当前位置: 首页 > 期刊 > 《齐齐哈尔医学院学报》 > 2006年第4期
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双歧杆菌对NOD小鼠1型糖尿病的免疫干预作用
http://www.100md.com 《齐齐哈尔医学院学报》 2006年第4期
双歧杆菌,,双歧杆菌,1型糖尿病,T细胞亚群,1材料与方法,2结果,3讨论,参考文献
     【摘要】 目的 了解早期应用双歧杆菌对非肥胖糖尿病(NOD)小鼠糖尿病发病的影响。方法 将4周龄雌性NOD小鼠随机分为两组:实验组(20只)给予双歧杆菌0.25mg/g体重/天(制备成活菌悬液0.5ml),对照组(20只)给予等量的磷酸盐缓冲液(PBS)。4周龄开始给药至30周龄,每周测体重,于15周龄时各组分别处死6只小鼠,取胰腺组织HE染色进行胰岛炎评分;其余小鼠30周龄时观察发病率,同时观察胰岛炎,脾脏T细胞亚群变化。结果 双歧杆菌组糖尿病发病率28.57%,明显低于对照组78.57%(P<0.05),发病时间也显著延缓,胰岛炎程度明显减轻,残存胰岛数目高于对照组;脾CD4+、CD8+T细胞亚群双歧杆菌组明显低于对照组(CD4+T细胞P<0.01,CD8+T细胞P<0.05)。结论 双歧杆菌对NOD小鼠1型糖尿病发病有预防和延迟的作用,其机制可能与调节小鼠CD4+、CD8+T细胞亚群有关。

    【关键词】 双歧杆菌 1型糖尿病 T细胞亚群

    Preventive Function of Bifidobacterium for Type I Diabetes in Female NOD Mice

    Zhang Mei,et al.

    (Biochemistry Department,Qiqihar Medical College,Heilongjiang Province 161042,China)

    【Abstract】 Objective To study whether bifidobacterium can prevent the onset of type 1 diabetes in female non-obese diabetic(NOD) mice.Methods 40 female NOD mice aged four weeks were divided into two groups.Experiment group(n=20)was orally administered bifidobacterium(0.25mg/gBM/d,prepared viable organism suspension 0.5ml),and the contrast group (n=20) was given PBS by the same regimen.Mice aged four weeks were administered until 30 weeks of age.At the age of fifteen weeks,the degree of insulitis was observed;The incidence of diabetes was detected at age of thirty weeks,at the same time,to observe insulitis and change of T cell subsets of spleen.Results Treatment with bifidobacterium reduced the total incidence of diabetes(28.57% Vs 78.57%,P<0.05) and delay its onset compared with control group.The level of insulitis were lessen than control group,but the number of survival areas of Langerhans were higher than control group;CD4+、CD8+T cell subsets of spleen were lower obviously than control group.(CD4+ T cell P<0.01,CD8+T cell P<0.05).Conclusions The data demonstrated the preventive effects of bifidobacterium on the onset of type 1 diabetes and the severity of insulitis in female NOD mice.The mechanisms of these effects may be related to the change of CD4+、CD8+T cell subsets. ......

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