INHIBITORY EFFECTS EVOKED FROM BOTH THE LATERAL AND VENTROLATERAL PERIAQUEDUCTAL GREY ARE SELECTIVE FOR THE NOCICEPTIVE RESPONSES OF RAT DORSAL HORN NEURONS
Aj. Waters et Bm. Lumb, INHIBITORY EFFECTS EVOKED FROM BOTH THE LATERAL AND VENTROLATERAL PERIAQUEDUCTAL GREY ARE SELECTIVE FOR THE NOCICEPTIVE RESPONSES OF RAT DORSAL HORN NEURONS, Brain research, 752(1-2), 1997, pp. 239-249
In rats anaesthetized with alphaxalone/alphadolone a comparative study
was made of the inhibitory effects on dorsal horn neurones evoked by
chemical stimulation at identified presser and depressor sites in the
lateral and ventrolateral periaqueductal grey (PAG). Stimulating micro
pipettes were inserted stereotaxically into the lateral or ventrolater
al PAG at sites where microinjection of DL-homocysteic acid (DLH) evok
ed increases or decreases respectively in mean arterial blood pressure
. The effects of DLH microinjection at these sites were tested against
the responses of dorsal horn neurones to noxious and innocuous stimul
i applied to their cutaneous receptive fields. Single unit extracellul
ar recordings were made from 15 Class 1 (low-threshold) and 37 Class 2
(wide dynamic range) dorsal horn neurones in laminae II-VI of the low
er lumbar spinal cord. The responses of Class 1 neurones to innocuous
prodding of their receptive fields were unaffected by neuronal activat
ion in either the lateral or ventrolateral PAG. The nociceptive (noxio
us pinch/heat) responses of most Class 2 neurones were strongly inhibi
ted by chemical stimulation in either sector of the PAG. The low thres
hold (prod) responses of the same neurones were generally unaffected o
r only weakly inhibited by identical stimulation, regardless of stimul
ation site. No significant differences were found between the effects
of lateral vs. ventrolateral PAG stimulation on the responses of dorsa
l horn neurones. These results do not support the view that dorsal hor
n neurones may be inhibited with different selectivities by hyper- and
hypotensive regions of the PAG. (C) 1997 Elsevier Science B.V.