CU ZN SUPEROXIDE-DISMUTASE, CATALASE AND GLUTATHIONE-PEROXIDASE MESSENGER-RNA EXPRESSION IN THE RAT TESTIS AFTER SURGICAL CRYPTORCHIDISM AND EFFERENT DUCT LIGATION/
A. Zini et Pn. Schlegel, CU ZN SUPEROXIDE-DISMUTASE, CATALASE AND GLUTATHIONE-PEROXIDASE MESSENGER-RNA EXPRESSION IN THE RAT TESTIS AFTER SURGICAL CRYPTORCHIDISM AND EFFERENT DUCT LIGATION/, The Journal of urology, 158(2), 1997, pp. 659-663
The testis is known to be highly sensitive to a number of physical str
esses. Previous investigations suggest that oxidative stress may be an
important mediator of testicular injury. The ability of the testis to
manage oxidative stress may be limited by enzymatic clearance of reac
tive oxygen species (ROS). To evaluate the ability of the testis to wi
thstand the common pathologic conditions of cryptorchidism and obstruc
tion, we measured mRNA levels of testicular antioxidant enzymes. Prepu
bertal rats were rendered unilaterally cryptorchid and 40 days after t
he procedure, cryptorchid, contralateral and control (sham) testes wer
e harvested for RNA extraction. Adult rats were subjected to unilatera
l efferent duct ligation and the obstructed testes harvested 1 to 28 d
ays after the procedure. Antioxidant enzyme mRNA expression was assess
ed by Northern blot analysis using P-32-labeled DNA probes for classic
al cellular glutathione peroxidase (GSHPx), phospholipid hydroperoxide
glutathione peroxidase (PHGPX), Cu/Zn superoxide dismutase (SOD) and
catalase, In both cryptorchid and contralateral testes, the germ cell-
specific 0.9 kb SOD and PHGPX mRNA transcript levels were significantl
y decreased compared to control testes (p <0.05). Similarly, after eff
erent duct ligation, the 0.9 kb SOD and PHGPX mRNA transcript levels a
lso decreased compared to control testes (p <0.05). These findings sug
gest that the overall decline in testicular mRNA transcript levels aft
er efferent duct ligation and cryptorchidism is primarily due to germ
cell depletion. Reduced levels of antioxidant enzyme mRNAs in cryptorc
hid testes have been documented. Further experiments may elucidate the
role of increased oxidative stress associated with decreased antioxid
ants in cryptorchidism. It remains to be determined whether oxidative
stress has a causative role in the abnormal spermatogenesis and tumori
genesis associated with cryptorchidism.