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Potential therapeutic roles of retinoids for prevention of neuroinflammation and neurodegeneration in Alzheimer’s disease

机译:维氏素治疗预防神经炎症和阿尔茨海默病中神经变性的潜在治疗作用

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All retinoids, which can be natural and synthetic, are chemically related to vitamin A. Both natural and synthetic retinoids use specific nuclear receptors such as retinoic acid receptors and retinoid X receptors to activate specific signaling pathways in the cells. Retinoic acid signaling is extremely important in the central nervous system. Impairment of retinoic acid signaling pathways causes severe pathological processes in the central nervous system, especially in the adult brain. Retinoids have major roles in neural patterning, differentiation, axon outgrowth in normal development, and function of the brain. Impaired retinoic acid signaling results in neuroinflammation, oxidative stress, mitochondrial malfunction, and neurodegeneration leading to progressive Alzheimer’s disease, which is pathologically characterized by extra-neuronal accumulation of amyloid plaques (aggregated amyloid-beta) and intra-neurofibrillary tangles (hyperphosphorylated tau protein) in the temporal lobe of the brain. Alzheimer’s disease is the most common cause of dementia and loss of memory in old adults. Inactive cholinergic neurotransmission is responsible for cognitive deficits in Alzheimer’s disease patients. Deficiency or deprivation of retinoic acid in mice is associated with loss of spatial learning and memory. Retinoids inhibit expression of chemokines and neuroinflammatory cytokines in microglia and astrocytes, which are activated in Alzheimer’s disease. Stimulation of retinoic acid receptors and retinoid X receptors slows down accumulation of amyloids, reduces neurodegeneration, and thereby prevents pathogenesis of Alzheimer’s disease in mice. In this review, we described chemistry and biochemistry of some natural and synthetic retinoids and potentials of retinoids for prevention of neuroinflammation and neurodegeneration in Alzheimer’s disease.
机译:所有含有天然和合成的类视黄曲面都与维生素A化学相关。天然和合成的类视黄醇都使用特定的核受体,例如视黄酸受体和视黄醇X受体,以激活细胞中的特异性信号传导途径。维甲酸信号传导在中枢神经系统中非常重要。视黄酸信号传导途径的损害导致中枢神经系统中严重的病理过程,特别是在成年脑中。维氏醇在神经图案化,分化,正常发育中的轴突过多和大脑的功能具有重要作用。视黄酸信号传递受损导致神经炎症,氧化应激,线粒体故障和神经变性,导致进步的阿尔茨海默病是病理学的,其具有淀粉样蛋白斑块(聚集淀粉样蛋白β)和神经纤维状缠结(超磷酸化Tau蛋白)的显神经元积累在大脑的颞叶中。阿尔茨海默病是痴呆症最常见的原因和老年人内存损失。无活性的胆碱能神经递质负责阿尔茨海默病患者的认知缺陷。小鼠中视黄酸的缺陷或剥夺与空间学习和记忆的损失有关。类视黄醇抑制了在阿尔茨海默病中激活的微胶质细胞和星形胶质细胞中趋化因子和神经炎细胞因子的表达。视黄酸受体和类视黄醇X受体的刺激减慢淀粉样蛋白的积累,减少神经变性,从而防止老年人疾病在小鼠中的发病机制。在本综述中,我们描述了一些天然和合成类化毒性的化学和生物化学以及类视黄醇的潜力,用于预防阿尔茨海默病的神经炎症和神经变性。

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