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BST-104, a Water Extract of Lonicera japonica , Has a Gastroprotective Effect via Antioxidant and Anti-Inflammatory Activities

机译:BST-104 是金银花的水提取物,具有抗氧化和抗炎活性的胃保护作用

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Lonicera japonica ) and the mechanisms involved were investigated in murine models of gastritis and peptic ulcer. The gastroprotective effects of BST-104 and its active components were evaluated in rat models of HCl/ethanol-induced gastritis and acetic acid-induced gastric ulcer. After orally administering BST-104, chlorogenic acid, rebamipide (positive control), or vehicle to each animal model, gastric lesion sizes, gastric mucus statuses, proinflammatory cytokine levels, and oxidative stress were measured. Superoxide dismutase (SOD), catalase, and malondialdehyde (MDA) levels and oxidized/reduced glutathione (GSH) ratios in gastric mucosal tissues were measured to evaluate oxidative stress. To clarify the action mechanism of BST-104, we investigated nuclear factor (NF)- κ B pathway involvement by real-time polymerase chain reaction (PCR). In the acetic acid-induced ulcer model, oral administration of BST-104 at 50, 100, or 200 mg/kg significantly reduced gastric lesions by 38, 43, and 55, respectively, compared with vehicle controls. BST-104 significantly increased gastric mucus contents and this was accompanied by higher levels of hexosamine, sialic acid, and prostaglandin E_(2) in gastric mucus. Furthermore, BST-104 treatment increased antioxidant activities, as evidenced by higher levels of catalase, SOD, and oxidized/reduced GSH and lower MDA levels. In addition, BST-104 significantly suppressed proinflammatory cytokine (tumor necrosis factor- α , interleukin IL-6, and IL-1 β ) increases, and real-time PCR showed that BST-104 significantly downregulated NF- κ B expression. In summary, BST-104 and its active component, chlorogenic acid, were found to have gastroprotective effects by virtue of their antioxidant and anti-inflammatory properties through downregulation of NF- κ B expression.
机译:Lonicera japonica)及其机制在胃炎和消化性溃疡小鼠模型中进行了研究。在HCl/乙醇诱导的胃炎和醋酸诱导的胃溃疡大鼠模型中评估了BST-104及其活性成分的胃保护作用。口服BST-104、绿原酸、瑞巴派特(阳性对照)或载体后,测量胃病变大小、胃粘液状态、促炎细胞因子水平和氧化应激。测量胃黏膜组织中的超氧化物歧化酶 (SOD)、过氧化氢酶和丙二醛 (MDA) 水平以及氧化/还原型谷胱甘肽 (GSH) 比率以评估氧化应激。为了阐明BST-104的作用机制,我们通过实时聚合酶链反应(PCR)研究了核因子(NF)-κ B通路的参与。在醋酸诱导的溃疡模型中,与载体对照组相比,口服 50、100 或 200 mg/kg 的 BST-104 可分别显着减少 38%、43% 和 55% 的胃病变。BST-104 显着增加胃粘液含量,并伴有胃粘液中己糖胺、唾液酸和前列腺素水平升高 E_(2)。此外,BST-104 处理增加了抗氧化活性,过氧化氢酶、SOD 和氧化/还原 GSH 水平较高,MDA 水平较低。此外,BST-104显著抑制促炎细胞因子(肿瘤坏死因子-α、白细胞介素[IL]-6和IL-1 β)的增加,实时荧光定量PCR显示BST-104显著下调NF-κ B表达。综上所述,BST-104及其活性成分绿原酸通过下调NF-κ B表达而具有抗氧化和抗炎特性,具有胃保护作用。

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