Literature DB >> 8136048

The periaqueductal gray and defensive behavior: functional representation and neuronal organization.

P Carrive1.   

Abstract

Recent findings suggest that the periaqueductal gray (PAG) can be subdivided on the basis of its anatomical connections and functional representation of cardiovascular and behavioral functions. This new scheme of subdivision postulates the existence of 4 major longitudinal columns located dorsomedial, dorsolateral, lateral and ventrolateral to the aqueduct. Attention has focussed on the lateral and ventrolateral columns, because they contain topographically distinct groups of neurons whose activation results in different forms of defensive or protective reactions. Reactions evoked from the lateral PAG column are associated with somatomotor and autonomic activation and are characteristic of an organism's response to superficial or cutaneous noxious stimuli, whereas reactions evoked from the ventrolateral PAG column are associated with somatomotor and autonomic inhibition and appear to correspond to an organism's response to deep or visceral noxious stimuli. Furthermore, the neurons of these two columns possess some degree of somatotopic and viscerotopic organization and send axon collaterals to multiple targets in the medulla. This model of PAG neuronal organization outlines the basic architectural features of a network involved in the coordinated expression of certain types of defensive/protective reactions.

Mesh:

Year:  1993        PMID: 8136048     DOI: 10.1016/0166-4328(93)90088-8

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  85 in total

1.  Lesion of the ventral periaqueductal gray reduces conditioned fear but does not change freezing induced by stimulation of the dorsal periaqueductal gray.

Authors:  D M Vianna; F G Graeff; J Landeira-Fernandez; M L Brandão
Journal:  Learn Mem       Date:  2001 May-Jun       Impact factor: 2.460

2.  Periaqueductal gray matter modulates the hypercapnic ventilatory response.

Authors:  Luana T Lopes; Luis G A Patrone; Kênia C Bícego; Norberto C Coimbra; Luciane H Gargaglioni
Journal:  Pflugers Arch       Date:  2012-06-05       Impact factor: 3.657

3.  Opioid receptors in the midbrain periaqueductal gray regulate extinction of pavlovian fear conditioning.

Authors:  Gavan P McNally; Michael Pigg; Gabrielle Weidemann
Journal:  J Neurosci       Date:  2004-08-04       Impact factor: 6.167

4.  Tracheal occlusions evoke respiratory load compensation and neural activation in anesthetized rats.

Authors:  Kathryn M Pate; Paul W Davenport
Journal:  J Appl Physiol (1985)       Date:  2011-11-10

5.  Connections of the lateral hypothalamic area juxtadorsomedial region in the male rat.

Authors:  Joel D Hahn; Larry W Swanson
Journal:  J Comp Neurol       Date:  2012-06-15       Impact factor: 3.215

6.  Differential involvement of the periaqueductal gray in multiple system atrophy.

Authors:  Eduardo E Benarroch; Ann M Schmeichel; Phillip A Low; Joseph E Parisi
Journal:  Auton Neurosci       Date:  2010-08-21       Impact factor: 3.145

7.  Periaqueductal gray c-Fos expression varies relative to the method of conditioned taste aversion extinction employed.

Authors:  G Andrew Mickley; Gina N Wilson; Jennifer L Remus; Linnet Ramos; Kyle D Ketchesin; Orion R Biesan; Joseph R Luchsinger; Suzanna Prodan
Journal:  Brain Res       Date:  2011-09-22       Impact factor: 3.252

8.  Social defeat, a paradigm of depression in rats that elicits 22-kHz vocalizations, preferentially activates the cholinergic signaling pathway in the periaqueductal gray.

Authors:  Roger A Kroes; Jeffrey Burgdorf; Nigel J Otto; Jaak Panksepp; Joseph R Moskal
Journal:  Behav Brain Res       Date:  2007-03-25       Impact factor: 3.332

Review 9.  Distinct patterns of neuronal inputs and outputs of the juxtaparaventricular and suprafornical regions of the lateral hypothalamic area in the male rat.

Authors:  Joel D Hahn; Larry W Swanson
Journal:  Brain Res Rev       Date:  2010-02-17

10.  Cardiovascular and thermal responses evoked from the periaqueductal grey require neuronal activity in the hypothalamus.

Authors:  Rodrigo C A de Menezes; Dmitry V Zaretsky; Marco A P Fontes; Joseph A DiMicco
Journal:  J Physiol       Date:  2009-01-26       Impact factor: 5.182

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