Induced luteolysis in the primate: rapid loss of luteinizing hormone receptors

Citation
Wc. Duncan et al., Induced luteolysis in the primate: rapid loss of luteinizing hormone receptors, HUM REPR, 13(9), 1998, pp. 2532-2540
Citations number
50
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
HUMAN REPRODUCTION
ISSN journal
02681161 → ACNP
Volume
13
Issue
9
Year of publication
1998
Pages
2532 - 2540
Database
ISI
SICI code
0268-1161(199809)13:9<2532:ILITPR>2.0.ZU;2-M
Abstract
The molecular mechanisms involved in luteolysis are still unclear in the pr imate. This study aimed to investigate the effect of induced luteolysis on the ovarian luteinizing hormone (LH) receptor and the steroidogenic enzyme, 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) in the marmoset monkey. L uteolysis was induced in the mid-luteal phase either directly by systemic p rostaglandin F-2 alpha (PGF(2 alpha)), or indirectly by LH withdrawal using systemic gonadotrophin releasing hormone antagonist (GnRH(ant)) treatment. The LH receptor was studied by isotopic mRNA in-situ hybridization and in- situ ligand binding and 3 beta-HSD expression was studied using isotopic mR NA in-situ hybridization and immunohistochemistry. Induced luteolysis was a ssociated with a reduction in the expression of LH receptor (P < 0.0001) an d 3 beta-HSD mRNA, closely followed by a reduction in the LB receptor (P < 0.05) and 3 beta-HSD protein concentrations within 24 h. There were no diff erences in the findings whether luteolysis was induced with PGF(2 alpha) or GnRH(ant). This study shows that disparate mechanisms to induce luteolysis in the primate result in an identical rapid loss of the LH receptor and 3 beta-HSD. In conclusion, induced luteolysis leads to rapid loss of the ster oidogenic pathway in luteal cells.