Ovarian follicular dynamics were studied during the breeding season, before and after ovulation in mink. Nulliparous female mink were stimulated to ovulate with an injection of 4 μg GnRH. Ovaries from three animals were collected on days 0, 2, 3, 4, 5, 6 and 7 after hormone treatment. A second dose of GnRH was administered on day 8 and ovaries were collected from three animals on day 9. Corpora lutea and follicles were identified in histological sections and follicles were classified by stage of development, healthy versus atretic, and by diameter. Preovulatory follicles (diameter 0.7–1.0 mm) were present in the ovaries of all animals on day 0 and these responded to GnRH treatment by ovulating. A synchronized wave of follicular development occurred following ovulation. Changes in follicle populations indicated that follicles are recruited from the small antral follicle class (0.2–0.4 mm) into the 0.4–0.6 mm class, with the first defined changes occurring between days 2 and 4. From the recruited group, a smaller cohort of follicles is selected to become the dominant follicles between days 4 and 6, and these acquire the ability to respond to a stimulus which induces ovulation at diameters of > 0.7 mm. The ovaries of unmated mink also contained substantial numbers of large, degenerating, luteinized, unruptured follicles. These degenerating, luteinized follicles are considered to represent the demise of large follicles that failed to receive an ovulatory stimulus.

Nulliparous heifers (n = 58) were studied to determine whether computer-assisted quantitative echotexture analysis of ultrasound images reflects the functional and histomorphological characteristics of the corpus luteum. The ovaries of heifers were examined daily by transrectal ultrasonography from day −2 (day 0 = ovulation) until the day of ovariectomy during metoestrus (day 3; n = 8), early dioestrus (day 6; n = 9), mid-dioestrus (mean, day 10; n = 7), or pro-oestrus (mean, day 18; n = 8; Expt 1). High resolution ultrasound images of corpora lutea were obtained in vitro, and were digitized and analysed using custom-developed computer algorithms optimized for ultrasonography. Cryostat sections of corpora lutea were examined for lipid distribution, and corpora lutea were homogenized to determine the content of progesterone, total protein, cholesterol and triglyceride. In Expt 2, heifers (n = 26) were ovariectomized as in Expt 1, and ovaries were prepared for histomorphometric evaluation. Pixel values (brightness of picture elements) of ultrasound images of corpora lutea were characterized as high during metoestrus, low during early and mid-dioestrus, and increasing again during pro-oestrus (P < 0.05). Changes (P < 0.001) in volume density of luteal cells were characterized as increasing from metoestrus (40.7 ± 0.4%) to mid-dioestrus (55.8 ± 2.8%) and decreasing again at pro-oestrus (41.5 ± 0.9%). The proportion of blood vascular components decreased (P < 0.001) progressively from 31.0 ± 1.0% in metoestrus to 15.6 ± 1.1% in pro-oestrus. Pixel values of ultrasound images of corpora lutea were correlated with luteal (r = −0.72, P < 0.05) and plasma (r = −0.71, P < 0.03) progesterone concentration, and to the volume densities of luteal cells (r = −0.75, P < 0.02) and connective tissue (r = 0.69, P < 0.03). Estimates of triglyceride, protein and cholesterol content of corpora lutea were not correlated with pixel values of ultrasound images. Protein and cholesterol content did not change while triglyceride concentration increased during pro-oestrus (P < 0.05). Results support the hypothesis that ultrasound images reflect luteal and plasma progesterone content, and histomorphological characteristics of the corpus luteum.

Progesterone, oestradiol and oestrone were measured in plasma from four captive muskoxen during three consecutive pregnancies (1983–1984, 1984–1985 and 1985–1986). Jugular blood samples were collected weekly (1983) or on an alternating 3:4 day schedule (1984–1986) during the first 12–15 weeks and last 6–10 weeks of pregnancy. Sampling during mid-pregnancy was at intervals of 2 weeks (1983 and 1985) or 1 week (1986). Duration of gestation was about 34 weeks (235 ± 4 (sd) days (n = 10), range 230–242 days). Progesterone remained at concentrations similar to those found during the luteal phase of the oestrous cycle for the first 10–12 weeks (mean ± sem 1.6 ± 0.1 ng ml⁻¹) after which it rose to a peak (mean 5.5 ± 0.65 ng ml⁻¹) between weeks 12 and 20. In all ten pregnancies progesterone concentrations declined dramatically between weeks 20 and 22 to luteal phase values where they remained until parturition. The decline was accompanied by an increase in oestradiol and oestrone concentrations which reached mean peak values of 199.23 ± 87.23 pg ml⁻¹ and 980.48 ± 203.91 pg ml⁻¹, respectively. Corpora lutea collected from wild muskoxen between 45 and 80 days gestation all showed histological evidence of regression, while corpora lutea from mid-gestation (112–125 days) were in advanced stages of involution. Repeated ovarian ultrasonography of captive muskoxen during the first 100 days of pregnancy confirmed these findings. The unusual, early regression of the corpus luteum of pregnancy indicates that progesterone and oestrogen of mid- and late pregnancy are probably of placental origin. The temporal relationship between the concentrations of these hormones during late pregnancy differs from those of domestic species and is apparently unique among ruminants.

Heifers were studied to determine whether computer-assisted quantitative echotexture analysis of ultrasound images reflect functional and endocrine characteristics of dominant and subordinate follicles at specific stages of development. Heifers were examined using transrectal ultrasonography each day until ovariectomy on day 3 (n = 8) and day 6 (n = 9) of wave 1, day 1 of wave 2 (n = 7), or after onset of pro-oestrus ≥ 17 days after ovulation (n = 8) to obtain growing, early-static, late-static and regressing dominant follicles of wave 1, subordinate follicles, preselection follicles and preovulatory dominant follicles. Ultrasound images of the follicles were obtained in vitro and analysed using custom-developed computer algorithms. Mean pixel (picture element) values (grey-scale: black = 0, white = 255) for the follicle wall and stroma increased (P < 0.05) progressively from the growing to the regressing phases of the dominant follicle of wave 1. The antrum and wall of subordinate follicles had higher (P < 0.05) mean pixel values than that of the corresponding dominant follicles. Pixel heterogeneity (a measure of variation of grey-scale values of pixels) of images of the follicle antrum and wall increased (P < 0.05) progressively during the early-static to regressing phases. A progressive increase (P < 0.05) in the slope of the regression line of pixel values for the follicle wall was detected from the growing to the regressing phases of the dominant follicle of wave 1. The regression line of the wall of the preovulatory dominant follicle had the lowest (P < 0.05) slope. Oestradiol concentration in the follicular fluid decreased (P < 0.05) from the growing to the late-static phase, while a marked decrease (P < 0.05) in the androstenedione concentration was recorded between the growing and the early-static phases of the dominant follicle. Progesterone content did not increase until follicles were in the final stages of regression. Pixel heterogeneity of the antrum and wall, and the slope of the follicle wall regression line were negatively correlated (P < 0.001) with oestradiol and the oestradiol:progesterone ratio in follicular fluid. The results of this study support the hypothesis that echotexture characteristics of ultrasound images of the follicle antrum and wall are correlated with the functional and endocrine status of a follicle.

Changes in systemic concentrations of FSH, LH, oestradiol and progesterone during the ovulatory follicular wave were compared between 30 mares and 30 women. Based on a previous study, the emergence of the future ovulatory follicle was defined as occurring at 13.0 mm in mares and 6.0 mm in women, and deviation in diameter between the two largest follicles was expected to begin at 22.7 mm in mares and 10.3 mm in women. Mean FSH concentrations were high in mares during the luteal phase, resulting from statistically identified FSH surges occurring in individuals on different days and in different numbers (mean, 1.5 ± 0.2 surges/mare); the internadir interval was 3.9 ± 0.3 days. In contrast, mean FSH in women was low during the luteal phase and increased to a prolonged elevation during the follicular phase. The prolonged elevation was apparent in each individual (internadir interval, 15.2 ± 0.4 days). Changes in LH or oestradiol concentrations encompassing deviation were not detected in mares, but both hormones increased slightly but significantly between emergence and deviation in women. The hypothesis that a greater number of growing follicles causes a greater predeviation decrease in FSH was supported for mares (r, −0.39; P< 0.04), but a similar negative correlation (r, −0.36) was not significant in women. The hypothesis that the increase in oestradiol during the luteal phase in women was at least partly attributable to luteal-phase anovulatory follicular waves was not supported. Normalization of FSH concentrations to the day of emergence showed maximum value on the day of emergence with a significant increase and decrease on each side of emergence in both species. The day of expected deviation occurred 3 days after emergence during the decline in FSH in both species. These results indicated that the previously reported striking similarities in emergence and deviation between mares and women during the ovulatory follicular wave are associated with species similarities in the temporal relationships between follicle events and FSH concentration changes. Thus, mares may be useful research models for studying the role and mechanism of the action of FSH in emergence and deviation during the ovulatory follicular wave in women.