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SLEEP 2011 Abstract Supplement

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A. Basic Science IV. Neurobiology<br />

habituation, activity of single neurons (3:1 signal: noise) was recorded in<br />

freely-behaving rats over multiple episodes of sleep-wake.<br />

Results: Eleven neurons in the PZ region, all of which showed either<br />

tonic/sustained activity or phasic/burst activity during sleep and firing<br />

rate higher than wake and REM sleep. This indicates that the PZ contains<br />

high density of sleep active neurons. The firing frequency for these<br />

neurons ranged from 0.2 to 2.3 Hz.<br />

Conclusion: This study for first time has identified a sleep active area in<br />

parafacial zone of the caudal brain stem.<br />

Support (If Any): NS062727 and NS061841<br />

0095<br />

BOOSTING SK2-TYPE K + CHANNEL ACTIVITY IN THE<br />

NUCLEUS RETICULARIS THALAMI CONSOLIDATES<br />

NREM <strong>SLEEP</strong><br />

Wimmer RD 1,2 , Bond CT 3 , Adelman JP 3 , Franken P 2 , Lüthi A 1<br />

1<br />

Department of Cell Biology and Morphology, University of Lausanne,<br />

Lausanne, Switzerland, 2 Center for Integrative Genomics, University<br />

of Lausanne, Lausanne, Switzerland, 3 Vollum Institute, Oregon Health<br />

and Science University, Portland, OR, USA<br />

Introduction: The nucleus reticularis thalami (nRT) is known for its<br />

pacemaking function during oscillatory brain activity related to non-rapid-eye-movement<br />

sleep (NREMS). Small conductance type-2 (SK2) K +<br />

channels are crucial for oscillatory bursting in nRT neurons and a loss of<br />

SK2 channels increased NREMS fragmentation and reduced EEG delta<br />

(1-4Hz) power during NREMS. We tested whether over-expressing SK2<br />

channels (SK2-OE) potentiates nRT oscillatory capacity and stabilizes<br />

NREMS.<br />

Methods: Whole-cell patch-clamp recordings in horizontal brain slices<br />

(300μm) were obtained from nRT and thalamocortical (TC) neurons of<br />

SK2-OE and wild-type (WT) littermates (C57Bl/6J background, P25-<br />

34). At P56-63, mice were implanted with EEG and EMG electrodes.<br />

After 8-12 days of recovery, spontaneous sleep and waking behavior<br />

was recorded for 48h.<br />

Results: SK2-current amplitudes were >2-fold greater and oscillatory<br />

bursting was strengthened in SK2-OE compared to WT nRT cells<br />

(p0.05). However, SK2 channel over-expression reduced action<br />

potential (AP) number per nRT burst and attenuated the efficacy<br />

of unitary burst-induced inhibitory postsynaptic currents in rebound AP<br />

generation in TC neurons (p

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