Wang Jing, Chen Meixia, Wang Sixin, Chu Xu, Ji Haifeng
Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China.
Sino-US Joint Laboratory of Animal Science, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China.
Antioxidants (Basel). 2022 Oct 28;11(11):2134. doi: 10.3390/antiox11112134.
Oxidative stress contributes to intestinal dysfunction. Plant extracts can have antioxidant action; however, the specific phytogenic active ingredients and their potential mechanisms are not well known. We screened 845 phytogenic compounds using a porcine epithelial cell (IPEC-J2) oxidative stress model to identify oxidative-stress-alleviating compounds. Calycosin and deoxyshikonin were evaluated for their ability to alleviate HO-induced oxidative stress by measuring their effects on malondialdehyde (MDA) accumulation, reactive oxygen species (ROS) generation, apoptosis, mitochondrial membrane potential (MMP), and antioxidant defense. Nrf2 pathway activation and the effect of knockdown on the antioxidative effects of hit compounds were investigated. Calycosin protected IPEC-J2 cells against HO-induced oxidative damage, likely by improving the cellular redox state and upregulating antioxidant defense via the Nrf2-Keap1 pathway. Deoxyshikonin alleviated the HO-induced decrease in cell viability, ROS production, and MMP reduction, but had no significant effect on MDA accumulation and apoptosis. knockdown did not weaken the effect of deoxyshikonin in improving cell viability, but it weakened its effect in suppressing ROS production. These results indicate that the mechanisms of action of natural compounds differ. The newly identified phytogenic compounds can be developed as novel antioxidant agents to alleviate intestinal oxidative stress in animals.
氧化应激会导致肠道功能障碍。植物提取物具有抗氧化作用;然而,具体的植物活性成分及其潜在机制尚不清楚。我们使用猪上皮细胞(IPEC-J2)氧化应激模型筛选了845种植物化合物,以确定具有减轻氧化应激作用的化合物。通过测量毛蕊异黄酮和脱氧紫草素对丙二醛(MDA)积累、活性氧(ROS)生成、细胞凋亡、线粒体膜电位(MMP)和抗氧化防御的影响,评估了它们减轻过氧化氢(HO)诱导的氧化应激的能力。研究了核因子E2相关因子2(Nrf2)途径的激活以及敲除对筛选出的化合物抗氧化作用的影响。毛蕊异黄酮可能通过改善细胞氧化还原状态并通过Nrf2-Keap1途径上调抗氧化防御,从而保护IPEC-J2细胞免受HO诱导的氧化损伤。脱氧紫草素减轻了HO诱导的细胞活力下降、ROS产生和MMP降低,但对MDA积累和细胞凋亡没有显著影响。敲除并没有削弱脱氧紫草素改善细胞活力的作用,但削弱了其抑制ROS产生的作用。这些结果表明天然化合物的作用机制不同。新鉴定出的植物化合物可开发为新型抗氧化剂,以减轻动物肠道氧化应激。