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首页> 外文期刊>Mediators of inflammation >Prophylactic Ozone Administration Reduces Intestinal Mucosa Injury Induced by Intestinal Ischemia-Reperfusion in the Rat
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Prophylactic Ozone Administration Reduces Intestinal Mucosa Injury Induced by Intestinal Ischemia-Reperfusion in the Rat

机译:预防性臭氧管理减少了大鼠肠缺血-再灌注引起的肠粘膜损伤

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Objectives. Intestinal ischemia-reperfusion injury is associated with mucosal damage and has a high rate of mortality. Various beneficial effects of ozone have been shown. The aim of the present study was to show the effects of ozone in ischemia reperfusion model in intestine.Material and Method. Twenty eight Wistar rats were randomized into four groups with seven rats in each group. Control group was administered serum physiologic (SF) intraperitoneally (ip) for five days. Ozone group was administered 1 mg/kg ozone ip for five days. Ischemia Reperfusion (IR) group underwent superior mesenteric artery occlusion for one hour and then reperfusion for two hours. Ozone + IR group was administered 1 mg/kg ozone ip for five days and at sixth day IR model was applied. Rats were anesthetized with ketamine∖xyzlazine and their intracardiac blood was drawn completely and they were sacrificed. Intestinal tissue samples were examined under light microscope. Levels of superoxide dismutase (SOD), catalase (CAT), glutathioneperoxidase (GSH-Px), malondyaldehide (MDA), and protein carbonyl (PCO) were analyzed in tissue samples. Total oxidant status (TOS), and total antioxidant capacity (TAC) were analyzed in blood samples. Data were evaluated statistically by Kruskal Wallis test.Results. In the ozone administered group, degree of intestinal injury was not different from the control group. IR caused an increase in intestinal injury score. The intestinal epithelium maintained its integrity and decrease in intestinal injury score was detected in Ozone + IR group. SOD, GSH-Px, and CAT values were high in ozone group and low in IR. TOS parameter was highest in the IR group and the TAC parameter was highest in the ozone group and lowest in the IR group.Conclusion. In the present study, IR model caused an increase in intestinal injury.In the present study, ozone administration had an effect improving IR associated tissue injury. In the present study, ozone therapy prevented intestine from ischemia reperfusion injury. It is thought that the therapeutic effect of ozone is associated with increase in antioxidant enzymes and protection of cells from oxidation and inflammation.
机译:目标。肠缺血再灌注损伤与粘膜损伤有关,死亡率很高。已经显示出臭氧的各种有益作用。本研究的目的是显示臭氧在肠缺血再灌注模型中的作用。材料与方法。将28只Wistar大鼠随机分为四组,每组七只。对照组腹膜内(ip)给予血清生理(SF)5天。臭氧组腹腔注射1 mg / kg臭氧,持续5天。缺血再灌注(IR)组先行肠系膜上动脉闭塞1小时,然后再进行2小时再灌注。臭氧+ IR组腹腔注射1μmg/ kg臭氧,持续5天,第6天采用IR模型。用氯胺酮∖嗪将大鼠麻醉,并完全抽出其心脏内血液并处死。在光学显微镜下检查肠组织样品。在组织样本中分析了超氧化物歧化酶(SOD),过氧化氢酶(CAT),谷胱甘肽过氧化物酶(GSH-Px),丙二醛(MDA)和羰基蛋白(PCO)的水平。在血液样本中分析了总氧化剂状态(TOS)和总抗氧化剂容量(TAC)。通过Kruskal Wallis检验对数据进行统计学评估。在臭氧给药组中,肠损伤程度与对照组没有差异。 IR导致肠道损伤评分增加。臭氧+ IR组肠上皮保持完整,肠损伤评分降低。臭氧组的SOD,GSH-Px和CAT值较高,而IR较低。 IR组的TOS参数最高,臭氧组的TAC参数最高,IR组的TAC参数最低。在本研究中,IR模型引起肠道损伤的增加。在本研究中,臭氧给药具有改善IR相关组织损伤的作用。在本研究中,臭氧疗法可防止肠缺血再灌注损伤。据认为,臭氧的治疗作用与抗氧化酶的增加和保护细胞免受氧化和炎症有关。

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