Effect of Heat Stress on Sperm DNA: Protamine Assessment in Ram Spermatozoa and Testicle.
Thais Rose Dos Santos HamiltonAdriano Felipe Perez SiqueiraLetícia Signori de CastroCamilla Mota MendesJuliana de Carvalho DelgadoPatrícia Monken de AssisLeonardo Pereira MesquitaPaulo César MaiorkaMarcílio NichiMarcelo Demarchi GoissisJosé Antonio VisintinMayra Elena Ortiz D'Avila AssumpçãoPublished in: Oxidative medicine and cellular longevity (2018)
Sperm DNA fragmentation is considered one of the main causes of male infertility. The most accepted causes of sperm DNA damage are deleterious actions of reactive oxygen species (ROS), defects in protamination, and apoptosis. Ram sperm are highly prone to those damages due to the high susceptibility to ROS and to oxidative stress caused by heat stress. We aimed to evaluate the effects of heat stress on the chromatin of ejaculated and epididymal sperm and the activation of apoptotic pathways in different cell types in ram testis. We observed higher percentages of ejaculated sperm with increased chromatin fragmentation in the heat stress group; a fact that was unexpectedly not observed in epididymal sperm. Heat stress group presented a higher percentage of spermatozoa with DNA fragmentation and increased number of mRNA copies of transitional protein 1. Epididymal sperm presented greater gene expression of protamine 1 on the 30th day of the spermatic cycle; however, no differences in protamine protein levels were observed in ejaculated sperm and testis. Localization of proapoptotic protein BAX or BCL2 in testis was not different. In conclusion, testicular heat stress increases ram sperm DNA fragmentation without changes in protamination and apoptotic patterns.
Keyphrases
- heat stress
- dna damage
- heat shock
- gene expression
- oxidative stress
- cell death
- reactive oxygen species
- circulating tumor
- single molecule
- dna methylation
- cell free
- type diabetes
- protein protein
- genome wide
- signaling pathway
- dna repair
- ischemia reperfusion injury
- single cell
- mesenchymal stem cells
- cell therapy
- small molecule
- metabolic syndrome
- nucleic acid
- clinical evaluation