We investigated on the mechanism responsible for the reduced ATP-sensitive K+(KATP) channel activity recorded from skeletal muscle of K+-depleted rats. Patch-clamp and gene expression measurements of KATP channel subunits were performed. A down-regulation of the KATP channel subunits Kir6.2(70%) and SUR2A(46%) in skeletal muscles of K+-depleted rats but no changes in the expression of Kir6.1, SUR1 and SUR2B subunits were observed. A reduced KATP channel currents of 69.5% in K+-depleted rats was observed. The Kir6.2/SUR2A-B agonist cromakalim showed similar potency in activating the KATP channels of normokalaemic and K+-depleted rats but reduced efficacy in K+-depleted rats. The Kir6.2/SUR1-2B agonist diazoxide activated KATP channels in normokalaemic and K+-depleted rats with equal potency and efficacy. The down-regulation of the Kir6.2 explains the reduced KATP channel activity in K+-depleted rats. The lower expression of SUR2A explains the reduced efficacy of cromakalim; preserved SUR1 expression accounts for the efficacy of diazoxide. Kir6.2/SUR2A deficiency is associated with impaired muscle function in K+-depleted rats and in hypoPP

We investigated on the mechanism responsible for the reduced ATP-sensitive K+(KATP) channel activity recorded from skeletal muscle of K+-depleted rats. Patch-clamp and gene expression measurements of KATP channel subunits were performed. A down-regulation of the KATP channel subunits Kir6.2(-70%) and SUR2A(-46%) in skeletal muscles of K+-depleted rats but no changes in the expression of Kir6.1, SUR1 and SUR2B subunits were observed. A reduced KATP channel currents of -69.5% in K+-depleted rats was observed. The Kir6.2/SUR2A-B agonist cromakalim showed similar potency in activating the KATP channels of normokalaemic and K+-depleted rats but reduced efficacy in K+-depleted rats. The Kir6.2/SUR1-2B agonist diazoxide activated KATP channels in normokalaemic and K+-depleted rats with equal potency and efficacy. The down-regulation of the Kir6.2 explains the reduced KATP channel activity in K+-depleted rats. The lower expression of SUR2A explains the reduced efficacy of cromakalim; preserved SUR1 expression accounts for the efficacy of diazoxide. Kir6.2/SUR2A deficiency is associated with impaired muscle function in K+-depleted rats and in hypoPP. © 2007 Elsevier B.V. All rights reserved.

Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted rats

Tricarico, Domenico;Mele, Antonietta;Conte Camerino, Diana
2008-01-01

Abstract

We investigated on the mechanism responsible for the reduced ATP-sensitive K+(KATP) channel activity recorded from skeletal muscle of K+-depleted rats. Patch-clamp and gene expression measurements of KATP channel subunits were performed. A down-regulation of the KATP channel subunits Kir6.2(-70%) and SUR2A(-46%) in skeletal muscles of K+-depleted rats but no changes in the expression of Kir6.1, SUR1 and SUR2B subunits were observed. A reduced KATP channel currents of -69.5% in K+-depleted rats was observed. The Kir6.2/SUR2A-B agonist cromakalim showed similar potency in activating the KATP channels of normokalaemic and K+-depleted rats but reduced efficacy in K+-depleted rats. The Kir6.2/SUR1-2B agonist diazoxide activated KATP channels in normokalaemic and K+-depleted rats with equal potency and efficacy. The down-regulation of the Kir6.2 explains the reduced KATP channel activity in K+-depleted rats. The lower expression of SUR2A explains the reduced efficacy of cromakalim; preserved SUR1 expression accounts for the efficacy of diazoxide. Kir6.2/SUR2A deficiency is associated with impaired muscle function in K+-depleted rats and in hypoPP. © 2007 Elsevier B.V. All rights reserved.
2008
We investigated on the mechanism responsible for the reduced ATP-sensitive K+(KATP) channel activity recorded from skeletal muscle of K+-depleted rats. Patch-clamp and gene expression measurements of KATP channel subunits were performed. A down-regulation of the KATP channel subunits Kir6.2(70%) and SUR2A(46%) in skeletal muscles of K+-depleted rats but no changes in the expression of Kir6.1, SUR1 and SUR2B subunits were observed. A reduced KATP channel currents of 69.5% in K+-depleted rats was observed. The Kir6.2/SUR2A-B agonist cromakalim showed similar potency in activating the KATP channels of normokalaemic and K+-depleted rats but reduced efficacy in K+-depleted rats. The Kir6.2/SUR1-2B agonist diazoxide activated KATP channels in normokalaemic and K+-depleted rats with equal potency and efficacy. The down-regulation of the Kir6.2 explains the reduced KATP channel activity in K+-depleted rats. The lower expression of SUR2A explains the reduced efficacy of cromakalim; preserved SUR1 expression accounts for the efficacy of diazoxide. Kir6.2/SUR2A deficiency is associated with impaired muscle function in K+-depleted rats and in hypoPP
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/203907
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