Jm. Christensen et Tr. Tiersch, CRYOPRESERVATION OF CHANNEL CATFISH SPERMATOZOA - EFFECT OF CRYOPROTECTANT, STRAW SIZE, AND FORMULATION OF EXTENDER, Theriogenology, 47(3), 1997, pp. 639-645
Various aspects of the cryopreservation of spermatozoa of channel catf
ish (Ictalurus punctatus) were studied in relation to spermatozoa moti
lity. The objectives were to evaluate 1) the efficacy of 5, 10 and 15%
of methanal or n,n-dimethyl acetamide (DMA) as cryoprotectants; 2) th
e acute toxicity of 5, 10 and 15% methanal or DMA; 3) the use of 0.5-m
l vs. 0.25-ml straws; 4) the efficacy of 5, 10 and 15% of methanal in
Hanks' balanced salt solution (HBSS) or HBSS without glucose, and 5) t
he use of HBSS with or without 5% methanal. We found that use of 5% me
thanol as a cryoprotectant resulted in significantly higher post-thaw
motility (P = 0.0001) than did 5, 10 or 15% DMA. The use of 5% of eith
er cryoprotectant resulted in significantly higher post-thaw motility
(P = 0.0001) than did 10 or 15% of the cryoprotectants. Samples contai
ning 10 or 15% DMA had significantly lower motility (P = 0.0001) after
30 min exposure than did samples containing 5, 10 or 15% methanol. Th
e use of 0.25-ml straws resulted in significantly higher post-thaw mot
ility (P = 0.0001) than that of 0.5-ml straws. No difference was found
in post-thaw motility between HBSS with and without glucose as the ex
tenders. Cryopreservation in HBSS without addition of cryoprotectant r
esulted in post-thaw motility values of about 1%. (C) 1997 by Elsevier
Science Inc.