Abstract

To evaluate effects of different concentrations of pentoxifylline, as phosphodiesterase inhibitor, on kinematic parameters, capacitation, and acrosome reaction, spermatozoa were separated from ram caudal epididymis. Epididymal sperm were incubated at concentrations of 0.01 mM, 0.1 mM, 1 mM, and 10 mM pentoxifylline for 60 min. Motion parameters were assessed using the CASA system. Capacitation and acrosome reaction were also evaluated by CTC staining. Pentoxifylline at 0.01 mM appeared significant (P < 0.05) in increasing progressive motility, straight line velocity (VSL), VCL, average path velocity (VAP), average amplitude of lateral head displacement in micrometers (ALH), and mean angular displacement (MAD) and significant (P < 0.05) in decreasing BCF in spermatozoa compared with controls. Pentoxifylline at 10 mM caused a significant (P < 0.05) decrease in progressive motility, VSL, VAP, ALH, LIN, and WOB compared with controls. There was a significant (P < 0.05) reduction in uncapacitated spermatozoa but an insignificant rise in capacitated and acrosome-reacted spermatozoa in 0.01 mM pentoxifylline when compared with controls. Capacitated spermatozoa were significantly (P < 0.05) lower in 0.1 mM pentoxifylline, whereas capacitated and acrosome-reacted spermatozoa were insignificantly higher than controls. In 10 mM pentoxifylline, significant increase was observed in capacitated and significant decrease in acrosome-reacted spermatozoa. In conclusion, a low concentration of pentoxifylline was able to increase most kinematic parameters while high concentration had the opposite effect. Pentoxifylline in high concentration increased capacitation but decreased acrosome reaction.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.