ANCILLARY FOLLICLE AND SECONDARY CORPORA-LUTEA FORMATION FOLLOWING EXOGENOUS GONADOTROPIN TREATMENT IN THE DOMESTIC CAT AND EFFECT OF PASSIVE TRANSFER OF GONADOTROPIN-NEUTRALIZING ANTISERA
Wf. Swanson et al., ANCILLARY FOLLICLE AND SECONDARY CORPORA-LUTEA FORMATION FOLLOWING EXOGENOUS GONADOTROPIN TREATMENT IN THE DOMESTIC CAT AND EFFECT OF PASSIVE TRANSFER OF GONADOTROPIN-NEUTRALIZING ANTISERA, Theriogenology, 45(3), 1996, pp. 561-572
A combination regimen of equine chorionic gonadotropin (eCG) and human
chorionic gonadotropin (hCG) was used to stimulate ovarian follicular
development in domestic cats. The rate of elimination of eCG from cir
culation was estimated, and, following follicular aspiration, the form
ation of ancillary follicles and secondary CL was characterized. The e
ffect of gonadotropin-neutralizing antisera on the development of seco
ndary ovarian structures, CL function and humoral immune responses als
o was evaluated. After intramuscular injection, initial serum eCG conc
entrations were variable, with the elimination half-life estimated at
39 to 55 h and eCG persisting in circulation for several days. Followi
ng follicular aspiration, queens formed CL equal to the number of aspi
rated follicles and exhibited a rapid increase in progesterone concent
ration but developed high numbers of ancillary follicles by 5 d post a
spiration. By 15 d post aspiration, all ancillary follicles had lutein
ized to form secondary CL. Treatment with neutralizing antisera at the
time of follicular aspiration slowed (P<0,05) CL formation but did no
t decrease (P>0.05) the number of ancillary follicles or secondary CL.
Progesterone concentrations did not differ (P>0.05) from control quee
ns while secondary humoral immune responses to eCG were qualitatively
similar between groups. In summary, eCG was eliminated slowly from cat
s following intramuscular injection and this persistence in circulatio
n may have contributed to the development of ancillary follicles and s
econdary CL. However, the administration of neutralizing antisera at t
he time of follicular aspiration was ineffective in preventing the for
mation of these secondary ovarian structures.