To assess whether stoichiometric manipulation of morphine (M) metaboli
sm can enhance analgesia or slow the development of M tolerance we co-
administered M-3- glucuronide (M3G) during single or repeated doses of
morphine in rats. Although M3G itself lacked analgesic activity, co-i
njection of M3G with M increased and prolonged analgesia beyond that s
een with M. In addition, diminution of the acute analgesic effect of M
after 3 once-daily doses of M did not occur after daily co-injection
of M3G and M. Thus the traditional view that tolerance to the effects
of M is due solely to effects mediated through opioid receptors must b
e broadened to include the contributions of enzyme induction or stoich
iometric equilibration of M3G in this process.