Y. Rhee, H. Ku, Hye-Ji Noh, Hyang-Hyun Cho, Hee-Kyong Kim, Jin-Chul Ahn
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引用次数: 3
摘要
目的研究钙螯合n -乙酰神经氨酸糖大肽(CaG-NANA)对幽门螺杆菌的杀菌作用。方法将钙(Ca)与糖大肽(GMP)螯合结合,以Ca-GMP为底物酶法合成n -乙酰神经氨酸(NANA)。各组分的最终浓度为5% Ca, 7% NANA, 85% GMP, 3%水。体外实验采用最低抑菌浓度(MIC)对不同浓度的CaG-NANA进行研究。在体内研究中,幽门螺杆菌感染后口服CaG-NANA 3周。采用酶联免疫吸附法分析血中炎症因子水平,采用组织学观察观察幽门螺杆菌根除情况。结果时间杀伤曲线显示细胞数量持续下降,且与剂量有关,体外对幽门螺杆菌的杀伤MIC为0.5%。组织病理学观察显示,CaG-NANA治疗组胃黏膜在体内无明显炎症及病理改变。经CaG-NANA处理后,幽门螺杆菌的定植量减少。白细胞介素(IL)-6、IL-1β、肿瘤坏死因子-α和IL-10的水平也被CaG-NANA降低。结论CaG-NANA对幽门螺杆菌具有较强的体外和体内抑菌活性。
Anti-Helicobacter pylori effect of CaG-NANA, a new sialic acid derivative
AIM To investigate the bactericidal effects of calcium chelated N-acetylneuraminic acid-glycomacropeptide (CaG-NANA) against Helicobacter pylori (H. pylori). METHODS For manufacture of CaG-NANA, calcium (Ca) was combined with glycomacropeptide (GMP) by chelating, and N-acetylneuraminic acid (NANA) was produced with Ca-GMP substrate by an enzymatic method. The final concentration of each component was 5% Ca, 7% NANA, 85% GMP, and 3% water. For in vitro study, various concentrations of CaG-NANA were investigated under the minimal inhibitory concentration (MIC). For in vivo study, CaG-NANA was administered orally for 3 wk after H. pylori infection. The levels of inflammatory cytokines in blood were analyzed by enzyme-linked immunosorbent assay and eradication of H. pylori was assessed by histological observation. RESULTS The time-kill curves showed a persistent decrease in cell numbers, which depended on the dose of CaG-NANA, and MIC of CaG-NANA against H. pylori was 0.5% in vitro. Histopathologic observation revealed no obvious inflammation or pathologic changes in the gastric mucosa in the CaG-NANA treatment group in vivo. The colonization of H. pylori was reduced after CaG-NANA treatment. The levels of interleukin (IL)-6, IL-1β, tumor necrosis factor-α, and IL-10 were also decreased by CaG-NANA. CONCLUSION CaG-NANA demonstrates effective anti-bactericidal activity against H. pylori both in vitro and in vivo.