The total ovarian follicular populations were studied in two breeds of ewes which differed greatly in their ovulation rates. Thus 8 Romanov (mean ovulation rate 3.1) and 12 Ile-de-France ewes (mean ovulation rate 1.4) were ovariectomized at oestrus during the breeding season. Each right ovary and 3 left ovaries were sectioned at 7 micron and examined microscopically. The number of small follicles, i.e. with 2 or less layers of granulosa cells, was estimated by a tested sampling procedure whilst all larger follicles were measured and arranged into classes. There were half as many small follicles but 1.5--2 times more large follicles in the ovaries of the Romanov ewes compared to those of the Ile-de-France ewes. The number of atretic follicles was approximately the same in both breeds and does not explain the difference observed in ovulation rate. It is concluded that the higher ovulation rate in the Romanov ewe is due to the greater number of large follicles available to be stimulated for ovulation.
To investigate the factors contributing to the different ovulation rates observed in two strains of sheep (Booroola 5.2, Merino 1.2), in-vivo monitoring of follicular kinetics followed by histological examination of both ovaries was performed during the late luteal and follicular phases. Ewes of both strains were either ovariectomized at Day 13, or had the 3 largest follicles of each ovary ink-labelled at Day 13 and were ovariectomized at Day 15, or had the 3 largest follicles of each ovary ink-labelled at Days 13 and 15 and were ovariectomized 16 h after the beginning of oestrus (N = 6 per time per strain). In another experiment, the age effects on the follicular populations of these two strains were also studied. There were 2-4 times more primordial follicles and 1.5-2 times more preantral follicles in the ovaries of Booroola than in control Merino ewes, although the number of antral follicles was the same. The percentage of normal follicles in this population was higher in Merino than Booroola ovaries. In Booroola ewes, there was no correlation between the number of antral follicles per ovary and the ovulation rate at the previous cycle (r = 0.22). This suggests that follicle numbers do not play a key role in the high ovulation rate of the Booroola strain. The number of follicles initiating growth from the primordial pool, the number of growing follicles disappearing at the preantral stage, the pattern of antrum development, granulosa cell multiplication and appearance of atresia differed between strains. The reasons for the high ovulation rate of the Booroola strain became clear when preovulatory enlargement was followed by ink labelling. An extended period of time during which recruitment of ovulatory follicles takes place, together with a low incidence of selection and the ability of the follicles to wait for ovulation are the features involved in this high ovulation rate.
Total follicular populations and peripheral plasma concentrations of LH, FSH, prolactin, oestradiol-17 beta and progesterone during the preceding cycle were studied in two breeds of sheep (Romanov and Ile-de-France) which differed widely in their ovulation rates (3.2 and 1.5 respectively). No LH parameters could be correlated with the follicular details measured. The second peak of FSH occurring 20-30 h after the preovulatory surge of LH was significantly larger in the Romanov ewes and the area under this peak was correlated (P less than 0.01) with the number of antral follicles present in the ovary 17 days later. This suggests that formation of the antrum during the follicular growth phase is under the control of FSH. The discharge of prolactin preceding the LH peak, although not significantly different between breeds, was correlated with several of the follicular classes measured, including the number of preantral follicles. The peak value of oestradiol-17 beta measured before the LH peak was significantly higher (P less than 0.05) in the Romanov ewes and was correlated with the number of the largest follicles present. There was no significant difference between breeds in the concentration of oestradiol at the onset of oestrus. The progesterone concentration during the luteal phase was highly correlated with the number of preovulatory follicles.
Follicular growth was studied in 16 ewes of different breeds (Romanov, mean ovulation rate 3.0, and Ile-de-France, mean ovulation rate 1.6), stage of cycle (Day 0 or 7) and season (December and June). The follicular growth rates, determined by measuring the mitotic index before and 2 h after colchicine treatment, varied greatly between animals studied and did not vary significantly between breeds, time of cycle or season. From 3 layers of granulosa cells until antrum formation the mitotic index increased slowly but then the follicles grew rapidly reaching maximum growth rate at a follicular diameter of 0.85 mm; thereafter the mitotic index decreased almost to zero in preovulatory follicles. The mean time for a follicle to pass from 3 layers of granulosa cells (200 cells) to preovulatory size (3 x 10(6) cells) was estimated to be about 6 months. The total number of normal follicles with > 3 layers of granulosa cells in Ile-de-France ewes was similar in the anoestrous (3 ovaries studied) and breeding (3 ovaries) seasons, but there were more antral follicles in the latter. Highly significant correlations existed in each ewe between the number of follicles and the mean mitotic index per class, suggesting the existence of an intraovarian mechanism regulating folliculogenesis.
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