Modulation of G protein-coupled receptors by an estrogen receptor that activates protein kinase A

Andre H. Lagrange, Oline K. Rønnekleiv, Martin J. Kelly

Research output: Contribution to journalArticlepeer-review

189 Scopus citations


17β-Estradiol (E2) rapidly (<20 min) attenuates the ability of μ- opioids to hyperpolarize guinea pig hypothalamic (β-endorphin) neurons. In the current study, we used intracellular recordings from guinea pig hypothalamic slices to characterize the receptor and intracellular effector system mediating the rapid effects of E2. E2 acted stereospecifically with physiologically relevant concentration dependence (EC50 = 8 nM) to cause a 4-fold reduction in the potency of a μ-opioid agonist to activate an inwardly rectifying K+ conductance. Using Schild analysis to estimate the affinity of the μ-opioid receptor for an antagonist (naloxone), we found that estrogen did not compete for the μ-opioid receptor or alter the affinity of the μ receptor. Both the nonsteroidal estrogen diethylstilbestrol and the 'pure' antiestrogen ICI 164,384 blocked the actions of E2, the latter with a subnanomolar affinity. The protein synthesis inhibitor cycloheximide did not block the estrogenic uncoupling of the μ-opioid receptor from its K+ channel, implying a nongenomic mechanism of action by E2. The actions of E2 were mimicked by the protein kinase A (PKA) activators forskolin and cAMP, Spisomer triethylammonium salt. Furthermore, the selective PKA antagonists cAMP, Rp-isomer triethylammonium salt and KT5720, which have different chemical structures and modes of action, both blocked the effects of E2. Thus, estrogen binds to a specific receptor that activates PKA to rapidly uncouple the μ-opioid receptor from its K+ channel. Because we have previously shown that γ-aminobutyric acid(B) receptors are also uncoupled by estrogen, this mechanism of action has the potential to alter synaptic transmission via G protein-coupled receptors throughout the brain.

Original languageEnglish (US)
Pages (from-to)605-612
Number of pages8
JournalMolecular pharmacology
Issue number4
StatePublished - Apr 1997

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology


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