◀ Back to AKT1
AKT1 — CPA1
Text-mined interactions from Literome
Germack et al., Br J Pharmacol 2000
(MAP Kinase Signaling System) :
The selective A ( 1 ) -adenosine receptor agonist N ( 6 )
-cyclopentyladenosine (CPA) stimulated time and concentration dependent increases in
PKB phosphorylation in DDT ( 1 ) MF-2 cells ( EC ( 50 ) 1.3+/-0.5 nM ) ...
CPA mediated increases in
PKB phosphorylation were antagonized by the A ( 1 ) -adenosine receptor selective antagonist 1,3-dipropylcyclopentylxanthine ( DPCPX ) yielding an apparent K ( D ) value of 2.3 nM ... Removal of extracellular Ca ( 2+ ) and chelation of intracellular Ca ( 2+ ) with BAPTA had no significant effect on
CPA induced
PKB phosphorylation ... Similarly, pretreatment ( 30 min ) with inhibitors of protein kinase C ( Ro 31-8220 ; 10 microM ), tyrosine kinase ( genistein ; 100 microM ), mitogen activated protein ( MAP ) kinase kinase ( PD 98059 ; 50 microM ) and p38 MAPK ( SB 203580 ; 20 microM ) had no significant effect on
CPA induced
PKB phosphorylation
Germack et al., J Mol Cell Cardiol 2004
(Myocardial Ischemia...) :
Adenosine ( non-selective agonist ),
CPA ( A ( 1 ) selective agonist ) and Cl-IB-MECA ( A ( 3 ) selective agonist ) all
increased PKB phosphorylation in a time- and concentration dependent manner
Migita et al., J Neurosci Res 2008
:
CPA also
induced phosphorylation of extracellular signal regulated kinase ( ERK ), mitogen activated protein kinase/ERK kinase ( MEK ), and
Akt , and their phosphorylation was inhibited by DPCPA