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[Abstract Title]. - Society for Neuroscience

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in polymodal nociceptors. CA and MO induce heat hyperalgesia and mechanical allodynia in<br />

human skin, and sensitize responses of wide dynamic range (WDR)-type dorsal horn neurons to<br />

noxious skin heating in rats. We presently tested if these TRPA1 agonists induce behavioral<br />

evidence of thermal hyperalgesia and mechanical allodynia in rats. After habituation training,<br />

adult male rats underwent baseline testing of hindpaw withdrawal latency to noxious heat<br />

(Hargreaves test), or the threshold <strong>for</strong> paw withdrawal elicited by a mechanical probe from<br />

below (electronic von Frey). In separate sessions, one hindpaw received intraplantar<br />

microinjection of CA (5-20%= 398 mM-1.56 M, 10 µl) or vehicle. Thermal withdrawal latencies<br />

or mechanical thresholds <strong>for</strong> both hindpaws were then obtained 3, 15, 30, 45, 60 and 120 min<br />

post-injection. CA induced a significant, concentration-dependent reduction in thermal paw<br />

withdrawal latencies on the injected side. The peak latency change (to 61.7% of pre-injection<br />

baseline) occurred by 30 min with partial recovery at 120 min. Thermal withdrawal latencies of<br />

the uninjected (contralateral) paw did not change significantly. CA also induced a significant,<br />

concentration-dependent reduction in mechanical withdrawal threshold of the injected paw that<br />

peaked sooner (3 min) and was more profound (44.4% <strong>for</strong> 20% CA). Mechanical withdrawal<br />

thresholds <strong>for</strong> the uninjected paw were not significantly affected. A similar series is being<br />

conducted with MO. The present results are consistent with reports of allodynia and thermal<br />

hyperalgesia induced by TRPA1 agonists in humans. The thermal hyperalgesia is consistent with<br />

CA and MO enhancement of rat WDR responses to noxious heat. However, the mechanical<br />

allodynia observed presently is inconsistent with the lack of effect of CA or MO on WDR<br />

responses to graded mechanical stimuli, possibly due to different routes of administration of the<br />

TRPA1 agonists (intraplantar vs. topical).<br />

Disclosures: M.G. Tsagareli , None; N. Tsiklauri, None; G. Gurtskai, None; E. Abzianidze,<br />

None; E. Carstens, None; M. Iodi Carstens, None; K. Zanotto, None.<br />

Poster<br />

266. Pain: Psychophysics and Behavior<br />

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

Program#/Poster#: 266.10/FF4<br />

Topic: D.08.h. Psychophysics and behavior<br />

Support: NINDS P01 NS047399.<br />

<strong>Title</strong>: Capsaicin and histamine produce itch when delivered via inactivated-cowhage spicules<br />

Authors: *P. SIKAND 1 , S. G. SHIMADA 1 , B. G. GREEN 2,3 , R. H. LAMOTTE 1 ;<br />

1 2 3<br />

Dept Anesthesiol, Dept Surgery, Yale Univ. Sch. Med., New Haven, CT; Sensory Neurosci.,<br />

The John B. Pierce Lab., New Haven, CT

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