P. Chemineau et al., RAM-INDUCED SHORT LUTEAL PHASES - EFFECTS OF HYSTERECTOMY AND CELLULAR COMPOSITION OF THE CORPUS-LUTEUM, Reproduction, nutrition, development, 33(3), 1993, pp. 253-261
Two experiments were conducted on Prealpes ewes to test 2 complementar
y hypotheses which may explain the short lifespan of corpora lutea obs
erved in some cases after ram-induced ovulation: i) the possible role
of the uterus was tested by determining the effects of hysterectomy on
the duration of luteal phases after the ram effect (RE); ii) the poss
ible difference due to characteristics of follicles before ovulation w
as tested by determining the cellular composition and characteristics
of corpora lutea (CL) induced by the RE compared to CL of the breeding
season (BS) when ovulation is synchronized by FGA-impregnated sponges
. In the first experiment, 9 ewes were hysterectomized (Hys) and intro
duced to rams at the same time as 1 0 control ewes. Plasma progesteron
e (P4) was analyzed each day for 17 consecutive d after the introducti
on of rams. The number of females ovulating was not different for the
2 groups (7/9 vs 9/10, respectively), but no Hys ewes experienced shor
t cycles compared to 5 of the 9 control ewes (P = 0.029). The second e
xperiment involved 16 ewes subjected to the RE in June, and 5 cyclic e
wes in January. The ewes were ovariectomized 82 h after the preovulato
ry LH surge, the CL were separated, weighed and the luteal cells enzym
atically dissociated to count the relative proportions of small (< 20
mu diameter) and large cells and assess in vitro P4 secretion both wit
h and without stimulation with 1 00 ng ovine LH. Plasma P4 concentrati
on increased significantly more slowly in RE than in BS ewes (P < 0.05
). The weight of twin RE CL did not differ from that of twin FGA-BS CL
(m +/- SD; 142-1 +/- 48.7 vs 139.1 +/- 23.0 mg). The percentage of la
rge luteal cells was lower in RE than in FGA-BS CL (10.7 +/- 4.6 vs 25
.0 +/- 6.6%; P < 0.001). The quantity of P4 secreted in vitro without
LH stimulation was lower in RE than in FGA-BS CL. (7.3 +/- 6.6 vs 13.8
+/- 9.8 ng/105 luteal cells/3 h; P < 0.05). The incubation of luteal
cells for 3 h with 100 ng oLH significantly increased P4 secretion in
RE but not in FGA-BS CL (+73% vs +9%; P < 0.05). It is concluded that
the uterus is essential for determining the lifespan of RE-induced CL
and that the cellular composition and characteristics of the RE CL are
very different from those of FGA-treated breeding season CL.