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首页> 外文期刊>European Journal of Obstetrics, Gynecology and Reproductive Biology: An International Journal >Protective effect of infliximab on ischemia/reperfusion injury in a rat ovary model: Biochemical and histopathologic evaluation
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Protective effect of infliximab on ischemia/reperfusion injury in a rat ovary model: Biochemical and histopathologic evaluation

机译:英夫利昔单抗对大鼠卵巢缺血/再灌注损伤的保护作用:生化和组织病理学评价

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Objective The aim of this study was to investigate the effect of infliximab on experimentally induced ovarian ischemia/reperfusion injury (IRi). Study design A total of 42 female rats were equally divided into 6 experimental groups; group 1: sham operation, group 2: 3-h ischemia, group 3 and 4: 3-h ischemia, 3-h reperfusion, group 5 and 6: 3-h ischemia, 24 h reperfusion. In group 4 and group 6, 30 min before reperfusion, infliximab was administered intraperitoneally at a dose of 5 mg/kg. Bilateral ovaries were removed for histopathologic and biochemical analysis. Serum MDA (sMDA), tissue MDA (tMDA), serum NO (sNO), tissue NO (tNO) and serum catalase concentrations were analyzed. Tissue damage of ovarian tissue was scored by histological examination. Results The infliximab administration significantly lowered the sNO, tNO and sMDA concentrations in group 4 compared to group 3 (p = 0.041, p = 0.025 and p = 0.035, respectively). sNO, tNO and sMDA concentrations were also lower in group 6 when compared to group 5, but this differences were not significant (p > 0.05). On the other hand, tMDA concentrations were lower in infliximab-applied groups when compared to ischemia/reperfusion groups (group 3 vs. 4 and 5 vs. 6) (p = 0.045 and p = 0.048, respectively). Moreover, histopathologic tissue damage scores in infliximab administration groups were significantly lower than in ischemia/reperfusion groups (p < 0.001). Conclusion Infliximab attenuates I/R-induced ovarian tissue injury in rats subjected to ischemia/reperfusion.
机译:目的本研究的目的是研究英夫利昔单抗对实验性卵巢缺血/再灌注损伤(IRi)的影响。研究设计将42只雌性大鼠平均分为6个实验组。组1:假手术,组2:3-h缺血,组3和4:3-h缺血,3-h再灌注,组5和6:3-h缺血,24h再灌注。在第4组和第6组中,再灌注前30分钟,腹膜内给予英夫利昔单抗,剂量为5 mg / kg。取出双侧卵巢进行组织病理学和生化分析。分析血清MDA(sMDA),组织MDA(tMDA),血清NO(sNO),组织NO(tNO)和血清过氧化氢酶浓度。通过组织学检查对卵巢组织的组织损伤进行评分。结果与第3组相比,英夫利昔单抗给药显着降低了第4组的sNO,tNO和sMDA浓度(分别为p = 0.041,p = 0.025和p = 0.035)。与第5组相比,第6组的sNO,tNO和sMDA浓度也较低,但这种差异并不显着(p> 0.05)。另一方面,英夫利昔单抗治疗组的tMDA浓度低于缺血/再灌注组(第3组,第4组和第5组与第6组)(分别为p = 0.045和p = 0.048)。此外,英夫利昔单抗给药组的组织病理学组织损伤评分显着低于缺血/再灌注组(p <0.001)。结论英夫利昔单抗可减轻缺血再灌注大鼠I / R引起的卵巢组织损伤。

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