Literature DB >> 12612020

Temporal and spatial profiles of pontine-evoked monoamine release in the rat's spinal cord.

Ian D Hentall1, Riza Mesigil, Alberto Pinzon, Brian R Noga.   

Abstract

In the spinal cord, the monoamine neurotransmitter norepinephrine, which is released mainly from fibers descending from the dorsal pons, has major modulatory effects on nociception and locomotor rhythms. To map the spatial and temporal patterns of this release, changes in monoamine level were examined in laminae I-VIII of lumbar segments L3-L6 of halothane-anesthetized rats during pontine stimulation. The changes were measured through a carbon fiber microelectrode at 0.5-s intervals by fast cyclic voltammetry, which presently is the method of best spatiotemporal resolution. When different pontine sites were tested with 20-s pulse trains (50-to 200-microA amplitude, 0.5-ms pulse width, and 50-Hz frequency) during measurement in the dorsal horn (lamina IV), the largest consistent increases were produced by the locus ceruleus, although effective pontine sites extended 1.5 mm dorsally and ventral from the locus ceruleus. When the locus ceruleus stimulus was used to map the spinal cord, increased levels were always seen in lamina I and laminae IV-VIII, whereas 50% of sites in laminae II and III showed substantial decreases and the rest showed increases. These increases typically had short latencies [4.5 +/- 0.4 (SE) s] and variable decay times (5-200 s), with peaks occurring during the stimulus train (mean rise-time: 12.0 +/- 0.6 s). The mean peak level was 544 +/- 82 nM as estimated from postexperimental calibration with norepinephrine. Other significant laminar differences included higher mean peak concentrations (805 nM) and rise times (14.9 s) in lamina I and shorter latencies in lamina VI (3.2 s). Peak concentrations were inversely correlated with latency. When stimulation frequency was varied, increases were disproportionately larger with faster frequencies (> or =50 Hz), hence extrajunctional overflow probably contributed most of the signal. We conclude, generally, that pontine noradrenergic control is exerted on widespread spinal laminae with a significant component of paracrine transmission after several seconds of sustained activity. Relatively stronger effects prevail where nociceptive transmission (lamina I) and locomotor rhythm generation (lamina VI) occur.

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Year:  2003        PMID: 12612020     DOI: 10.1152/jn.00608.2002

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


  19 in total

1.  Effect of chrysin on nociception in formalin test and serum levels of noradrenalin and corticosterone in rats.

Authors:  Tahereh Farkhondeh; Saeed Samarghandian; Mohsen Azimin-Nezhad; Fariborz Samini
Journal:  Int J Clin Exp Med       Date:  2015-02-15

2.  Locomotor-activated neurons of the cat. I. Serotonergic innervation and co-localization of 5-HT7, 5-HT2A, and 5-HT1A receptors in the thoraco-lumbar spinal cord.

Authors:  Brian R Noga; Dawn M G Johnson; Mirta I Riesgo; Alberto Pinzon
Journal:  J Neurophysiol       Date:  2009-07-01       Impact factor: 2.714

3.  Spatial and temporal patterns of serotonin release in the rat's lumbar spinal cord following electrical stimulation of the nucleus raphe magnus.

Authors:  I D Hentall; A Pinzon; B R Noga
Journal:  Neuroscience       Date:  2006-08-04       Impact factor: 3.590

4.  Activation of NK₁ receptors in the locus coeruleus induces analgesia through noradrenergic-mediated descending inhibition in a rat model of neuropathic pain.

Authors:  Y Muto; A Sakai; A Sakamoto; H Suzuki
Journal:  Br J Pharmacol       Date:  2012-06       Impact factor: 8.739

5.  Noradrenergic innervation of the rat spinal cord caudal to a complete spinal cord transection: effects of olfactory ensheathing glia.

Authors:  Aya Takeoka; Marc D Kubasak; Hui Zhong; Jennifer Kaplan; Roland R Roy; Patricia E Phelps
Journal:  Exp Neurol       Date:  2009-12-16       Impact factor: 5.330

6.  Locomotor-activated neurons of the cat. II. Noradrenergic innervation and colocalization with NEα 1a or NEα 2b receptors in the thoraco-lumbar spinal cord.

Authors:  Brian R Noga; Dawn M G Johnson; Mirta I Riesgo; Alberto Pinzon
Journal:  J Neurophysiol       Date:  2011-02-09       Impact factor: 2.714

7.  Glial cell line-derived neurotrophic factor-mediated enhancement of noradrenergic descending inhibition in the locus coeruleus exerts prolonged analgesia in neuropathic pain.

Authors:  M Kimura; A Sakai; A Sakamoto; H Suzuki
Journal:  Br J Pharmacol       Date:  2015-02-27       Impact factor: 8.739

Review 8.  The use of viral gene transfer in studies of brainstem noradrenergic and serotonergic neurons.

Authors:  S Kasparov; A G Teschemacher
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-09-12       Impact factor: 6.237

9.  Retrograde viral vector-mediated inhibition of pontospinal noradrenergic neurons causes hyperalgesia in rats.

Authors:  Patrick W Howorth; Simon R Thornton; Victoria O'Brien; Wynne D Smith; Natalia Nikiforova; Anja G Teschemacher; Anthony E Pickering
Journal:  J Neurosci       Date:  2009-10-14       Impact factor: 6.167

10.  Serotonin concentrations in the lumbosacral spinal cord of the adult rat following microinjection or dorsal surface application.

Authors:  Michele R Brumley; Ian D Hentall; Alberto Pinzon; Brijesh H Kadam; Anthony Blythe; Francisco J Sanchez; Annette M Taberner; Brian R Noga
Journal:  J Neurophysiol       Date:  2007-07-18       Impact factor: 2.714

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