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1.
Expert Opin Investig Drugs ; 13(5): 461-4, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-15155121

RESUMO

Pharmacology is at a crucial point, because we now have access to sequences, by homology, for almost all of the receptors in the human genome. The International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification (NC-IUPHAR) has set up > 50 subcommittees to define the receptors, and their recommendations, when approved, are posted on a website freely available to all scientists. A major new effort is to functionally define relevant receptor polymorphisms. This initiative is open to all, and works only because of the freely given voluntary effort of scientists.


Assuntos
Receptores de Droga/classificação , Terminologia como Assunto , Guias como Assunto/normas , Humanos , Agências Internacionais , Sociedades Farmacêuticas
2.
J Biol Chem ; 278(13): 11312-9, 2003 Mar 28.
Artigo em Inglês | MEDLINE | ID: mdl-12496283

RESUMO

GPR41 and GPR43 are related members of a homologous family of orphan G protein-coupled receptors that are tandemly encoded at a single chromosomal locus in both humans and mice. We identified the acetate anion as an agonist of human GPR43 during routine ligand bank screening in yeast. This activity was confirmed after transient transfection of GPR43 into mammalian cells using Ca(2+) mobilization and [(35)S]guanosine 5'-O-(3-thiotriphosphate) binding assays and by coexpression with GIRK G protein-regulated potassium channels in Xenopus laevis oocytes. Other short chain carboxylic acid anions such as formate, propionate, butyrate, and pentanoate also had agonist activity. GPR41 is related to GPR43 (52% similarity; 43% identity) and was activated by similar ligands but with differing specificity for carbon chain length, with pentanoate being the most potent agonist. A third family member, GPR42, is most likely a recent gene duplication of GPR41 and may be a pseudogene. GPR41 was expressed primarily in adipose tissue, whereas the highest levels of GPR43 were found in immune cells. The identity of the cognate physiological ligands for these receptors is not clear, although propionate is known to occur in vivo at high concentrations under certain pathophysiological conditions.


Assuntos
Ácidos Carboxílicos/farmacologia , Propionatos/farmacologia , Receptores de Superfície Celular/agonistas , Receptores Acoplados a Proteínas G , Sequência de Aminoácidos , Animais , Primers do DNA , Humanos , Imuno-Histoquímica , Dados de Sequência Molecular , Receptores de Superfície Celular/metabolismo , Proteínas Recombinantes/efeitos dos fármacos , Proteínas Recombinantes/metabolismo , Xenopus laevis
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