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Potent inhibition of non-opioid defeat analgesia in male mice by benzodiazepine antagonist Ro15-3505.

作者信息

Rodgers R J, Randall J I

机构信息

Pharmacoethology Laboratory, School of Psychology, University of Bradford, U.K.

出版信息

Physiol Behav. 1988;42(5):461-4. doi: 10.1016/0031-9384(88)90177-1.

DOI:10.1016/0031-9384(88)90177-1
PMID:3393607
Abstract

In male mice, defeat in social encounters is associated with an acute non-opioid analgesia, a reaction that may also be seen in response to the scent of a territorial conspecific. As this form of pain inhibition is blocked by diazepam and Ro15-1788, benzodiazepine receptor mediation has been proposed. To further test this hypothesis, the effects of a novel benzodiazepine receptor antagonist (Ro15-3505; 0.625-20 mg/kg) on basal nociception and defeat analgesia have been examined. Results show that, although devoid of intrinsic activity on the mouse tail-flick assay, Ro15-3505 totally blocks the analgesic consequences of defeat at doses above 1.25 mg/kg. Despite certain inconsistencies in the literature, present data provide further support for benzodiazepine receptor mediation of this ecologically-relevant form of pain inhibition.

摘要

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1
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引用本文的文献

1
Blockade of non-opioid analgesia in intruder mice by selective neuronal and non-neuronal benzodiazepine recognition site ligands.通过选择性神经元和非神经元苯二氮䓬识别位点配体对入侵小鼠非阿片类镇痛的阻断作用。
Psychopharmacology (Berl). 1988;96(1):45-54. doi: 10.1007/BF02431532.
2
5HT1A agonist, 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT), inhibits non-opioid analgesia in defeated mice: influence of route of administration.
Psychopharmacology (Berl). 1989;97(2):163-5. doi: 10.1007/BF00442242.