Inhibition of protein kinase C, but not of protein kinase A, blocks the development of acute antinociceptive tolerance to an intrathecally administered mu-opioid receptor agonist in the mouse.

Abstract:

:A specific protein kinase C inhibitor, calphostin C, which injected alone had no effect on the antinociception induced by intrathecal (i.t.) administration of a selective mu-opioid receptor agonist, [D-Ala2,NMePhe4,Gly(ol)5]enkephalin (DAMGO), dose-dependently attenuated the development of acute tolerance to the i.t. DAMGO-induced antinociception in male ICR mice. On the other hand, a selective protein kinase A inhibitor, KT5720, did not have any effect on the development of acute tolerance to DAMGO antinociception. These findings suggest that protein kinase C, but not protein kinase A, plays an important role in the development of acute tolerance to the mu-opioid receptor agonist-induced antinociception.

journal_name

Eur J Pharmacol

authors

Narita M,Narita M,Mizoguchi H,Tseng LF

doi

10.1016/0014-2999(95)00322-c

subject

Has Abstract

pub_date

1995-07-04 00:00:00

pages

R1-3

issue

2

eissn

0014-2999

issn

1879-0712

pii

0014-2999(95)00322-C

journal_volume

280

pub_type

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