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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of Cellular ...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of Cellular Physiology
Article . 2008 . Peer-reviewed
License: Wiley Online Library User Agreement
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Adenosine A1 and A2A receptor regulation of protein phosphatase 2A in the murine heart

Authors: Tikh, Eugene I.; Fenton, Richard A.; Chen, Jiang-Fan; Schwarzschild, Michael A.; Dobson, James G.;

Adenosine A1 and A2A receptor regulation of protein phosphatase 2A in the murine heart

Abstract

AbstractAdenosine plays a role in regulating the contractile function of the heart. This includes a positive ionotropic action via the adenosine A2A receptor (A2AR) and an inhibition of β1‐adrenergic receptor‐induced ionotropy (antiadrenergic action) via the adenosine A1 receptor (A1R). Phosphatase activity has also been shown to influence contractile function by affecting the level of protein phosphorylation. Protein phosphatase 2A (PP2A) plays a significant role in mediating the A1R antiadrenergic effect. The purpose of this study was to investigate the effects of A2AR and A1R on the activities of PP2A in hearts obtained from wild‐type (WT) and A2AR knockout (A2AR‐KO) mice. PP2A activities were examined in myocardial particulate and cytoplasmic extract fractions. Treatment of wild‐type hearts with the A1R agonist CCPA increased the total PP2A activity and increased the particulate:cytoplasmic PP2A activity ratio. Treatment with the A2AR agonist CGS‐21680 (CGS) decreased the total PP2A activity and decreased the particulate:cytoplasmic PP2A activity ratio. This indicated a movement of PP2A activity between cell fractions. The effect of CCPA was inhibited by CGS. In A2AR‐KO hearts the response to A1R activation was markedly enhanced whereas the response to A2AR activation was absent. These data show that A2AR and A1R regulate PP2A activity, thus suggesting an important mechanism for modulating myocardial contractility. J. Cell. Physiol. 216: 83–90, 2008. © 2008 Wiley‐Liss, Inc.

Keywords

Male, Mice, Knockout, Adenosine, Adenosine A2 Receptor Agonists, Receptor, Adenosine A2A, Receptor, Adenosine A1, Myocardium, 610, Heart, Myocardial Contraction, Adenosine A1 Receptor Agonists, Enzyme Activation, Mice, Inbred C57BL, Mice, Phenethylamines, Animals, Tyrosine, Protein Phosphatase 2

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
15
Average
Average
Top 10%