氧化应激
糖基化
愤怒(情绪)
糖尿病
医学
疾病
活性氮物种
活性氧
糖基化终产物
生物信息学
内科学
内分泌学
生物
神经科学
细胞生物学
出处
期刊:Biomedicines
[Multidisciplinary Digital Publishing Institute]
日期:2023-10-29
卷期号:11 (11): 2925-2925
被引量:264
标识
DOI:10.3390/biomedicines11112925
摘要
-carboxymethyllysine (CML) serve as markers for disease progression. AGEs, through interaction with receptors for advanced glycation end products (RAGE), initiate a cascade of deleterious signaling events to form inflammatory cytokines, and thereby further exacerbate oxidative stress in a vicious cycle. AGE inhibitors, AGE breakers, and RAGE inhibitors are therefore potential therapeutic agents for multiple diseases, including diabetes and AD. The complexity of the AGEs and the lack of well-established mechanisms for AGE formation are largely responsible for the lack of effective therapeutics targeting oxidative stress and AGE-related diseases. This review addresses the role of oxidative stress in the pathogenesis of AGE-related chronic diseases, including diabetes and neurological disorders, and recent progress in the development of therapeutics based on antioxidants, AGE breakers and RAGE inhibitors. Furthermore, this review outlines therapeutic strategies based on single-atom nanozymes that attenuate oxidative stress through the sequestering of reactive oxygen species (ROS) and reactive nitrogen species (RNS).
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