Advancing the understanding of diabetic encephalopathy through unravelling pathogenesis and exploring future treatment perspectives

神经炎症 医学 神经保护 神经科学 神经退行性变 神经化学 生物信息学 氧化应激 疾病 糖尿病 药理学 心理学 内科学 生物 内分泌学
作者
Aarti Nagayach,Rakesh Bhaskar,Shampa Ghosh,Krishna Kumar Singh,Sung Soo Han,Jitendra Kumar Sinha
出处
期刊:Ageing Research Reviews [Elsevier]
卷期号:100: 102450-102450 被引量:32
标识
DOI:10.1016/j.arr.2024.102450
摘要

Diabetic encephalopathy (DE), a significant micro-complication of diabetes, manifests as neurochemical, structural, behavioral, and cognitive alterations. This condition is especially dangerous for the elderly because aging raises the risk of neurodegenerative disorders and cognitive impairment, both of which can be made worse by diabetes. Despite its severity, diagnosis of this disease is challenging, and there is a paucity of information on its pathogenesis. The pivotal roles of various cellular pathways, activated or influenced by hyperglycemia, insulin sensitivity, amyloid accumulation, tau hyperphosphorylation, brain vasculopathy, neuroinflammation, and oxidative stress, are widely recognized for contributing to the potential causes of diabetic encephalopathy. We also reviewed current pharmacological strategies for DE encompassing a comprehensive approach targeting metabolic dysregulations and neurological manifestations. Antioxidant-based therapies hold promise in mitigating oxidative stress-induced neuronal damage, while anti-diabetic drugs offer neuroprotective effects through diverse mechanisms, including modulation of insulin signaling pathways and neuroinflammation. Additionally, tissue engineering and nanomedicine-based approaches present innovative strategies for targeted drug delivery and regenerative therapies for DE. Despite significant progress, challenges remain in translating these therapeutic interventions into clinical practice, including long-term safety, scalability, and regulatory approval. Further research is warranted to optimize these approaches and address remaining gaps in the management of DE and associated neurodegenerative disorders.
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