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[Abstract Title]. - Society for Neuroscience

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decrease in REM sleep in humans between birth and puberty, and between 10-30 days in the rat.<br />

This study aimed at identifying responses of Pf cells to cholinergic input during this critical<br />

period. Whole-cell patch clamp recordings were per<strong>for</strong>med in Pf neurons in 9-20 day rat<br />

parasagittal slices in artificial CSF, and their responses to the mixed cholinergic agonist<br />

carbachol (CAR) determined. Three types of cholinergic responses were identified: inhibitory<br />

(55.34%), excitatory (31.07%) and biphasic (fast inhibitory followed by a slow excitatory,<br />

6.8%). 6.8% of cells showed no response. The proportion of CAR-inhibited Pf neurons increased<br />

with development, conversely, the proportion of excited cells decreased during this period.<br />

Experiments using cholinergic antagonists revealed that M2 receptors were responsible <strong>for</strong> all<br />

inhibitory modulation, however, the excitatory modulation required the participation of M1,<br />

nicotinic and probably M3 or M5 receptors. Analyses of the current-voltage relationship under<br />

both voltage- and current-clamp modes showed significant differences in certain intrinsic<br />

membrane properties of Pf neurons. In general, CAR-excited Pf cells demonstrated 1) smaller<br />

time constants, 2) higher density of rebound currents (normalized to membrane capacitance), 3)<br />

higher density of normalized hyperpolarization-activated inward (Ih) current, 4) lower input<br />

resistance, 5) lower action potential threshold, and 6) shorter halfwidth duration of action<br />

potentials. Some Pf cells exhibited spikelets, which are rhythmic, subthreshold depolarizing<br />

potentials thought to reflect firing in the electrically coupled neurons, and all were excited by<br />

CAR. These studies suggest that PPN modulation of Pf neurons differentially affects separate<br />

populations, including electrically coupled cells, tending to show decreased activation during the<br />

developmental decrease in REM sleep.<br />

Disclosures: M. Ye , None; E. Garcia-Rill, None.<br />

Poster<br />

285. Sleep: Molecular, Cellular and Pharmacology I<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 285.20/QQ36<br />

Topic: E.08.c. Sleep: Molecular, cellular, and pharmacology<br />

Support: NIH Grant MH57434<br />

VA Merit Review<br />

<strong>Title</strong>: GABAA receptor subunits implicated in REM sleep control in pontine reticular <strong>for</strong>mation<br />

of rat

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