Department of Clinical Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Pathobiology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Arch Razi Inst. 2021 Jul;76(2):371-384. doi: 10.22092/ari.2020.128136.1406. Epub 2021 Jul 1.
The current study aimed to determine the effect of metformin (MET) on histopathologic evaluation and antioxidant enzyme activity in experimental varicocele-induced rats. A total of 60 rats were randomly divided into six experimental groups. Group 1 (control) received no medication and underwent no surgery. In group 2 (sham), the rats received no medication and the abdominal cavity was opened; however, there was no varicocele induction. In group 3 (varicocele), the abdominal cavity was opened and the rats underwent varicocele induction and received no medication. In group 4, the abdominal cavity was opened and the animals received 25 mg/kg of MET for 42 days and were varicocele-induced. Groups 5 and 6 were similar to group 4 except that the animals received 50 and 100 mg/kg of MET, respectively. At the end of the 21st and 42nd days, the rats were euthanized and the left testis was removed for histological analysis and measurement of superoxide dismutase (SOD), malondialdehyde (MDA), glutathione peroxidase (GPx), and total antioxidant status levels. According to the results, a dose-dependent difference was observed in testis damage grade in the MET treated groups, compared to that reported for the varicocele group (p <0.05). No difference was observed between 25 and 50 mg/kg of MET (P>0.05). Tissue MDA levels significantly increased in varicocele rats (p <0.05); however, MET (25, 50, and 100 mg/kg) in a dose-dependent manner decreased varicocele-induced MDA (p <0.05). Experimental varicocele significantly decreased SOD activity, compared to that reported for the control group (p <0.05). The administration of MET (25, 50, and 100 mg/kg) significantly increased tissue SOD activity in varicocele rats (p <0.05). The MET (25, 50, and 100 mg/kg) in a dose-dependent manner increased GPx activity in varicocele rats (p <0.05). There was no difference in MDA, SOD, and GPx levels between 25 and 50 mg/kg MET groups (P>0.05). The aforementioned findings suggested that MET treatment had beneficial effects on varicocele.
当前研究旨在探讨二甲双胍(MET)对实验性精索静脉曲张诱导大鼠的组织病理学评估和抗氧化酶活性的影响。将 60 只大鼠随机分为 6 个实验组。第 1 组(对照组)未接受任何药物治疗且未进行手术。第 2 组(假手术组)大鼠未接受任何药物治疗且仅行腹腔开放,但不诱导精索静脉曲张。第 3 组(精索静脉曲张组)大鼠仅行腹腔开放并诱导精索静脉曲张,但不接受任何药物治疗。第 4 组大鼠接受 25mg/kg 的 MET 治疗 42 天,并同时诱导精索静脉曲张。第 5 组和第 6 组与第 4 组相似,不同之处在于动物分别接受 50mg/kg 和 100mg/kg 的 MET。在第 21 天和第 42 天结束时,处死大鼠并取出左侧睾丸进行组织学分析和测量超氧化物歧化酶(SOD)、丙二醛(MDA)、谷胱甘肽过氧化物酶(GPx)和总抗氧化状态水平。结果显示,与精索静脉曲张组相比,MET 治疗组的睾丸损伤程度存在剂量依赖性差异(p < 0.05)。25mg/kg 和 50mg/kg 的 MET 之间无差异(P > 0.05)。精索静脉曲张大鼠的组织 MDA 水平显著升高(p < 0.05);然而,MET(25、50 和 100mg/kg)以剂量依赖性方式降低了精索静脉曲张诱导的 MDA(p < 0.05)。与对照组相比,实验性精索静脉曲张显著降低了 SOD 活性(p < 0.05)。MET(25、50 和 100mg/kg)的给药显著增加了精索静脉曲张大鼠的组织 SOD 活性(p < 0.05)。MET(25、50 和 100mg/kg)以剂量依赖性方式增加了精索静脉曲张大鼠的 GPx 活性(p < 0.05)。25mg/kg 和 50mg/kg MET 组之间 MDA、SOD 和 GPx 水平无差异(P > 0.05)。上述研究结果表明,MET 治疗对精索静脉曲张具有有益作用。