Does in vitro capacitation alter chromatin stability of ejaculated human spermatozoa? cytochemical studies

In vitro capacitation of human spermatozoa is commonly evaluated by the progressive motility percent. However its effects on sperm chromatin have hardly been studied. Our aim was to determine the extent to which in vitro capacitation with two treatments (B2 or human follicular fluid) alters the chromatin of human spermatozoa, by using two analytical methods, acridine orange staining and Feulgen‐DNA cytophotometric measures. Ejaculates were obtained from 23 men participating in our in vitro fertilization program, and several measurements were made on the same ejaculate for each subject. No alteration was observed for the percent of native DNA after capacitation in B2, but spermatozoa incubation during the same time in human follicular fluid was followed by a significant decrease of the percent of native DNA (P < 0.01). Feulgen‐DNA content significantly increased after capacitation in either B2 or follicular fluid (P < 0.05, P < 0.001 respectively), and so did sperm nuclear surface area (P < 0.001). In this study we observed a negative correlation between Feulgen‐DNA content and fertilization rate (P < 0.02). Moreover, the greater effects on Feulgen‐DNA content were observed in men with abnormal sperm, whose spontaneous percent of native DNA was lower (P < 0.05) and Feulgen‐DNA content higher (P < 0.05) than in men with normal sperm. These results indicate that capacitation in B2 as well as in human follicular fluid may alter the chromatin stability of human spermatozoa. Such results suggest a partial decondensation state of human spermatozoa during in vitro capacitation. However, beyond some level of decondensation, the fertilizing ability could be altered.