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[Abstract Title]. - Society for Neuroscience

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<strong>Society</strong> <strong>for</strong> <strong>Neuroscience</strong> <strong>Abstract</strong>s, 2007). In that work, we assumed the classical and<br />

modulatory inputs were co-distributed in the dendrites. In the current work, we discarded this<br />

assumption based on recent evidence from modeling and experimental studies of layer 5<br />

pyramidal cells showing that nonlinear "summation" of two inputs to the basal dendrites depends<br />

strongly on their absolute and relative locations (Behabadi et al., <strong>Society</strong> <strong>for</strong> <strong>Neuroscience</strong><br />

<strong>Abstract</strong>s, 2007). We found that "scaling competence" was significantly improved when the<br />

modulatory input was delivered to the proximal portion of the dendritic branch. In that case, an<br />

accurate and repeatable multiplicative scaling of the classical response could be achieved over<br />

multiple octaves of input and output dynamic range. This finding supports the proposal of<br />

Behabadi et al. (2007) that attentional, contextual and other scaling inputs may target more<br />

proximal regions of neocortical basal dendrites. This work was supported by NIMH grant<br />

MH065918-01.<br />

Disclosures: M. Jadi , None; B.W. Mel, None.<br />

Poster<br />

240. Intrinsic Membrane Properties: Modulation of Neuronal Firing Properties by Inputs<br />

and Activity<br />

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

Program#/Poster#: 240.2/E24<br />

Topic: B.10.b. Modulation of neuronal firing properties<br />

Support: NIH grant NS045248<br />

<strong>Title</strong>: Electrophysiological characterization of sympathetic preganglionic neurons in HB9-GFP<br />

transgenic mice<br />

Authors: *A. L. ZIMMERMAN 1 , S. HOCHMAN 1,2 ;<br />

1 Biomed. Engin., Georgia Tech/Emory Univ., Atlanta, GA; 2 Physiol., Emory Univ., Atlanta, GA<br />

<strong>Abstract</strong>: Spinal cord sympathetic preganglionic neurons (SPNs) are the final common output of<br />

the sympathetic nervous system. Intracellular recordings have characterized several<br />

electrophysiological properties of SPNs in rat and cat, and here we extend these studies to<br />

mouse. We undertook whole-cell recordings of fluorescently-identified GFP + -HB9 SPNs in the<br />

intermediolateral column in young mice using horizontal and transverse slices.<br />

Preliminary results using a combination of current and voltage step protocols suggest that the<br />

active and passive membrane properties are comparable to those reported in neonatal rat. Action<br />

potentials exhibited the characteristic inflection during repolarization and prolonged<br />

afterhyperpolarization typical of SPNs (Pickering et al, <strong>Neuroscience</strong> Letters, 1991. 130: 237-

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