Literature DB >> 30388470

Effect of different freezing rates and thawing temperatures on cryosurvival of dromedary camel spermatozoa.

Clara Malo1, Bodil Elwing2, Linn Soederstroem2, Nils Lundeheim2, Jane M Morrell2, Julian A Skidmore3.   

Abstract

The objective of this study was to evaluate the effect of different freezing rates and thawing temperatures on the post-thaw quality of camel spermatozoa. Ten ejaculates from five male camels were frozen at five different freezing rates, achieved by placing the straws at specific heights above the surface of liquid nitrogen for different lengths of time (4 cm for 15 min; 1 cm for 15 min; 7 cm for 15 min; 7 cm for 5 min + 4 cm for 3 min; 4 cm for 5 min + 1 cm for 3 min) followed by storage in liquid nitrogen. Two thawing temperatures (37° for 30 s and 60 °C for 10 s) were subsequently tested. Post-thawing, the samples were evaluated for total and progressive motility, kinematics, membrane and acrosome integrity, and membrane functionality (hypoosmotic swelling test) at zero and 1 h post thawing. Total and progressive motility were significantly higher for the fastest freezing rate (at 1 cm) at 0 h (p < 0.01 for both), as were VCL (p < 0.01), VSL (p < 0.05) and STR (p < 0.05). Freezing at 4 cm produced the lowest values of STR compared to other treatments (p < 0.05). At 1 h, no differences in total motility were observed between freezing at 4 cm and 1 cm, both being significantly better than freezing rate 7 cm + 4 cm (p < 0.01). For progressive motility and VSL, only freezing at 1 cm was superior to the 7 cm + 4 cm combination (p < 0.001 and p < 0.05 respectively). Membrane integrity at 1 h was higher for freezing at 7 cm than at 1 cm (p < 0.01). For thawing temperatures, total motility and progressive motility at 0 h and 1 h (p < 0.001), and acrosome integrity at 1 h (p < 0.01) were higher for 60 °C thawing temperature than 37 °C. The kinematics VCL (p < 0.001), VSL and STR (p < 0.01), and VAP (p < 0.05) showed higher values for 60 °C thawing temperature than 37 °C at 0 h. After 1 h, higher values for VSL, VCL and VAP (p < 0.05) were observed for 60 °C than for 37 °C. In conclusion, a fast freezing rate would probably be beneficial for camel semen, and thawing should be conducted at 60 °C.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  Acrosome integrity; Colloids; Cryopreservation; HOST; Kinematics; Semen

Mesh:

Year:  2018        PMID: 30388470     DOI: 10.1016/j.theriogenology.2018.07.037

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  4 in total

1.  Impact on using cryopreservation of testicular or epididymal sperm upon intracytoplasmic sperm injection outcome in men with obstructive azoospermia: a systematic review and meta-analysis.

Authors:  Hanchao Liu; Yun Xie; Linzhi Gao; Xiangzhou Sun; Xiaoyan Liang; Chunhua Deng; Yong Gao; Guihua Liu
Journal:  J Assist Reprod Genet       Date:  2020-09-15       Impact factor: 3.412

2.  Cryo-banking of human spermatozoa by aseptic cryoprotectants-free vitrification in liquid air: Positive effect of elevated warming temperature.

Authors:  Maria Diaz-Jimenez; Mengying Wang; Wanxue Wang; Evgenia Isachenko; Gohar Rahimi; Pradeep Kumar; Peter Mallmann; Melanie von Brandenstein; Manuel Hidalgo; Vladimir Isachenko
Journal:  Cell Tissue Bank       Date:  2021-02-19       Impact factor: 1.522

3.  Optimization of the Thawing Protocol for Iberian Boar Sperm.

Authors:  Cristina Tomás-Almenar; Eduardo de Mercado
Journal:  Animals (Basel)       Date:  2022-09-28       Impact factor: 3.231

4.  Strategy on Persisting in Distinct Activity of Plasmon-Activated Water.

Authors:  Chih-Ping Yang; Hui-Yen Tsai; Ching-Li Tseng; Pei-Jun Hao; Yu-Chuan Liu
Journal:  ACS Omega       Date:  2019-12-03
  4 in total

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