Administration of opiate agonists and antagonists has been shown to in
crease and decrease alcohol consumption, respectively. Because opioids
can affect gastric emptying and decrease intestinal motility, the pre
sent experiments were done to determine whether changes in alcohol con
sumption following opioid administration might be due to opioid-induce
d changes in the pharmacokinetics of alcohol. rn experiment 1, morphin
e in doses ranging from 1.5 to 4.5 mg/kg dose dependently decreased th
e absorption of alcohol induced by oral intubation (I g/kg) and reduce
d peak blood alcohol levels (BALs). Naltrexone in doses ranging from 1
.5 to 4.5 mg/kg produced a small, but significant, reduction in the ab
sorption of alcohol, but the effects were not dose related. Similar ef
fects of morphine and naltrexone on alcohol absorption were observed i
n rats infused with alcohol (1 g/kg) through an implanted intragastric
cannula. The effects of morphine on alcohol absorption were observed
whether alcohol levels were determined from tail vein or arterial bloo
d samples or from brain samples. The effects of morphine on alcohol ab
sorption were not blocked by pretreatment with methyl-naltrexone. Howe
ver, the peripherally acting opioid agonist loperamide reduced BALs in
a manner similar to morphine. These studies indicate that although op
iate agonists and antagonists modify alcohol absorption to different e
xtents, their effects on BALs are not a sufficient condition to induce
changes in alcohol consumption. (C) 1997 Elsevier Science Inc.