Gou Zhongyong, Jiang Shouqun, Zheng Chuntian, Tian Zhimei, Lin Xiajing
Cell Physiol Biochem. 2015;36(2):611-21. doi: 10.1159/000430124.
BACKGROUND/AIMS: There has been increasing recent attention on the antioxidative capacity of equol. This study tested the effect of equol on oxidative stress induced by lipopolysaccharide (LPS) and regulation of immunity in chicken macrophages.
Chicken HD11 macrophages were challenged with LPS (100 ng/mL) alone or with LPS (100 ng/mL) and (±)equol (10, 20, 40, 80, 160 μmol/L) together for 24h. Evaluated responses included the contents of malondialdehyde (MDA) and reduced glutathione (GSH), activities of total superoxide dismutase (T-SOD) and inducible nitric oxide synthase (iNOS), transcript abundance of superoxide dismutase 2 (SOD2), catalase (CAT), glutathione transferase (GST), Toll-like receptor 4 (TLR4), tumor necrosis factor alpha (TNFα) and interleukin-1 beta (IL-1β), and contents of the cytokines TNFα, IL-1β, interleukin-2 (IL-2) and interferon beta (IFNβ).
Exposure to LPS induced oxidative stress as contents of MDA increased and GSH decreased in LPS-treated cells (P < 0.05) compared to those in control cells. Compared to LPS alone, co-treatment with equol (20 μmol/L, 40 μmol/L or 80 μmol/L) reduced contents of MDA and increased those of GSH (both P < 0.05). Activity of T-SOD increased (P < 0.05) in cells treated with the higher contentration of equol (80 μmol/L or 160 μmol/L), however, all concentrations (20 μmol/L to 160 μmol/L) increased activity of iNOS (P < 0.05). The highest concentration of equol (160 μmol/L) increased SOD2 and GST transcripts (P < 0.05). Equol treatment increased transcripts of TLR4, TNFα and IL-1β (P < 0.05). And there were similar changes in contents of IL-1β, IL-2, IFNβ and TNFα in the cells (P < 0.05).
It concluded that equol can protect chicken HD11 macrophages from oxidative stress induced by LPS through reducing lipid peroxidation products and enhancing contents of antioxidants, and activities of relevant antioxidase enzymes; effects were also seen in gene expression related to the immune response and increased contents of cytokines. The optimal concentration of equol on antioxidation and immune enhancement in chicken macrophages was 40 μmol/L.
背景/目的:近来,人们对雌马酚的抗氧化能力越来越关注。本研究检测了雌马酚对脂多糖(LPS)诱导的鸡巨噬细胞氧化应激及免疫调节的影响。
用LPS(100 ng/mL)单独处理鸡HD11巨噬细胞,或用LPS(100 ng/mL)与(±)雌马酚(10、20、40、80、160 μmol/L)共同处理24小时。评估的反应指标包括丙二醛(MDA)和还原型谷胱甘肽(GSH)的含量、总超氧化物歧化酶(T-SOD)和诱导型一氧化氮合酶(iNOS)的活性、超氧化物歧化酶2(SOD2)、过氧化氢酶(CAT)、谷胱甘肽转移酶(GST)、Toll样受体4(TLR4)、肿瘤坏死因子α(TNFα)和白细胞介素-1β(IL-1β)的转录丰度,以及细胞因子TNFα、IL-1β、白细胞介素-2(IL-2)和干扰素β(IFNβ)的含量。
与对照细胞相比,LPS处理的细胞中MDA含量增加而GSH含量降低,表明LPS诱导了氧化应激(P < 0.05)。与单独使用LPS相比,雌马酚(20 μmol/L、40 μmol/L或80 μmol/L)共同处理可降低MDA含量并增加GSH含量(均P < 0.05)。较高浓度雌马酚(80 μmol/L或160 μmol/L)处理的细胞中T-SOD活性增加(P < 0.05),然而,所有浓度(20 μmol/L至160 μmol/L)均增加了iNOS的活性(P < 0.05)。最高浓度的雌马酚(160 μmol/L)增加了SOD2和GST的转录本(P < 0.05)。雌马酚处理增加了TLR4、TNFα和IL-1β的转录本(P < 0.05)。并且细胞中IL-1β、IL-2、IFNβ和TNFα的含量也有类似变化(P < 0.05)。
得出结论,雌马酚可通过减少脂质过氧化产物、提高抗氧化剂含量及相关抗氧化酶的活性,保护鸡HD11巨噬细胞免受LPS诱导的氧化应激;在与免疫反应相关的基因表达及细胞因子含量增加方面也有作用。雌马酚对鸡巨噬细胞抗氧化和免疫增强的最佳浓度为40 μmol/L。