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Cryopreservation of epididymal spermatozoa collected by needle biopsy from cynomolgus monkeys ( Macaca fascicularis )
Author(s) -
Feradis A.H.,
Pawitri D.,
Suatha I.K.,
Amin M.R.,
Yusuf T.L.,
Sajuthi D.,
Budiarsa I.N.,
Hayes E.S.
Publication year - 2001
Publication title -
journal of medical primatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.31
H-Index - 42
eISSN - 1600-0684
pISSN - 0047-2565
DOI - 10.1034/j.1600-0684.2001.300205.x
Subject(s) - extender , cryopreservation , cryoprotectant , andrology , sperm , biology , motility , sperm motility , epididymis , anatomy , chemistry , embryo , medicine , microbiology and biotechnology , organic chemistry , polyurethane
We have examined the motility, morphology, and cryopreservation of epididymal spermatozoa collected by needle biopsy from cynomolgus monkeys ( Macaca fascicularis ). At collection, epididymal sperm (23×10 6 ±4×10 6 sperm/sample; 611×10 6 ±116×10 6 sperm/ml; n=18) were alive (79±2%), motile (67±2%), and exhibited intact membranes (65±2%). Sperm maintained at room temperature in handling medium exhibited decreased motility over time, but head‐to‐head agglutination was limited. Tris egg‐yolk extender containing 6% glycerol and dimethylsulfoxide (DMSO) did not significantly affect functional morphology, whereas extender containing propanediol significantly reduced motility, survival, and membrane integrity. Cryostorage reduced all measures of functional morphology independent of cryoprotectant. Post‐thaw motility was superior for glycerol and DMSO compared to propanediol. Variation in glycerol concentration (4, 6, and 8%) produced equivocal effects on sperm functional morphology post‐thaw. Needle biopsy may be a useful technique for laboratory and field‐based collection of spermatozoa from nonhuman primates.