2005
DOI: 10.1007/s11302-005-0778-6
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LY 294002 inhibits adenosine receptor activation by a mechanism independent of effects on PI-3 kinase or casein kinase II

Abstract: Adenosine reduces both evoked and spontaneous calcium-dependent acetylcholine (ACh) release through a mechanism downstream of calcium entry at amphibian motor nerve endings (Silinsky EM. J Physiol 1984; 346: 243Y56). LY 294002 (2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one), an inhibitor of both phosphoinositide-3 kinase (PI-3 kinase) and casein kinase II, has been reported to increase spontaneous ACh release reflected in miniature endplate potential (MEPP) frequencies independently of intraterminal calcium… Show more

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Cited by 8 publications
(3 citation statements)
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“…Since LY may also target other signaling pathways [31], we directly assessed the impact of Akt upon Oct4 by treatment with Akti1/2, a potent and specific Akt inhibitor [32]. Treatment of mESCs with increasing amounts of Akti1/2 resulted in a dose‐dependent reduction in pAkt Thr308 and Ser473 (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Since LY may also target other signaling pathways [31], we directly assessed the impact of Akt upon Oct4 by treatment with Akti1/2, a potent and specific Akt inhibitor [32]. Treatment of mESCs with increasing amounts of Akti1/2 resulted in a dose‐dependent reduction in pAkt Thr308 and Ser473 (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…LY294002 [pan PI3K inhibitor ( 24 , 25 )], and CP-724714 [selective HER2 inhibitor ( 26 , 27 )] were diluted to the concentrations of 3 and 10 μ M and 0.1 and 1 μ M in SFIHE medium, respectively, according to previous data. SFIHE medium with either concentration of the PI3K inhibitor, the HER2 inhibitor, or both inhibitors at both concentrations were added to only the MCF10A cell line expressing both the mutant PIK3CA -H1047R and the HER2 gene in a 96-well plate for cell growth, and in 6-well plates for colony formation with 2.5×10 4 cells/well.…”
Section: Methodsmentioning
confidence: 99%
“…Since in others systems, it was shown that ADP stimulates phosphoinositide-3 kinase (PI3K) through P2Y 12 receptors, and this pathways have been implicated in integrin activation (see discussion, Kauffenstein et al, 2001;Dorsam and Kunapuli, 2004;Jackson et al, 2004;Sun et al, 2005), we studied the effect of LY-294002, a reversible inhibitor of PI3K and casein kinase II, upon the modulation of the hypertonic response induced by CCPA and 2-Me-SADP. At frog neuromuscular junctions, it was found that LY-294002 increases MEPP frequency through a mechanism independent of internal calcium concentration (Rizzoli and Betz, 2002;Searl and Silinsky, 2005), this action being transient at high concentrations of the drug (Rizzoli and Betz 2002). Thus, we first tested the time-dependent action of LY-294002 on MEPP frequency.…”
Section: Mechanism Of Action Of Adenosine and Adenine Nucleotides Act...mentioning
confidence: 99%