Mathematical Engineering Academy of Chinese Medicine, and School of Pharmaceutical Science, Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong, PR China.
Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an 223001, Jiangsu, PR China.
Carbohydr Polym. 2018 Apr 15;186:321-331. doi: 10.1016/j.carbpol.2018.01.075. Epub 2018 Jan 31.
The purpose of this study was to investigate the effects of Ostrea rivularis polysaccharide (ORP) against testicular oxidative stress injury via kelch-like ECH-associated protein 1-nuclear erythroid 2-related factor 2/antioxidant response element (Keap1-Nrf2/ARE) pathway. In pharmacological experiments in vivo, ORP administration could dose-dependently inhibit body and testicular weight loss, ameliorate epididymal sperm quality and protect reproductive impairment in cyclophosphamide-induced male Balb/c mice. Moreover, the mechanism in vivo might be elucidated that ORP could increase expression level of Nrf2 and its downstream ARE gene battery in the testis, promote production of corresponding antioxidative enzymes and protein, and enhance Keap1-Nrf2/ARE signaling pathway to avoid male reproductive dysfunction. In addition, ORP treatment could improve survival capacity of HO-induced TM4 cells and its antioxidant mechanism in vitro also had been verified to activate Keap1-Nrf2/ARE signaling pathway. Overall, these results showed that ORP as a potent antioxidant could reduce reproductive oxidative stress damage related to Keap1-Nrf2/ARE pathway.
本研究旨在探讨牡蛎多糖(ORP)通过 Kelch 样 ECH 相关蛋白 1-核红细胞 2 相关因子 2/抗氧化反应元件(Keap1-Nrf2/ARE)通路对睾丸氧化应激损伤的影响。在体内药理学实验中,ORP 给药可剂量依赖性地抑制体质量和睾丸质量减轻,改善附睾精子质量,并保护环磷酰胺诱导的雄性 Balb/c 小鼠的生殖损伤。此外,体内机制可能被阐明,即 ORP 可以增加睾丸中 Nrf2 及其下游 ARE 基因簇的表达水平,促进相应抗氧化酶和蛋白质的产生,并增强 Keap1-Nrf2/ARE 信号通路,以避免男性生殖功能障碍。此外,ORP 处理可提高 HO 诱导的 TM4 细胞的存活能力,其体外抗氧化机制也已被验证可激活 Keap1-Nrf2/ARE 信号通路。总的来说,这些结果表明,ORP 作为一种有效的抗氧化剂,可以减少与 Keap1-Nrf2/ARE 通路相关的生殖氧化应激损伤。