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[Abstract Title]. - Society for Neuroscience

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<strong>Title</strong>: In C57BL/6J (B6) mouse the GABAA receptor antagonist bicuculline blocks the increase<br />

in wakefulness and decrease in sleep caused by the GABAA receptor agonist muscimol<br />

Authors: *R. R. FLINT 1,2 , R. LYDIC 1 , H. A. BAGHDOYAN 1,2 ;<br />

1 Dept. of Anesthesiol., 2 Dept. of Pharmacol., Univ. of Michigan, Ann Arbor, MI<br />

<strong>Abstract</strong>: The pontine reticular <strong>for</strong>mation contributes to the generation of wakefulness and rapid<br />

eye movement sleep (REM) (Anesthesiology 103:1268, 2005). GABAergic transmission and<br />

GABAA receptors in the pontine reticular nucleus, oral part (PnO) promote wakefulness in both<br />

cat and rat (J Neurophysiol 82:2015, 1999; Neurosci Lett 129:95, 1991; Sleep 31:453, 2008) but<br />

no studies have systematically examined the sleep effects of GABAergic transmission in mouse<br />

PnO. Muscimol microinjected into the PnO of B6 mouse causes a concentration dependent<br />

increase in wakefulness and decrease in sleep (Soc Neurosci Abstr Prog No 631.5, 2007). As a<br />

further ef<strong>for</strong>t to determine whether the sleep and wake responses to PnO muscimol in B6 mouse<br />

are mediated by GABAA receptors, the present study is testing the hypothesis that coadministration<br />

of bicuculline with muscimol blocks the increase in wakefulness and decrease in<br />

sleep caused by muscimol. Adult, male B6 mice (n = 3) were implanted with electrodes <strong>for</strong><br />

recording the electroencephalogram and electromyogram, and with a microinjection guide tube<br />

stereotaxically aimed <strong>for</strong> the PnO. Each mouse received randomized microinjections (50 nL) of<br />

muscimol (5.71 ng; 1 mM), muscimol and bicuculline (2.5 ng; 0.1 mM), and saline (vehicle<br />

control) followed by a 4 h recording. States of wakefulness, non-REM sleep (NREM), and REM<br />

were digitized and analyzed manually in 10 s bins using Icelus Data Acquisition and Analysis<br />

software (Physiol Behav 63:67, 1998). The data were evaluated <strong>for</strong> statistical significance using<br />

ANOVA and Tukey/Kramer multiple comparisons test. All microinjection sites were<br />

histologically localized to the PnO. Muscimol caused a significant (p

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