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核因子红细胞生成 2 相关因子 2(Nrf2)信号通路是乳清蛋白在衰老大鼠模型前额叶皮层抗衰老作用的重要分子途径(组织学和生化研究)。

Nuclear factor erythrogen-2 associated factor 2 (Nrf2) signaling is an essential molecular pathway for the anti-aging effect of whey protein in the prefrontal cortex of aging rat model (Histological and Biochemical Study).

机构信息

Medical Histology and Cell Biology Department, Faculty of Medicine, Mansoura University, Egypt; Medical Histology and Cell Biology Department, Faculty of Medicine, Horus University - Egypt.

Department of Anatomy, college of Medicine, King Khalid University, Abha 61421, Saudi Arabia.

出版信息

Tissue Cell. 2023 Oct;84:102192. doi: 10.1016/j.tice.2023.102192. Epub 2023 Aug 9.

Abstract

Aging is a highly complicated natural process. Brain aging is associated with remarkable neurodegenerative changes and oxidative damage. Whey protein (WP) has been mentioned to have an antioxidant property. Nuclear factor erythrogen-2 associated factor 2 (Nrf2) signaling pathway is an antioxidant defense system. Nrf2 activity declines with age so, its activation could be a promising therapeutic strategy for aging. This study aimed to explore the anti-aging role of WP against D-galactose (D-gal) induced age-related degenerative changes and oxidative damage in the prefrontal cortex (PFC) and investigate its underlying mechanisms. Forty adult male rats were divided into 4 groups; control, WP group received WP (28.77 mg/kg/day) by gastric tube on the 4 experimental week; D-gal (model group) received D-gal (300 mg/kg/day) intraperitoneally for 8 weeks and D-gal +WP group received WP on the 4 week of D-gal treatment. Specimens from PFC were obtained for biochemical, histological, immunohistochemical and western blot analysis. WP treatment in D-gal +WP group reduced lipid peroxidation, enhanced antioxidant enzyme activities, decreased advanced glycation end products level and improved the histological and ultrastructural alterations. Moreover, the number of neurons expressed the senescence marker; p21 and percentage area of the astrocytic marker; glial fibrillary acidic protein were significantly reduced. WP also enhanced Nrf2 pathway and its downstream targets; heme oxygenase-1 and NADPH quinone oxidoreductase 1. In conclusion WP alleviates the D-gal-induced PFC aging through activating Nrf2 pathway, reducing cell senescence and gliosis. So, it may be a potential therapeutic target to retard the aging process.

摘要

衰老是一个高度复杂的自然过程。大脑衰老与显著的神经退行性变化和氧化损伤有关。乳清蛋白(WP)具有抗氧化特性。核因子红细胞生成素 2 相关因子 2(Nrf2)信号通路是一种抗氧化防御系统。Nrf2 活性随年龄增长而下降,因此激活它可能是衰老的一种有前途的治疗策略。本研究旨在探讨 WP 对 D-半乳糖(D-gal)诱导的前额叶皮质(PFC)与年龄相关的退行性变化和氧化损伤的抗衰老作用,并探讨其潜在机制。40 只成年雄性大鼠分为 4 组;对照组、WP 组通过胃管给予 WP(28.77mg/kg/天);D-gal(模型组)腹腔内给予 D-gal(300mg/kg/天)8 周;D-gal+WP 组在 D-gal 处理的第 4 周给予 WP。从 PFC 中获取标本进行生化、组织学、免疫组织化学和 Western blot 分析。D-gal+WP 组的 WP 治疗可降低脂质过氧化,增强抗氧化酶活性,降低晚期糖基化终产物水平,并改善组织学和超微结构改变。此外,神经元表达衰老标志物;p21 的数量和星形胶质细胞标志物的百分比区域;胶质纤维酸性蛋白明显减少。WP 还增强了 Nrf2 通路及其下游靶标;血红素加氧酶-1 和 NADPH 醌氧化还原酶 1。总之,WP 通过激活 Nrf2 通路、减少细胞衰老和神经胶质增生,减轻 D-gal 诱导的 PFC 衰老。因此,它可能是延缓衰老过程的潜在治疗靶点。

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