Abstract
A cyclic AMP response element (CRE)-luciferase reporter gene assay was used to characterise the functional responses of human melatonin mt(1) and human melatonin MT2 receptors, stably expressed in the human embryonic kidney cell line HEK293, to a series of six naphthalenic analogues of melatonin. By comparison to the observed melatonin-mediated inhibition of stimulated luciferase levels the naphthalenic series was identified as comprising agonists, partial agonists and one antagonist of melatonin mt(1) and melatonin MT2 receptor function. Three of the agonist/partial agonist members of this series were also identified as displaying a functional selectivity for the melatonin MT2 receptor. Competitive displacement of 2-[I-125]iodomelatonin binding to the ovine pars tuberalis melatonin ML1 receptor demonstrated a close correlation to the observed functional luciferase responses of the human melatonin mt(1) receptor. We conclude that the CRE-luciferase reporter gene assay provides an effective functional screening method for the pharmacological characterisation of human melatonin receptor subtypes. (C) 2000 Elsevier Science B.V. All rights reserved.
Original language | English |
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Pages (from-to) | 15-24 |
Number of pages | 10 |
Journal | European Journal of Pharmacology |
Volume | 390 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 25 Feb 2000 |
Keywords
- melatonin receptor
- cAMP response element
- luciferase
- reporter gene assay
- HEK293 cell
- ovine pars tuberalis
- naphthalenic ligands
- high-affinity
- cloning
- expression
- inhibition
- MEL(1A)
- gene
- pharmacology
- localization
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From melatonin receptors to Valdoxan
Peter Morgan (Coordinator), Lynda Williams (Coordinator), Perry Barrett (Coordinator) & A D Strosberg (Coordinator)
Impact: Health and Wellbeing