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Estrogenic Compounds or Adiponectin Inhibit Cyclic AMP Response to Human Luteinizing Hormone in Mouse Leydig Tumor Cells

Overview
Journal Biology (Basel)
Publisher MDPI
Specialty Biology
Date 2019 Jun 20
PMID 31212720
Citations 2
Authors
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Abstract

Mouse Leydig Tumor cells (mLTC), transiently expressing cAMP-dependent luciferase, were used to study the influence of sexual steroids and of adiponectin (ADPN) on the cAMP response to luteinizing hormones (LH). While testosterone and progesterone had no significant effect, several molecules with estrogenic activity (17β-estradiol, ethynylestradiol, and bisphenol A) provoked a decrease in intracellular cyclic AMP accumulation under 0.7 nM human LH stimulation. Adiponectin exhibited a bimodal dose-effect on LH response: synergistic between 2-125 ng/mL and inhibitory between 0.5-5 µg/mL. In brief, our data indicate that estrogens and ADPN separately exert rapid (<1 h) inhibitory and/or synergistic effects on cAMP response to LH in mLTC-1 cells. As the inhibitory effect of each estrogenic molecule was observed after only 1-h preincubation, it might be mediated through the G protein-coupled estrogen receptor (GPER) membrane receptor, but this remains to be demonstrated. The synergistic effect with low concentrations of ADPN with human Luteinizing Hormone (hLH) was observed with both fresh and frozen/thawed ADPN. In contrast, the inhibitory effect with high concentrations of ADPN was lost with frozen/thawed ADPN, suggesting deterioration of its polymeric structure.

Citing Articles

Knowledge Gap in Understanding the Steroidogenic Acute Regulatory Protein Regulation in Steroidogenesis Following Exposure to Bisphenol A and Its Analogues.

Jefferi N, Shamhari A, Abd Hamid Z, Budin S, Zulkifly A, Roslan F Biomedicines. 2022; 10(6).

PMID: 35740303 PMC: 9219931. DOI: 10.3390/biomedicines10061281.


Bisphenols and Leydig Cell Development and Function.

Li X, Wen Z, Wang Y, Mo J, Zhong Y, Ge R Front Endocrinol (Lausanne). 2020; 11:447.

PMID: 32849262 PMC: 7411000. DOI: 10.3389/fendo.2020.00447.

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