Reduced SIRT1 and SIRT3 and Lower Antioxidant Capacity of Seminal Plasma Is Associated with Shorter Sperm Telomere Length in Oligospermic Men.
Varinderpal S DhillonMohammad ShahidPermal DeoMichael FenechPublished in: International journal of molecular sciences (2024)
Infertility affects millions of couples worldwide and has a profound impact not only on their families, but also on communities. Telomere attrition has been associated with infertility, DNA damage and fragmentation. Oxidative stress has been shown to affect sperm DNA integrity and telomere length. Sirtuins such as SIRT1 and SIRT3 are involved in aging and oxidative stress response. The aim of the present study is to determine the role of SIRT1 and SIRT3 in regulating oxidative stress, telomere shortening, and their association with oligospermia. Therefore, we assessed the protein levels of SIRT1 and SIRT3, total antioxidant capacity (TAC), superoxide dismutase (SOD), malondialdehyde (MDA) and catalase activity (CAT) in the seminal plasma of 272 patients with oligospermia and 251 fertile men. We also measured sperm telomere length (STL) and leukocyte telomere length (LTL) using a standard real-time quantitative PCR assay. Sperm chromatin and protamine deficiency were also measured as per standard methods. Our results for oligospermic patients demonstrate significant reductions in semen parameters, shorter STL and LTL, lower levels of SOD, TAC, CAT, SIRT1 and SIRT3 levels, and also significant protamine deficiency and higher levels of MDA and DNA fragmentation. We conclude that a shorter TL in sperms and leukocytes is associated with increased oxidative stress that also accounts for high levels of DNA fragmentation in sperms. Our results support the hypothesis that various sperm parameters in the state of oligospermia are associated with or caused by reduced levels of SIRT1 and SIRT3 proteins.
Keyphrases
- oxidative stress
- ischemia reperfusion injury
- dna damage
- diabetic rats
- gene expression
- induced apoptosis
- type diabetes
- circulating tumor
- transcription factor
- metabolic syndrome
- signaling pathway
- hydrogen peroxide
- high throughput
- cell proliferation
- single molecule
- nitric oxide
- chronic kidney disease
- dna repair
- intellectual disability
- breast cancer cells
- polycystic ovary syndrome
- mass spectrometry
- insulin resistance
- amino acid
- skeletal muscle
- pi k akt
- peritoneal dialysis