The domestic blue fox (Alopex lagopus) is extensively farmed in Scandi
navia, and represents a genetic reserve, as well as a model for basic
reproductive studies for the wild arctic fox, which is a canid species
threatened by extinction. The development of in vitro techniques may
be a way to preserve genetic material from the wild fox population. Th
e scope of this paper was to review the authors' first experiments wit
h maturation and fertilization in vitro (IVM, IVF) of fox oocytes. IVF
was attempted after collection of in vivo matured oocytes 2 days afte
r maximum vaginal electrical resistance, from 6 farmed blue fox female
s in natural oestrus. IVM was carried out in oocytes collected from ov
aries of 29 vixens in pro-oestrus, i.e. prior to the preovulatory LH p
eak. The oocytes for IVM were cultured in bovine IVM media (M199, 10%
FCS, w/wo FSH), but without LH. In the IVF experiment, 2 of 36 insemin
ated ova developed beyond the 4-cell stage. One embryo developed to a
morula 144 h after insemination. In the IVM experiment 325 oocytes wer
e evaluated, 91% (w/FSH) vs 78% showed germinal vesicle breakdown. GVB
D was observed after 24 h in culture (19% w/FSH vs 27%), MI was reache
d at 48 h (70% vs 40%), MII at 48-72 h (48% vs 22%), but the majority
of MII were seen at 96 h after insemination (73% vs 66%). Duration of
IVM (96 h) was somewhat longer than observed in vivo (72 h). Although
dissociation of cumulus cells was observed, corona radiata cells were
tightly connected with the oocytes, suggesting incomplete cytoplasmati
c maturation.