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NEUROPHARMACOLOGY

Pharmacologic Characterization of the Cloned Human Trace Amine-Associated Receptor1 (TAAR1) and Evidence for Species Differences with the Rat TAAR1

Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana

The hemagglutinin-tagged human trace amine-associated receptor1 (TAAR1) was stably coexpressed with rat G_s in the AV12-664 cell line, and receptor activation was measured as the stimulation of cAMP formation. After blockade of endogenously expressed ₂- and -adrenoceptors with 2-[2-(2-methoxy-1,4-benzodioxanyl)]-imidazoline hydrochloride (2-methoxyidazoxan, RX821002) and alprenolol, respectively, the resulting pharmacology was consistent with that of a unique receptor subtype. -Phenylethylamine (-PEA), the putative endogenous ligand, gave an EC₅₀ of 106 ± 5 nM in the assay. For a series of -PEA analogs used to explore the pharmacophore, small substituents at ring positions 3 and/or 4 generally resulted in compounds having lower potency than -PEA, although several were as potent as -PEA. However, small substituents at ring position 2 resulted in a number of compounds having potencies as good as or better than -PEA. A number of nonselective antagonists known to share affinity for multiple monoaminergic receptors were evaluated for their ability to inhibit -PEA stimulation of the human TAAR1. None had an IC₅₀ <10 µM. For comparison, the rat TAAR1 receptor was expressed in the AV12-664 cell line. A number of agonist compounds had significantly different relative potencies between the rat and human TAAR1, demonstrating a significant species difference between the rat and human TAAR1. The TAAR1 receptor exhibits a pharmacologic profile uniquely different from those of classic monoaminergic receptors, consistent with the structural information that places them in a distinct family of receptors. This unique pharmacologic profile suggests the potential for development of TAAR-selective agonists and antagonists to study their physiologic roles.

Address correspondence to: David B. Wainscott, Eli Lilly and Company, Lilly Corporate Center, Mail Drop 0510, Indianapolis, IN 46285. E-mail: dbwainscott{at}lilly.com

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