Department of Animal Sciences and Technology, Qingdao Agricultural University, Qingdao 266109, China.
Department of Animal Sciences and Technology, Shandong Agricultural University, Taian 271018, China.
Toxins (Basel). 2022 Nov 14;14(11):793. doi: 10.3390/toxins14110793.
This study aims to examine the impact of zearalenone (ZEA) on glucose nutrient absorption and the role of the Kelch-like erythroid cell-derived protein with CNC homology-associated protein 1 (Keap1)-nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway in zearalenone-induced oxidative stress of porcine jejunal epithelial cells (IPEC-J2). For 24 and 36 h, the IPEC-J2 cells were exposed to ZEA at concentrations of 0, 10, 20, and 40 (Control, ZEA10, ZEA20, ZEA40) mol/L. With the increase of ZEA concentration and prolongation of the action time, the apoptosis rate and malondialdehyde level and relative expression of sodium-dependent glucose co-transporter 1 (Sglt1), glucose transporter 2 (Glut2), Nrf2, quinone oxidoreductase 1 (Nqo1), and hemeoxygenase 1 (Ho1) at mRNA and protein level, fluorescence intensity of Nrf2 and reactive oxygen species increased significantly ( < 0.05), total superoxide dismutase and glutathione peroxidase activities and relative expression of Keap1 at mRNA and protein level, fluorescence intensity of Sglt1 around the cytoplasm and the cell membrane of IPEC-J2 reduced significantly ( < 0.05). In conclusion, ZEA can impact glucose absorption by affecting the expression of Sglt1 and Glut2, and ZEA can activate the Keap1-Nrf2 signaling pathway by enhancing Nrf2, Nqo1, and Ho1 expression of IPEC-J2.
本研究旨在探讨玉米赤霉烯酮(ZEA)对葡萄糖营养吸收的影响,以及 Kelch 样红细胞衍生蛋白与 CNC 同源相关蛋白 1(Keap1)-核因子红细胞 2 相关因子 2(Nrf2)信号通路在 ZEA 诱导猪空肠上皮细胞(IPEC-J2)氧化应激中的作用。在 24 和 36 小时,IPEC-J2 细胞暴露于 0、10、20 和 40(对照、ZEA10、ZEA20、ZEA40)mol/L 的 ZEA 浓度下。随着 ZEA 浓度的增加和作用时间的延长,细胞凋亡率和丙二醛水平以及钠依赖性葡萄糖协同转运蛋白 1(Sglt1)、葡萄糖转运蛋白 2(Glut2)、Nrf2、醌氧化还原酶 1(Nqo1)和血红素加氧酶 1(Ho1)的 mRNA 和蛋白水平的相对表达、Nrf2 和活性氧的荧光强度均显著增加(<0.05),总超氧化物歧化酶和谷胱甘肽过氧化物酶活性以及 Keap1 的 mRNA 和蛋白水平的相对表达、IPEC-J2 细胞质和细胞膜周围 Sglt1 的荧光强度均显著降低(<0.05)。综上所述,ZEA 可以通过影响 Sglt1 和 Glut2 的表达来影响葡萄糖吸收,并且可以通过增强 IPEC-J2 的 Nrf2、Nqo1 和 Ho1 表达来激活 Keap1-Nrf2 信号通路。