Journal of Biological Chemistry · 1987 · 105 citations · 21 references
MedicineNeurobiologyPharmacologyBiochemical PharmacologyMolecular PharmacologyNeuropharmacologyNeurotransmissionNeurotransmitter ReceptorsReceptor PharmacologySodium HomeostasisAdrenergic AntagonistsAdrenergic Receptor AgonistsAdrenergic Receptor AntagonistsAdrenergic SignalingAlpha-adrenergic AgonistsLigand-receptor AffinityReceptor Affinity RegulationReceptors
Previous reports from this laboratory have demonstrated that alpha 2-adrenergic receptors accelerate Na+/H+ exchange in NG108-15 neuroblastoma X glioma cells and evoke platelet secretion via a pathway involving Na+/H+ exchange. The present studies were designed to examine whether agents that interact with Na+/H+ antiporters also might influence alpha 2-adrenergic receptor-ligand interactions. We observed that Na+ decreases receptor affinity for the agonists epinephrine, norepinephrine, and UK14304 and slightly increases receptor affinity for the antagonists yohimbine and idazoxan in digitonin-solubilized preparations from porcine brain cortex. Increases in [H+] also decrease receptor affinity for agonists and cause either a slight increase or no change in receptor affinity for antagonists. Amiloride analogs accelerate the rate of [3H] yohimbine dissociation from digitonin-solubilized receptors with a relative effectiveness that parallels their ability to block Na+/H+ exchange in other systems. Interestingly, these modulatory effects of Na+,H+ and 5-amino-substituted analogs of amiloride are retained in homogeneous preparations of the alpha 2-adrenergic receptor, suggesting that the allosteric-binding sites for these agents are on the receptor-binding protein itself.
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Jeffrey M. Besterman, W. Stratford May, Harry LeVine et al. · Journal of Biological Chemistry · 1985 · 203 citations · Full text