IndraLab

Statements



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"In this regard, of the 15 members of the K2P K + channels family, only TREK-1 and TREK-2 are inhibited by cAMP."

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"Because cAMP analogs inhibited increase of the PDBu elicited K2P currents produced by divalent cataions, we suggest that cAMP may inhibit TREK1 channel without PKA activation."

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"TREK channels are also inhibited by an increase in cAMP, which is counteracted in case of Gi signaling [XREF_BIBR]."

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"Accordingly, it was previously reported that TREK-1 inhibition by cAMP is voltage dependent and less effective at positive potentials."

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"Previously, it had been shown that TREK-1 inhibition by cAMP was voltage dependent and less effective at positive potentials."

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"This hypothesis is supported by an earlier report that suggested that cAMP might inhibit the TREK1 channel independently from PKA in bovine adrenal zona fasciculata cells XREF_BIBR."

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"The decrease in cAMP concentration (as a result of reduced adenylate cyclase activity) in 5-HT neurons is also thought to induce TREK-1 opening because of a consequent reduction of phosphorylation of Ser333 by PKA XREF_BIBR."

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"TREK-1 and TREK-2 (which was not represented on the original Affymetrix chip) are inhibited by cAMP via PKA and exhibit outward rectification in physiological solutions [XREF_BIBR]."

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"Conversely, TREK-1 channels are inhibited by cAMP and following Gαq and Gαs activation [16,22,26]."

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"Adrenocorticotropic hormone and cAMP may inhibit TREK-1 by a PKA independent signaling pathway XREF_BIBR."