ANTINOCICEPTION PRODUCED BY MICROINJECTION OF MORPHINE IN THE RAT PERIAQUEDUCTAL GRAY IS ENHANCED IN THE FOOT, BUT NOT THE TAIL, BY INTRATHECAL INJECTION OF ALPHA-1-ADRENOCEPTOR ANTAGONISTS
F. Fang et Hk. Proudfit, ANTINOCICEPTION PRODUCED BY MICROINJECTION OF MORPHINE IN THE RAT PERIAQUEDUCTAL GRAY IS ENHANCED IN THE FOOT, BUT NOT THE TAIL, BY INTRATHECAL INJECTION OF ALPHA-1-ADRENOCEPTOR ANTAGONISTS, Brain research, 790(1-2), 1998, pp. 14-24
Antinociception produced by microinjection of morphine in the ventrola
teral periaqueductal gray is mediated in part by alpha(2)-adrenoceptor
s in the spinal cord dorsal horn. However, several recent reports demo
nstrate that microinjection of morphine in the ventrolateral periaqued
uctal gray inhibits nociceptive responses to noxious heating of the ta
il by activating descending neuronal systems that are different from t
hose that inhibit the nociceptive responses to noxious heating of the
feet. More specifically, alpha(2)-adrenoceptors appear to mediate the
antinociception produced by morphine using the tail-flick test, but no
t that using the foot-withdrawal or hot-plate tests. The present study
extended these findings and determined the role of alpha(1)-adrenocep
tors in mediating the antinociceptive effects of morphine microinjecte
d into the ventrolateral periaqueductal gray using both the foot-withd
rawal and the tail-flick responses to noxious radiant heating in light
ly anesthetized rats. Intrathecal injection of selective antagonists w
as used to determine whether the antinociceptive effects of morphine w
ere modulated by alpha(1)-adrenoceptors. Injection of the selective al
pha(1)-adrenoceptor antagonists prazosin or WB4101 potentiated the inc
rease in the foot-withdrawal response latency produced by microinjecti
on of morphine in the ventrolateral periaqueductal gray. In contrast,
either prazosin or WB4101 partially reversed the increase in the tail-
flick response latency produced by morphine. These results indicate th
at microinjection of morphine in the ventrolateral periaqueductal gray
modulates nociceptive responses to noxious heating of the feet by act
ivating descending neuronal systems that are different from those that
inhibit the nociceptive responses to noxious heating of the tail. Mor
e specifically, alpha(1)-adrenoceptors mediate a pro-nociceptive actio
n of morphine using the foot-withdrawal response, but in contrast, alp
ha(1)-adrenoceptors appear to mediate part of the antinociceptive effe
ct of morphine determined using the tail-flick test. (C) 1998 Elsevier
Science B.V.