Bg. Green et H. Rentmeisterbryant, TEMPORAL CHARACTERISTICS OF CAPSAICIN DESENSITIZATION AND STIMULUS-INDUCED RECOVERY IN THE ORAL CAVITY, Physiology & behavior, 65(1), 1998, pp. 141-149
It was recently discovered that capsaicin desensitization of the tongu
e can be temporarily reversed during recurrent stimulation (''stimulus
-induced recovery,'' SIR). The effects of concentration and the tempor
al pattern of stimulation on desensitization and SIR were studied in f
our experiments. In Experiment 1, three different concentrations of ca
psaicin (3.3, 33; or 330 mu M) were delivered to the tongue in blocks
of twelve stimuli at the rate of one per minute (treatment block) foll
owed by a block of 20 exposures to 33 mu M capsaicin (test block). The
33- and 330-mu M treatments both caused significant desensitization,
but by the end of the test block recovery was substantial only for the
33-mu M condition. Experiment 2 provided a second test of the effect
of concentration while also exploring whether intermittent stimulation
was a requirement for SIR, i.e., stimuli were refreshed on the tongue
every six minutes rather than every 60 s. SIR occurred but was pronou
nced only when the concentration of the test stimulus equaled or excee
ded that of the treatment stimulus. In the third experiment we deliver
ed capsaicin in a candy formulation to examine SIR under conditions in
which stimulation was not interrupted at all. Although desensitizatio
n was evident during the first few minutes of succeeding exposures to
the candy, peak irritation was unchanged throughout nine exposures ove
r 3 days. In the final experiment, we returned to intermittent stimula
tion to examine the effect of lengthening ISI on SIR. The results show
ed that SIR remained virtually complete until ISI was lengthened to 60
s. We conclude that SIR is a robust phenomenon that is maximized by r
apid exposure to capsaicin in a concentration at least as high as that
of the desensitizing stimulus. The implications of these findings for
hypotheses about the mechanism of SIR, its function in endogenous che
monociception, and for clinical use of capsaicin as a topical analgesi
c are discussed. (C) 1998 Elsevier Science Inc.