Sleep in <it>Kcna2 </it>knockout mice

<p>Abstract</p> <p>Background</p> <p><it>Shaker </it>codes for a <it>Drosophila </it>voltage-dependent potassium channel. Flies carrying <it>Shaker </it>null or hypomorphic mutations sleep 3–4 h/day instead of 8–14 h/day as their wild...

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Main Authors: Messing Albee, Chiu Shing-Yan, Southard Teresa, Vyazovskiy Vladyslav, Douglas Christopher L, Tononi Giulio, Cirelli Chiara
Format: Article
Language:English
Published: BMC 2007-10-01
Series:BMC Biology
Online Access:http://www.biomedcentral.com/1741-7007/5/42
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spelling doaj-bba66559df4d4c7583309aebb7bbf20d2020-11-25T01:32:30ZengBMCBMC Biology1741-70072007-10-01514210.1186/1741-7007-5-42Sleep in <it>Kcna2 </it>knockout miceMessing AlbeeChiu Shing-YanSouthard TeresaVyazovskiy VladyslavDouglas Christopher LTononi GiulioCirelli Chiara<p>Abstract</p> <p>Background</p> <p><it>Shaker </it>codes for a <it>Drosophila </it>voltage-dependent potassium channel. Flies carrying <it>Shaker </it>null or hypomorphic mutations sleep 3–4 h/day instead of 8–14 h/day as their wild-type siblings do. Shaker-like channels are conserved across species but it is unknown whether they affect sleep in mammals. To address this issue, we studied sleep in <it>Kcna2 </it>knockout (KO) mice. <it>Kcna2 </it>codes for Kv1.2, the alpha subunit of a Shaker-like voltage-dependent potassium channel with high expression in the mammalian thalamocortical system.</p> <p>Results</p> <p>Continuous (24 h) electroencephalograph (EEG), electromyogram (EMG), and video recordings were used to measure sleep and waking in <it>Kcna2 </it>KO, heterozygous (HZ) and wild-type (WT) pups (P17) and HZ and WT adult mice (P67). Sleep stages were scored visually based on 4-s epochs. EEG power spectra (0–20 Hz) were calculated on consecutive 4-s epochs. KO pups die by P28 due to generalized seizures. At P17 seizures are either absent or very rare in KO pups (< 1% of the 24-h recording time), and abnormal EEG activity is only present during the seizure. KO pups have significantly less non-rapid eye movement (NREM) sleep (-23%) and significantly more waking (+21%) than HZ and WT siblings with no change in rapid eye movement (REM) sleep time. The decrease in NREM sleep is due to an increase in the number of waking episodes, with no change in number or duration of sleep episodes. Sleep patterns, daily amounts of sleep and waking, and the response to 6 h sleep deprivation are similar in HZ and WT adult mice.</p> <p>Conclusion</p> <p>Kv1.2, a mammalian homologue of Shaker, regulates neuronal excitability and affects NREM sleep.</p> http://www.biomedcentral.com/1741-7007/5/42
collection DOAJ
language English
format Article
sources DOAJ
author Messing Albee
Chiu Shing-Yan
Southard Teresa
Vyazovskiy Vladyslav
Douglas Christopher L
Tononi Giulio
Cirelli Chiara
spellingShingle Messing Albee
Chiu Shing-Yan
Southard Teresa
Vyazovskiy Vladyslav
Douglas Christopher L
Tononi Giulio
Cirelli Chiara
Sleep in <it>Kcna2 </it>knockout mice
BMC Biology
author_facet Messing Albee
Chiu Shing-Yan
Southard Teresa
Vyazovskiy Vladyslav
Douglas Christopher L
Tononi Giulio
Cirelli Chiara
author_sort Messing Albee
title Sleep in <it>Kcna2 </it>knockout mice
title_short Sleep in <it>Kcna2 </it>knockout mice
title_full Sleep in <it>Kcna2 </it>knockout mice
title_fullStr Sleep in <it>Kcna2 </it>knockout mice
title_full_unstemmed Sleep in <it>Kcna2 </it>knockout mice
title_sort sleep in <it>kcna2 </it>knockout mice
publisher BMC
series BMC Biology
issn 1741-7007
publishDate 2007-10-01
description <p>Abstract</p> <p>Background</p> <p><it>Shaker </it>codes for a <it>Drosophila </it>voltage-dependent potassium channel. Flies carrying <it>Shaker </it>null or hypomorphic mutations sleep 3–4 h/day instead of 8–14 h/day as their wild-type siblings do. Shaker-like channels are conserved across species but it is unknown whether they affect sleep in mammals. To address this issue, we studied sleep in <it>Kcna2 </it>knockout (KO) mice. <it>Kcna2 </it>codes for Kv1.2, the alpha subunit of a Shaker-like voltage-dependent potassium channel with high expression in the mammalian thalamocortical system.</p> <p>Results</p> <p>Continuous (24 h) electroencephalograph (EEG), electromyogram (EMG), and video recordings were used to measure sleep and waking in <it>Kcna2 </it>KO, heterozygous (HZ) and wild-type (WT) pups (P17) and HZ and WT adult mice (P67). Sleep stages were scored visually based on 4-s epochs. EEG power spectra (0–20 Hz) were calculated on consecutive 4-s epochs. KO pups die by P28 due to generalized seizures. At P17 seizures are either absent or very rare in KO pups (< 1% of the 24-h recording time), and abnormal EEG activity is only present during the seizure. KO pups have significantly less non-rapid eye movement (NREM) sleep (-23%) and significantly more waking (+21%) than HZ and WT siblings with no change in rapid eye movement (REM) sleep time. The decrease in NREM sleep is due to an increase in the number of waking episodes, with no change in number or duration of sleep episodes. Sleep patterns, daily amounts of sleep and waking, and the response to 6 h sleep deprivation are similar in HZ and WT adult mice.</p> <p>Conclusion</p> <p>Kv1.2, a mammalian homologue of Shaker, regulates neuronal excitability and affects NREM sleep.</p>
url http://www.biomedcentral.com/1741-7007/5/42
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