Alsegiani Amsha S, Shah Zahoor A
Department of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH, USA.
Neural Regen Res. 2020 Aug;15(8):1451-1459. doi: 10.4103/1673-5374.274330.
Aging brain becomes susceptible to neurodegenerative diseases due to the shifting of microglia and astrocyte phenotypes to an active "pro-inflammatory" state, causing chronic low-grade neuroinflammation. Despite the fact that the role of neuroinflammation during aging has been extensively studied in recent years, the underlying causes remain unclear. The identification of relevant proteins and understanding their potential roles in neuroinflammation can help explain their potential of becoming biomarkers in the aging brain and as drug targets for prevention and treatment. This will eventually reduce the chances of developing neurodegenerative diseases and promote healthier lives in the elderly. In this review, we have summarized the morphological and cellular changes in the aging brain, the effects of age-related neuroinflammation, and the potential role of cofilin-1 during neuroinflammation. We also discuss other factors contributing to brain aging and neuroinflammation.
由于小胶质细胞和星形胶质细胞表型转变为活跃的“促炎”状态,导致慢性低度神经炎症,衰老的大脑易患神经退行性疾病。尽管近年来对衰老过程中神经炎症的作用进行了广泛研究,但其潜在原因仍不清楚。识别相关蛋白质并了解它们在神经炎症中的潜在作用,有助于解释它们成为衰老大脑生物标志物以及作为预防和治疗药物靶点的潜力。这最终将减少患神经退行性疾病的几率,并促进老年人更健康的生活。在这篇综述中,我们总结了衰老大脑中的形态学和细胞变化、与年龄相关的神经炎症的影响以及丝切蛋白-1在神经炎症中的潜在作用。我们还讨论了导致大脑衰老和神经炎症的其他因素。