C. Labbe et G. Maisse, INFLUENCE OF RAINBOW-TROUT THERMAL-ACCLIMATION ON SPERM CRYOPRESERVATION - RELATION TO CHANGE IN THE LIPID-COMPOSITION OF THE PLASMA-MEMBRANE, Aquaculture, 145(1-4), 1996, pp. 281-294
The ability of rainbow trout (Oncorhynchus mykiss) spermatozoa to with
stand cryopreservation was tested after the fish and sperm were expose
d to various temperature conditions, In the first experiment, trout we
re acclimated at either 8 degrees C or 18 degrees C during gametogenes
is, and transferred to 13 degrees C at the beginning of the spawning s
eason, Following this 13 degrees C transfer, the fertilizing ability o
f frozen-thawed sperm from the fish reared at 18 degrees C was found t
o be twice as better (60-80% fertilization rate) than that of the fish
reared at 8 degrees C (20-30% fertilization rate) up to 42 days after
the transfer. A low membrane cholesterol/phospholipid ratio was stron
gly correlated (P < 0.002) with the better freezing resistance of the
corresponding sperm. The relevance of this parameter in predicting spe
rm ability to survive cryopreservation is discussed, In another experi
ment, fish with the same thermal background during gametogenesis were
transferred to 13 degrees C or to 5 degrees C before the beginning of
the spawning season, The same fertilization rates after freeze-thawing
were observed between the two groups (30-35%), Weekly or bi-weekly st
ripping frequencies did not alter the fertilization rates. Thus, no da
mage can be attributed to a long in vivo storage of sperm at a relativ
ely high temperature, In an in vitro experiment, the storage temperatu
re (0 degrees C to 25 degrees C) of sperm before freezing was shown to
have little influence on the fertilizing results after thawing althou
gh membrane fluidity was higher in sperm stored at 24 degrees C compar
ed with those stored at 4 degrees C. It is concluded from this study t
hat the quality of sperm cryopreservation can be improved by appropria
te broodstock handling. A high rearing temperature during gametogenesi
s followed by transfer to colder water improves sperm resistance durin
g cryopreservation. The stripping frequency of the fish does not influ
ence sperm quality at the temperature tested. Storing sperm in vitro b
elow 5 degrees C is recommended, although higher temperatures are not
markedly deleterious.