Literature DB >> 8185943

Dualistic behavior of ATP-sensitive K+ channels toward intracellular nucleoside diphosphates.

A Terzic1, I Findlay, Y Hosoya, Y Kurachi.   

Abstract

ATP-sensitive K+ (KATP) channels are intracellular ligand-gated channels which regulate diverse cellular functions. Intracellular nucleoside diphosphates (NDPs) are essential for the physiological opening of KATP channels which would otherwise be permanently closed by their overt sensitivity to intracellular ATP. We find that KATP channels exhibit dualistic behavior toward NDPs depending on their operative condition. When channels are in the spontaneous operative condition, NDPs antagonize channel inhibition by intracellular ATP. When channels have "run down", NDPs induce channel opening but no longer antagonize intracellular ATP. The switch of the KATP channel response to the same ligand, i.e., NDPs, is controlled by a Mg-ATP-dependent reaction. The condition of the target protein therefore determines the effect of the ligand. This property provides a novel basis to evaluate the dynamic regulation of ion channels by their ligands.

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Year:  1994        PMID: 8185943     DOI: 10.1016/0896-6273(94)90313-1

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  21 in total

1.  Concerted gating mechanism underlying KATP channel inhibition by ATP.

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Journal:  Biophys J       Date:  2004-04       Impact factor: 4.033

2.  Evidence for direct physical association between a K+ channel (Kir6.2) and an ATP-binding cassette protein (SUR1) which affects cellular distribution and kinetic behavior of an ATP-sensitive K+ channel.

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Journal:  Mol Cell Biol       Date:  1998-03       Impact factor: 4.272

3.  Cardiac ATP-sensitive K+ channel: a target for diadenosine 5',5''-P1,P5-pentaphosphate.

Authors:  A Jovanovic; A E Alekseev; A Terzic
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1996-01       Impact factor: 3.000

4.  Diadenosine tetraphosphate-induced inhibition of ATP-sensitive K+ channels in patches excised from ventricular myocytes.

Authors:  A Jovanovic; A Terzic
Journal:  Br J Pharmacol       Date:  1996-01       Impact factor: 8.739

5.  Actin microfilament disrupters enhance K(ATP) channel opening in patches from guinea-pig cardiomyocytes.

Authors:  A Terzic; Y Kurachi
Journal:  J Physiol       Date:  1996-04-15       Impact factor: 5.182

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Journal:  Environ Sci Pollut Res Int       Date:  2016-02-09       Impact factor: 4.223

7.  Ligand-insensitive state of cardiac ATP-sensitive K+ channels. Basis for channel opening.

Authors:  A E Alekseev; P A Brady; A Terzic
Journal:  J Gen Physiol       Date:  1998-02       Impact factor: 4.086

8.  The sulphonylurea receptor SUR1 regulates ATP-sensitive mouse Kir6.2 K+ channels linked to the green fluorescent protein in human embryonic kidney cells (HEK 293).

Authors:  S A John; J R Monck; J N Weiss; B Ribalet
Journal:  J Physiol       Date:  1998-07-15       Impact factor: 5.182

9.  The new antihypertensive drug iptakalim activates ATP-sensitive potassium channels in the endothelium of resistance blood vessels.

Authors:  Su-yang Wang; Wen-yu Cui; Hai Wang
Journal:  Acta Pharmacol Sin       Date:  2015-11-23       Impact factor: 6.150

10.  A dual mechanism of cytoprotection afforded by M-LDH in embryonic heart H9C2 cells.

Authors:  Sofija Jovanović; Qingyou Du; Andriy Sukhodub; Aleksandar Jovanović
Journal:  Biochim Biophys Acta       Date:  2009-05-04
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