ryanodine and 6-fluoro-5-7-dibromo-2-methyl-1-formyl-1-2-3-4-tetrahydroquinoline

ryanodine has been researched along with 6-fluoro-5-7-dibromo-2-methyl-1-formyl-1-2-3-4-tetrahydroquinoline* in 1 studies

Other Studies

1 other study(ies) available for ryanodine and 6-fluoro-5-7-dibromo-2-methyl-1-formyl-1-2-3-4-tetrahydroquinoline

ArticleYear
Ca2+ influx through L-type Ca2+ channels and Ca2+-induced Ca2+ release regulate cAMP accumulation and Epac1-dependent ERK 1/2 activation in INS-1 cells.
    Molecular and cellular endocrinology, 2016, Jan-05, Volume: 419

    We previously reported that INS-1 cells expressing the intracellular II-III loop of the L-type Ca(2+) channel Cav1.2 (Cav1.2/II-III cells) are deficient in Ca(2+)-induced Ca(2+) release (CICR). Here we show that glucose-stimulated ERK 1/2 phosphorylation (GSEP) is slowed and reduced in Cav1.2/II-III cells compared to INS-1 cells. This parallels a decrease in glucose-stimulated cAMP accumulation (GS-cAMP) in Cav1.2/II-III cells. Influx of Ca(2+) via L-type Ca(2+) channels and CICR play roles in both GSEP and GS-cAMP in INS-1 cells since both are inhibited by nicardipine or ryanodine. Further, the Epac1-selective inhibitor CE3F4 abolishes glucose-stimulated ERK activation in INS-1 cells, as measured using the FRET-based sensor EKAR. The non-selective Epac antagonist ESI-09 but not the Epac2-selective antagonist ESI-05 nor the PKA antagonist Rp-cAMPs inhibits GSEP in both INS-1 and Cav1.2/II-III cells. We conclude that L-type Ca(2+) channel-dependent cAMP accumulation, that's amplified by CICR, activates Epac1 and drives GSEP in INS-1 cells.

    Topics: Animals; Benzene Derivatives; Calcium; Calcium Channels, L-Type; Cyclic AMP; Glucose; Guanine Nucleotide Exchange Factors; MAP Kinase Signaling System; Nicardipine; Phosphorylation; Quinolines; Rats; Ryanodine; Sulfones

2016