Do GH, IGF-I and oxytocin interact by regulating the secretory activity of porcine ovarian cells?

J Endocrinol. 2001 Dec;171(3):475-80. doi: 10.1677/joe.0.1710475.

Abstract

The aims of this study on porcine ovarian granulosa cells were to examine the effect of GH on oxytocin (OT), IGF-I and IGF-I receptors, IGF-binding protein-3 (IGFBP-3), progesterone and prostaglandin E (PGE), as well as to determine whether IGF-I and/or OT may be mediators of GH action. The cells were cultured either with porcine GH (pGH) (1 ng/ml to 10 microg/ml or 100 ng/ml only), antiserum against IGF-I (0.1%), antiserum against OT (0.1%) or a combination of GH (10 ng/ml) with antiserum against IGF-I or antiserum against OT (0.1%). The secretion of IGF-I, OT, IGFBP-3, progesterone and PGE was determined using RIA/IRMA, whilst the IGF-I binding sites were measured using a radioreceptor assay. It was observed that pGH increased the secretion of IGF-I and the abundance of IGF-I binding sites in granulosa cells. Furthermore, GH inhibited OT release, stimulated progesterone and PGE output, but had no significant effect on IGFBP-3 secretion. Immunoneutralization of IGF-I by antiserum against IGF-I inhibited PGE secretion, but it did not influence progesterone or IGFBP-3 secretion. Binding of OT by antiserum suppressed IGFBP-3, PGE, but not progesterone secretion. Neither immunoneutralization of IGF-I nor OT substantially prevented the effects of GH on progesterone, IGFBP and PGE. These observations demonstrate the involvement of GH, IGF-I and OT in the control of porcine ovarian secretory activity and the ability of GH to regulate IGF-I and OT production and IGF-I reception. Nevertheless, lack of correlation between the effects of GH, antiserum against IGF-I and antiserum against OT, as well as the inability of blockade of IGF-I or OT to prevent the effects of GH, suggests that IGF-I and OT, despite their dependence on GH, do not mediate GH action on ovarian cells.

MeSH terms

  • Animals
  • Cell Culture Techniques
  • Culture Media, Conditioned
  • Female
  • Granulosa Cells / drug effects*
  • Granulosa Cells / metabolism
  • Growth Hormone / pharmacology*
  • Growth Hormone / physiology
  • Immune Sera
  • Insulin-Like Growth Factor Binding Protein 3 / biosynthesis
  • Insulin-Like Growth Factor I / antagonists & inhibitors
  • Insulin-Like Growth Factor I / biosynthesis
  • Insulin-Like Growth Factor I / physiology
  • Oxytocin / antagonists & inhibitors
  • Oxytocin / biosynthesis
  • Oxytocin / physiology
  • Progesterone / biosynthesis
  • Prostaglandins E / biosynthesis
  • Swine / metabolism*

Substances

  • Culture Media, Conditioned
  • Immune Sera
  • Insulin-Like Growth Factor Binding Protein 3
  • Prostaglandins E
  • Progesterone
  • Oxytocin
  • Insulin-Like Growth Factor I
  • Growth Hormone