Glycogen Synthase Kinase 3 Enzyme Gene Expression of Infertile Men Before and After Sperm Activation in vitro
Background: Infertility is characterized by the inability to achieve pregnancy after engaging in unprotected sexual intercourse for at least one year. Objective: This study aims to examine the expression levels of the GSK3A gene in infertile men, both before and after in vitro sperm activation. Methodology: Semen samples from 100 men: 50 with (oligozoospermia and oligoasthenozoospermia) as patients or infertile men and 50 healthy controls were collected at Al-Najaf Fertility Center. In vitro sperm activation was performed using FertiCult™ flushing medium with the swim-up technique, and GSK3A gene expression was measured by RT-qPCR. Results: The data of this study demonstrated significant improvement in progressive sperm motility (P < 0.006) and morphologically normal sperm (P < 0.001) in both the control and infertile men following in vitro activation compared to pre-activation values. The expression levels of GSK3A gene after activation showed a significant difference (P<0.01, P<0.035) in oligozoospermia and oligoasthenozoospermia subgroups compared to before activation, while the gene expression of control group after activation showed non- significant difference (P>0.05) compared to before activation. Conclusion: The study showed that after swim-up activation, sperm quality improved with higher progressive motility and normal morphology, while GSK3A expression improved significantly only the oligoasthenozoospermia subgroup.
Authors
- Ismail H. Aziz (ORCID: https://orcid.org/0000-0003-0263-3357)
- Saad S. Al-Dujaily (ORCID: https://orcid.org/0000-0002-6945-7442)
- Noor Hani Al-Naji
Institutions
- University of Baghdad (IQ)
- University of Kufa (IQ)
- Nahrain University (IQ)
Publication Details
- Journal
- The Egyptian Journal of Medical Microbiology
- Published
- 2025-08-25
- DOI
- https://doi.org/10.21608/ejmm.2025.412713.1826
- Primary Topic
- Reproductive Biology and Fertility
- Type
- article
- Field-Weighted Citation Impact
- 0.00