1982
DOI: 10.1530/jrf.0.0660169
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Relationship between LH receptor concentrations in thecal and granulosa cells and in-vivo and in-vitro steroid secretion by ovine follicles during the preovulatory period

Abstract: Summary. Ewes were ovariectomized before (Group 1, N = 5) or after (Group 2, N = 6) the peak of the preovulatory gonadotrophin surge. Ovarian secretion rates of oestradiol and testosterone were significantly higher in Group 1 than in Group 2. The presence of high levels of LH receptors in both thecal and granulosa cells was used to identify ovulatory from non-ovulatory follicles. There was a significant fall in the LH receptor concentration in the thecal and granulosa cells of ovulatory follicles after the pea… Show more

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Cited by 53 publications
(35 citation statements)
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References 31 publications
(61 reference statements)
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“…Normal secretion of oestradiol requires both the stimulation by LH of androgen production, principally androstenedione and testosterone, from the theca and its conversion to oestradiol by an active aromatase system induced by FSH and possibly LH in the granulosa cell layer of the follicle (Moor, 1977;Armstrong, Weiss, Selstam & Seamark, 1981;McNatty, Gibb, Dobson, Thurley & Findlay, 1981 (Dorrington & Gore-Langton, 1981) and LH-induced androgen production from ovarian thecal and interstitial cells in vitro (Magoffin & Erickson, 1982 (Carson, Findlay, Burger & Trounson, 1979;Webb & England, 1982). However, this seems unlikely as most studies of the rat indicate that prolactin is part of the hormonal complex necessary for the induction and maintenance of LH receptors in the follicle and corpus luteum (Richards & Williams, 1976;Holt, Richards, Midgley & Reichert, 1976).…”
Section: Discussionmentioning
confidence: 99%
“…Normal secretion of oestradiol requires both the stimulation by LH of androgen production, principally androstenedione and testosterone, from the theca and its conversion to oestradiol by an active aromatase system induced by FSH and possibly LH in the granulosa cell layer of the follicle (Moor, 1977;Armstrong, Weiss, Selstam & Seamark, 1981;McNatty, Gibb, Dobson, Thurley & Findlay, 1981 (Dorrington & Gore-Langton, 1981) and LH-induced androgen production from ovarian thecal and interstitial cells in vitro (Magoffin & Erickson, 1982 (Carson, Findlay, Burger & Trounson, 1979;Webb & England, 1982). However, this seems unlikely as most studies of the rat indicate that prolactin is part of the hormonal complex necessary for the induction and maintenance of LH receptors in the follicle and corpus luteum (Richards & Williams, 1976;Holt, Richards, Midgley & Reichert, 1976).…”
Section: Discussionmentioning
confidence: 99%
“…overall, the total population of lh-receptive gc in the follicles in the BMp15 mutant is similar to that in the wild-type follicle(s). Follicles with lh-receptive gc are the putative ovulatory follicles, 59 and are the dominant ovarian sources of estradiol and inhibin. 54 since the major sources of these hormones are the gc, the total ovarian secretions do not differ between these genotypes and consequently the ovulation rate differences occur without any differences in the plasma concentrations of pituitary gonadotropins.…”
Section: Can Gene Expression Profiles In Cumulus Cells (Cc) Isolated mentioning
confidence: 99%
“…More recently, Kanai et al (1995) found that heat stress did not change the pituitary LH secretion in long-day-treated anoestrous goats that were injected with exogenous gonadotrophin-releasing hormone (GnRH) to induce artificial LH pulses, whereas it reduced the follicular responsiveness to LH. Follicular LH responsiveness is attributed to the expression of LH receptors on the follicles (Webb & England 1982). Therefore, it appears probable that heat stress induces alterations in the follicular LH receptors.…”
Section: Introductionmentioning
confidence: 99%