Kang Ji Sook, Han Min Ho, Kim Gi-Young, Kim Cheol Min, Kim Byung Woo, Hwang Hye Jin, Hyun Yung
Blue-Bio Industry Regional Innovation Center and Anti-Aging Research Center, Dongeui University, Busan 614-714, Korea.
Nutrients. 2014 Dec;6(12):5667-78. doi: 10.3390/nu6125667.
This study was designed to confirm the protective effect of Schisandrae Fructus, which are the dried fruits of Schisandra chinensis (Turcz.) Baill, against oxidative stress-induced cellular damage and to elucidate the underlying mechanisms in C2C12 myoblasts. Preincubating C2C12 cells with a Schisandrae Fructus ethanol extract (SFEE) significantly attenuated hydrogen peroxide (H2O2)-induced inhibition of growth and induced scavenging activity against intracellular reactive oxygen species (ROS) induced by H2O2. SFEE also inhibited comet tail formation and phospho-histone γH2A.X expression, suggesting that it prevents H2O2-induced cellular DNA damage. Furthermore, treating C2C12 cells with SFEE significantly induced heme oxygenase-1 (HO-1) and phosphorylation of nuclear factor-erythroid 2 related factor 2 (Nrf2). However, zinc protoporphyrin IX, a potent inhibitor of HO-1 activity, significantly reversed the protective effects of SFEE against H2O2-induced growth inhibition and ROS generation in C2C12 cells. Additional experiments revealed that the potential of the SFEE to induce HO-1 expression and protect against H2O2-mediated cellular damage was abrogated by transient transfection with Nrf2-specific small interfering RNA, suggesting that the SFEE protected C2C12 cells against oxidative stress-induced injury through the Nrf2/HO-1 pathway.
本研究旨在证实五味子(即五味子科植物五味子Schisandra chinensis (Turcz.) Baill的干燥果实)对氧化应激诱导的细胞损伤的保护作用,并阐明其在C2C12成肌细胞中的潜在机制。用五味子乙醇提取物(SFEE)预孵育C2C12细胞可显著减轻过氧化氢(H2O2)诱导的生长抑制,并诱导对H2O2诱导的细胞内活性氧(ROS)的清除活性。SFEE还抑制彗星尾形成和磷酸化组蛋白γH2A.X表达,表明其可预防H2O2诱导的细胞DNA损伤。此外,用SFEE处理C2C12细胞可显著诱导血红素加氧酶-1(HO-1)和核因子红细胞2相关因子2(Nrf2)的磷酸化。然而,HO-1活性的有效抑制剂锌原卟啉IX可显著逆转SFEE对C2C12细胞中H2O2诱导的生长抑制和ROS生成的保护作用。进一步的实验表明,用Nrf2特异性小干扰RNA瞬时转染可消除SFEE诱导HO-1表达和保护细胞免受H2O2介导的细胞损伤的潜力,这表明SFEE通过Nrf2/HO-1途径保护C2C12细胞免受氧化应激诱导的损伤。