Cyclooxygenase‐2 Protects Germ Cells Against Spermatogenesis Disturbance in Experimental Cryptorchidism Model Mice

H Kubota, S Sasaki, Y Kubota, Y Umemoto… - Journal of …, 2011 - Wiley Online Library
H Kubota, S Sasaki, Y Kubota, Y Umemoto, Y Yanai, K Tozawa, Y Hayashi, K Kohri
Journal of andrology, 2011Wiley Online Library
The role of cyclooxygenases (COX) in the male reproductive organ remains unclear.
However, there are some reports suggesting that COX‐2 might have an effect on
spermatogenesis or steroidogenesis. In this study, we examined whether COX‐2 was
induced in impaired testes, and we also investigated the possible role of COX in the testes
using experimental cryptorchidism model mice. Five‐week‐old male mice underwent an
operation to induce unilateral cryptorchidism via an abdominal incision and suturing of the …
Abstract
The role of cyclooxygenases (COX) in the male reproductive organ remains unclear. However, there are some reports suggesting that COX‐2 might have an effect on spermatogenesis or steroidogenesis. In this study, we examined whether COX‐2 was induced in impaired testes, and we also investigated the possible role of COX in the testes using experimental cryptorchidism model mice. Five‐week‐old male mice underwent an operation to induce unilateral cryptorchidism via an abdominal incision and suturing of the left testes to the lateral abdominal wall, and they were then divided into 3 groups: 1) experimental cryptorchidism plus SC560 (selective COX‐1 inhibitor) administration; 2) experimental cryptorchidism plus NS398 (selective COX‐2 inhibitor) administration; 3) and experimental cryptorchidism alone. The expression levels of COX‐1 and COX‐2 were determined by immunohistologic staining and quantitative reverse transcription–polymerase chain reaction (RT‐PCR). The influence of COX inhibitors on the testes was assessed by measuring the concentration of serum testosterone and evaluating the seminiferous tubules according to the Johnsen score. Terminal deoxynucleotidyl transferase–mediated dUTP‐biotin nick‐end labeling (TUNEL) staining was also performed to detect apoptosis in the testes. Immunohistologic staining and RT‐PCR revealed that the expression of COX‐2 was increased in the experimental cryptorchid testes (groups 1–3). The concentration of serum testosterone was significantly lower in group 2 at 5 weeks after surgery than in the other groups. The Johnsen score of the cryptorchid testes in group 2 was significantly lower than those in other groups at 5 weeks after surgery. TUNEL staining revealed that the number of apoptotic cells was significantly increased in group 2 compared with the other groups. However, the COX‐1 inhibitor did not appear to affect spermatogenesis in the experimental cryptorchid testes. These results suggest that the COX‐2 inhibitor provoked testicular damage in experimental cryptorchidism by inducing germ cell apoptosis. The expression of COX‐2 might be induced to protect germ cells from heat stress caused by experimental cryptorchidism.
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