Unsal Ali, Eroglu Muzaffer, Avci Asli, Cimentepe Ersin, Guven Cengiz, Derya Balbay M, Durak Ilker
Department of Urology, Fatih University, Ankara, Turkey.
Scand J Urol Nephrol. 2006;40(1):17-22. doi: 10.1080/00365590500407514.
To investigate the impact of garlic extract (GE), which is known for its antioxidant activity, on a testicular torsion/detorsion model in animals and to help understand how to prevent both ischemic and reperfusion injuries after testicular torsion and detorsion.
Six groups of rats (n=7 in each group) were used. The animals in the control group (Group I) did not receive any treatment. The animals in the sham group (Group II) underwent scrotal incision and testicular fixation only. The animals in Groups III-VI underwent 720 degrees of left testicular torsion for 2 h; subsequent detorsion was performed for 2h in Groups IV and VI only. Animals in Groups V and VI were treated exactly the same as those in Groups III and IV, respectively except that they were pretreated with oral GE for 5 days at a dosage of 5 ml/kg. Both testicles in all rats were removed and tissue malondialdehyde (MDA) levels and enzymatic activities of xanthine oxidase (XO) were studied, in addition to a histological evaluation after hematoxylin-eosin staining.
Testicular MDA levels and XO activities were higher in Group III compared to Group II (p<0.05). Pretreatment with GE prevented these increases. Detorsion caused more damage and resulted in a further increase in MDA levels but MDA levels were not increased in animals pretreated with GE. Histologically, torsion caused some separation between germinative cells in the seminiferous tubules, which became much more prominent in Group IV and was attenuated by GE pretreatment. There were no significant changes in any of the above-mentioned enzymatic activities or histopathologic changes in the contralateral testicle in any of the groups.
We believe that both testicular torsion and detorsion result in testicular tissue damage by means of lipid peroxidation, which is evident by an increase in the tissue levels of MDA. Dietary supplementation with GE seems to attenuate the generation of toxic free radicals, as evidenced indirectly by low tissue MDA levels.
研究以其抗氧化活性而闻名的大蒜提取物(GE)对动物睾丸扭转/复位模型的影响,并有助于了解如何预防睾丸扭转和复位后的缺血性损伤和再灌注损伤。
使用六组大鼠(每组n = 7)。对照组(I组)动物未接受任何治疗。假手术组(II组)动物仅接受阴囊切开和睾丸固定。III - VI组动物进行左侧睾丸720度扭转2小时;仅IV组和VI组随后进行2小时的复位。V组和VI组动物分别与III组和IV组动物的治疗完全相同,只是它们以5 ml/kg的剂量口服GE预处理5天。切除所有大鼠的双侧睾丸,研究组织丙二醛(MDA)水平和黄嘌呤氧化酶(XO)的酶活性,此外还进行苏木精 - 伊红染色后的组织学评估。
与II组相比,III组的睾丸MDA水平和XO活性更高(p<0.05)。GE预处理可防止这些升高。复位造成了更多损伤并导致MDA水平进一步升高,但GE预处理的动物MDA水平未升高。组织学上,扭转导致生精小管中生发细胞之间出现一些分离,这在IV组中更为明显,而GE预处理可使其减轻。任何组的对侧睾丸中上述酶活性或组织病理学变化均无显著变化。
我们认为睾丸扭转和复位均通过脂质过氧化导致睾丸组织损伤,这可通过组织MDA水平升高得到证明。膳食补充GE似乎可减轻有毒自由基的产生,低组织MDA水平间接证明了这一点。