Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Q J Exp Psychol B ; 43(3): 323-46, 1991 Aug.
Article in English | MEDLINE | ID: mdl-1658853

ABSTRACT

Five experiments used rats to examine the conditioned hypoalgesia induced by exposure to a heated floor. Experiments 1 and 2 demonstrated that this hypoalgesia is mediated by non-opioid mechanisms of pain control, as evidenced by insensitivity to the opioid antagonist naloxone and by the absence of cross-tolerance with the opioid agonist morphine. Although non-opioid in nature, the acquisition of conditioned hypoalgesia was facilitated by naloxone and impaired by morphine (Experiments 3 and 4). These effects did not appear to be due to an opioid regulation of pain. (1) Pairing morphine with the heated floor attenuated acquisition in drug-tolerant rats. (2) This attenuation by morphine was removed when naloxone was given after exposure to the heated floor. (3) Conditioning was facilitated when naloxone was given after exposure to the heated floor (Experiment 5). The results were discussed in terms of an opioid regulation of (a) surprise, (b) arousal of an aversive motivational system, and (c) the affective component of pain.


Subject(s)
Habituation, Psychophysiologic/drug effects , Morphine/pharmacology , Naloxone/pharmacology , Nociceptors/drug effects , Reaction Time/drug effects , Thermosensing/drug effects , Animals , Brain/drug effects , Dose-Response Relationship, Drug , Male , Rats , Rats, Inbred Strains , Receptors, Opioid/drug effects
2.
J Exp Psychol Anim Behav Process ; 17(3): 219-30, 1991 Jul.
Article in English | MEDLINE | ID: mdl-1653814

ABSTRACT

Hypoalgesia and fear co-occurred in rats trained on a heated floor and tested for their latencies to paw lick on that floor and to step down onto a nonheated floor. These responses were extinguished, suggesting a mediation by aversive conditioning processes. A benzodiazepine impaired the acquisition of aversive conditioning, but it did not attenuate the expression of conditioned hypoalgesia. The opioid agonist morphine also impaired acquisition across a range of drug doses and variations in hypoalgesic tolerance, whereas the opioid antagonist naloxone facilitated acquisition. The results are discussed in terms of the perceptual-defensive-recuperative (Fanselow, 1986) and working memory (Grau, 1987) models of the mechanisms for the co-occurrence of conditioned hypoalgesia and fear.


Subject(s)
Avoidance Learning/drug effects , Conditioning, Classical/drug effects , Fear/drug effects , Midazolam/pharmacology , Morphine/pharmacology , Naloxone/pharmacology , Nociceptors/drug effects , Receptors, GABA-A/drug effects , Receptors, Opioid/drug effects , Animals , Arousal/drug effects , Brain/drug effects , Dose-Response Relationship, Drug , Male , Rats , Rats, Inbred Strains , Reaction Time/drug effects , Sensory Thresholds/drug effects , Thermosensing/drug effects
SELECTION OF CITATIONS
SEARCH DETAIL
...