Exp Clin Endocrinol Diabetes 1993; 101(4): 255-261
DOI: 10.1055/s-0029-1211241
Original

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Different Steroidogenic Response of Young and Aged Porcine Small and Large Luteal Cells to Prostaglandin F, Oxytocin and Estradiol

L. Pitzel, H. Jarry, W. Wuttke
  • Division of Clinical and Experimental Endocrinology, Department of Obstetrics/Gynecology, University of Göttingen/Germany
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Publication History

Publication Date:
15 July 2009 (online)

Summary

The role of oxytocin (OXT) and prostaglandin F (PGF) in the process of luteal regulation, particularly their function in the early luteal phase is poorly understood. Therefore the effects of both compounds on in vitro steroid release of porcine luteal cells harvested from young/milddleaged (day 4-6, day 0 = 1st estrous day) or old (day 12-14) corpora lutea were tested. As corpora lutea (CL) contain at least two different steroidogenic cell populations, fractions of the so called small (SLC) and large (LLC) luteal cells were prepared and tested in separate experiments. In SLC as well as LLC from young CL OXT and PGF inhibited progesterone (P) production but induced a strong increase of estradiol (E2) release. In old SLC and LLC OXT and PGF were still inhibitory to P release but OXT was ineffective and PGF had a moderate stimulatory effect on luteal E2 secretion. In SLC cultures from young but not from old CL E2 exerted a powerful stimulatory effect on progesterone (P) secretion, i.e. E2 has strong luteotrophic effects in the early luteal phase. Indeed, the pronounced inhibitory effect of OXT and PGF on P release from SLC could be counteracted by the addition of exogenous E2 to the culture media. Therefore, we suggest that in the early luteal phase OXT as well as PGF have an indirect, E2-mediated luteotrophic effect on P release which is stronger than the direct inhibitory action on P secretion. Indeed, under in vivo conditions we have demonstrated these stimulatory effects of OXT and PGF on luteal P secretion in the early luteal phase. Although in old CL the direct inhibitory effect of OXT and PGF on P release was less pronounced than in young CL the reduced luteotrophic power of E2 may sum up to an inhibitory effect on luteal P release. In conclusion, our experiments support the concept of a dual action of OXT and/or PGF in the regulation of the CL, with a luteotrophic effect in the early luteal phase and a luteolytic effect in the late luteal phase.

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