Thiopurines exert harmful effects on spermatogenesis in Nudt15R138C knock-in mice

Background The association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect testicular functions based on the NUDT15 genotypes using Nudt15 R138C knock-in mice. Methods The male Nudt15 R138C knock-in mice (9–12 we...

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Published inJournal of gastroenterology Vol. 59; no. 2; pp. 109 - 118
Main Authors Yokota, Yoshihiro, Imai, Takayuki, Kawahara, Masahiro, Inatomi, Osamu, Nishida, Atsushi, Kakuta, Yoichi, Masamune, Atsushi, Andoh, Akira
Format Journal Article
LanguageEnglish
Published Singapore Springer Nature Singapore 01.02.2024
Springer Nature B.V
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ISSN0944-1174
1435-5922
1435-5922
DOI10.1007/s00535-023-02059-7

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Abstract Background The association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect testicular functions based on the NUDT15 genotypes using Nudt15 R138C knock-in mice. Methods The male Nudt15 R138C knock-in mice (9–12 weeks) were treated with mercaptopurine (MP: 0.5 mg/kg/day) for 4 or 12 weeks. To examine reversibility, some mice were maintained for a further 12 weeks under MP-free condition. Results After MP treatment for 4 weeks, Nudt15 R138C/R138C mice exhibited a significant reduction of testis weight compared to Nudt15 + / + mice and Nudt15 + / R138C mice. The epithelial height and diameter of seminiferous tubules were significantly reduced in Nudt15 R138C/R138C mice compared to Nudt15 + / + and Nudt15 + / R138C mice. Apoptotic cells were significantly increased in Nudt15 R138C/R138C mice, and most of apoptotic cells were spermatogonia. There were no significant changes in sperm counts and sperm morphology in MP-treated Nudt15 R138C/R138C mice after 4-week MP treatment. On the other hand, after MP treatment for 12 weeks, the Nudt15 + / R138C mice, but not Nudt15 + / + mice, exhibited a significant reduction in the testis weight and atrophic changes of seminiferous tubules, but these changes disappeared after 12-week rearing under MP-free condition. Despite a significant increase in abnormal sperm rate, there were no changes in the ability to conceive. No differences in serum levels of follicle-stimulating hormone or testosterone were observed between MP-treated Nudt15 +/ R138C and Nudt15 + / + mice after 12-week MP treatment. Conclusions Thiopurines exert harmful effects on testicular reproductive function according to host NUDT15 genotypes.
AbstractList The association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect testicular functions based on the NUDT15 genotypes using Nudt15R138C knock-in mice.BACKGROUNDThe association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect testicular functions based on the NUDT15 genotypes using Nudt15R138C knock-in mice.The male Nudt15R138C knock-in mice (9-12 weeks) were treated with mercaptopurine (MP: 0.5 mg/kg/day) for 4 or 12 weeks. To examine reversibility, some mice were maintained for a further 12 weeks under MP-free condition.METHODSThe male Nudt15R138C knock-in mice (9-12 weeks) were treated with mercaptopurine (MP: 0.5 mg/kg/day) for 4 or 12 weeks. To examine reversibility, some mice were maintained for a further 12 weeks under MP-free condition.After MP treatment for 4 weeks, Nudt15R138C/R138C mice exhibited a significant reduction of testis weight compared to Nudt15+/+ mice and Nudt15+/R138C mice. The epithelial height and diameter of seminiferous tubules were significantly reduced in Nudt15R138C/R138C mice compared to Nudt15+/+ and Nudt15+/R138C mice. Apoptotic cells were significantly increased in Nudt15R138C/R138C mice, and most of apoptotic cells were spermatogonia. There were no significant changes in sperm counts and sperm morphology in MP-treated Nudt15R138C/R138C mice after 4-week MP treatment. On the other hand, after MP treatment for 12 weeks, the Nudt15+/R138C mice, but not Nudt15+/+ mice, exhibited a significant reduction in the testis weight and atrophic changes of seminiferous tubules, but these changes disappeared after 12-week rearing under MP-free condition. Despite a significant increase in abnormal sperm rate, there were no changes in the ability to conceive. No differences in serum levels of follicle-stimulating hormone or testosterone were observed between MP-treated Nudt15+/R138C and Nudt15+/+ mice after 12-week MP treatment.RESULTSAfter MP treatment for 4 weeks, Nudt15R138C/R138C mice exhibited a significant reduction of testis weight compared to Nudt15+/+ mice and Nudt15+/R138C mice. The epithelial height and diameter of seminiferous tubules were significantly reduced in Nudt15R138C/R138C mice compared to Nudt15+/+ and Nudt15+/R138C mice. Apoptotic cells were significantly increased in Nudt15R138C/R138C mice, and most of apoptotic cells were spermatogonia. There were no significant changes in sperm counts and sperm morphology in MP-treated Nudt15R138C/R138C mice after 4-week MP treatment. On the other hand, after MP treatment for 12 weeks, the Nudt15+/R138C mice, but not Nudt15+/+ mice, exhibited a significant reduction in the testis weight and atrophic changes of seminiferous tubules, but these changes disappeared after 12-week rearing under MP-free condition. Despite a significant increase in abnormal sperm rate, there were no changes in the ability to conceive. No differences in serum levels of follicle-stimulating hormone or testosterone were observed between MP-treated Nudt15+/R138C and Nudt15+/+ mice after 12-week MP treatment.Thiopurines exert harmful effects on testicular reproductive function according to host NUDT15 genotypes.CONCLUSIONSThiopurines exert harmful effects on testicular reproductive function according to host NUDT15 genotypes.
Background The association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect testicular functions based on the NUDT15 genotypes using Nudt15 R138C knock-in mice. Methods The male Nudt15 R138C knock-in mice (9–12 weeks) were treated with mercaptopurine (MP: 0.5 mg/kg/day) for 4 or 12 weeks. To examine reversibility, some mice were maintained for a further 12 weeks under MP-free condition. Results After MP treatment for 4 weeks, Nudt15 R138C/R138C mice exhibited a significant reduction of testis weight compared to Nudt15 + / + mice and Nudt15 + / R138C mice. The epithelial height and diameter of seminiferous tubules were significantly reduced in Nudt15 R138C/R138C mice compared to Nudt15 + / + and Nudt15 + / R138C mice. Apoptotic cells were significantly increased in Nudt15 R138C/R138C mice, and most of apoptotic cells were spermatogonia. There were no significant changes in sperm counts and sperm morphology in MP-treated Nudt15 R138C/R138C mice after 4-week MP treatment. On the other hand, after MP treatment for 12 weeks, the Nudt15 + / R138C mice, but not Nudt15 + / + mice, exhibited a significant reduction in the testis weight and atrophic changes of seminiferous tubules, but these changes disappeared after 12-week rearing under MP-free condition. Despite a significant increase in abnormal sperm rate, there were no changes in the ability to conceive. No differences in serum levels of follicle-stimulating hormone or testosterone were observed between MP-treated Nudt15 +/ R138C and Nudt15 + / + mice after 12-week MP treatment. Conclusions Thiopurines exert harmful effects on testicular reproductive function according to host NUDT15 genotypes.
BackgroundThe association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect testicular functions based on the NUDT15 genotypes using Nudt15R138C knock-in mice.MethodsThe male Nudt15R138C knock-in mice (9–12 weeks) were treated with mercaptopurine (MP: 0.5 mg/kg/day) for 4 or 12 weeks. To examine reversibility, some mice were maintained for a further 12 weeks under MP-free condition.ResultsAfter MP treatment for 4 weeks, Nudt15R138C/R138C mice exhibited a significant reduction of testis weight compared to Nudt15+/+ mice and Nudt15+/R138C mice. The epithelial height and diameter of seminiferous tubules were significantly reduced in Nudt15R138C/R138C mice compared to Nudt15+/+ and Nudt15+/R138C mice. Apoptotic cells were significantly increased in Nudt15R138C/R138C mice, and most of apoptotic cells were spermatogonia. There were no significant changes in sperm counts and sperm morphology in MP-treated Nudt15R138C/R138C mice after 4-week MP treatment. On the other hand, after MP treatment for 12 weeks, the Nudt15+/R138C mice, but not Nudt15+/+ mice, exhibited a significant reduction in the testis weight and atrophic changes of seminiferous tubules, but these changes disappeared after 12-week rearing under MP-free condition. Despite a significant increase in abnormal sperm rate, there were no changes in the ability to conceive. No differences in serum levels of follicle-stimulating hormone or testosterone were observed between MP-treated Nudt15+/R138C and Nudt15+/+ mice after 12-week MP treatment.ConclusionsThiopurines exert harmful effects on testicular reproductive function according to host NUDT15 genotypes.
Author Inatomi, Osamu
Kakuta, Yoichi
Masamune, Atsushi
Yokota, Yoshihiro
Andoh, Akira
Imai, Takayuki
Kawahara, Masahiro
Nishida, Atsushi
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  organization: Department of Medicine, Shiga University of Medical Science
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  surname: Nishida
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  organization: Department of Medicine, Shiga University of Medical Science
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Keywords Inflammatory bowel disease
NUDT15
Spermatogenesis
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SSID ssj0013058
Score 2.4089067
Snippet Background The association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines...
BackgroundThe association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines...
The association between thiopurine use and testicular reproductive functions remains unclear. In this study, we investigated whether thiopurines affect...
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SubjectTerms 6-Mercaptopurine
Abdominal Surgery
Apoptosis
Colorectal Surgery
Follicle-stimulating hormone
Gastroenterology
Genotypes
Hepatology
Medicine
Medicine & Public Health
Original Article—Alimentary Tract
Serum levels
Sperm
Spermatogenesis
Spermatogonia
Surgical Oncology
Testes
Testosterone
Tubules
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Title Thiopurines exert harmful effects on spermatogenesis in Nudt15R138C knock-in mice
URI https://link.springer.com/article/10.1007/s00535-023-02059-7
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Volume 59
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