Optimization of sperm alkaline single-cell gel electrophoresis.
- Author:
Shuang DENG
;
Lang FAN
;
Xi-yan WU
;
Yan ZHU
;
Ke-qian XU
- Publication Type:Journal Article
- MeSH: Asthenozoospermia; genetics; Comet Assay; standards; DNA Damage; DNA Fragmentation; Humans; Hydrogen Peroxide; toxicity; Male; Oligospermia; genetics; Oxidants; toxicity; Reproducibility of Results; Sperm Count; Spermatozoa; drug effects; enzymology; Time Factors
- From: National Journal of Andrology 2015;21(2):124-131
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the main factors that influence the results of sperm alkaline single-cell gel electrophoresis (SCGE), optimize the conditions, and standardize its procedures.
METHODSUsing alkaline SCGE, we detected the DNA fragments of sperm treated with different concentrations of H2O2 and determined the influences of the number of agarose gel layers, pH during DNA unwinding and electrophoresis, the time of DNA unwinding and electrophoresis, and cumulative sperm number on the results of sperm alkaline SCGE. Then we optimized the procedures, analyzed the repeatability of the optimized method, and examined 40 semen samples using the method.
RESULTSThree agarose gel layers could reduce the background. The optimal pH during DNA unwinding and electrophoresis was 10, and the best times for DNA unwinding and electrophoresis were 40 min and 30 min, respectively. Fifty sperm were adequate to ensure the reliability of the results. Based on the percentage of tail DNA, the intra- and inter-assay repeatabilities of the optimized sperm alkaline SCGE were 3.12% and 7.13%, and by the DNA damage score, they were 2.38% and 6.09%, respectively. Sperm DNA fragments were significantly increased in the infertile patients with oligoasthenoteratozoospermia as compared with healthy fertile males (P <0.05).
CONCLUSIONThe optimized sperm alkaline SCGE, highly repeatable and easy to be standardized, can be applied to the clinical detection of sperm DNA fragmentation in infertile men.