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[Abstract Title]. - Society for Neuroscience

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Poster<br />

269. Pain: Visceral Pain II<br />

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

Program#/Poster#: 269.6/GG21<br />

Topic: D.08.n. Visceral pain<br />

Support: NHMRC Grant 400053<br />

<strong>Title</strong>: Vagal afferent neurons innervating the adult mouse jejunum differ from spinal afferents in<br />

their neurochemical and structural features<br />

Authors: L. L. TAN 1 , J. C. BORNSTEIN 1 , *C. R. ANDERSON 2 ;<br />

1 Dept Physiol., 2 Dept Anat. & Cell Biol, Univ. Of Melbourne, Parkville 3010, Australia<br />

<strong>Abstract</strong>: Sensory in<strong>for</strong>mation from the gastrointestinal tract is conveyed to the central nervous<br />

system by primary afferent fibres originating from the vagal sensory (nodose ganglion) and<br />

dorsal root ganglion (DRG) neurons. We have recently shown that the cell bodies of spinal<br />

afferents projecting to the jejunum of the adult mouse are medium-sized and are neurochemically<br />

defined by combinations of transient receptor potential vanilloid type 1 (TRPV1), nitric oxide<br />

synthase (NOS), calcitonin-gene related peptide (CGRP) and substance P (SP). It is unknown if<br />

vagal afferent neurons innervating the small intestine have similar characteristics. Multiple subserosal<br />

injections (each 0.1 κL) of cholera toxin B (CTB) were made into the jejunum of<br />

anesthetized C57Bl/6 mice (ketamine 100 mg/kg and xylazine 10 mg/kg; n=13). A thin layer of<br />

cyanoacrylate glue was applied over each injection site to prevent dye leakage. Multi-labelling<br />

immunofluorescence of CTB-labelled nodose cells with antibodies specific <strong>for</strong> TRPV1, CGRP,<br />

SP, NOS as well as binding to isolectin B4 (IB4) were per<strong>for</strong>med 7 days post-operative. Soma<br />

sizes were assessed by measuring the cross-sectional areas of nucleated cell profiles using Image<br />

J software (NIH). CTB-labelled nodose ganglion neurons supplying the jejunum are significantly<br />

smaller than DRG neurons supplying the same region (median areas: 295 vs 540κm 2<br />

respectively; p

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