Published online 2014-08-28. doi: 10.11569/wcjd.v22.i24.3632
修回日期: 2014-06-23
接受日期: 2014-07-15
在线出版日期: 2014-08-28
目的: 观察双歧杆菌黏附素对大鼠肠缺血再灌注损伤(intestinal ischemia reperfusion injury, I/R)后肠道菌群和细菌易位的影响.
方法: SD大鼠72只随机分为假手术组(对照组, 24只)、I/R模型组(24只)和黏附素实验组(24只). 建模成功后6 h及1、4、7 d, 各组分别取6只大鼠剖杀, 观察肠道菌群和细菌易位的变化情况, 并检测各时间点血浆内毒素水平.
结果: I/R组各时点大鼠粪便中肠球菌(6.63 lgN/g±1.06 lgN/g vs 5.26 lgN/g±1.08 lgN/g, 9.44 lgN/g±1.37 lgN/g vs 5.30 lgN/g±1.12 lgN/g, 8.56 lgN/g±1.35 lgN/g vs 4.99 lgN/g±0.96 lgN/g, 8.23 lgN/g±1.01 lgN/g vs 5.18 lgN/g±1.03 lgN/g, P<0.05)和肠杆菌(7.86 lgN/g±1.17 lgN/g vs 6.39 lgN/g±0.85 lgN/g, 9.49 lgN/g±1.23 lgN/g vs 6.64 lgN/g±1.44 lgN/g, 8.76 lgN/g±0.86 lgN/g vs 6.52 lgN/g±1.13 lgN/g, 8.89 lgN/g±1.09 lgN/g vs 6.71 lgN/g±0.98 lgN/g, P<0.05)数量较对照组均明显升高, 产气荚膜梭菌数量在1 d(6.47 lgN/g±1.43 lgN/g vs 4.51 lgN/g±1.22 lgN/g, P<0.05)、4 d(6.70 lgN/g±1.16 lgN/g vs 4.71 lgN/g±0.89 lgN/g, P<0.05)、7 d(6.55 lgN/g±1.29 lgN/g vs 4.46 lgN/g±0.79 lgN/g, P<0.05)时较对照组均明显升高, 双歧杆菌(6.13 lgN/g±1.28 lgN/g vs 9.02 lgN/g±1.10 lgN/g, 5.59 lgN/g±1.22 lgN/g vs 8.66 lgN/g±0.99 lgN/g, P<0.05)、乳杆菌数量(6.07 lgN/g±1.09 lgN/g vs 9.08 lgN/g±1.04 lgN/g, 5.35 lgN/g±1.26 lgN/g vs 8.89 lgN/g±0.97 lgN/g, P<0.05)在4、7 d时较对照组明显降低; 实验组粪便中肠球菌(6.37 lgN/g±1.04 lgN/g vs 8.56 lgN/g±1.35 lgN/g, 5.42 lgN/g±0.92 lgN/g vs 8.23 lgN/g±1.01 lgN/g, P<0.05)和肠杆菌数量(7.55 lgN/g±1.03 lgN/g vs 8.76 lgN/g±0.86 lgN/g, 7.16 lgN/g±0.86 lgN/g vs 8.89 lgN/g±1.09 lgN/g, P<0.05)在4、7 d时均明显低于I/R组, 在1、4、7 d时粪便中产气荚膜梭菌数量虽仍高于对照组(5.95 lgN/g±1.24 lgN/g vs 4.51 lgN/g±1.22 lgN/g, 6.08 lgN/g±1.07 lgN/g vs 4.71 lgN/g±0.89 lgN/g, 5.87 lgN/g±0.82 lgN/g vs 4.46 lgN/g±0.79 lgN/g, P<0.05), 但较I/R组已有所下降, 各时点双歧杆菌(8.56 lgN/g±0.85 lgN/g vs 8.45 lgN/g±0.86 lgN/g, 7.89 lgN/g±1.47 lgN/g vs 8.78 lgN/g±1.06 lgN/g, 8.67 lgN/g±1.13 lgN/g vs 9.02 lgN/g±1.10 lgN/g, 8.75 lgN/g±0.96 lgN/g vs 8.66 lgN/g±0.99 lgN/g, P>0.05)和乳杆菌数量(9.16 lgN/g±0.94 lgN/g vs 8.91 lgN/g±1.06 lgN/g, 8.56 lgN/g±1.21 lgN/g vs 9.11 lgN/g±1.13 lgN/g, 9.16 lgN/g±1.08 lgN/g vs 9.08 lgN/g±1.04 lgN/g, 9.01 lgN/g±0.95 lgN/g vs 8.89 lgN/g±0.97 lgN/g, P>0.05)则较对照组均无显著变化; I/R组各时点血浆内毒素水平(1.43 EU/mL±0.32 EU/mL vs 0.21 EU/mL±0.18 EU/mL, 1.84 EU/mL±0.24 EU/mL vs 0.30 EU/mL±0.23 EU/mL, 1.69 EU/mL±0.35 EU/mL vs 0.26 EU/mL±0.21 EU/mL, 1.73 EU/mL±0.31 EU/mL vs 0.28 EU/mL±0.19 EU/mL, P<0.05)及肝(50% vs 0, 66.67% vs 16.67%, 83.33% vs 0, 83.33% vs 0, P<0.05)、脾(33.33% vs 0, 50% vs 0, 66.67% vs 0, 66.67% vs 0, P<0.05)和肠系膜淋巴结(66.67% vs 0, 83.33% vs 0, 100% vs 16.67%, 100% vs 0, P<0.05)细菌易位率均明显高于对照组, 实验组各时点血浆内毒素水平(0.57 EU/mL±0.23 EU/mL vs 1.43 EU/mL±0.32 EU/mL, 0.71 EU/mL±0.16 EU/mL vs 1.84 EU/mL±0.24 EU/mL, 0.41 EU/mL±0.22 EU/mL vs 1.69 EU/mL±0.35 EU/mL, 0.35 EU/mL±0.12 EU/mL vs 1.73 EU/mL±0.31 EU/mL, P<0.05)及肝(16.67% vs 50%, 33.33% vs 66.67%, 50% vs 83.33%, 33.33% vs 83.33%, P<0.05)、脾(0 vs 33.33%, 16.67% vs 50%, 33.33% vs 66.67%, 33.33% vs 66.67%, P<0.05)和肠系膜淋巴结(50% vs 66.67%, 50% vs 83.33%, 50% vs 100%, 33.33% vs 100%, P<0.05)细菌易位率均明显低于I/R组.
结论: 双歧杆菌分泌型黏附素可改善I/R后肠道菌群失衡, 减少肠道细菌易位及内毒素血症的发生, 保护肠黏膜屏障功能.
核心提示: 本文观察了双歧杆菌黏附素对大鼠肠道缺血再灌注损伤(intestine ischemia/reperfusion injury, I/R)后肠道菌群和细菌易位的影响, 发现双歧杆菌分泌型黏附素可改善I/R后肠道菌群失衡, 减少肠道细菌易位及内毒素血症的发生. 作为一种菌体成分, 黏附素保存、运输方便, 又避免了益生菌的其他一些不足之处, 因此为肠屏障功能障碍的防护提供了一条崭新的临床思路.