GABAergic modulation of descending inhibitory systems from the rostral ventromedial medulla (RVM). Dose-response analysis of nociception and neurological deficits

Citation
Ak. Gilbert et Kbj. Franklin, GABAergic modulation of descending inhibitory systems from the rostral ventromedial medulla (RVM). Dose-response analysis of nociception and neurological deficits, PAIN, 90(1-2), 2001, pp. 25-36
Citations number
61
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
PAIN
ISSN journal
03043959 → ACNP
Volume
90
Issue
1-2
Year of publication
2001
Pages
25 - 36
Database
ISI
SICI code
0304-3959(20010201)90:1-2<25:GMODIS>2.0.ZU;2-5
Abstract
We have examined the effects of muscimol and bicuculline microinjected in t he rostral ventromedial medulla (RVM) on motor function and on nociception in three pain tests. In Exp. I microinjection of muscimol (6.25-400 ng in 1 mul) in the RVM dose-dependently decreased pain threshold of rats and the ED50 for muscimol was the same in both the hot plate and tail immersion pai n tests. In the hot plate test, but not in the tail immersion test, paw wit hdrawal latencies increased again with high doses of muscimol (75-400 ng). High doses also produced catalepsy. Exp. 2 examined the effects of muscimol (50 ng) and bicuculline (50 ng) over a range of formalin concentrations (0 .25-4%) in the formalin test. Muscimol increased responsiveness to formalin and reduced the slope of the formalin dose-response relation. Bicuculline decreased responses to formalin and reduced the slope of the formalin dose- response relation. It is suggested that RVM cells with inhibitory projectio ns to the dorsal horn are not subject to strong GABAergic influence under m ild noxious stimulation. RVM cells are thus active, and spinal dorsal horn relay neurons are inhibited. On the other hand, intense noxious peripheral stimulation may stimulate the release of GABA onto RVM cells, which in turn shuts off descending inhibitory fibers to allow transmission of nociceptor input through the dorsal hem. (C) 2001 International Association for the S tudy of Pain. Published by Elsevier Science B.V. All rights reserved.