Department of Occupational and Environmental Health, Tokyo University of Science, Noda 278-8510, Japan.
Genetics and Genetic Engineering in Department of Animal Husbandry and Animal Wealth Development, Faculty of Veterinary Medicine, Alexandria University, Alexandria 21500, Egypt.
Int J Mol Sci. 2021 Jun 1;22(11):5995. doi: 10.3390/ijms22115995.
Acrylamide is a well characterized neurotoxicant known to cause neuropathy and encephalopathy in humans and experimental animals. To investigate the role of nuclear factor erythroid 2-related factor 2 (Nrf2) in acrylamide-induced neuropathy, male C57Bl/6JJcl adult mice were exposed to acrylamide at 0, 200 or 300 ppm in drinking water and co-administered with subcutaneous injections of sulforaphane, a known activator of the Nrf2 signaling pathway at 0 or 25 mg/kg body weight daily for 4 weeks. Assessments for neurotoxicity, hepatotoxicity, oxidative stress as well as messenger RNA-expression analysis for Nrf2-antioxidant and pro-inflammatory cytokine genes were conducted. Relative to mice exposed only to acrylamide, co-administration of sulforaphane protected against acrylamide-induced neurotoxic effects such as increase in landing foot spread or decrease in density of noradrenergic axons as well as hepatic necrosis and hemorrhage. Moreover, co-administration of sulforaphane enhanced acrylamide-induced mRNA upregulation of Nrf2 and its downstream antioxidant proteins and suppressed acrylamide-induced mRNA upregulation of tumor necrosis factor alpha (TNF-α) and inducible nitric oxide synthase (iNOS) in the cerebral cortex. The results demonstrate that activation of the Nrf2 signaling pathway by co-treatment of sulforaphane provides protection against acrylamide-induced neurotoxicity through suppression of oxidative stress and inflammation. Nrf2 remains an important target for the strategic prevention of acrylamide-induced neurotoxicity.
丙烯酰胺是一种特征明确的神经毒物,已知会导致人类和实验动物的周围神经病和脑病。为了研究核因子红细胞 2 相关因子 2(Nrf2)在丙烯酰胺诱导的周围神经病中的作用,雄性 C57Bl/6JJcl 成年小鼠暴露于饮用水中的 0、200 或 300ppm 丙烯酰胺中,并每日接受皮下注射已知的 Nrf2 信号通路激活剂萝卜硫素,剂量为 0 或 25mg/kg 体重,持续 4 周。评估神经毒性、肝毒性、氧化应激以及 Nrf2-抗氧化和促炎细胞因子基因的信使 RNA 表达分析。与仅暴露于丙烯酰胺的小鼠相比,萝卜硫素的共同给药可预防丙烯酰胺引起的神经毒性作用,如着陆足间距增加或去甲肾上腺素能轴密度降低,以及肝坏死和出血。此外,萝卜硫素的共同给药增强了丙烯酰胺诱导的大脑皮层 Nrf2 及其下游抗氧化蛋白的 mRNA 上调,并抑制了丙烯酰胺诱导的肿瘤坏死因子-α(TNF-α)和诱导型一氧化氮合酶(iNOS)的 mRNA 上调。结果表明,通过共同给予萝卜硫素激活 Nrf2 信号通路可通过抑制氧化应激和炎症来提供丙烯酰胺诱导的神经毒性的保护作用。Nrf2 仍然是丙烯酰胺诱导的神经毒性的战略预防的重要靶点。