Literature DB >> 6308696

Social conflict activates status-dependent endogenous analgesic or hyperalgesic mechanisms in male mice: effects of naloxone on nociception and behaviour.

R J Rodgers, C A Hendrie.   

Abstract

The concept of environmentally-induced activation of endogenous analgesia mechanisms rests, almost exclusively, upon studies which have involved the use of rather intense artificial stimuli. The current study was therefore designed to assess the validity of this concept under the more naturalistic conditions of social conflict between isolated resident mice and group-housed intruders. Agonistic experience was found to result in a potent, naloxone-reversible (10 mg/kg) analgesia in intruder mice while, in residents, it produced a moderate hyperalgesic reaction which was very sensitive to naloxone antagonism (0.1 mg/kg). Detailed videotape analyses revealed that only the behaviour of residents was significantly altered by naloxone treatment, with a highly selective inhibition of attack observed at 10 mg/kg. These data suggest that (1) social conflict in mice is a potent, and biologically-relevant, stimulus in the activation of endogenous naloxone-sensitive pain control mechanisms, (2) social status is an important determinant of nociceptive response to such experience and (3) inescapability from attack may be a critical factor in the development of encounter-induced analgesia.

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Year:  1983        PMID: 6308696     DOI: 10.1016/0031-9384(83)90177-4

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  21 in total

1.  Social stress in hamsters: defeat activates specific neurocircuits within the brain.

Authors:  S Kollack-Walker; S J Watson; H Akil
Journal:  J Neurosci       Date:  1997-11-15       Impact factor: 6.167

2.  Aggression during morphine withdrawal: effects of method of withdrawal, fighting experience, and social role.

Authors:  K M Kantak; K A Miczek
Journal:  Psychopharmacology (Berl)       Date:  1986       Impact factor: 4.530

Review 3.  Modulation of nociception by social factors in rodents: contribution of the opioid system.

Authors:  Francesca R D'Amato; Flaminia Pavone
Journal:  Psychopharmacology (Berl)       Date:  2012-09-20       Impact factor: 4.530

4.  Prevention of the analgesic consequences of social defeat in male mice by 5-HT1A anxiolytics, buspirone, gepirone and ipsapirone.

Authors:  R J Rodgers; J K Shepherd
Journal:  Psychopharmacology (Berl)       Date:  1989       Impact factor: 4.530

5.  Relationship between behavioral and nociceptive changes in attacked mice: effects of opiate antagonists.

Authors:  H R Frischknecht; B Siegfried
Journal:  Psychopharmacology (Berl)       Date:  1989       Impact factor: 4.530

Review 6.  Mechanisms of placebo analgesia: A dual-process model informed by insights from cross-species comparisons.

Authors:  Scott M Schafer; Stephan Geuter; Tor D Wager
Journal:  Prog Neurobiol       Date:  2017-11-03       Impact factor: 11.685

7.  Analgesia and decrement in operant performance in socially defeated mice: selective cross-tolerance to morphine and antagonism by naltrexone.

Authors:  K A Miczek; J T Winslow
Journal:  Psychopharmacology (Berl)       Date:  1987       Impact factor: 4.530

8.  Diazepam and gepirone selectively attenuate either 20-32 or 32-64 kHz ultrasonic vocalizations during aggressive encounters.

Authors:  J A Vivian; K A Miczek
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

9.  Physiological evidence for genetically mediated sibling recognition in mice.

Authors:  F R D'Amato
Journal:  Behav Genet       Date:  1994-11       Impact factor: 2.805

Review 10.  Alcohol and violence: neuropeptidergic modulation of monoamine systems.

Authors:  Klaus A Miczek; Joseph F DeBold; Lara S Hwa; Emily L Newman; Rosa M M de Almeida
Journal:  Ann N Y Acad Sci       Date:  2015-08-18       Impact factor: 5.691

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