TY - JOUR
T1 - Antinociceptive, subjective and behavioral effects of smoked marijuana in humans
AU - Greenwald, Mark K.
AU - Stitzer, Maxine L.
N1 - Funding Information:
This research was supported by US Public Health Service Research Grant DA-05880 and Research Training Grant DA-07209 from the National Institute on Drug Abuse. The authors are grateful to David Ginn for medical screening, Rolley E. Johnson for drug preparation, John Yingling for technical assistance, Paula Pakulski for data collection, Valerie Schindler of RTI for analyses of plasma THC, and Mike DiMarino for consultation in statistical analysis.
PY - 2000/6/1
Y1 - 2000/6/1
N2 - The purpose of this study was to determine whether marijuana produced dose-dependent antinociception in humans and, if so, whether endogenous opiates modulate this effect. A total of five male regular marijuana users participated in three test sessions during which they smoked cigarettes containing 0% (placebo) and 3.55% Δ9-tetrahydrocannabinol (Δ9-THC) (active). Each of four controlled smoking bouts per session, spaced at 40-min intervals, consisted of nine puffs from active and placebo cigarettes (three cigarettes, three puffs per cigarette, one puff per min). During successive bouts, participants smoked 0, 3, 6 and 9 (0, 3, 9 and 18 cumulative) puffs from active marijuana cigarettes, with the remainder of puffs from placebo cigarettes. Test sessions were identical, except for naltrexone 0, 50 or 200 mg p.o. (randomized, double-blind) administration 1 h before the first smoking bout on the different days. Before smoking, between smoking bouts and postsmoking, participants completed an assessment battery that included antinociceptive (finger withdrawal from radiant heat stimulation), biological, subjective, observer-rated signs and performance measures. Marijuana produced significant dose-dependent antinociception (increased finger withdrawal latency) and biobehavioral effects. Naltrexone did not significantly influence marijuana dose-effect curves, suggesting no role of endogenous opiates in marijuana-induced antinociception under these conditions. (C) 2000 Elsevier Science Ireland Ltd.
AB - The purpose of this study was to determine whether marijuana produced dose-dependent antinociception in humans and, if so, whether endogenous opiates modulate this effect. A total of five male regular marijuana users participated in three test sessions during which they smoked cigarettes containing 0% (placebo) and 3.55% Δ9-tetrahydrocannabinol (Δ9-THC) (active). Each of four controlled smoking bouts per session, spaced at 40-min intervals, consisted of nine puffs from active and placebo cigarettes (three cigarettes, three puffs per cigarette, one puff per min). During successive bouts, participants smoked 0, 3, 6 and 9 (0, 3, 9 and 18 cumulative) puffs from active marijuana cigarettes, with the remainder of puffs from placebo cigarettes. Test sessions were identical, except for naltrexone 0, 50 or 200 mg p.o. (randomized, double-blind) administration 1 h before the first smoking bout on the different days. Before smoking, between smoking bouts and postsmoking, participants completed an assessment battery that included antinociceptive (finger withdrawal from radiant heat stimulation), biological, subjective, observer-rated signs and performance measures. Marijuana produced significant dose-dependent antinociception (increased finger withdrawal latency) and biobehavioral effects. Naltrexone did not significantly influence marijuana dose-effect curves, suggesting no role of endogenous opiates in marijuana-induced antinociception under these conditions. (C) 2000 Elsevier Science Ireland Ltd.
KW - Analgesia
KW - Antinociception
KW - Endogenous opioids
KW - Heart rate
KW - Humans
KW - Marijuana smoking
KW - Naltrexone
KW - Performance
KW - Subjective effects
KW - Δ- Tetrahydrocannabinol
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U2 - 10.1016/S0376-8716(99)00128-3
DO - 10.1016/S0376-8716(99)00128-3
M3 - Article
C2 - 10812286
AN - SCOPUS:0034212169
SN - 0376-8716
VL - 59
SP - 261
EP - 275
JO - Drug and alcohol dependence
JF - Drug and alcohol dependence
IS - 3
ER -