Korean J Physiol Pharmacol.
2001 Feb;5(1):71-78.
DAMGO, a micro-opioid agonist and cholecystokinin-octapeptide have dual
modulatory effects on capsaicin-activated current in rat dorsal root
ganglion neurons
- Affiliations
-
- 1Department of Physiology and Biophysics, Seoul National University
College of Medicine, 28 Yongon-dong, Chongno-gu, Seoul, South Korea.
Kimjun@plaza.snu.ac.kr
Abstract
- Capsaicin, a pungent ingredient of hot pepper, elicits an intense
burning pain when applied cutaneously and intradermally. Activation of
capsaicin-gated channel in. C-type dorsal root ganglion (DRG) neurons
produces nonselective cationic currents. Although electrophysiological
and biochemical properties of capsaicin-activated current (ICAP) were
studied, the regulatory mechanism and intracellular signaling pathway
are still unclear. In the present study, we investigated the
modulations of ICAP by DAMGO (micro-opioid agonist) and cholecystokinin
octapeptide (CCK-8). In 18 out of 86 cells, the amplitude of ICAP was
significantly increased by DAMGO and completely reversed after washout,
while ICAP was decreased by DAMGO in 25 cells. In 43 cells, DAMGO had
no effect on ICAP. Mean action potential duration was significantly
different between 'increased-by-DAMGO' group and 'decreased-by-DAMGO'
group. Mean amplitudes of IH were not significantly different between
both groups. CCK-8 reversibly enhanced the amplitude of ICAP (5/13).
DAMGO also increased ICAP amplitude significantly in the same cells.
The amplitude of ICAP was increased in additive manner by combined
applications of DAMGO and CCK-8 in these cells. These results suggest
that DAMGO and CCK-8 can either increase or decrease ICAP presumably
depending on the subtypes of DRG cells and classified by
electrophysiological properties.