Department of General Medicine, Xiamen Changgeng Hospital Affiliated to Huaqiao University, Xiamen 361000, China.
Department of Critical Care Medicine, Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou 362000, China.
Int J Biol Macromol. 2024 Nov;280(Pt 4):135924. doi: 10.1016/j.ijbiomac.2024.135924. Epub 2024 Sep 23.
This study aimed to explore the mechanism that Lycium barbarum polysaccharides (LBP) suppress hypoxia/reoxygenation (H/R)-caused pyroptosis in cardiomyocytes (H9C2) via the Nrf2/HO-1 pathway. Initially, we established the cell model of H/R (6 h hypoxia plus with 24 h reoxygenation), and found that 90 μg/mL LBP was the optimal concentration. Subsequently, we confirmed that LBP reduced the apoptosis rate of cells after H/R, the activity of LDH, the inflammatory factors IL-1β and IL-18, and the levels of pyroptosis-specific markers ASC, NLRP3, and Caspase-1 (mRNAs and proteins). It increased the cell survival rate and the mRNA levels of the Nrf2/HO-1 pathway markers Nrf2 and HO-1, and allowed cytoplasmic Nrf2 protein to enter the nucleus to activate HO-1 protein. The Nrf2 siRNA2 caused the following events in H/R model: (1) the increases of the apoptosis rate, LDH activity, the levels of inflammatory factors (IL-1β and IL-18), the levels of ACS, NLRP3, and Caspase-1 (mRNAs and proteins); and (2) the decreases of the cell survival rate, the mRNA levels of Nrf2 and HO-1, and the protein levels of cytoplasm-Nrf2, nucleus-Nrf2, and HO-1. Therefore we concluded that 90 μg/mL LBP suppressed H/R-induced H9C2 cardiomyocyte pyroptosis via the Nrf2/HO-1 pathway.
本研究旨在探讨枸杞多糖(LBP)通过 Nrf2/HO-1 通路抑制心肌细胞(H9C2)缺氧/复氧(H/R)引起细胞焦亡的机制。首先,我们建立了 H/R 细胞模型(6 h 缺氧加 24 h 复氧),发现 90 μg/mL 的 LBP 是最佳浓度。随后,我们证实 LBP 降低了 H/R 后细胞的凋亡率、LDH 活性、炎症因子 IL-1β 和 IL-18 的水平,以及细胞焦亡特异性标志物 ASC、NLRP3 和 Caspase-1(mRNA 和蛋白)的水平。它增加了细胞存活率和 Nrf2/HO-1 通路标志物 Nrf2 和 HO-1 的 mRNA 水平,并使细胞质 Nrf2 蛋白进入细胞核激活 HO-1 蛋白。Nrf2 siRNA2 在 H/R 模型中引起以下事件:(1)凋亡率、LDH 活性、炎症因子(IL-1β 和 IL-18)水平、ACS、NLRP3 和 Caspase-1(mRNA 和蛋白)水平的增加;(2)细胞存活率、Nrf2 和 HO-1 的 mRNA 水平以及细胞质-Nrf2、细胞核-Nrf2 和 HO-1 蛋白水平的降低。因此,我们得出结论,90 μg/mL 的 LBP 通过 Nrf2/HO-1 通路抑制 H/R 诱导的 H9C2 心肌细胞焦亡。