» Articles » PMID: 23883298

The Therapeutic Potential of Small-conductance KCa2 Channels in Neurodegenerative and Psychiatric Diseases

Overview
Publisher Informa Healthcare
Specialty Pharmacology
Date 2013 Jul 26
PMID 23883298
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: KCa2 or small-conductance Ca(2+)-activated K(+) channels (SK) are expressed in many areas of the central nervous system where they participate in the regulation of neuronal afterhyperpolarization and excitability, and also serve as negative feedback regulators on the glutamate-NMDA pathway.

Areas Covered: This review focuses on the role of KCa2 channels in learning and memory and their potential as therapeutic targets for Alzheimer's and Parkinson's disease, ataxia, schizophrenia and alcohol dependence.

Expert Opinion: There currently exists relatively solid evidence supporting the use of KCa2 activators for ataxia. Genetic KCa2 channel suppression in deep cerebellar neurons induces ataxia, while KCa2 activators like 1-EBIO, SKA-31 and NS13001 improve motor deficits in mouse models of episodic ataxia (EA) and spinal cerebellar ataxia (SCA). Use of KCa2 activators for ataxia is further supported by a report that riluzole improves ataxia in a small clinical trial. Based on accumulating literature evidence, KCa2 activators further appear attractive for the treatment of alcohol dependence and withdrawal. Regarding Alzheimer's disease, Parkinson's disease and schizophrenia, further research, including long-term studies in disease relevant animal models, will be needed to determine whether KCa2 channels constitute valid targets and whether activators or inhibitors would be needed to positively affect disease outcomes.

Citing Articles

Potassium and calcium channels in different nerve cells act as therapeutic targets in neurological disorders.

Qiu Q, Yang M, Gong D, Liang H, Chen T Neural Regen Res. 2024; 20(5):1258-1276.

PMID: 38845230 PMC: 11624876. DOI: 10.4103/NRR.NRR-D-23-01766.


Oxidative stress and ion channels in neurodegenerative diseases.

Orfali R, Alwatban A, Orfali R, Lau L, Chea N, Alotaibi A Front Physiol. 2024; 15:1320086.

PMID: 38348223 PMC: 10859863. DOI: 10.3389/fphys.2024.1320086.


K 2.2 (KCNN2): A physiologically and therapeutically important potassium channel.

Rahman M, Orfali R, Dave N, Lam E, Naguib N, Nam Y J Neurosci Res. 2023; 101(11):1699-1710.

PMID: 37466411 PMC: 10932612. DOI: 10.1002/jnr.25233.


Activation of small conductance Ca -activated K channels suppresses Ca transient and action potential alternans in ventricular myocytes.

Kanaporis G, Blatter L J Physiol. 2022; 601(1):51-67.

PMID: 36426548 PMC: 9878619. DOI: 10.1113/JP283870.


The modulation of potassium channels by estrogens facilitates neuroprotection.

Li X Front Cell Dev Biol. 2022; 10:998009.

PMID: 36393851 PMC: 9643774. DOI: 10.3389/fcell.2022.998009.


References
1.
Stocker M, Krause M, Pedarzani P . An apamin-sensitive Ca2+-activated K+ current in hippocampal pyramidal neurons. Proc Natl Acad Sci U S A. 1999; 96(8):4662-7. PMC: 16389. DOI: 10.1073/pnas.96.8.4662. View

2.
Steketee J, Kalivas P . Effect of microinjections of apamin into the A10 dopamine region of rats: a behavioral and neurochemical analysis. J Pharmacol Exp Ther. 1990; 254(2):711-9. View

3.
Shakkottai V, Chou C, Oddo S, Sailer C, Knaus H, Gutman G . Enhanced neuronal excitability in the absence of neurodegeneration induces cerebellar ataxia. J Clin Invest. 2004; 113(4):582-90. PMC: 338266. DOI: 10.1172/JCI20216. View

4.
Ren Y, Barnwell L, Alexander J, Lubin F, Adelman J, Pfaffinger P . Regulation of surface localization of the small conductance Ca2+-activated potassium channel, Sk2, through direct phosphorylation by cAMP-dependent protein kinase. J Biol Chem. 2006; 281(17):11769-79. DOI: 10.1074/jbc.M513125200. View

5.
Walter J, Alvina K, Womack M, Chevez C, Khodakhah K . Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia. Nat Neurosci. 2006; 9(3):389-97. DOI: 10.1038/nn1648. View