising from brain insulin resistance and deficiency, ultimately highlighting the need for new approaches capable of preventing the development of AD in type 2 diabetic patients. This review provides an update on overlapping pathophysiological mechanisms and pathways in T2D and AD, such as amyloidogenic events, oxidative stress, endothelial dysfunction, aberrant enzymatic activity, and even shared genetic background. These events will be presented as puzzle pieces put together, thus establishing potential therapeutic targets for drug discovery and development against T2D and diabetes‐induced cognitive decline—a heavyweight contributor to the increasing incidence of dementia in developed countries. Hoping to pave the way in this direction, we will present some of the most promising and well‐studied drug leads with potential against both pathologies, including their respective bioactivity reports, mechanisms of action, and structure–activity relationships.
机译:摘要2型糖尿病(T2D)和阿尔茨海默病(AD)是两个与全球数百万人口相关的淀粉样症疾病。广泛支持流行病学数据,2型糖尿病患者的AD发病率较高,导致T2D作为广告发展的有形危险因素的识别。实际上,现在有关于脑胰岛素抵抗力和缺乏产生的脑结构和功能异常的证据,最终突出了能够预防2型糖尿病患者患者的新方法的需求。该综述提供了关于T2D和AD中的重叠病理生理机制和途径的更新,例如淀粉化事件,氧化应激,内皮功能障碍,异常酶活性,甚至共享遗传背景。这些事件将被呈现为拼凑的碎片,从而建立潜在的治疗目标,用于针对T2D和糖尿病诱导的认知拒绝的药物发现和发育的潜在治疗目标 - 这是发达国家痴呆症越来越多的痴呆症发病率的重量级贡献。希望朝着这个方向铺平道路,我们将展示一些最有前途和学习的药物导致具有潜在的药物,包括各自的生物活性报告,行动机制和结构 - 活动关系。

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