» Articles » PMID: 17292462

Effect of Lactose and Glycerol on the Motility, Normal Apical Ridge, Chromatin Condensation and Chromatin Stability of Frozen Boar Spermatozoa

Overview
Journal Theriogenology
Publisher Elsevier
Date 2007 Feb 13
PMID 17292462
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

The effect of lactose and glycerol concentration, as well as the equilibration time with glycerol was studied on motility, normal apical ridge (NAR), and chromatin state of boar spermatozoa after the freezing and thawing process. In the first experiment, samples were frozen in first and second extenders containing different concentrations of lactose (11, 12 and 14%). In the second experiment samples were frozen using second extenders with different concentrations of glycerol (4, 6, 8 and 10%) and were incubated at 5 degrees C for 0 and 30 min. Motility, motility after caffeine treatment, NAR, chromatin condensation and stability (susceptibility to de-condense after heparin treatment) were evaluated. The results indicated that freezing spermatozoa in extenders with increasing concentrations of lactose adversely affected motility but provided a protective effect on acrosomes. Increased lactose concentration induced higher chromatin condensation but maintained the same stability. Increasing the glycerol concentration in the second extender from 4-6 to 8% led to higher motility and NAR as well as lower chromatin condensation and stability. When 30 min equilibration time was allowed after dilution with the same extenders, spermatozoa showed higher NAR and lower chromatin condensation and stability. The longer equilibration time was detrimental for motility when freezing in the 8% glycerol extender but favourable when using the 4% glycerol extender. Compared to the 8% glycerol, spermatozoa frozen in the 10% glycerol extender showed similar motility and increased chromatin condensation and stability, as well as low values of NAR that did not improve by longer incubation time.

Citing Articles

Cryopreservation of pig spermatozoa using carboxylated poly-L-lysine as cryoprotectant.

Jin H, Choi W, Matsumura K, Hyon S, Gen Y, Hayashi M J Reprod Dev. 2022; 68(5):312-317.

PMID: 35908977 PMC: 9558810. DOI: 10.1262/jrd.2022-058.


Type III antifreeze protein (AFP) improves the post-thaw quality and in vivo fertility of rooster spermatozoa.

Mehdipour M, Daghigh-Kia H, Najafi A, Martinez-Pastor F Poult Sci. 2021; 100(8):101291.

PMID: 34217904 PMC: 8260870. DOI: 10.1016/j.psj.2021.101291.


Improvement of the in vitro fertilization and embryo development using frozen-thawed spermatozoa of microminipigs.

Namula Z, Isumi Y, Sato Y, Le Q, Lin Q, Takebayashi K Arch Anim Breed. 2021; 64(1):265-271.

PMID: 34189254 PMC: 8223014. DOI: 10.5194/aab-64-265-2021.


Saccharin consumption increases sperm DNA fragmentation and apoptosis in mice.

Rahimipour M, Talebi A, Anvari M, Sarcheshmeh A, Omidi M Iran J Reprod Med. 2014; 12(5):307-12.

PMID: 25031574 PMC: 4094655.


Egg yolk and glycerol requirements for freezing boar spermatozoa treated with methyl β-cyclodextrin or cholesterol-loaded cyclodextrin.

Blanch E, Tomas C, Hernandez M, Roca J, Martinez E, Vazquez J J Reprod Dev. 2014; 60(2):143-9.

PMID: 24492655 PMC: 3999393. DOI: 10.1262/jrd.2013-073.