H. Alm et K. Hinrichs, EFFECT OF CYCLOHEXIMIDE ON NUCLEAR MATURATION OF HORSE OOCYTES AND ITS RELATION TO INITIAL CUMULUS MORPHOLOGY, Journal of Reproduction and Fertility, 107(2), 1996, pp. 215-220
The period of protein synthesis necessary for meiotic maturation in ho
rse oocytes initially having compact or expanded cumulus cells was stu
died. Oocytes incubated in the presence of cycloheximide after 0, 4, 8
, 12 or 16 h maturation in vitro (total incubation time 24 h) were mat
ured for 24 h, or were incubated with cycloheximide for 24 h and then
matured for 24 h. Incubation with cycloheximide from 0 h was effective
in suppressing maturation (no significant increase in maturing oocyte
s compared with controls fixed directly after removal from the follicl
e) in both expanded and compact groups and was completely reversible,
as there was no difference in the proportion of oocytes reaching metap
hase II between controls and treatment groups of either cumulus type.
Addition of cycloheximide after 4 h maturation resulted in no signific
ant difference in distribution of oocytes compared with addition at 0
h in either cumulus group. A significant decrease in the proportion of
germinal vesicle stage oocytes, and an increase in oocytes in metapha
se I occurred in oocytes with expanded cumulus cells in the 8 h treatm
ent and in oocytes with compact cumulus cells in the 12 h treatment, c
ompared with oocytes treated after 0 h. A significant increase in the
proportion of oocytes at metaphase II occurred in the 12 h treatment f
or expanded cumulus-oocyte complexes and in the 16 h treatment for com
pact cumulus-oocyte complexes. These data show that nuclear maturation
of horse oocytes can be reversibly suppressed by incubation with cycl
oheximide from the onset of culture. Oocytes with different initial cu
mulus type differed in the time required for protein synthesis essenti
al for maturation: expanded cumulus-oocyte complexes required less tim
e to prepare for germinal vesicle breakdown, maturation to metaphase I
, and maturation to metaphase II, than did compact cumulus-oocyte comp
lexes.