Literature DB >> 7287930

Afferent connections of the rostral medulla of the cat: a neural substrate for midbrain-medullary interactions in the modulation of pain.

I A Abols, A I Basbaum.   

Abstract

In order to study the organization of the rostral medulla of the cat and its contribution to pain control mechanisms, we have examined the afferent connections of the midline nucleus raphe magnus (NRM), the laterally located nucleus reticularis magnocellularis (Rmc), and the nucleus reticularis gigantocellularis (Rgc) located dorsal to Rmc. Iontophoretic injections of HRP were made into the three regions; the distribution of retrogradely labeled neurons in brainstem and spinal cord was then mapped. While significant differences characterize the source of afferents to Rgc and NRM/Rmc, there is little to distinguish that between NRM and Rmc. The predominant spinal projection is to Rgc; fewer labeled neurons were recorded after injections into Rmc. In contrast, no significant direct spinal projection to NRM was found. All three regions receive input from widespread areas within the medullary and pontine reticular formation. The most pronounced differences in the distribution of retrogradely labeled neurons were found in the midbrain. The major projection to both NRM and Rmc derives from the periaqueductal gray (PAG) and from the adjacent nucleus cuneiformis. Labeled cells are concentrated in the dorsal and lateral PAG; few are found in the ventrolateral PAG. In contrast, Rgc receives few afferents from the PAG; however, after Rgc injections, many cells were recorded in the deep layers of the contralateral tectum. None of the injection sites produced significant labeling of the catecholamine-rich dorsolateral pontine tegmentum or of the nucleus raphe dorsalis. The demonstration of significant PAG projections to NRM/Rmc provides anatomical evidence for the hypothesis that opiate and stimulation-produced analgesia involves connections from PAG to neurons of NRM and Rmc which, in turn, inhibit spinal nociceptors.

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Year:  1981        PMID: 7287930     DOI: 10.1002/cne.902010211

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  28 in total

1.  Ascending projections from the area around the spinal cord central canal: A Phaseolus vulgaris leucoagglutinin study in rats.

Authors:  C C Wang; W D Willis; K N Westlund
Journal:  J Comp Neurol       Date:  1999-12-20       Impact factor: 3.215

2.  Responses of neurons in the caudal medullary raphe nuclei of the cat to stimulation of the vestibular nerve.

Authors:  B J Yates; T Goto; P S Bolton
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

3.  Roles for pain modulatory cells during micturition and continence.

Authors:  Madelyn A Baez; Thaddeus S Brink; Peggy Mason
Journal:  J Neurosci       Date:  2005-01-12       Impact factor: 6.167

4.  Sex differences in the anatomical and functional organization of the periaqueductal gray-rostral ventromedial medullary pathway in the rat: a potential circuit mediating the sexually dimorphic actions of morphine.

Authors:  Dayna R Loyd; Anne Z Murphy
Journal:  J Comp Neurol       Date:  2006-06-10       Impact factor: 3.215

5.  Genetically expressed transneuronal tracer reveals direct and indirect serotonergic descending control circuits.

Authors:  João Manuel Braz; Allan I Basbaum
Journal:  J Comp Neurol       Date:  2008-04-20       Impact factor: 3.215

Review 6.  Central modulation of pain.

Authors:  Michael H Ossipov; Gregory O Dussor; Frank Porreca
Journal:  J Clin Invest       Date:  2010-11-01       Impact factor: 14.808

7.  The periaqueductal gray in the cat projects to lamina VIII and the medial part of lamina VII throughout the length of the spinal cord.

Authors:  L J Mouton; G Holstege
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

8.  A lateralized deficit in morphine antinociception after unilateral inactivation of the central amygdala.

Authors:  B H Manning
Journal:  J Neurosci       Date:  1998-11-15       Impact factor: 6.167

9.  Dorsal border periaqueductal gray neurons project to the area directly adjacent to the central canal ependyma of the C4-T8 spinal cord in the cat.

Authors:  L J Mouton; L Kerstens; J Van der Want; G Holstege
Journal:  Exp Brain Res       Date:  1996-11       Impact factor: 1.972

10.  Descending control of spinal nociceptive transmission. Actions produced on spinal multireceptive neurones from the nuclei locus coeruleus (LC) and raphe magnus (NRM).

Authors:  S S Mokha; J A McMillan; A Iggo
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

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