Literature DB >> 16564622

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

George S Borszcz1.   

Abstract

The ventromedial hypothalamus (VMH) is a core structure underlying the generation of affective behaviors to threats. The prototypical threat to an individual is exposure to a noxious stimulus and the dorsomedial division of the VMH (dmVMH) receives nociceptive input. The present study evaluated the contribution of the dmVMH to generation of the affective reaction to pain in rats. Noxious tailshock elicits from rats vocalization afterdischarges (VADs) that have distinct spectrographic characteristics and are a validated model of the affective reaction to pain. VAD-like vocalizations (vocalizations with the same spectral characteristics of VADs) were elicited by stimulation (electrical or chemical) of the dmVMH. Stimulation in the vicinity of the dmVMH was ineffective in eliciting VADs. Manipulation of GABA(A) neurochemistry within the dmVMH altered the threshold for elicitation of VADs by dmVMH stimulation or tailshock. Administration of the GABA(A) antagonist bicuculline or the GABA(A) agonist muscimol into the dmVMH lowered and elevated VAD thresholds, respectively. These treatments did not alter thresholds of other tailshock elicited responses (vocalizations during tailshock or spinal motor reflexes). Bicuculline and muscimol administered into the dmVMH also elevated and lowered the asymptotic level of fear conditioning supported by dmVMH stimulation or tailshock. These findings demonstrate that the dmVMH contributes to the processing of pain affect and that the affective dimension of pain belongs to a broader class of sensory experience that represents threat to the individual.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16564622      PMCID: PMC1534121          DOI: 10.1016/j.pain.2006.02.026

Source DB:  PubMed          Journal:  Pain        ISSN: 0304-3959            Impact factor:   6.961


  68 in total

1.  Vocalization as an emotional indicator. A neuroethological study in the squirrel monkey.

Authors:  U Jürgens
Journal:  Behaviour       Date:  1979       Impact factor: 1.991

2.  Role of the periaqueductal grey in vocal expression of emotion.

Authors:  U Jürgens; R Pratt
Journal:  Brain Res       Date:  1979-05-11       Impact factor: 3.252

Review 3.  Brain function and behavior. I. Emotion and sensory phenomena in psychotic patients and in experimental animals.

Authors:  R G Heath
Journal:  J Nerv Ment Dis       Date:  1975-03       Impact factor: 2.254

4.  Validity and sensitivity of ratio scales of sensory and affective verbal pain descriptors: manipulation of affect by diazepam.

Authors:  R H Gracely; P McGrath; R Dubner
Journal:  Pain       Date:  1978-06       Impact factor: 6.961

5.  Threat, attack and flight elicited by electrical stimulation of the ventromedial hypothalamus of the marmoset monkey Callithrix jacchus.

Authors:  H P Lipp; R W Hunsperger
Journal:  Brain Behav Evol       Date:  1978       Impact factor: 1.808

Review 6.  Central mechanisms of chronic pain (neuralgias and certain other neurogenic pain).

Authors:  W H Sweet
Journal:  Res Publ Assoc Res Nerv Ment Dis       Date:  1980

7.  A psychophysical analysis of morphine analgesia.

Authors:  D D Price; A Von der Gruen; J Miller; A Rafii; C Price
Journal:  Pain       Date:  1985-07       Impact factor: 6.961

8.  Defensive behavior of laboratory and wild Rattus norvegicus.

Authors:  R J Blanchard; K J Flannelly; D C Blanchard
Journal:  J Comp Psychol       Date:  1986-06       Impact factor: 2.231

9.  Mental and behavioral effects of brain stem and hypothalamic stimulation in man.

Authors:  R P Iacono; B S Nashold
Journal:  Hum Neurobiol       Date:  1982

10.  Identification of pain processing systems by electrical stimulation of the brain.

Authors:  R R Tasker
Journal:  Hum Neurobiol       Date:  1982
View more
  18 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.  Nuclei-and condition-specific responses to pain in the bed nucleus of the stria terminalis.

Authors:  Tania J Morano; Nicole J Bailey; Catherine M Cahill; Eric C Dumont
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2007-11-12       Impact factor: 5.067

3.  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

4.  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

Review 5.  Pain and emotion: a biopsychosocial review of recent research.

Authors:  Mark A Lumley; Jay L Cohen; George S Borszcz; Annmarie Cano; Alison M Radcliffe; Laura S Porter; Howard Schubiner; Francis J Keefe
Journal:  J Clin Psychol       Date:  2011-06-06

6.  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

7.  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

8.  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

9.  Neural substrates for expectation-modulated fear learning in the amygdala and periaqueductal gray.

Authors:  Joshua P Johansen; Jason W Tarpley; Joseph E LeDoux; Hugh T Blair
Journal:  Nat Neurosci       Date:  2010-07-04       Impact factor: 24.884

10.  Social defeat stress activates medial amygdala cells that express type 2 corticotropin-releasing factor receptor mRNA.

Authors:  E M Fekete; Y Zhao; C Li; V Sabino; W W Vale; E P Zorrilla
Journal:  Neuroscience       Date:  2009-04-07       Impact factor: 3.590

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.