Unsal Ali, Devrim Erdinc, Guven Cengiz, Eroglu Muzaffer, Durak Ilker, Bozoklu Ayca, Balbay M Derya
Department of Urology, Fatih University, P.K 5, Emek 06510, Ankara, Turkey.
World J Urol. 2004 Dec;22(6):461-5. doi: 10.1007/s00345-004-0451-7. Epub 2004 Dec 4.
Propofol, which is widely used as an intravenous anesthetic, has been shown to have an antioxidant activity on several tissues. This study was designed to investigate the prevention of reperfusion injury with propofol after testicular torsion. Five groups of rats (seven in each group) were used. Animals in the control group (group I) did not received any treatment, while animals in the sham group (group II) underwent scrotal incision and testicular fixation only. After 2 h of 720 degrees left testicular torsion in groups III, IV and V, subsequent detorsion was done for 2 h in groups IV and V. Propofol (50 mg/kg) was injected transperitoneally 30 min prior to detorsion in group V. Both testicles in all rats were retrieved and tissue malondialdeyhde (MDA) level, which is a measure of the amount of free oxygen radicals, and enzymatic activity of xanthine oxidase (XO), which converts hypoxanthine to xanthine and uric acid were studied. In addition, tissue catalase (CAT) and glutathione peroxidase (GSH-Px) activities, which are endogenous scavenger enzymes, protecting tissues against free radicals, were studied. Additionally, histological evaluations were performed after hematoxylin and eosin staining. Testicular MDA levels, and XO and CAT activities were higher in the torsion group compared to sham control group (P<0.05). Detorsion caused a further increase in MDA levels, contrasting with a decrease in the levels of XO activity, while CAT activity was not changed. Pretreatment with propofol prevented a further increase in MDA levels and significantly decreased CAT activity following detorsion. GSH-Px activities were not effected either by torsion/detorsion or propofol pretreatment. Histologically, torsion caused some separation between germinal cells in the seminiferous tubules, which became much more prominent in the detorsion group and attenuated with propofol pretreatment. There was no significant change in any of the above-mentioned enzymatic activities nor were there histopathological changes in the contralateral testicle in any groups. It is concluded that biochemically and histologically reperfusion injury occurs in the ipsilateral testis following detorsion up to 2 h. Preference of propofol for anaesthesia during the detorsion procedure may attenuate such reperfusion injury.
丙泊酚作为一种广泛应用的静脉麻醉剂,已被证明对多种组织具有抗氧化活性。本研究旨在探讨丙泊酚对睾丸扭转后再灌注损伤的预防作用。实验使用了五组大鼠(每组七只)。对照组(I组)动物未接受任何处理,而假手术组(II组)动物仅进行阴囊切开和睾丸固定。III组、IV组和V组大鼠左侧睾丸进行720度扭转2小时后,IV组和V组随后进行2小时的扭转复位。V组在扭转复位前30分钟经腹腔注射丙泊酚(50mg/kg)。取出所有大鼠的双侧睾丸,研究组织丙二醛(MDA)水平(衡量游离氧自由基量的指标)以及黄嘌呤氧化酶(XO,将次黄嘌呤转化为黄嘌呤和尿酸)的酶活性。此外,还研究了组织过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GSH-Px)的活性,它们是内源性清除酶,可保护组织免受自由基损伤。另外,在苏木精和伊红染色后进行组织学评估。与假手术对照组相比,扭转组睾丸MDA水平以及XO和CAT活性更高(P<0.05)。扭转复位导致MDA水平进一步升高,与XO活性水平降低形成对比,而CAT活性未改变。丙泊酚预处理可防止扭转复位后MDA水平进一步升高,并显著降低CAT活性。GSH-Px活性不受扭转/扭转复位或丙泊酚预处理的影响。组织学上,扭转导致生精小管中生精细胞之间出现一些分离,在扭转复位组中这种分离更加明显,而丙泊酚预处理可使其减轻。上述任何酶活性在任何组的对侧睾丸中均无显著变化,也未出现组织病理学改变。结论是,扭转复位后长达2小时,同侧睾丸在生化和组织学上会发生再灌注损伤。在扭转复位过程中选择丙泊酚进行麻醉可能会减轻这种再灌注损伤。