Frozen cashmere goat embryos were imported from Scotland to the Czech
Republic. Embryos were recovered surgically from superovulated (pFSH t
reated) donors on day 6 of their cycle. Embryos were cultured in ovum
culture medium (OCM) and then serially equilibrated in 0.5M, 1.0M and
1.5M ethylene glycol in OCM and aspirated into straws. Embryos were fr
ozen by a routine method with seeding at -7-degrees-C and cooled at 0.
3-degrees-C/min to -37-degrees-C utilising a programmable freezer. Tha
wing was effected in air for 7 seconds and in a water bath at 35-degre
es-C for 25 seconds, cryoprotective agent was eluted in 0.75M ethylene
glycol together with 0.5M sucrose in OCM (10 minutes) and in 0.5M suc
rose in OCM (10 minutes). Embryos were then washed in pure OCM (in two
steps), examined morphologically, and transferred in pairs by endosco
py (Wolf, Germany) into synchronised recipients either ipsilaterally o
r bilaterally (two groups in the reproductive season, one group out of
season). Those recipients receiving embryos during the breeding seaso
n had a pregnancy rate of 85.7%, this was significantly higher (P < 0.
05) than the pregnancy rate which resulted from the transfer of embryo
s out of season (50%). It is concluded that cryopreservation of embryo
s and their movement between countries is an effective method of estab
lishing a novel breed within an importing country and is thereby a use
ful method for establishment of a new genetic pool.