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pubmed-article:15271349pubmed:dateCreated2004-7-23lld:pubmed
pubmed-article:15271349pubmed:abstractTextA large collection of bioactive compounds with diverse biological effects can be used as probes to elucidate new biological mechanisms that influence a particular cellular process. Here we analyze the effects of 880 well-known small-molecule bioactives or drugs on the insulin-induced adipogenesis of 3T3-L1 fibroblasts, a cell-culture model of fat cell differentiation. Our screen identified 86 compounds as modulators of the adipogenic differentiation of 3T3-L1 cells. Examination of their chemical and pharmacological information revealed that antihistamine drugs with distinct chemical scaffolds inhibit differentiation. Histamine H1 receptor is expressed in 3T3-L1 cells, and its knockdown by small interfering RNA impaired the insulin-induced adipogenic differentiation. Histamine receptors and histamine-like biogenic amines may play a role in inducing adipogenesis in response to insulin.lld:pubmed
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pubmed-article:15271349pubmed:authorpubmed-author:TanakaSatoshi...lld:pubmed
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pubmed-article:15271349pubmed:authorpubmed-author:KawazoeYoshin...lld:pubmed
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pubmed-article:15271349pubmed:pagination907-13lld:pubmed
pubmed-article:15271349pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:15271349pubmed:year2004lld:pubmed
pubmed-article:15271349pubmed:articleTitleChemical genetic identification of the histamine H1 receptor as a stimulator of insulin-induced adipogenesis.lld:pubmed
pubmed-article:15271349pubmed:affiliationThe Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX 77030, USA.lld:pubmed
pubmed-article:15271349pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15271349pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:15271349pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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