Department of Microbiology, College of Medicine, Soonchunhyang University, Cheonan, Chungnam 330-721, Republic of Korea.
Mol Med Rep. 2013 Dec;8(6):1852-60. doi: 10.3892/mmr.2013.1736. Epub 2013 Oct 16.
The extract of sea buckthorn (SBT) [Hippophae rhamnoides L. (Elaeagnaceae)], is used as a food supplement and traditional medicine in numerous countries. This study investigated the protective effects of the functional extract of SBT against paraquat (PQ)-induced toxicity via antioxidant mechanisms in A549 cells. The methanol extract of SBT (25-200 µg/ml) was used to protect cells against PQ (200 µM)-induced cell death. A viability assay was conducted using 3-(4,5-dimethylthioazol-2-ly)-2,5-diphenyltetrazolium bromide and lactate dehydrogenase (LDH). Total intracellular reactive oxygen species (ROS) were measured and plotted. For validation of the SBT-induced expression of nuclear factor-E2-related factor 2 (Nrf2) and its target genes, western blot analysis and qPCR were performed. The present study showed that pretreatment of A549 cells with SBT extract significantly attenuated PQ (200 µM)-induced cellular toxicity. The maximum cytoprotective effect was identified using 200 µg/ml SBT extract; it began 24 h following exposure and was sustained up to 120 h (P<0.05). SBT extract significantly reduced LDH activity by 35.63% and ROS levels by 30.90% (P<0.05). Pretreatment with SBT extract activated Nrf2 mRNA and protein expression and its nuclear translocation. The SBT extract effectively induced Nrf2 target genes, such as NAD(P)H dehydrogenase quinone 1, glutathione peroxidase 1, glutathione reductase and catalase following treatment with PQ. Based on these results, it was hypothesized that SBT extract may be used as a potential therapeutic agent for the treatment of various oxidative stress-related diseases.
沙棘(SBT)[ Hippophae rhamnoides L.(Elaeagnaceae)]提取物在许多国家被用作食品补充剂和传统药物。本研究通过抗氧化机制研究了 SBT 的功能提取物对百草枯(PQ)诱导的毒性的保护作用在 A549 细胞中。使用甲醇提取物 SBT(25-200μg/ml)保护细胞免受 PQ(200μM)诱导的细胞死亡。使用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐和乳酸脱氢酶(LDH)进行活力测定。测量并绘制总细胞内活性氧(ROS)。为了验证 SBT 诱导的核因子-E2 相关因子 2(Nrf2)及其靶基因的表达,进行了 Western blot 分析和 qPCR。本研究表明,SBT 提取物预处理 A549 细胞可显著减轻 PQ(200μM)诱导的细胞毒性。使用 200μg/ml SBT 提取物鉴定出最大的细胞保护作用;它在暴露后 24 小时开始,并持续至 120 小时(P<0.05)。SBT 提取物可将 LDH 活性降低 35.63%,ROS 水平降低 30.90%(P<0.05)。SBT 提取物预处理可激活 Nrf2 mRNA 和蛋白表达及其核转位。SBT 提取物在用 PQ 处理后有效诱导 Nrf2 靶基因,如 NAD(P)H 脱氢酶醌 1、谷胱甘肽过氧化物酶 1、谷胱甘肽还原酶和过氧化氢酶。基于这些结果,假设 SBT 提取物可作为治疗各种氧化应激相关疾病的潜在治疗剂。