Studies on the basic issues relevant to sperm cryopreservation in humans

Rapid freezing and vitrification are becoming popular for sperm freezing in humans; however, basic and critical issues relevant to sperm cryopreservation remain to be resolved. The aims of the present study were to study the effects of osmolality of freezing medium, sperm concentrations, thawing met...

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Main Authors: Huanhuan Hu, Xiaowei Shi, Guojie Ji, Rui Liu, Jing Zhang, Han Zhang, Mingwen Li
Format: Article
Language:English
Published: SAGE Publishing 2020-05-01
Series:Therapeutic Advances in Reproductive Health
Online Access:https://doi.org/10.1177/2633494120909375
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spelling doaj-f50bf2fbe45a43a5a5749c2f6b77ce552020-11-25T02:26:16ZengSAGE PublishingTherapeutic Advances in Reproductive Health2633-49412020-05-011410.1177/2633494120909375Studies on the basic issues relevant to sperm cryopreservation in humansHuanhuan HuXiaowei ShiGuojie JiRui LiuJing ZhangHan ZhangMingwen LiRapid freezing and vitrification are becoming popular for sperm freezing in humans; however, basic and critical issues relevant to sperm cryopreservation remain to be resolved. The aims of the present study were to study the effects of osmolality of freezing medium, sperm concentrations, thawing methods, and sugars (sucrose and trehalose) on sperm motility and DNA integrity by rapid freezing using 0.5 ml standard straws loaded with 100 µl sperm each. The results showed that (1) the post-thaw recovery rates of total motility and progressive motility of sperm cryopreserved in freezing medium containing 0.25 M sucrose with 442 mOsm/kg osmolality were significantly higher ( p  < 0.05) than that of sperm cryopreserved in freezing medium containing 0.25 M sucrose with 536 mOsm/kg osmolality (36.5 ± 2.8% and 36.9 ± 1.7% versus 30.4 ± 1.9% and 30.3 ± 2.9%, respectively), (2) cryopreservation of both total and progressive motilities was not significantly affected ( p  > 0.05) by sperm concentrations in the range from 5 to 20 × 10 6  sperm/ml, (3) thawing method 37°C for 2 min was better than 42°C for 15 s in terms of post-thaw recovery rates of both total and progressive motilities ( p  < 0.05), (4) 0.25 M trehalose was better than 0.25 M sucrose in cryopreserving both total and progressive motilities ( p  < 0.05), and (5) sperm nuclear DNA is relatively resistant to the changes of the above factors compared with sperm motility. It was concluded that human sperm can be best cryopreserved by rapid freezing using 0.25 M sucrose or trehalose with osmolality 442 to 457 mOsm/kg at high sperm concentration followed by thawing at 37°C. Trehalose is a stronger cryoprotectant than sucrose for sperm cryopreservation.https://doi.org/10.1177/2633494120909375
collection DOAJ
language English
format Article
sources DOAJ
author Huanhuan Hu
Xiaowei Shi
Guojie Ji
Rui Liu
Jing Zhang
Han Zhang
Mingwen Li
spellingShingle Huanhuan Hu
Xiaowei Shi
Guojie Ji
Rui Liu
Jing Zhang
Han Zhang
Mingwen Li
Studies on the basic issues relevant to sperm cryopreservation in humans
Therapeutic Advances in Reproductive Health
author_facet Huanhuan Hu
Xiaowei Shi
Guojie Ji
Rui Liu
Jing Zhang
Han Zhang
Mingwen Li
author_sort Huanhuan Hu
title Studies on the basic issues relevant to sperm cryopreservation in humans
title_short Studies on the basic issues relevant to sperm cryopreservation in humans
title_full Studies on the basic issues relevant to sperm cryopreservation in humans
title_fullStr Studies on the basic issues relevant to sperm cryopreservation in humans
title_full_unstemmed Studies on the basic issues relevant to sperm cryopreservation in humans
title_sort studies on the basic issues relevant to sperm cryopreservation in humans
publisher SAGE Publishing
series Therapeutic Advances in Reproductive Health
issn 2633-4941
publishDate 2020-05-01
description Rapid freezing and vitrification are becoming popular for sperm freezing in humans; however, basic and critical issues relevant to sperm cryopreservation remain to be resolved. The aims of the present study were to study the effects of osmolality of freezing medium, sperm concentrations, thawing methods, and sugars (sucrose and trehalose) on sperm motility and DNA integrity by rapid freezing using 0.5 ml standard straws loaded with 100 µl sperm each. The results showed that (1) the post-thaw recovery rates of total motility and progressive motility of sperm cryopreserved in freezing medium containing 0.25 M sucrose with 442 mOsm/kg osmolality were significantly higher ( p  < 0.05) than that of sperm cryopreserved in freezing medium containing 0.25 M sucrose with 536 mOsm/kg osmolality (36.5 ± 2.8% and 36.9 ± 1.7% versus 30.4 ± 1.9% and 30.3 ± 2.9%, respectively), (2) cryopreservation of both total and progressive motilities was not significantly affected ( p  > 0.05) by sperm concentrations in the range from 5 to 20 × 10 6  sperm/ml, (3) thawing method 37°C for 2 min was better than 42°C for 15 s in terms of post-thaw recovery rates of both total and progressive motilities ( p  < 0.05), (4) 0.25 M trehalose was better than 0.25 M sucrose in cryopreserving both total and progressive motilities ( p  < 0.05), and (5) sperm nuclear DNA is relatively resistant to the changes of the above factors compared with sperm motility. It was concluded that human sperm can be best cryopreserved by rapid freezing using 0.25 M sucrose or trehalose with osmolality 442 to 457 mOsm/kg at high sperm concentration followed by thawing at 37°C. Trehalose is a stronger cryoprotectant than sucrose for sperm cryopreservation.
url https://doi.org/10.1177/2633494120909375
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