Comparison Between Human Sperm Preservation Medium and TEST‐Yolk Buffer on Protecting Chromatin and Morphology Integrity of Human Spermatozoa in Fertile and Subfertile Men After Freeze‐Thawing Procedure
Journal Articles
Overview
Research
Identity
Additional Document Info
View All
Overview
abstract
ABSTRACT: The aim of this study was to identify the detrimental effect of the freeze‐thaw process on chromatin integrity and morphology of human spermatozoa, and to determine whether human sperm preservation medium (HSPM) or TEST‐yolk buffer (TYB) offers a better protection to spermatozoa from cryodamage after the freeze‐thaw procedure. Thirty‐five semen samples obtained from couples childless because of male factor infertility (subfertile men, group 1) and 25 semen samples from healthy, normal volunteers of proven fertility (group 2) were included in the study. Each semen sample was divided into 2 parts, the first part was mixed with HSPM and the other with TYB (1:1), and frozen with a controlled slow‐stage freezer, before plunging into liquid nitrogen. Twelve smears from each semen sample were made before (n = 4) and after (n = 8) the freeze‐thaw process. Chromatin structure was evaluated after staining using the acridine orange (AO) test, whereas morphology was analyzed according to strict criteria. The mean percentage of spermatozoa that exhibited normal morphology and intact chromatin structure was decreased after freeze‐thaw in all samples treated with HSPM or TYB in comparison with the value observed in the native semen samples of both groups. However, TYB preserved chromatin and morphology significantly better than HSPM did (9.3% ± 5.6% and 88.7% ± 11.2% vs. 7.8% ± 4.2% and 85.5% ± 12.5%, respectively). Therefore, TYB could be recommended as a first choice cryoprotectant for semen preservation in order to avoid extra chromatin structure damage and morphology alterations of spermatozoa not only for patients pursuing assisted reproduction, but also for donor samples.
