目的 研究植物乳杆菌对肠道细菌易位的抑制作用。方法 将SD大鼠随机分为4组,即假手术对照组,乳杆菌L2灌胃组,缺血再灌注(Ischemia/Reperfusion, I/R)组,乳杆菌预处理+缺血再灌注组。观察各组动物肠黏膜形态病理学变化、肠道菌群变化、细菌易位、血浆细胞因子的水平。结果 与假手术对照组相比,缺血再灌注组大鼠肠黏膜有明显病理损伤改变,肠黏膜出现坏死、脱落。肠道内厌氧菌数量显著下降,肠杆菌数量也有所下降。在肝、脾、肾及肠系膜淋巴结中有细菌存在,其易位率达87.5%(P<0.01)。乳杆菌灌胃组大鼠各项指标无显著变化,乳杆菌预处理+I/R组其变化程度较之缺血再灌注组显著减弱。结论 植物乳杆菌L2能够抑制肠道缺血再灌注损伤引起的细菌易位,减弱其对肠黏膜屏障的损伤。
Abstract
Objective To investigate the ability of Lactobacillus plantarum L2 to prevent intestinal ischemia and reperfusion induced bacterial translocation.Methods 32 SD rats were randomly divided into four groups: sham, Lactobacillus intragastric administration, ischemia and reperfusion (I/R) model, Lactobacillus pre-treatment and I/R model. The bacterial translocation, changes of gut microflora, levels of proinflammatory cytokines in plasma and intestinal morphology were observed.Results The increase in bacterial translocation was significant after 4 h I/R treatment (P<0.01) as compared with sham-operated group. There were obvious pathological changes of mucosal morphology in I/R rats and the number of anaerobic bacteria such as Bifidobacteria, Lactobacillus and Bacteroides was significantly reduced. The level of TNF-α in plasma was increased after I/R injury. Lactobacillus plantarum treatment alone had no effect on intestinal barrier function. However, pretreatment of rats with Lactobacillus plantarum L2 significantly abrogated I/R induced intestinal mucosal injury and prevented translocation of bacteria to mesenteric lymph nodes or to remote organs.Conclusions Lactobacillus plantarum L2 has the ability to prevent bacterial translocation and attenuate I/R induced intestinal injury.
关键词
植物乳杆菌 /
抑制 /
肠道 /
缺血再灌注 /
细菌易位
Key words
Lactobacillus plantarum /
prevent /
gut /
ischemia and reperfusion /
bacterial translocation
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参考文献
[1] Steinberg S M. Bacterial translocation: what it is and what it is not[J]. Am J Surg, 2003, 186 (3): 301-305.
[2] Shimizu K, Ogura H, Goto M, et al. Altered gut flora and environment in patients with severe SIRS[J]. J Trauma, 2006, 60 (1):126-133.
[3] Gatt M, Reddy B S, MacFie J. Bacterial translocation in the critically ill-evidence and methods of prevention[J]. Aliment Pharmacol Ther, 2007, 25 (7): 741-757.
[4] Reddy B S, MacFie J, Gatt M, et al. Commensal bacteria do translocate across the intestinal barrier in surgical patients[J]. Clin Nutr, 2007, 26 (2): 208-215.
[5] Yüksek Y N, Kologlu M, Daglar G, et al. Intestinal ischemia-reperfusion injury augments intestinal mucosal injury and bacterial translocation in jaundiced rats[J]. Hepatogastroenterology, 2004, 51 (55): 171-175.
[6] Matthijsen R A, Derikx J P, Kuipers D, et al. Enterocyte shedding and epithelial lining repair following ischemia of the human small intestine attenuate inflammation[J]. PLoS One, 2009, 4 (9): e7045.
[7] Amaral F A, Fagundes C T, Guabiraba R, et al. The role of macrophage migration inhibitory factor in the cascade of events leading to reperfusion-induced inflammatory injury and lethality[J]. Am J Pathol, 2007, 171 (6):1887-1893.
[8] Souza D G, Amaral F A, Fagundes C T, et al. The long pentraxin PTX3 is crucial for tissue inflammation after intestinal ischemia and reperfusion in mice[J]. Am J Pathol, 2009, 174 (4): 1309-1318.
[9] Stefanutti G, Pierro A, Parkinson EJ, et al. Moderate hypothermia as a rescue therapy against intestinal ischemia and reperfusion injury in the rat[J]. Crit Care Med, 2008, 36 (5):1564-1572.
[10] Stefanutti G, Pierro A, Vinardi S, et al. Moderate hypothermia protects against systemic oxidative stress in a rat model of intestinal ischemia and reperfusion injury[J]. Shock, 2005, 24 (2):159-164.
[11] Leaphart C L, Tepas J J.The gut is a motor of organ system dysfunction [J]. Surgery,2007,141(5):563-569.
[12] Fagundes C T, Amaral F A, Souza A L, et al. ST2, an IL-1R family member, attenuates inflammation and lethality after intestinal ischemia and reperfusion[J]. J Leukoc Biol, 2007, 81 (2): 492-499.
[13] Tadros T, Traber D L, Heggers J P, et al. Effects of interleukin-1alpha administration on intestinal ischemia and reperfusion injury, mucosal permeability, and bacterial translocation in burn and sepsis[J]. Ann Surg, 2003, 237 (1): 101-109.
[14] Wang Bin, Li Jieshou, Li Qiurong,et al. Isolation of adhesive strains and evaluation of the colonization and immune response by Lactobacillus plantarum L2 in the rat gastrointestinal tract [J]. Int J Food Microbiol, 2009, 132 (1): 59-66.