Differential acute tolerance development to effects of nitrous oxide in humans

被引:13
作者
Zacny, JP
Cho, AM
Coalson, DW
Rupani, G
Young, CJ
Klafta, JM
Klock, PA
Apfelbaum, JL
机构
[1] Dept. Anesthesia and Critical Care, MC 4028, University of Chicago, Chicago, IL 60637
关键词
acute tolerance; nitrous oxide; analgesia; mood; psychomotor; human;
D O I
10.1016/0304-3940(96)12626-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The analgesic, subjective, and psychomotor effects of 0, 10, 20, 30, and 40% nitrous oxide in oxygen were studied in 10 volunteers to determine if acute tolerance developed differentially to;these variables. In this prospective, randomized, crossover, double-blind study, volunteers inhaled either placebo (100% oxygen) or one of the aforementioned doses of nitrous oxide for 120 min. During this period, volunteers immersed their non-dominant forearm, for 3 min, in ice-cold water at 25, 70 and 115 min from the onset of the inhalation. At other prescribed time intervals throughout the session, mood and psychomotor performance were assessed. Subjects reported less pain intensity from the cold-water stimulus and reported the pain bothered them less as a function of increasing nitrous oxide dose; in addition, this analgesia was significantly less as the inhalation period progressed (i.e., acute tolerance). Some subjective effects of nitrous oxide that could be considered hedonic in nature (elation, drug liking) also showed evidence of acute tolerance, In contrast, other subjective effects and the psychomotor-impairing effects of nitrous oxide did not change significantly during the inhalation period (i.e., no acute tolerance). The differential acute tolerance observed in this study suggests that different effects of nitrous oxide may be mediated by different neurochemical substrates.
引用
收藏
页码:73 / 76
页数:4
相关论文
共 23 条
[1]   NITROUS-OXIDE ANALGESIA - RESEMBLANCE TO OPIATE ACTION [J].
BERKOWITZ, BA ;
NGAI, SH ;
FINCK, AD .
SCIENCE, 1976, 194 (4268) :967-968
[2]  
BERKOWITZ BA, 1977, J PHARMACOL EXP THER, V203, P539
[3]   HUMAN PAIN RESPONSIVITY IN A TONIC PAIN MODEL - PSYCHOLOGICAL DETERMINANTS [J].
CHEN, ACN ;
DWORKIN, SF ;
HAUG, J ;
GEHRIG, J .
PAIN, 1989, 37 (02) :143-160
[4]  
EGER EI, 1994, ANESTHESIA, P309
[5]   ONSET OF PEAK IMPAIRMENT AFTER DIAZEPAM AND AFTER ALCOHOL [J].
ELLINWOOD, EH ;
LINNOILA, M ;
EASLER, ME ;
MOLTER, DW .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1981, 30 (04) :534-538
[6]   NITROUS-OXIDE ANXIOLYTIC EFFECT IN MICE IN THE ELEVATED PLUS-MAZE - MEDIATION BY BENZODIAZEPINE RECEPTORS [J].
EMMANOUIL, DE ;
JOHNSON, CH ;
QUOCK, RM .
PSYCHOPHARMACOLOGY, 1994, 115 (1-2) :167-172
[7]  
KALANT H, 1971, PHARMACOL REV, V23, P135
[8]  
KISSIN I, 1993, LIFE SCI, V52, P55
[9]  
KOBLIN DD, 1994, ANESTHESIA, P51
[10]   CENTRAL-NERVOUS-SYSTEM EFFECTS OF MECLIZINE AND DIMENHYDRINATE - EVIDENCE OF ACUTE TOLERANCE TO ANTIHISTAMINES [J].
MANNING, C ;
SCANDALE, L ;
MANNING, EJ ;
GENGO, FM .
JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 32 (11) :996-1002