Anim J T, Kehinde E O, Prasad Asa, Varghese R
Department of Pathology, Faculty of Medicine, Kuwait University, Safat, Kuwait.
Urol Int. 2005;75(3):258-63. doi: 10.1159/000087805.
To investigate the morphological effects of free radical injury on spermatogenic cells in both testes of the rabbit experimental model of testicular torsion.
The left testes of 8 peripubertal NZW rabbits (3-6 months) were subjected to 0, 15, 30, 60, 90, 120, and 180 min of ischemia by applying a clamp to the spermatic cord, followed by reperfusion. Another set of 8 rabbits was subjected to 60 min of ischemia and administered antioxidants (acetylsalicylic acid, ascorbic acid, allopurinol, quercetin, superoxide dismutase) before reperfusion. Both testes of 4 animals per group were harvested at 24 h and the remaining 4 at 3 months. Johnsen scores for spermatogenic activity and other changes were assessed histologically and these were compared with testicular malondialdehyde (MDA), a measure of free radical damage, assayed on testicular homogenates using the thiobarbiturate method.
In the 24-hour reperfusion group, apoptotic bodies and giant cells were more prominent in the seminiferous tubules of the left testes compared to the right, and were maximal after 90 min. In the 3-month reperfusion group, giant cells were absent, and apoptotic bodies were reduced in both testes. Testicular MDA showed an increase only in the left testes in the 24-hour reperfusion group, while the 3-month group showed increased MDA levels in both testes, but more on the left. The Johnsen score fell only to 8.0 in the left testes in the 24-hour reperfusion group, but dropped to 2.3 in the 3-month reperfusion group. Only in the 3-month reperfusion group, did antioxidant-treated animals show a fall in Johnsen scores in the left testes, regardless of the type of antioxidant.
These findings confirm a role for reactive oxygen species (ROS) in damage to spermatogenic cells in both the ipsilateral and contralateral testes following torsion, with longer term effects in the torted testis. Currently available antioxidants do not provide any significant long-term protection against morphological damage to the testis by ROS generated in testicular torsion.
研究睾丸扭转兔实验模型中自由基损伤对双侧睾丸生精细胞的形态学影响。
对8只青春期前新西兰白兔(3 - 6个月)的左侧睾丸,通过钳夹精索分别进行0、15、30、60、90、120和180分钟的缺血处理,随后再灌注。另一组8只兔子在缺血60分钟后,再灌注前给予抗氧化剂(乙酰水杨酸、抗坏血酸、别嘌呤醇、槲皮素、超氧化物歧化酶)。每组4只动物的双侧睾丸在24小时时摘取,其余4只在3个月时摘取。通过组织学评估生精活性的约翰森评分及其他变化,并与睾丸丙二醛(MDA)进行比较,MDA是自由基损伤的一个指标,采用硫代巴比妥酸法在睾丸匀浆中进行检测。
在24小时再灌注组中,左侧睾丸生精小管中的凋亡小体和巨细胞比右侧更明显,90分钟时达到最大值。在3个月再灌注组中,巨细胞消失,双侧睾丸中的凋亡小体减少。睾丸MDA仅在24小时再灌注组的左侧睾丸中升高,而3个月组双侧睾丸MDA水平均升高,但左侧更高。24小时再灌注组左侧睾丸的约翰森评分仅降至8.0,但在3个月再灌注组中降至2.3。仅在3个月再灌注组中,无论抗氧化剂类型如何,经抗氧化剂处理的动物左侧睾丸的约翰森评分均下降。
这些发现证实了活性氧(ROS)在扭转后同侧和对侧睾丸生精细胞损伤中的作用,对扭转睾丸有更长期的影响。目前可用的抗氧化剂不能对睾丸扭转产生的ROS所致的睾丸形态学损伤提供任何显著的长期保护。