Journal article

Adiponectin gene expression is inhibited by beta-adrenergic stimulation via protein kinase A in 3T3-L1 adipocytes


Authors listFasshauer, M; Klein, J; Neumann, S; Eszlinger, M; Paschke, R

Publication year2001

Pages142-146

JournalFEBS Letters

Volume number507

Issue number2

ISSN0014-5793

DOI Linkhttps://doi.org/10.1016/S0014-5793(01)02960-X

PublisherWiley


Abstract
Recently, it has been shown that the fat-derived factor adiponectin is downregulated in insulin resistance and obesity and that replenishment of this adipocytokine reverses insulin resistance in mice. Growing evidence, on the other hand, suggests that raised levels of catecholamines due to increased activity of the sympathetic nervous system are an integral part in the development of insulin resistance. To clarify whether catecholamines might exert their insulin resistance-inducing effects at least partly via downregulation of adiponectin gene expression, 3T3-L1 adipocytes were treated with isoproterenol, and adiponectin mRNA was measured by quantitative real-time reverse transcription-polymerase chain reaction. In fact, isoproterenol treatment reduced the level of adiponectin mRNA by about 75% in a dose-dependent fashion with significant inhibition detectable at concentrations as low as 10 nM isoproterenol. Furthermore, the inhibitory effect of isoproterenol was almost completely reversed by pretreatment of 3T3-L1 cells with the beta -adrenergic antagonist propranolol and the protein kinase A (PKA) inhibitor H-89. Moreover, the effects of isoproterenol could be mimicked by stimulation of stimulatory guanine nucleotide-binding (Gs)proteins with cholera toxin and adenylyl cyclase with forskolin. Thus, our results suggest that adiponectin gene expression is severely suppressed by beta -adrenergic agents via activation of a Gs-protein-PKA-dependent pathway. The data support a possible role of adiponectin in catecholamine-induced insulin resistance. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.



Citation Styles

Harvard Citation styleFasshauer, M., Klein, J., Neumann, S., Eszlinger, M. and Paschke, R. (2001) Adiponectin gene expression is inhibited by beta-adrenergic stimulation via protein kinase A in 3T3-L1 adipocytes, FEBS Letters, 507(2), pp. 142-146. https://doi.org/10.1016/S0014-5793(01)02960-X

APA Citation styleFasshauer, M., Klein, J., Neumann, S., Eszlinger, M., & Paschke, R. (2001). Adiponectin gene expression is inhibited by beta-adrenergic stimulation via protein kinase A in 3T3-L1 adipocytes. FEBS Letters. 507(2), 142-146. https://doi.org/10.1016/S0014-5793(01)02960-X


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