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Abstracts - Association for Chemoreception Sciences

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innervated by the trigeminal nerve and when stimulated evoke<br />

protective airway reflexes such as sneezing, apnea and local<br />

inflammation (Tizzano et al., 2010; AChemS 2012). We have<br />

begun investigating SCCs in human sinonasal epithelium and<br />

their clinical implications. Previously we and others reported<br />

that cells resembling SCCs occur in human biopsy material<br />

near the vestige of the vomeronasal organ (Braun et al., 2011)<br />

as well as within the turbinates (Barham et al 2013; AChemS<br />

2012). However, the exact distribution and abundance of SCCs<br />

in humans is unknown. To map the distribution of SCCs, we<br />

obtained middle and inferior turbinate mucosa from human<br />

patients that were free of sinonasal disease, but were undergoing<br />

surgical procedures requiring removal of this tissue. Whole<br />

mount tissue was stained with antibodies against TRPM5 and<br />

villin, which is expressed at the apex of microvillous, but not<br />

ciliated, epithelial cells. TRPM5-immunoreactive cells were<br />

scattered heterogeneously in the sinonasal tissue. The cells were<br />

most abundant on the ridges of the turbinates and less abundant<br />

on the lateral margins. Many TRPM5 immunoreactive cells<br />

also labeled with the villin antibody, suggesting that TRPM5 is<br />

present in microvillous but not ciliated cells of the epithelium.<br />

Studies are in progress to determine if disease state alters the<br />

distribution or abundance of these cells and whether SCCs in<br />

humans are innervated by the trigeminal nerve, as in rodents.<br />

Acknowledgements: R01 DC009820 (TEF and SCK) P30<br />

DC04657 (to D. Restrepo)<br />

#P116 POSTER SESSION III:<br />

TRIGEMINAL; HUMAN OLFACTORY<br />

PSYCHOPHYSICS; TASTE PERIPHERY<br />

Responses to change in oral temperature by neurons in the<br />

mouse medullary dorsal horn and nucleus of the solitary tract<br />

Yi Kang, Christian Lemon<br />

St. Louis University St. Louis, MO, USA<br />

Psychophysical data show the temperature of sapid solutions<br />

influences flavor. However, it is not entirely clear how central<br />

neural circuits <strong>for</strong> oral sensation encode temperature input.<br />

The trigeminal subnucleus caudalis (Vc) is a brainstem somatic<br />

relay receiving temperature signals from the oro-facial region<br />

and implicated <strong>for</strong> oral thermosensation. Additionally, the<br />

solitary tract nucleus (NTS), the first central taste relay, also<br />

receives thermal input from the mouth. Here we compared<br />

neural responses of NTS and Vc to intraoral thermal stimulation<br />

in anesthetized mice to assess the contribution of activity in<br />

these structures to oral temperature responses in brain stem.<br />

Extracellular single-unit activities of NTS thermo-gustatory<br />

neurons and Vc thermo-somatic cells were recorded after<br />

application of different temperature stimuli to tongue, including<br />

cold (5 and 10 °C), cool/ambient (17 and 23 °C), and warm/<br />

hot (30, 45, and 48 °C). Temperature stimulation was achieved<br />

rapidly by oral flow of thermally varied water. Seventytwo<br />

neurons were obtained; 34 from Vc and 38 from NTS.<br />

Analyses revealed significant differences between NTS and<br />

Vc in responses to thermal stimuli [F(1, 70) = 5.80, P ATP > acetylcholine<br />

(ACh)). Because of the low percentage of ACh-sensitive MCs<br />

and SCCs, ACh released from these cells may play a role in<br />

paracrine regulation to influence neighboring cells. Using Ca 2+<br />

imaging on intact epithelial preparations, we found that AChinduced<br />

increases in intracellular Ca 2+ levels in epithelial cells<br />

surrounding the MCs and SCCs were inhibited by muscarinic<br />

ACh antagonist atropine. Our results suggest that MCs and<br />

SCCs share common physiological roles in sensing chemical<br />

stimuli and may release ACh to influence surrounding nonsensory<br />

cells via paracrine mechanism. Because MCs lack<br />

afferent innervation, this cholinergic paracrine regulation could<br />

be especially important <strong>for</strong> chemoreception-mediated regulation<br />

of MOE activities. Acknowledgements: Supported by research<br />

grants NIH/NIDCD 009269, 012831 and ARRA administrative<br />

supplement to WL<br />

POSTER PRESENTATIONS<br />

<strong>Abstracts</strong> are printed as submitted by the author(s).<br />

73

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