Associative and non-associative fentanyl tolerance in the rat: evaluation of cross tolerance with mu-and kappa-specific opioids

被引:4
作者
Carter, BL [1 ]
Tiffany, ST [1 ]
Conklin, CA [1 ]
机构
[1] Purdue Univ, W Lafayette, IN 47907 USA
关键词
fentanyl tolerance; cross tolerance; classical conditioning; associative; non-associative; morphine; U50,488H;
D O I
10.1007/s002130050067
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Associative tolerance to the analgesic effects of morphine is most pronounced when morphine is paired with a distinctive context at a long interdose interval (IDI). In contrast, morphine administered at a short IDI promotes the development of non-associative tolerance and disrupts the acquisition of associative tolerance. The impact of LDI an the development of associative tolerance to opioids other than morphine has not been investigated previously. Objectives: This research examined associative and non-associative tolerance to the analgesic effects of fentanyl in rats. Cross tolerance for these two forms of tolerance with morphine (mu-receptor agonist) and U50,488H (kappa-receptor agonist) analgesia was also investigated. Methods: Animals were given eight fentanyl injections (0.10 mg/kg) paired or unpaired with a distinctive context at either a 3-h (short) or 96-h (long) IDI. Subjects were then tested for tolerance in the distinctive context using the tail-flick procedure and dose-response curve methodology. Results: At the short IDI, animals eveloped non-associative tolerance to fentanyl that was receptor specific, i.e., cross tolerant with morphine analgesia but not with U50.488H analgesia. At the long LDI, fentanyl-tested animals displayed tolerance that appeared to be controlled primarily by associative processes. This associative form of tolerance was also receptor specific, displaying cross tolerance with morphine but not with U50,388H. Conclusions: The impact of IDI on the development of non-associative and associative fentanyl tolerance is consistent with findings obtained with morphine showing that conditions conducive to the development of non-associative tolerance disrupt the acquisition of associative tolerance. The cross-tolerance data, however, did not parallel previous research examining the cross-tolerance profiles of associative and non-associative morphine tolerance.
引用
收藏
页码:384 / 392
页数:9
相关论文
共 39 条
[1]  
ADAMS JU, 1990, J PHARMACOL EXP THER, V255, P1027
[3]  
[Anonymous], 1975, APPL MULTIPLE CORREL
[4]  
[Anonymous], 1989, Psychoactive Drugs: tolerance and sensitization. Eds
[5]   MORPHINE-TOLERANCE AS HABITUATION [J].
BAKER, TB ;
TIFFANY, ST .
PSYCHOLOGICAL REVIEW, 1985, 92 (01) :78-108
[6]  
BHARGAVA HN, 1989, J PHARMACOL EXP THER, V251, P21
[7]   Competitive and non-competitive NMDA antagonists block the development of antinociceptive tolerance to morphine, but not to selective mu or delta opioid agonists in mice [J].
Bilsky, EJ ;
Inturrisi, CE ;
Sadee, W ;
Hruby, VJ ;
Porreca, F .
PAIN, 1996, 68 (2-3) :229-237
[9]   Cross-tolerance of associative and nonassociative morphine tolerance in the rat with mu- and kappa-specific opioids [J].
Carter, BL ;
Tiffany, ST .
PSYCHOPHARMACOLOGY, 1996, 123 (03) :289-296
[10]   Context-specific morphine tolerance on the paw-pressure and tail-shock vocalization tests: evidence of associative tolerance without conditioned compensatory responding [J].
Cepeda-Benito, A ;
Tiffany, ST ;
Cox, LS .
PSYCHOPHARMACOLOGY, 1999, 145 (04) :426-432