Dasatinib and quercetin increase testosterone and sperm concentration in mice

Author:

Garcia Driele N.1,Hense Jéssica D.1,Zanini Bianka M.2,Isola José V. V.3,Pradiee Jorgea2,Prosczek Juliane B.1,Alvarado-Rincón Joao A.4,Mondadori Rafael G.5,Mason Jeffrey B.6,Brieño-Enríquez Miguel A.7,Barros Carlos C.1,Stout Michael B.3,Masternak Michal M.89,Schneider Augusto1ORCID

Affiliation:

1. Faculdade de Nutrição, Universidade Federal de Pelotas, Pelotas-RS, Brazil

2. Faculdade de Veterinária, Universidade Federal de Pelotas, Pelotas-RS, Brazil

3. Aging & Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA

4. Facultad de Ciencias Agropecuarias, Universidad de La Salle, Campus Utopía, Yopal, Casanare, Colombia

5. Instituto de Biologia, Universidade Federal de Pelotas, Pelotas, RS, Brazil

6. Department of Animal, Dairy and Veterinary Sciences, Center for Integrated BioSystems, School of Veterinary Medicine, Utah State University, Logan, UT, USA

7. Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Research Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA

8. College of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, USA

9. Department of Head and Neck Surgery, Poznan University of Medical Sciences, Poznan, Poland

Abstract

AbstractCellular senescence is a defense mechanism to arrest proliferation of damaged cells. The number of senescent cells increases with age in different tissues and contributes to the development of age-related diseases. Old mice treated with senolytics drugs, dasatinib and quercetin (D+Q), have reduced senescent cells burden. The aim of this study was to evaluate the effects of D+Q on testicular function and fertility of male mice. Mice (n = 9/group) received D (5 mg kg−1) and Q (50 mg kg−1) via gavage every moth for three consecutive days from 3 to 8 months of age. At 8 months mice were breed with young non-treated females and euthanized. The treatment of male mice with D+Q increased serum testosterone levels and sperm concentration and decreased abnormal sperm morphology. Sperm motility, seminiferous tubule morphometry, testicular gene expression and fertility were not affected by treatment. There was no effect of D+Q treatment in β-galactosidase activity and in lipofuscin staining in testes. D+Q treatment also did not affect body mass gain and testes mass. In conclusion, D+Q treatment increased serum testosterone levels and sperm concentration and decreased abnormal sperm morphology, however did not affect fertility. Further studies with older mice and different senolytics are necessary to elucidate the effects in the decline of sperm output (quality and quantity) associated with aging.

Funder

CAPES

CNPq

FAPERGS

National Institute on Aging of the National Institutes of Health

Publisher

Akademiai Kiado Zrt.

Subject

Physiology (medical)

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