Literature DB >> 7886094

Comparison of motor reflex and vocalization thresholds following systemically administered morphine, fentanyl, and diazepam in the rat: assessment of sensory and performance variables.

G S Borszcz1, C P Johnson, K A Fahey.   

Abstract

The relative influence of systemically administered morphine, fentanyl, and diazepam on the thresholds of spinal motor reflexes (SMRs), vocalizations elicited during stimulation (VDSs), and vocalization afterdischarges (VADs) was assessed. Responses were elicited by applying graded electric current to the tail. Performance (latency and amplitude) of all three responses was monitored to determine whether elevations in threshold were confounded by performance decrements. All three drugs were found to elevate VAD thresholds more readily than VDS and SMR thresholds. VADs were also most susceptible to the deleterious effects of these drugs on motor performance. Nevertheless, across the dose range of morphine and fentanyl that elevated thresholds of all three responses without disrupting the performance of any response, the order of susceptibility to threshold increases remained VAD, VDS, and SMR. Diazepam also elevated VAD thresholds more readily than VDS thresholds across a dose range that failed to disrupt performance of either response. SMR thresholds were only elevated by diazepam when administered in doses that significantly disrupted performance. Results are discussed in terms of supporting the validity of VADs as a model of the affective-motivational dimension of pain.

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Year:  1994        PMID: 7886094     DOI: 10.1016/0091-3057(94)90230-5

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  10 in total

1.  Functional interaction between medial thalamus and rostral anterior cingulate cortex in the suppression of pain affect.

Authors:  S E Harte; C A Spuz; G S Borszcz
Journal:  Neuroscience       Date:  2010-10-27       Impact factor: 3.590

2.  NMDA or non-NMDA receptor antagonism within the amygdaloid central nucleus suppresses the affective dimension of pain in rats: evidence for hemispheric synergy.

Authors:  Catherine A Spuz; George S Borszcz
Journal:  J Pain       Date:  2012-03-15       Impact factor: 5.820

3.  N-methyl-D-aspartate receptor agonism and antagonism within the amygdaloid central nucleus suppresses pain affect: differential contribution of the ventrolateral periaqueductal gray.

Authors:  Catherine A Spuz; Michelle L Tomaszycki; George S Borszcz
Journal:  J Pain       Date:  2014-09-23       Impact factor: 5.820

4.  Developing Improved Translational Models of Pain: A Role for the Behavioral Scientist.

Authors:  Sarah L Withey; David R Maguire; Brian D Kangas
Journal:  Perspect Behav Sci       Date:  2020-01-03

5.  Contribution of the ventromedial hypothalamus to generation of the affective dimension of pain.

Authors:  George S Borszcz
Journal:  Pain       Date:  2006-03-29       Impact factor: 6.961

Review 6.  Aggression, anxiety and vocalizations in animals: GABAA and 5-HT anxiolytics.

Authors:  K A Miczek; E M Weerts; J A Vivian; H M Barros
Journal:  Psychopharmacology (Berl)       Date:  1995-09       Impact factor: 4.530

7.  Contribution of the periaqueductal gray to the suppression of pain affect produced by administration of morphine into the intralaminar thalamus of rat.

Authors:  Elizabeth M Munn; Steven E Harte; Alexander Lagman; George S Borszcz
Journal:  J Pain       Date:  2009-02-23       Impact factor: 5.820

8.  Separating analgesia from reward within the ventral tegmental area.

Authors:  E Schifirneţ; S E Bowen; G S Borszcz
Journal:  Neuroscience       Date:  2014-01-13       Impact factor: 3.590

9.  Affective analgesia following muscarinic activation of the ventral tegmental area in rats.

Authors:  Robert G Kender; Steven E Harte; Elizabeth M Munn; George S Borszcz
Journal:  J Pain       Date:  2008-04-03       Impact factor: 5.820

10.  Mice Lacking Serotonin 2C Receptors Have increased Affective Responses to Aversive Stimuli.

Authors:  Stephen J Bonasera; A Katrin Schenk; Evan J Luxenberg; Xidao Wang; Allan Basbaum; Laurence H Tecott
Journal:  PLoS One       Date:  2015-12-02       Impact factor: 3.240

  10 in total

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