Department of General Surgery, Faculty of Medicine, Abant İzzet Baysal University, Bolu, Emek Mah. 8. Cad 75.Sok No: 53/2, 06510, Emek, Ankara, Turkey.
Dig Dis Sci. 2011 Mar;56(3):707-14. doi: 10.1007/s10620-010-1362-7. Epub 2010 Aug 4.
BACKGROUND: Oxidative stress plays a role in disease initiation and progression in inflammatory bowel disease (IBD) and manipulation of this pathway may attenuate disease progress. In this study, the effect of exopolysaccharide (EPS)-producing probiotic bacteria on gut oxidative damage was evaluated in a rat model of experimental colitis. METHODS: Colitis was induced by intracolonic administration of acetic acid. Rats were treated daily with two probiotic strains, L. delbrueckii subsp. bulgaricus B3 strain (EPS of 211 mg/l; high-EPS group) or L. delbrueckii subsp. bulgaricus A13 strain (EPS of 27 mg/l; low-EPS group), which were given directly into the stomach. Non-colitis-fed control and preventative groups were only treated with the high-EPS producing strain. Antioxidant enzyme activities (superoxide dismutase, catalase, total glutathione, reduced glutathione, glutathione disulfide) and lipid peroxidation were measured in colonic tissue samples after a treatment period of 7 days. RESULTS: Significant oxidative damage was associated with a higher level of malondialdehyde (MDA) activity and reduced antioxidant enzyme activities in the colitis model group. All antioxidant enzyme activities were higher in both probiotic-treated groups compared with those of the colitis model group (P < 0.001). Lipid peroxidation was significantly ameliorated in both probiotic groups. The improvement of oxidative stress parameters was significantly more in the high-EPS group than in the low-EPS group (P < 0.001). CONCLUSIONS: EPS-producing probiotic bacteria significantly attenuate oxidative stress in experimental colitis. Increased EPS production gives rise to a better probiotic function. These results suggest that EPS molecules could revaluate probiotic strains and exert their beneficial effects on the host and this may have a therapeutic potential.
背景:氧化应激在炎症性肠病(IBD)的发病和进展中起作用,对该途径的干预可能会减轻疾病进展。在这项研究中,我们评估了产胞外多糖(EPS)益生菌对实验性结肠炎大鼠模型肠道氧化损伤的影响。
方法:通过结肠内给予乙酸诱导结肠炎。每天用两种益生菌菌株(EPS 为 211mg/L 的 L. delbrueckii subsp. bulgaricus B3 菌株[高 EPS 组]或 EPS 为 27mg/L 的 L. delbrueckii subsp. bulgaricus A13 菌株[低 EPS 组])直接给药到胃中治疗大鼠。非结肠炎喂养的对照和预防组仅用高 EPS 产生菌株治疗。在治疗 7 天后,测量结肠组织样品中的抗氧化酶活性(超氧化物歧化酶、过氧化氢酶、总谷胱甘肽、还原型谷胱甘肽、谷胱甘肽二硫化物)和脂质过氧化。
结果:在结肠炎模型组中,丙二醛(MDA)活性升高和抗氧化酶活性降低与显著的氧化损伤相关。与结肠炎模型组相比,所有益生菌治疗组的所有抗氧化酶活性均升高(P<0.001)。在两种益生菌组中,脂质过氧化均得到显著改善。高 EPS 组的氧化应激参数改善明显大于低 EPS 组(P<0.001)。
结论:产 EPS 的益生菌可显著减轻实验性结肠炎中的氧化应激。增加 EPS 产量可提高益生菌的功能。这些结果表明,EPS 分子可以重新评估益生菌菌株,并对宿主发挥有益作用,这可能具有治疗潜力。
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