The effect of glycerol on the viability, mitochondrial function and acrosomal integrity of bovine spermatozoa

Citation
Dl. Garner et al., The effect of glycerol on the viability, mitochondrial function and acrosomal integrity of bovine spermatozoa, REPROD DOM, 34(5), 1999, pp. 399-404
Citations number
12
Categorie Soggetti
Animal Sciences
Journal title
REPRODUCTION IN DOMESTIC ANIMALS
ISSN journal
09366768 → ACNP
Volume
34
Issue
5
Year of publication
1999
Pages
399 - 404
Database
ISI
SICI code
0936-6768(199910)34:5<399:TEOGOT>2.0.ZU;2-Y
Abstract
Eight bull ejaculates were split to evaluate the effects of glycerol on spe rm organelle function. Although glycerol protects sperm membranes during cr yopreservation, preliminary data suggested that glycerol was detrimental to sperm organelles to varying degrees. To assess the compartmental effects, three organelle-specific fluorophores were used to analyze with (G+) and wi thout glycerol (G-) in spermatozoa stored for 24h at 5 degrees C in an egg- yolk-based extender. The mitochondrial probe, 5,5',6,6'-tetrachloro-1,1',3, 3'-tetraethyl benzimidazolylcarbocyanine iodide (JC-I) was used to examine the level of mitochondrial metabolic function by it's discrimination betwee n high (J-aggregate staining, red-orange) and low membrane potentials (JC-I monomeric staining, green); while acosomal reacted spermatozoa were identi fied using fluorescein-labelled lectin from arachis hypogaea, PNA-FITC. The proportions of living and dead spermatozoa were determined by staining wit h the combination of SYBR-14 and propidium iodide (PI). Split-plot analysis of variance revealed that within bulls, glycerol altered the proportions o f sperm staining with each organelle-specific fluorophore to varying degree s. The proportion of spermatozoa labelled with SYBR-14, indicating intact p lasmalemmae, were not affected by the addition of glycerol (p = 0.11). Alth ough the total proportion of JC-1-labeled spermatozoa were similar in G- an d G+ samples (p = 0.90), the presence of glycerol decreased the proportion of spermatozoa that exhibited J-aggregate staining (p < 0.01) while produci ng an increase in monomeric staining (p = 0.02). The proportions of acrosom e-reacted spermatozoa, however, were greater in the G- samples than in the G+ samples as indicated by PNA-FITC (p = 0.03). These findings suggest that mitochondria, acrosomes and the plasmalemmae of unfrozen spermatozoa vary in their response to the addition of the cryoprotectant glycerol.