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机构地区:[1]苏州大学医学部,江苏省苏州市215325 [2]上海交通大学附属上海第六人民医院普外科,上海市200233
出 处:《世界华人消化杂志》2012年第33期3203-3210,共8页World Chinese Journal of Digestology
基 金:黎介寿院士肠道屏障研究专项基金资助项目;No.LJS-2009001~~
摘 要:目的:探讨不同两歧双歧杆菌菌株(Bifidobacterium bifidum,B.bifidumS17)干预周期对IL-10-/-小鼠结肠上皮肠屏障功能保护作用的影响.方法:分成4组:WT组、WT+BBf(B.bifidum)组、IL-10-/-组和IL-10-/-+BBf组,周期设为2、4、6wk,5只/组,分别灌饲PBS液或B.bifidum溶液,检测结肠组织肿瘤坏死因子α(tumornecrosisfactor-α,TNF-α)、白介素1β(interleukin-1β,IL-1β)和干扰素ν(interferon-ν,INF-ν)浓度,小鼠结肠上皮通透性和TER,紧密连接蛋白的表达.结果:B.bifidum干预4wk的小鼠结肠组织TNF-α、IL-1β、INF-ν浓度,结肠黏膜上皮通透性、TER和紧密连接蛋白表达较对照组、干预2wk有显著性差异(均P<0.01),与干预6wk相比较无显著性差异.结论:B.bifidum干预4wk可检测明确的肠屏障保护作用,增加干预周期,并不能增加肠屏障保护效果.AIM: To explore the protective effect of different cycles of intervention with Bifidobacterium bifidum (B. bifidum) on colonic epithelial mucosal barrier in IL-10 knockout mice. METHODS: Female IL-10 knockout (IL-10/) mice and wild type (WT) mice were divided into four groups: WT group, WT + B. biJidum (BBf) group, IL-10/ group, and IL-10/ + B. bifidum group. The WT + B. bifidum and IL-10-/ + B. b/fi- dum groups were administered with B. bifidum by gavage at a dose of 109 cells/d per mice for 2 wk, 4 wk, and 6 wk. The other groups were giv-en phosphate buffered saline solution. The ex- pression of tumor necrosis factor (TNF)-~, inter- leukin (IL)-I~, and interferon (INF)~y in the co- lon was measured at the end of the experiment. Colonic tissues were collected for measurement of colonic epithelial permeability, transepithelial electrical resistance (TER), and expression of tight junction protein. RESULTS: The expression of TNF-~, IL-I~, and INF-~, and tight junction protein, colonic epithe- lial permeability, and TER in mice treated with B. biJidum for 4 wk were significantly different from those in control mice and mice treated with B. bifidum for 2 wk (all P 〈 0.01), but showed no significant differences with those in mice treated with B. bifidum for 6 wk. CONCLUSION: B. bifidum intervention for 4 wk had a significant protective effect on colonic epi- thelial mucosal barrier in IL-10 knockout mice, and prolonged intervention did not significantly improve the protective effect of B. bifidum.
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