Literature DB >> 6178807

The sites of origin brain stem neurotensin and serotonin projections to the rodent nucleus raphe magnus.

A J Beitz.   

Abstract

The combined horseradish peroxidase retrograde transport-peroxidase-antiperoxidase immunohistochemical procedure was utilized in the present study to ascertain the sites of origin of serotonin and neurotensin projections to the rodent nucleus raphe magnus. The major serotonin inputs to the raphe magnus arise from the B-8 and B-9 groups of Dahlstrom and Fuxe (Dahlstrom, A., and K. Fuxe (1964) Acta Physiol. Scand. Suppl. 232 62: 1-55), the nucleus reticularis paragigantocellularis, and the nucleus reticularis gigantocellularis pars alpha. Neurotensinergic projections to the raphe magnus originate predominantly from the periaqueductal gray, the nucleus solitarius, the dorsal and ventral parabrachial nuclei, and the nucleus cuneiformis. The periaqueductal gray and the nucleus paragigantocellularis were found to provide both a neurotensin and a serotonin projection to this raphe nucleus. The present results indicate that several brain stem nuclei, which have been implicated previously in endogenous analgesia mechanisms, provide serotonergic and neurotensinergic input to the nucleus raphe magnus.

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Year:  1982        PMID: 6178807      PMCID: PMC6564387     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  25 in total

1.  Joint manipulation reduces hyperalgesia by activation of monoamine receptors but not opioid or GABA receptors in the spinal cord.

Authors:  D A Skyba; R Radhakrishnan; J J Rohlwing; A Wright; K A Sluka
Journal:  Pain       Date:  2003-11       Impact factor: 6.961

Review 2.  The role of neurotensin in central nervous system pathophysiology: what is the evidence?

Authors:  Fannie St-Gelais; Claudia Jomphe; Louis-Eric Trudeau
Journal:  J Psychiatry Neurosci       Date:  2006-07       Impact factor: 6.186

3.  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

4.  The projection from superior colliculus to cuneiform area in the rat. I. Anatomical studies.

Authors:  P Redgrave; P Dean; I J Mitchell; A Odekunle; A Clark
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

5.  Hypothalamic control of nocireceptive and other neurons in the marginal layer of the dorsal horn of the medulla (trigeminal nucleus caudalis) in the rat.

Authors:  S S Mokha; G E Goldsmith; R F Hellon; R Puri
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

6.  [Central pain processing in chronic low back pain. Evidence for reduced pain inhibition].

Authors:  T Giesecke; R H Gracely; D J Clauw; A Nachemson; M H Dück; R Sabatowski; H J Gerbershagen; D A Williams; F Petzke
Journal:  Schmerz       Date:  2006-09       Impact factor: 1.107

7.  Alterations in nociception following adrenal medullary transplants into the rat periaqueductal gray.

Authors:  J Sagen; G D Pappas; M J Perlow
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

8.  mu-Opioid and delta-opioid receptors are expressed in brainstem antinociceptive circuits: studies using immunocytochemistry and retrograde tract-tracing.

Authors:  A E Kalyuzhny; U Arvidsson; W Wu; M W Wessendorf
Journal:  J Neurosci       Date:  1996-10-15       Impact factor: 6.167

9.  Pirenperone does not attenuate morphine analgesia in spinal rats.

Authors:  D Paul; J P Pinel
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

10.  Inputs to serotonergic neurons revealed by conditional viral transneuronal tracing.

Authors:  João M Braz; Lynn W Enquist; Allan I Basbaum
Journal:  J Comp Neurol       Date:  2009-05-10       Impact factor: 3.215

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