Literature DB >> 6854362

Descending inhibitory influences from periaqueductal gray, nucleus raphe magnus, and adjacent reticular formation. I. Effects on lumbar spinal cord nociceptive and nonnociceptive neurons.

B G Gray, J O Dostrovsky.   

Abstract

1. This study examined the inhibitory effects of conditioning stimuli delivered to the periaqueductal gray (PAG), nucleus cuneiformis (CU), nucleus raphe magnus (NRM), nucleus reticularis gigantocellularis (NGC), and nucleus reticularis magnocellularis (NMC) on functionally identified neurons of the lumbar spinal cord dorsal horn in chloralose-anesthetized or decerebrate cats. 2. Neurons were classified according to their responses to a variety of cutaneous stimuli as low-threshold mechanoreceptive (LTM), wide dynamic range (WDR), or nociceptive specific (NS). The major aim of this study was to determine whether there was a difference in the effectiveness of the brain stem stimulation-produced inhibition of nociceptive (noci) neurons (consisting of both WDR and NS neurons) and the LTM non-nociceptive (nonnoci) neurons. There were no statistical differences in the susceptibility of WDR and NS neurons to brain stem-induced inhibition. 3. Most neurons tested could be inhibited by stimulation of any of the brain stem regions tested. In all cases the percentage of noci neurons inhibited from a given region was higher than the percentage of nonnoci neurons; however, this difference was only statistically significant in the case of NMC stimulation. 4. Threshold current intensities necessary to produce inhibition were determined for each neuron from each stimulation site. Although there was a trend for noci neurons to require slightly lower current intensities, there was in fact no statistically significant difference in the inhibitory thresholds between noci and nonnoci neurons for any of the regions tested. 5. A comparison of the mean threshold currents for the five regions studied revealed that the lowest stimulation currents were obtained in NMC with NRM, CU, NGC, and PAG, each requiring progressively higher current intensities in order to produce inhibition. 6. These results indicate that stimulation in PAG and NRM not only inhibits the responses of noci neurons but also those of nonnoci neurons. Moreover, stimulation in reticular regions adjacent to these two regions is effective in inhibiting the responses of both noci and nonnoci neurons.

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Mesh:

Year:  1983        PMID: 6854362     DOI: 10.1152/jn.1983.49.4.932

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  10 in total

1.  Sensory suppression during feeding.

Authors:  H Foo; Peggy Mason
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-07       Impact factor: 11.205

2.  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

Review 3.  Neurobiological mechanisms for the regulation of mammalian sleep-wake behavior: reinterpretation of historical evidence and inclusion of contemporary cellular and molecular evidence.

Authors:  Subimal Datta; Robert Ross Maclean
Journal:  Neurosci Biobehav Rev       Date:  2007-03-12       Impact factor: 8.989

4.  A Golgi study of the periaqueductal gray matter in the cat. Neuronal types and their distribution.

Authors:  M Gioia; G Tredici; R Bianchi
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

Review 5.  Descending control of nociception: Specificity, recruitment and plasticity.

Authors:  M M Heinricher; I Tavares; J L Leith; B M Lumb
Journal:  Brain Res Rev       Date:  2008-12-25

6.  Anterior pretectal stimulation alters the responses of spinal dorsal horn neurones to cutaneous stimulation in the rat.

Authors:  H Rees; M H Roberts
Journal:  J Physiol       Date:  1987-04       Impact factor: 5.182

7.  Inhibition of the responses of cat dorsal horn neurons to noxious skin heating by stimulation in medial or lateral medullary reticular formation.

Authors:  S Pretel; M J Guinan; E Carstens
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

8.  Studies of brain structures involved in diffuse noxious inhibitory controls in the rat: the rostral ventromedial medulla.

Authors:  D Bouhassira; Z Bing; D Le Bars
Journal:  J Physiol       Date:  1993-04       Impact factor: 5.182

9.  The developmental emergence of differential brainstem serotonergic control of the sensory spinal cord.

Authors:  F Schwaller; A H Kanellopoulos; M Fitzgerald
Journal:  Sci Rep       Date:  2017-05-22       Impact factor: 4.379

Review 10.  The role of the periaqueductal gray in the modulation of pain in males and females: are the anatomy and physiology really that different?

Authors:  Dayna R Loyd; Anne Z Murphy
Journal:  Neural Plast       Date:  2009-01-28       Impact factor: 3.599

  10 in total

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