Isolated porcine ovarian follicles as a model for the study of hormone and growth factor action on ovarian secretory activity.

The aim of our in vitro experiments with isolated porcine ovarian follicles was to study the effects of gonadotropins, GH, IGF-I and oxytocin (OT) on release of ovarian steroid, OT, IGF-I, insulin-like growth factor-binding protein-3 (IGFBP-3), prostaglandin F (PGF), prostaglandin E (PGE) and cAMP. It was found that quarters of ovarian follicles cultured for 8 days produced significant amounts of progesterone, estradiol-17 beta, OT and IGFBP-3 with peaks of accumulation from the 3rd to the 8th day of culture. Addition of serum promoted progesterone, estradiol and OT release, whilst accumulation of IGFBP-3 was maintained to a greater extent in serum-free medium. GH (10 ng/ml or above) was able to inhibit androstenedione, OT, PGF and IGFBP-3, to stimulate IGF-I and cAMP, and to alter testosterone and PGE release by follicles cultured in serum-supplemented and/or serum-free medium. IGF-I (10 ng/ml or more) inhibited androstenedione and PGF secretion, stimulated testosterone, estradiol, OT and cAMP production, but did not influence progesterone, IGFBP-3 or PGE output in these conditions. OT (100 ng/ml) was able to inhibit androstenedione and to stimulate testosterone, IGF-I, PGF and PGE, but not estradiol or IGFBP-3 release. A stimulatory effect of LH on progesterone and OT and an inhibitory influence of LH on estradiol secretion in the serum-supplemented medium were observed. FSH in these conditions stimulated OT, but not progesterone or estradiol secretion. The use of this experimental model suggests the involvement of gonadotropins, OT, GH and IGF-I in the control of ovarian steroid and nonapeptide hormone, growth factor, growth factor-binding protein, prostaglandin and cyclic nucleotide production. The stimulatory effect of GH on IGF-I, and the stimulatory influence of IGF-I on OT, as well as coincidence of the majority of effects of IGF-I and OT, suggest the existence of a GH-IGF-I-OT axis. On the other hand, the different patterns of action of GH and IGF-I on OT, estrogen and IGFBP-3 suggest that part of the GH effect on ovarian cells is IGF-I independent.

[1]  D. Schams Luteal peptides and intercellular communication. , 2019, Journal of reproduction and fertility. Supplement.

[2]  A. Sirotkin,et al.  The release of insulin-like growth factor-I by luteinized human granulosa cells in vitro: regulation by growth hormone, oxytocin, steroids and cAMP-dependent intracellular mechanisms. , 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[3]  A. Sirotkin Inter-relationships between nonapeptide hormones and cyclic nucleotides within cultured porcine granulosa cells. , 1996, The Journal of endocrinology.

[4]  H. Kwon,et al.  Prostaglandin production and ovulation during exposure of amphibian ovarian follicles to gonadotropin or phorbol ester in vitro. , 1995, General and comparative endocrinology.

[5]  A. Sirotkin In vitro Effects of Oxytocin and Vasopressin on Cyclic Nucleotide Production by Bovine Granulosa Cells , 1995 .

[6]  L. Spicer,et al.  The ovarian insulin and insulin-like growth factor system with an emphasis on domestic animals. , 1995, Domestic animal endocrinology.

[7]  G. Erickson,et al.  Ovarian control of follicle development. , 1995, American journal of obstetrics and gynecology.

[8]  A. Sirotkin,et al.  Growth hormone and prolactin affect oxytocin, vasopressin, progesterone and cyclic nucleotide secretion by bovine granulosa cells in vitro. , 1994, The Journal of endocrinology.

[9]  A. Sirotkin,et al.  Cooperation between LH-RH and LH in the direct action on the ovary: LH-RH stimulation of LH/hCG receptors, basal and LH-induced cAMP and cGMP release by porcine granulosa cells in vitro. , 1994, Cellular signalling.

[10]  G. Webley,et al.  Cellular mechanisms of luteolysis , 1994, Molecular and Cellular Endocrinology.

[11]  J. Grassi,et al.  Subpicogram determination of oxytocin by an enzyme immunoassay using acetylcholinesterase as label. , 1994, Journal of immunoassay.

[12]  H. Leese,et al.  Pattern of lactate production and steroidogenesis during growth and maturation of mouse ovarian follicles in vitro. , 1993, Biology of reproduction.

[13]  J. Kotwica,et al.  Influence of oxytocin removal from the corpus luteum on secretory function and duration of the oestrous cycle in cattle. , 1993, Journal of reproduction and fertility.

[14]  L. Giudice Insulin-like growth factors and ovarian follicular development. , 1992, Endocrine reviews.

[15]  D. Baird,et al.  Hormone production in vivo and in vitro from follicles at different stages of the oestrous cycle in the sheep. , 1992, The Journal of endocrinology.

[16]  S. Dieleman,et al.  Intrinsic and extrinsic factors influencing steroid production in vitro by bovine follicles. , 1989, Theriogenology.

[17]  B. Tsang,et al.  Gonadotropic regulation of prostaglandin production by ovarian follicular cells of the pig. , 1988, Biology of reproduction.

[18]  A. Hsueh,et al.  Growth hormone enhances follicle-stimulating hormone-induced differentiation of cultured rat granulosa cells. , 1986, Endocrinology.

[19]  B. Tsang,et al.  Prostaglandin production by dispersed granulosa and theca interna cells from porcine preovulatory follicles. , 1984, Biology of reproduction.

[20]  R. Webb,et al.  Estrogen secretion and gonadotropin binding by individual bovine follicles during estrus. , 1982, Journal of animal science.

[21]  F. Goetz,et al.  Ovarian and plasma prostaglandin E and F levels in brook trout (Salvelinus fontinalis) during pituitary-induced ovulation. , 1982, Biology of reproduction.

[22]  R. Furlanetto,et al.  Estimation of somatomedin-C levels in normals and patients with pituitary disease by radioimmunoassay. , 1977, The Journal of clinical investigation.

[23]  A. Sirotkin,et al.  Oxytocin affects the release of steroids, insulin-like growth factor-I, prostaglandin F2alpha and cyclic nucleotides by human granulosa cells in vitro. , 1996, Human reproduction.

[24]  Sirotkin Av Direct action of growth hormone on bovine ovarian cells: effects on estradiol, oxytocin, vasopressin release by granulosa cells and on oocyte maturation and cleavage in vitro. , 1996 .

[25]  N. Spears,et al.  The establishment of follicular dominance in co-cultured mouse ovarian follicles. , 1996, Journal of reproduction and fertility.

[26]  A. Sirotkin,et al.  The puberty-related changes in hormone secretion and responsibility of porcine granulosa cells to LH and dbcAMP in vitro , 1994 .

[27]  A. C. Paton,et al.  Differentiation processes of granulosa cells. , 1992, Oxford reviews of reproductive biology.

[28]  Collins Wp,et al.  Differentiation processes of granulosa cells. , 1992 .

[29]  D. Wathes Oxytocin and vasopressin in the gonads. , 1989, Oxford reviews of reproductive biology.

[30]  Wathes Dc Oxytocin and vasopressin in the gonads. , 1989 .

[31]  M. Driancourt,et al.  Morphological and functional features of ovine follicles in perifusion with pulsatile hormone delivery. , 1988, Reproduction, nutrition, development.

[32]  E. Adashi,et al.  Somatomedin-C as an amplifier of follicle-stimulating hormone action: enhanced accumulation of adenosine 3',5'-monophosphate. , 1986, Endocrinology.

[33]  O. Tsutsumi,et al.  Prostaglandins and ovulation. , 1985, Advances in prostaglandin, thromboxane, and leukotriene research.

[34]  P. Janson,et al.  Aspects concerning the role of prostaglandins for ovarian function. , 1983, Acta obstetricia et gynecologica Scandinavica. Supplement.

[35]  J. Watson,et al.  Effect of oestradiol-17 beta and gonadotrophins on prostaglandin production by pre-ovulatory pig follicles superfused in vitro. , 1979, Advances in experimental medicine and biology.