4.7 Article

Effects of human follicular fluid on the capacitation and motility of human spermatozoa

Journal

FERTILITY AND STERILITY
Volume 73, Issue 4, Pages 680-686

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S0015-0282(99)00637-8

Keywords

spermatozoa; capacitation; acrosome reaction; motility; human follicular fluid

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Objective: To investigate the capacitation and motility kinetics of spermatozoa treated with human follicular fluid (FF). Design: Controlled, experimental laboratory study. Setting: University-based gynecology unit. Patient(s): Human FF was collected from women undergoing assisted reproductive treatment. Semen samples were obtained from men visiting subfertility clinics. Intervention(s): Spermatozoa were incubated with human FF under various experimental conditions. Spermatozoa incubated with Earle's balanced salt solution were used as the control. Main Outcome Measure(s): Chlortetracycline staining patterns and sperm motility parameters. Result(s): The rate of capacitation in the human FF-treated spermatozoa was significantly higher than that in the control spermatozoa after 1 hour and 3 hours of treatment. The percentage of acrosome-reacted spermatozoa also was significantly higher after human FF treatment than after control treatment. These effects of human FF were dose-dependent. Human FF-treated spermatozoa maintained their velocities at the zero-hour level for 5 hours, whereas the velocities of the control spermatozoa decreased significantly after 1 hour. Human FF treatment significantly increased the beat cross-frequency above the rate at zero hour for 5 hours. The hyperactivation of the human FF-treated spermatozoa remained stable for 3 hours, whereas that of the control spermatozoa decreased significantly after 1 hour of incubation. Significantly more human FF-treated spermatozoa underwent hyperactivation than did control spermatozoa after I hour and 3 hours of treatment. The effects of human FF on beat cross-frequency and hyperactivation were dose-dependent. Conclusion(s): Human FF promotes capacitation and the acrosome reaction within a short period. It also stimulates or maintains various sperm motility parameters.

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