4.7 Article

Effects of Age and Lifelong Moderate-Intensity Exercise Training on Rats' Testicular Function

期刊

出版社

MDPI
DOI: 10.3390/ijms231911619

关键词

aging; physical exercise; testicular atrophy; mitochondrial function; protein synthesis; stress response; rodent model

资金

  1. FCT-Portuguese Foundation of Science and Technology [PTDC/DTP-DES/6077/2014]
  2. Institute for Biomedicine (iBiMED) [UIDB/04501/2020]
  3. UMIB [PEst-OE/SAU/UI0215/2019]
  4. QOPNA [FCT UID/QUI/00062/2019]
  5. European Investment Funds by FEDER/COMPETE/POCI-Operational Competitiveness and Internationalization Program
  6. FCT-Portuguese Foundation for Science and Technology [UIDB/04033/2020]
  7. FCT of the Portuguese Ministry of Science and Higher Education [SFRH/BPD/123155/2016, SFRH/BD/136896/2018]

向作者/读者索取更多资源

This study examined the effects of age and lifelong moderate-intensity exercise on rat testis. The results showed that aging is associated with testicular atrophy and alterations in stress response and mitochondrial biogenesis and function. Exercise did not protect against age-induced testicular atrophy and led to deleterious effects on sperm morphology.
Aging is associated with testicular morphological and functional alterations, but the underlying molecular mechanisms and the impact of physical exercise are poorly understood. In this study, we examined the effects of age and lifelong moderate-intensity exercise on rat testis. Mature adults (35 weeks) and middle-aged (61 weeks) Wistar Unilever male rats were maintained as sedentary or subjected to a lifelong moderate-intensity treadmill training protocol. Testis weight and histology, mitochondrial biogenesis and function, and proteins involved in protein synthesis and stress response were evaluated. Our results illustrate an age-induced testicular atrophy that was associated with alterations in stress response, and mitochondrial biogenesis and function. Aging was associated with increased testicular levels of heat shock protein beta-1 (HSP27) and antioxidant enzymes. Aging was also associated with decreased mRNA abundance of the nuclear respiratory factor 1 (Nrf1), a key transcription factor for mitochondrial biogenesis, which was accompanied by decreased protein levels of the oxidative phosphorylation system (OXPHOS) complexes subunits in the testes of older animals. On the other hand, exercise did not protect against age-induced testicular atrophy and led to deleterious effects on sperm morphology. Exercise led to an even more pronounced decrease in the Nrf1 mRNA levels in testes of both age groups and was associated with decreased mRNA abundance of other mitochondrial biogenesis markers and decreased protein levels of OXPHOS complexes subunits. Lifelong moderate-intensity exercise training was also associated with an increase in testicular oxidative stress markers and possibly with reduced translation. Together, our results indicate that exercise did not protect against age-induced testicular atrophy and was not associated with beneficial changes in mitochondria and stress response, further activating mechanisms of protein synthesis inhibition.

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