OBJECTIVE: To investigate the effects of thawing temperature on sperm function after cryopreservation. The technical aspects of sperm cryopreservation have significantly improved over the last few decades. However, a standard protocol designed to optimize sperm motility recovery after thawing has not yet been established. DESIGN: Prospective study. SETTING: Private infertility institute and university-based research laboratory. PATIENT(S): Eighty consenting normozoospermic patients consulting for infertility. INTERVENTION(S): Spermatozoa from donor semen samples were thawed at different temperatures. MAIN OUTCOME MEASURE(S): Sperm motility, viability, adenosine-5'-triphosphate (ATP) content, acrosomal status, and DNA integrity were evaluated as a function of thawing temperature in cryopreserved human sperm samples. RESULT(S): Thawing at 40 degrees C resulted in a statistically significant increase in sperm motility recovery compared with thawing at temperatures between 20 degrees C and 37 degrees C. There were no statistically significant differences in sperm viability, acrosomal status, ATP content, and DNA integrity after thawing at 40 degrees C compared with thawing at temperatures between 20 degrees C and 37 degrees C. CONCLUSION(S): Sperm thawing at 40 degrees C could be safely used to improve motility recovery after sperm cryopreservation. Copyright 2010 American Society for Reproductive Medicine. All rights reserved.
OBJECTIVE: To investigate the effects of thawing temperature on sperm function after cryopreservation. The technical aspects of sperm cryopreservation have significantly improved over the last few decades. However, a standard protocol designed to optimize sperm motility recovery after thawing has not yet been established. DESIGN: Prospective study. SETTING: Private infertility institute and university-based research laboratory. PATIENT(S): Eighty consenting normozoospermic patients consulting for infertility. INTERVENTION(S): Spermatozoa from donor semen samples were thawed at different temperatures. MAIN OUTCOME MEASURE(S): Sperm motility, viability, adenosine-5'-triphosphate (ATP) content, acrosomal status, and DNA integrity were evaluated as a function of thawing temperature in cryopreserved human sperm samples. RESULT(S): Thawing at 40 degrees C resulted in a statistically significant increase in sperm motility recovery compared with thawing at temperatures between 20 degrees C and 37 degrees C. There were no statistically significant differences in sperm viability, acrosomal status, ATP content, and DNA integrity after thawing at 40 degrees C compared with thawing at temperatures between 20 degrees C and 37 degrees C. CONCLUSION(S): Sperm thawing at 40 degrees C could be safely used to improve motility recovery after sperm cryopreservation. Copyright 2010 American Society for Reproductive Medicine. All rights reserved.
Authors: Nick S Strelchenko; Jenna Kropp Schmidt; Katherine D Mean; Michele L Schotzko; Thaddeus G Golos; Igor I Slukvin Journal: J Am Assoc Lab Anim Sci Date: 2020-09-02 Impact factor: 1.232
Authors: Mohammad Baqer Minaei; Mohammad Barbarestani; Saeid Nekoonam; Mir Abbas Abdolvahabi; Nasrin Takzare; Mohammad Hossein Asadi; Azim Hedayatpour; Fardin Amidi Journal: Iran J Reprod Med Date: 2012-03