Biol Reprod Keystone Symposia Conference on Frontiers in Reproductive Biology & Regulation of Fertility.
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Biology of Reproduction, Vol 21, 1175-1183, Copyright © 1979 by Society for the Study of Reproduction

Studies on the Mechanism of Action of the Inhibitory Effect of Prostaglandin F2agr on Cyclic AMP Accumulation in Rat Corpora Lutea of Various Ages

M. IQBAL KHAN 1, STEN ROSBERG 1, MICHAL LAHAV 1, SERGIO A. LAMPRECHT 1, GUNNAR SELSTAM 1, HANS HERLITZ 1, , and KURT AHRÉN 1

1 Department of Physiology, University of Göteborg, Göteborg, Sweden


In vivo administration of prostaglandin F2agr (PGF2agr) to PMSG treated immature rats drastically reduced the in vitro effect of LH on cAMP accumulation in 7-day-old corpora lutea (CL) but failed to do so in 3-day-old CL.

In vitro administration of PGF2agr added simultaneously with LH, reduced the LH effect on cAMP accumulation in 7- and 3-day-old CL but not in 1-day-old CL. A concentration of PGF2agr as low as 0.05 µM significantly inhibited the LH induced rise in cAMP accumulation in 7-day-old CL. A 100 times higher concentration of PGF2agr was needed to reduce the LH effect in 3-day-old CL, while 1-day-old CL were completely resistant to the inhibitory effect of PGF2agr.

A potent phosphodiesterase inhibitor, IBMX, had no effect on the PGF2agr-induced decrease of the LH effect. Furthermore, no change in the phosphodiesterase enzyme activity was observed in the CL after PGF2agr treatment. PGF2agr, when tested in combination with PGE2, did not inhibit the increase in cAMP produced by PGE2.

The present results illustrate that the inhibitory effect of PGF2agr on the LH-induced rise in cAMP accumulation is highly dependent upon the age of the CL and that this effect of PGF2agr is not exerted through changes in the phosphodiesterase enzyme activity. These results give further support to the possibility that changes in the cAMP response are one of the earliest steps in PGF2 agr-induced luteolysis.

Note:
ACKNOWLEDGMENTS We express our thanks to Miss Barbro Henskog and Stina Öberg for their expert technical assistance, Mrs. Gun Derevall and Mrs. Britt-Marie Udder for typing the manuscript and NIH, USA for the generous supply of LH. Michal Lahav and Sergio Lainprecht gratefully acknowledge the travel grant from EMBO. This work was supported by grants from the Swedish Medical Research Council (14X-00027), the Ford Foundation (76-0082), AB Leo Research Foundation, the Magnus Bergvall's Foundation and the Medical Faculty, University of Göteborg, Sweden.

Submitted on May 24, 1979
Accepted on September 5, 1979




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Copyright © 1979 by the Society for the Study of Reproduction.