The Different Effects of Testicular Torsion on the Contralateral Testis between Pubertal and Adult Rats

Seong Jin Jeong; Woo Seok Choi; Seung Beom Ha; Min Soo Jeong; Jae-Seung Chung; Minki Baek; Sung Kyu Hong; Hwang Choi

doi:10.4111/kju.2009.50.7.704

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Jeong, Choi, Ha, Jeong, Chung, Baek, Hong, and Choi: The Different Effects of Testicular Torsion on the Contralateral Testis between Pubertal and Adult Rats

Original Article

Korean J Urol 2009;50(7):704-710.

Published online: 19 July 2009

DOI: https://doi.org/10.4111/kju.2009.50.7.704

The Different Effects of Testicular Torsion on the Contralateral Testis between Pubertal and Adult Rats

Seong Jin Jeong, Woo Seok Choi¹, Seung Beom Ha¹, Min Soo Jeong¹, Jae-Seung Chung², Minki Baek³, Sung Kyu Hong¹, Hwang Choi^1,

¹From the Department of Urology, Seoul National University Bundang Hospital, Korea

²Pochon CHA Seoul National University College of Medicine, Seoul, Seongnam, Korea

³Konkuk University Medical University Bundang CHA Hospital, Seongnam, Center, Seoul, Korea

Correspondence to: Hwang Choi Department of Urology, Seoul National University Hospital, 28, Yongon-dong, Chongno-gu, Seoul 110-744, Korea TEL: 02-2072-3644 FAX: 02-742-4665 E-mail: hchoi@snu.ac.kr

Received 12 May 2009 Accepted 17 June 2009

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose:

Our study aimed to determine whether the severity of damage to the contralateral testis by ipsilateral testicular torsion/detorsion in pubertal rats, which have an incomplete blood-testis barrier, is different from that in adult rats.

Materials and Methods:

We divided pubertal (6 weeks, n=17) and adult (10 weeks, n=17) Sprague-Dawley (SD) rats into group S (sham; n=5), group O (orchiectomy; n=6), and group D (detorsion; n=6). After 4 hours' torsion of the ipsilateral testis, we applied orchiectomy (group O) and detorsion (group D) depending on the group and compared the histopathologic changes and germ cell apoptosis of the contralateral testis at the age of 13 weeks.

Results:

In each age group, increased interstitial area, edema, and germ cell sloughing were observed in group D. The mean seminiferous tubule diameter decreased more in group D than in group S or O in each age group (p＜0.05). The mean germ cell layer thickness and number of spermatids per tubule decreased more in group D than in group S or O in each age group; additionally, in group D, values decreased more in pubertal rats than in adult ones (p＜0.05, respectively). The mean numbers of terminal deoxyuridine nick-end labeling (TUNEL)-positive cells were less than 1.0 in groups S and O, which was smaller than in group D (p＜0.05); additionally, in group D, this value tended to be higher in pubertal rats than in adult ones (p=0.057).

Conclusions:

SD rats with a detorsioned testis had more severe damage to the contralateral testis than did those undergoing orchiectomy of the torsioned testis. Also, when comparing the severity of damage to the contralateral testis after ipsilateral torsion/detorsion between pubertal and adult rats, rats at a pubertal age, when most testicular torsions occur in clinical situations, had more severe damage than did those at an adult age.

Keywords: Spermatic cord torsion, Age factors, Testis

REFERENCES

1.Melekos MD., Asbach HW., Markou SA. Etiology of acute scrotum in 100 boys with regard to age distribution. J Urol. 1988. 139:1023–5.

2.Krarup T. The testes after torsion. Br J Urol. 1978. 50:43–6.

3.Williamson RC. Torsion of the testis and allied conditions. Br J Surg. 1976. 63:465–76.

4.Anderson JB., Williamson RC. The fate of the human testes following unilateral torsion of the spermatic cord. Br J Urol. 1986. 58:698–704.

5.Akgür FM., Kilinc K., Aktug T. Reperfusion injury after detorsion of unilateral testicular torsion. Urol Res. 1993. 21:395–9.

6.Cerasaro TS., Nachtsheim DA., Otero F., Parsons CL. The effect of testicular torsion on the contralateral testis and the production of antisperm antibodies in rabbits. J Urol. 1984. 132:577–9.

7.Kosar A., Sarica K., Kupeli B., Alçiǧir G., Süzer O., Küpeli S. Testicular torsion: evaluation of contralateral testicular histology. Int Urol Nephrol. 1997. 29:351–6.

8.Hadziselimovic F., Geneto R., Emmons LR. Increased apoptosis in the contralateral testis in patients with testicular torsion. Lancet. 1997. 350:118.

9.Turner TT. Acute experimental testicular torsion. No effect on the contralateral testis. J Androl. 1985. 6:65–72.

10.Becker EJ Jr., Turner TT. Endocrine and exocrine effects of testicular torsion in the prepubertal and adult rat. J Androl. 1995. 16:342–51.

11.Gang JW., Yang KY. Comparisons of the effects of testicular torsion through a scrotal wall incision and an abdominal wall incision on the contralateral testis in prepubertal rats. Korean J Urol. 1992. 33:816–21.

12.Clermont Y., Perey B. Quantitative study of the cell population of the seminiferous tubules in immature rats. Am J Anat. 1957. 100:241–67.

13.Steinberger A., Steinberger E. Replication pattern of Sertoli cells in maturing rat testis in vivo and in organ culture. Biol Reprod. 1971. 4:84–7.

14.Heindel RM., Pakyz RE., Consentino MJ. Spermatic cord torsion. Contralateral testicular degeneration at various ages in the rat. J Androl. 1990. 11:506–13.

15.Shin HS., Cho CK., Moon KH. The effect of testicular torsion on the histologic findings and apoptosis of the contralateral testis at various ages in rats. Korean J Urol. 2002. 43:693–8.

16.Nagler HM., White RD. The effect of testicular torsion on the contralateral testis. J Urol. 1982. 128:1343–8.

17.Sarica K., Kupeli B., Budak M., Koşar A., Kavukçu M., Durak I, et al. Influence of experimental spermatic cord torsion on the contralateral testis in rats. Evaluation of tissue free oxygen radical scavenger enzyme levels. Urol Int. 1997. 58:208–12.

18.Park EC., Kwak C., Son H., Oh SJ., Lee SE., Choi H. The role of clusterin in apoptosis induced by testicular torsion. Korean J Urol. 2004. 45:380–9.

19.Turner TT., Tung KS., Tomomasa H., Wilson LW. Acute testicular ischemia results in germ cell-specific apoptosis in the rat. Biol Reprod. 1997. 57:1267–74.

20.Werns SW., Lucchesi BR. Free radicals and ischemic tissue injury. Trends Pharmacol Sci. 1990. 11:161–6.

21.Chemes HE., Dym M., Fawcett DW., Javadpour N., Sherins RJ. Patho-physiological observations of Sertoli cells in patients with germinal aplasia or severe germ cell depletion. Ultrastructural findings and hormone levels. Biol Reprod. 1977. 17:108–23.

22.Russell LD., Malone JP. A study of Sertoli-spermatid tubulo-bulbar complexes in selected mammals. Tissue Cell. 1980. 12:263–85.

23.Hadziselimovic F., Geneto R., Emmons LR. Increased apoptosis in the contralateral testes of patients with testicular torsion as a factor for infertility. J Urol. 1998. 160:1158–60.

Fig. 1

Histology of contralateral testes sectioned 7 weeks (A, pubertal rats) and 3 weeks (B, adult rats) after ipsilateral 4 hour 720^o torsion (H&E, x400). Whereas there were no abnormalities in groups S and O, a dilated interstitial space, edema, and sloughing of germ cells were observed in group D. When compared within group D, mean germ cell layer thickness and number of spermatids per tubule decreased more in pubertal rats than in adult ones. S: sham group, O: orchiectomy group, D: detorsion group.

Fig. 2

Terminal deoxyuridine nick-end labeling (TUNEL) immunohistochemical staining of contralateral testes sectioned 7 weeks (A, pubertal rats) and 3 weeks (B, adult rats) after ipsilateral 4 hour 720^o torsion (x400). Whereas there were few TUNEL-positive cells in groups S and O, some TUNEL-positive cells were observed in group D. When compared within group D, there was a tendency for more TUNEL-positive cells in pubertal rats than in adult ones. S: sham group, O: orchiectomy group, D: detorsion group.

Fig. 3

Mean seminiferous tubule diameter for contralateral testes of rats aged 13 weeks after unilateral testicular torsion/detorsion induced at pubertal (black) and adult (gray) ages. Each bar is Mean±SD. S: sham group, O: orchiectomy group, D: detorsion group, ^a: p=0.046 for pubertal age and 0.032 for adult age: significantly decreased compared with S and O group.

Fig. 5

Mean numbers of spermatids per tubule for contralateral testes of rats aged 13 weeks after unilateral testicular torsion/ detorsion induced at pubertal (black) and adult (gray) ages. Each bar is Mean±SD. S: sham group, O: orchiectomy group, D: detorsion group, ^a: p=0.010 for pubertal age and 0.009 for adult age: significantly decreased compared with S and O group, ^b: p=0.045: significantly different between pubertal and adult rats.

Fig. 4

Mean germ cell layer thickness for contralateral testes of rats aged 13 weeks after unilateral testicular torsion/detorsion induced at pubertal (black) and adult (gray) ages. Each bar is Mean±SD. S: sham group, O: orchiectomy group, D: detorsion group, ^a: p=0.008 for pubertal age and 0.043 for adult age: signi-^b: p=0.038: ficantly decreased compared with S and O group, significantly different between pubertal and adult rats.

Fig. 6

Mean numbers of terminal deoxyuridine nick-end labeling (TUNEL)-positive cells per tubule for contralateral testes of rats aged 13 weeks after unilateral testicular torsion/detorsion induced at pubertal (black) and adult (gray) ages. Each bar is Mean±SD. ^a: S: sham group, O: orchiectomy group, D: detorsion group, p=0.014 for pubertal age and 0.011 for adult age: significantly ^b: p=0.057: different increased compared with S and O group, tendency between pubertal and adult rats.

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