期刊
FASEB JOURNAL
卷 21, 期 7, 页码 1597-1608出版社
WILEY
DOI: 10.1096/fj.06-7474com
关键词
thyronamines; signal transduction; G protein-coupled receptors; myocardial function
资金
- NIDDK NIH HHS [DK-52798] Funding Source: Medline
3-iodothyronamine T(1)AM is a novel endogenous thyroid hormone derivative that activates the G protein-coupled receptor known as trace anime-associated receptor 1 (TAAR1). In the isolated working rat heart and in rat cardiomyocytes, T(1)AM produced a reversible, dose-dependent negative inotropic effect (e.g., 27 +/- 5, 51 +/- 3, and 65 +/- 2% decrease in cardiac output at 19, 25, and 38 mu M concentration, respectively). An independent negative chronotropic effect was also observed. The hemodynamic effects of T(1)AM were remarkably increased in the presence of the tyrosine kinase inhibitor genistein, whereas they were attenuated in the presence of the tyrosine phosphatase inhibitor vanadate. No effect was produced by inhibitors of protein kinase A, protein kinase C, calcium-calmodulin kinase II, phosphatidylinositol-3-kinase, or MAP kinases. Tissue cAMP levels were unchanged. In rat ventricular tissue, Western blot experiments with antiphosphotyrosine antibodies showed reduced phosphorylation of microsomal and cytosolic proteins after perfusion with synthetic T(1)AM; reverse transcriptase-polymerase chain reaction experiments revealed the presence of transcripts for at least 5 TAAR subtypes; specific and saturable binding of [I-125] T(1)AM was observed, with a dissociation constant in the low micromolar range ( 5 mu M); and endogenous T(1)AM was detectable by tandem mass spectrometry. In conclusion, our findings provide evidence for the existence of a novel aminergic system modulating cardiac function.
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