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.
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.
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.
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).
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.
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。
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。
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)。
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。