Literature DB >> 24582665

A mutation causing increased KATP channel activity leads to reduced anxiety in mice.

Carolina Lahmann1, Rebecca H Clark1, Michaela Iberl1, Frances M Ashcroft2.   

Abstract

Activating mutations in the Kir6.2 (KCNJ11) subunit of the ATP-sensitive potassium channel cause neonatal diabetes. Many patients also suffer from neurological complications. By using mice carrying a human Kir6.2 mutation (Val(59) to Met(59); nV59M mice) targeted to neurones, we show that these mutations also result in altered anxiety behaviour. The light/dark box, successive alleys and elevated plus maze tasks revealed that nV59M mice have reduced anxiety related responses. Additionally, nV59M mice displayed enhanced basal locomotor activity and exploratory behaviour, as assessed by the low anxiety open-field test. These findings, in combination with previously reported hyperactivity of nV59M mice, appear to correlate with the increased impulsivity and inattentiveness reported in iDEND/DEND patients.
Copyright © 2014. Published by Elsevier Inc.

Entities:  

Keywords:  Anxiety; Hyperactivity; K(ATP) channels; Neonatal diabetes

Mesh:

Substances:

Year:  2014        PMID: 24582665      PMCID: PMC5576528          DOI: 10.1016/j.physbeh.2014.02.031

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  40 in total

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8.  Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.

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3.  Psychiatric morbidity in children with KCNJ11 neonatal diabetes.

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Review 4.  Neonatal Diabetes and the KATP Channel: From Mutation to Therapy.

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  6 in total

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