Department of Medical Cell Biology and Genetics, Health Science Center, Shenzhen University, Shenzhen 518060, China; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Jiangsu Key Laboratory of Sericultural Biology and Biotechnology, School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212018, China.
Mol Immunol. 2022 Aug;148:54-67. doi: 10.1016/j.molimm.2022.05.121. Epub 2022 Jun 4.
Mastitis, an inflammation of the mammary gland, is a complex disease that affects the health of dairy cows worldwide. Sodium butyrate (SB) is a short-chain fatty acid that has recently been shown to have antioxidant, anti-inflammatory and anti-apoptotic potential in various cells types, although its role in bovine mammary epithelial cells (bMECs) has not been comprehensively reported. Therefore, the aim of this study was to assess the protective effect of sodium butyrate on Lipopolysaccharide (LPS)-induced mastitis model in vitro and to elucidate the possible underlying molecular mechanisms. The in vitro mastitis model was designed to investigate the regulatory effect of SB on LPS-induced inflammatory conditions in bMECs, with particular emphasis on oxidative stress, inflammatory response, apoptosis, and mitochondrial dysfunction. The results showed that SB co-treatment markedly prevented LPS-induced death of bMECs in a concentration-dependent manner. In addition, SB attenuated LPS-induced oxidative stress (OS) (Increased Intracellular ROS, MDA, and decreased SOD, GSH-Px and CAT activity), thereby reduced inflammation (increased expression of IL-6, IL-Iβ, and TNF-α), and apoptosis (Increased the expression of caspases and Bax and decreased Bcl-2) via inhibiting NF-kB and caspase/bax signaling pathways. Furthermore, the protective effect of SB was also associated with the activation of endogenous antioxidant system (Nrf2, Keap1, NQO-1 and HO-1). Nrf2 silencing significantly abolished the protective effect of SB on bMECs. In conclusion, our findings suggest that SB has a significant protective effect on LPS-induced OS, inflammatory responses and apoptosis by activating Nrf2 and inhibiting NF-kB and ROS-mediated mitochondrial dysfunction. These results propose that SB may be an important regulator of OS and its subsequent inflammatory responses, and thus could be used as a therapeutic agent for bovine mastitis.
乳腺炎是一种乳腺炎症,是一种影响全球奶牛健康的复杂疾病。丁酸钠(SB)是一种短链脂肪酸,最近已被证明在各种细胞类型中具有抗氧化、抗炎和抗细胞凋亡作用,尽管其在奶牛乳腺上皮细胞(bMEC)中的作用尚未得到全面报道。因此,本研究旨在评估丁酸钠对 LPS 诱导的体外乳腺炎模型的保护作用,并阐明可能的潜在分子机制。体外乳腺炎模型旨在研究 SB 对 LPS 诱导的 bMECs 炎症状态的调节作用,特别强调氧化应激、炎症反应、细胞凋亡和线粒体功能障碍。结果表明,SB 共同处理以浓度依赖性方式显着防止 LPS 诱导的 bMEC 死亡。此外,SB 减弱了 LPS 诱导的氧化应激(OS)(增加细胞内 ROS、MDA,降低 SOD、GSH-Px 和 CAT 活性),从而减少炎症(增加 IL-6、IL-1β 和 TNF-α 的表达)和凋亡(增加 caspase 和 Bax 的表达并降低 Bcl-2 的表达)通过抑制 NF-kB 和 caspase/bax 信号通路。此外,SB 的保护作用还与内源性抗氧化系统(Nrf2、Keap1、NQO-1 和 HO-1)的激活有关。Nrf2 沉默显着消除了 SB 对 bMECs 的保护作用。总之,我们的研究结果表明,SB 通过激活 Nrf2 并抑制 NF-kB 和 ROS 介导的线粒体功能障碍,对 LPS 诱导的 OS、炎症反应和细胞凋亡具有显著的保护作用。这些结果表明,SB 可能是 OS 及其随后的炎症反应的重要调节剂,因此可作为奶牛乳腺炎的治疗剂。