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首页> 外文期刊>Archivio Italiano di Urologia e Andrologia >Protective effect of chlorogenic acid on renal ischemia/reperfusion injury in rats
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Protective effect of chlorogenic acid on renal ischemia/reperfusion injury in rats

机译:绿原酸对大鼠肾缺血/再灌注损伤的保护作用

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Objectives: Ischemia/reperfusion (I/R) injury is a common cause of renal injury and to date, many pharmacological agents have been identified to decrease I/R injury. One of the potential compound that can target I/R injury is chlorogenic acid (CGA). It has potent antiinflammatory, antibacterial, anti-oxidant, analgesic and antipyretic activities in in vitro experiments and in vivo animal models. The aim of the study was to investigate the protective characteristic of CGA on renal I/R injury. Material and Methods: 24 rats were randomly allocated to three groups (n = 8): Sham, I/R+CGA and I/R groups. CGA was administered intraperitoneally at a dose of 20 mg/kg, 10 min before reperfusion. I/R injury was achieved by clamping the left renal artery for 45 minutes, followed by reperfusion for 4 hours. The left kidneys of the rats were examined for tissue damage by histopathological and biochemical examination. For histological evaluation, EGTI scoring system was used. For biochemical examination total oxidant status, total antioxidant status and oxidative stress index were used. The power analysis indicated that 8 subjects per group would be required to produce 80% chance of achieving statistical significance at p 0.05 level. The results are expressed as mean ± SD. Mann- Whitney U was performed for statistical analysis. Results: Histopathological examination of the tissue damage revealed that all kidneys in the sham group were normal. I-R group had significantly higher histopathological scores than other groups. Histopathological improvement was seen after CGA treatment. TAS, TOS and OSI values of I-R group were significantly higher than sham group (0.88 vs 0.76 (p: 0.004), 13.8 vs 7.04 (p: 0.021) and 0.15 vs 0.09 (p: 0.034), respectively). In CGA treated group TAS, TOS and OSI levels were 0.84, 6.47 and 0.07, respectively. CGA treatment resulted in significant improvement in TOS and OSI parameters. Conclusions: CGA treatment provided marked improvement in renal histology and suppressed oxidative stress. Thus, CGA may have a protective effect in renal tissue against I/R injury.
机译:目的:缺血/再灌注(I / R)损伤是肾脏损伤的常见原因,并迄今为止,已鉴定出许多药理学药物以降低I / R损伤。可以靶向I / R损伤的潜在化合物之一是绿原酸(CGA)。它在体外实验中具有有效的抗炎,抗菌,抗氧化剂,镇痛和解热活性和体内动物模型。该研究的目的是探讨CGA对肾I / R损伤的保护性特征。材料和方法:将24只大鼠随机分配给三组(n = 8):假,I / R + CGA和I / R组。在再灌注前,在20mg / kg的剂量为10mm,10分钟,CGA腹膜内给药。通过将左肾动脉夹紧45分钟,然后再灌注4小时来实现I / R损伤。通过组织病理学和生物化学检查检查大鼠的左肾进行组织损伤。对于组织学评估,使用EGTI评分系统。对于生化检查总氧化剂状态,使用总抗氧化状态和氧化应激指数。功率分析表明,每组8个受试者需要在P <0.05水平下产生80%的统计学意义的几率。结果表示为平均值±SD。曼 - 惠特尼u是对统计分析进行的。结果:组织损伤的组织病理学检查显示,假手术中的所有肾脏都是正常的。 I-R组的组织病理学分数明显高于其他群体。 CGA治疗后观察组织病理学改善。 I-R组的TAS,TOS和OSI值明显高于假组(0.88 Vs 0.76(P:0.004),13.8 Vs 7.04(P:0.021)和0.15 Vs 0.09(P:0.034))。在CGA治疗组中,TOS,TOS和OSI水平分别为0.84,6.47和0.07。 CGA治疗导致TOS和OSI参数显着改善。结论:CGA治疗提供了肾组织学和抑制氧化应激的显着改善。因此,CGA可能对肾组织的保护作用免于I / R损伤。

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