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HERO ID
4116897
Reference Type
Journal Article
Title
A SIMPLE STAINING METHOD FOR EVALUATING ACROSOMAL STATUS OF CAT SPERMATOZOA
Author(s)
Pope, CE; Zhang, YZ; Dresser, BL
Year
1991
Is Peer Reviewed?
1
Journal
Journal of Zoo and Wildlife Medicine
ISSN:
1042-7260
Volume
22
Issue
1
Page Numbers
87-95
Web of Science Id
WOS:A1991FJ42700010
Abstract
The purpose of this study was to develop a simple staining procedure for determining the acrosomal status of felid spermatozoa. Previously, only a modified triple-stain technique successfully differentiated the acrosomal reaction; however the complexity of the technique limited its usefulness. The single-step staining technique uses a solution of 1% fast green FCF, 1% rose bengal, and 40% ethyl alcohol in 0.1 M citric acid-0.2 M disodium phosphate buffer. Semen was diluted with 2.9% sodium citrate, and an equal volume of staining solution was added and incubated for 70 sec at room temperature. Ten microliters of the mixture then was pipetted onto a microslide, smeared with anther slide, and air dried at 37-degrees-C. Acrosomal status was evaluated using bright field microscopy (x 1,000). An intact acrosome was indicated by the purplish-blue staining over the anterior portion of the sperm head. If acrosomal loss had occurred, the anterior caput was almost colorless to light pink. The postacrosomal region of the head was pale pink in spermatozoa with and without intact acrosomes. There was no difference in percentage of intact acrosomes in a comparison of three media used for semen dilution (Experiment Ia) or in a comparison of fresh versus premixed (stored) staining solution (Experiment Ib). The percentage of intact acrosomes as determined by the single stain was higher (P < 0.001) than that determined by the modified triple stain in all four cat species studied (Experiment II). This technique can be used to evaluate the daily rate of acrosome loss in domestic cat semen during storage at 4-degrees-C (Experiment III). The single-step acrosome staining technique as described is useful for quantifying acrosome loss in felid spermatozoa because it is simple, unaltered by dilution medium or storage of stain, and results in a higher percentage of intact acrosomes than does a modified triple stain.
Keywords
DOMESTIC CAT; EXOTIC CAT; SPERMATOZOA; ACROSOME; STAINING TECHNIQUE
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