Literature DB >> 22803826

Potentiation of the Kv1 family K(+) channel by cortisone analogues.

Yaping Pan1, Elena J Levin, Matthias Quick, Ming Zhou.   

Abstract

The Kv1 family voltage-dependent K(+) channels are essential for termination of action potentials in neurons and myocytes. These channels form a stable complex with their beta subunits (Kvβ), some of which inhibit channel activity. Cortisone potentiates Kv1 channel by binding to Kvβ and promoting its dissociation from the channel, but its half-maximum effective concentration is ∼46 μM. To identify corticosteroids that are more efficient than cortisone, we examined 25 cortisone analogues and found that fluticasone propionate potentiates channel current with a half-maximum effective concentration (EC(50)) of 37 ± 1.1 nM. Further studies showed that fluticasone propionate potentiates channel current by inducing dissociation of Kvβ, and docking of fluticasone propionate into the cortisone binding site reveals potential interactions that enhance the EC(50) value. Thus, fluticasone propionate provides a starting point for rational design of more efficient small-molecule compounds that increase Kv1 activity and affect the integrity of the Kv1-Kvβ complex.

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Year:  2012        PMID: 22803826      PMCID: PMC3567311          DOI: 10.1021/cb300233y

Source DB:  PubMed          Journal:  ACS Chem Biol        ISSN: 1554-8929            Impact factor:   5.100


  28 in total

1.  Regulation of fast inactivation of cloned mammalian IK(A) channels by cysteine oxidation.

Authors:  J P Ruppersberg; M Stocker; O Pongs; S H Heinemann; R Frank; M Koenen
Journal:  Nature       Date:  1991-08-22       Impact factor: 49.962

2.  Episodic ataxia results from voltage-dependent potassium channels with altered functions.

Authors:  J P Adelman; C T Bond; M Pessia; J Maylie
Journal:  Neuron       Date:  1995-12       Impact factor: 17.173

3.  Potassium channel alpha and beta subunits assemble in the endoplasmic reticulum.

Authors:  N Nagaya; D M Papazian
Journal:  J Biol Chem       Date:  1997-01-31       Impact factor: 5.157

4.  Kv beta 1 subunit binding specific for shaker-related potassium channel alpha subunits.

Authors:  S Sewing; J Roeper; O Pongs
Journal:  Neuron       Date:  1996-02       Impact factor: 17.173

5.  NAB domain is essential for the subunit assembly of both alpha-alpha and alpha-beta complexes of shaker-like potassium channels.

Authors:  W Yu; J Xu; M Li
Journal:  Neuron       Date:  1996-02       Impact factor: 17.173

6.  Beta subunits promote K+ channel surface expression through effects early in biosynthesis.

Authors:  G Shi; K Nakahira; S Hammond; K J Rhodes; L E Schechter; J S Trimmer
Journal:  Neuron       Date:  1996-04       Impact factor: 17.173

7.  Primary structure of a beta subunit of alpha-dendrotoxin-sensitive K+ channels from bovine brain.

Authors:  V E Scott; J Rettig; D N Parcej; J N Keen; J B Findlay; O Pongs; J O Dolly
Journal:  Proc Natl Acad Sci U S A       Date:  1994-03-01       Impact factor: 11.205

8.  Shaker K+ channel beta subunits belong to an NAD(P)H-dependent oxidoreductase superfamily.

Authors:  T McCormack; K McCormack
Journal:  Cell       Date:  1994-12-30       Impact factor: 41.582

9.  Expression and function of voltage-dependent potassium channel genes in human airway smooth muscle.

Authors:  S Adda; B K Fleischmann; B D Freedman; M Yu; D W Hay; M I Kotlikoff
Journal:  J Biol Chem       Date:  1996-05-31       Impact factor: 5.157

10.  A potassium channel beta subunit related to the aldo-keto reductase superfamily is encoded by the Drosophila hyperkinetic locus.

Authors:  S W Chouinard; G F Wilson; A K Schlimgen; B Ganetzky
Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-18       Impact factor: 11.205

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  4 in total

1.  Blocking the mineralocorticoid receptor improves effectiveness of steroid treatment for low back pain in rats.

Authors:  Ling Ye; Wenrui Xie; Judith A Strong; Jun-Ming Zhang
Journal:  Anesthesiology       Date:  2014-09       Impact factor: 7.892

2.  Corticosteroids and aldose reductase inhibitor Epalrestat modulates cardiac action potential via Kvβ1.1 (AKR6A8) subunit of voltage-gated potassium channel.

Authors:  Jared Tur; Sachin L Badole; Feng Cheng; Aparoop Das; Rakesh C Kukreja; Srinivas M Tipparaju
Journal:  Mol Cell Biochem       Date:  2017-06-05       Impact factor: 3.396

3.  Discovery of a small molecule modulator of the Kv1.1/Kvβ1 channel complex that reduces neuronal excitability and in vitro epileptiform activity.

Authors:  Isabelle Niespodziany; Brice Mullier; Véronique Marie André; Philippe Ghisdal; Eric Jnoff; David Moreno-Delgado; Dominique Swinnen; Zara Sands; Martyn Wood; Christian Wolff
Journal:  CNS Neurosci Ther       Date:  2018-09-21       Impact factor: 5.243

4.  Stapled Voltage-Gated Calcium Channel (CaV) α-Interaction Domain (AID) Peptides Act As Selective Protein-Protein Interaction Inhibitors of CaV Function.

Authors:  Felix Findeisen; Marta Campiglio; Hyunil Jo; Fayal Abderemane-Ali; Christine H Rumpf; Lianne Pope; Nathan D Rossen; Bernhard E Flucher; William F DeGrado; Daniel L Minor
Journal:  ACS Chem Neurosci       Date:  2017-03-17       Impact factor: 4.418

  4 in total

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