Literature DB >> 7085928

The origin of the spinomesencephalic tract in the rat: an anatomical study using the retrograde transport of horseradish peroxidase.

D Menétrey, A Chaouch, D Binder, J M Besson.   

Abstract

An anatomical technique based on the retrograde transport of horseradish peroxidase (HRP) was used to investigate the projections of spinal cord neurons to the mesencephalic tegmentum in the rat. Restricted unilateral injections were confined to central grey, cuneiformis areas, and superior colliculus. Injections into all these loci produced labeling in similar spinal areas. Only quantitative differences were noted. In the spinal grey matter, numerous labeled cells were regularly encountered in the marginal zone, the lateral part of the neck of the dorsal horn, and the dorsal grey commissure. Projections from the marginal zone and neck of the dorsal horn were predominantly contralateral. In the white matter, a pronounced bilateral labeling was observed in the nucleus of the dorsolateral funiculus, thus confirming our previous electrophysiological findings (Menétrey et al., '80). This distribution of labeled cells was commonly observed throughout the whole length of the cord. Additional sites of projecting cells have also been identified at the most rostral levels (obex, C1, C2). They mostly derived from spinal extensions of the dorsal column nuclei and lateral cervical nucleus contralaterally; from the lateral ventral horns bilaterally and from the nucleus commissuralis ipsilaterally. This study is thus a clear confirmation that the mesencephalic tegmentum constitutes a target for various somatosensory inputs originating from spinal cord, dorsal column nuclei, and lateral cervical nucleus. Moreover, from these results together with those obtained for the spinothalamic tract in the rat, it appears that marginal and dorsolateral funiculus neurons preferentially project to the mesencephalic tegmentum. The importance of marginal zone projections underlines the involvement of the spinomesencephalic tract in pain mechanisms.

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Year:  1982        PMID: 7085928     DOI: 10.1002/cne.902060208

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


  32 in total

1.  Lamina-specific membrane and discharge properties of rat spinal dorsal horn neurones in vitro.

Authors:  Ruth Ruscheweyh; Jürgen Sandkühler
Journal:  J Physiol       Date:  2002-05-15       Impact factor: 5.182

2.  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

3.  Disabled-1 dorsal horn spinal cord neurons co-express Lmx1b and function in nociceptive circuits.

Authors:  Griselda M Yvone; Hannah H Zhao-Fleming; Joe C Udeochu; Carmine L Chavez-Martinez; Austin Wang; Megumi Hirose-Ikeda; Patricia E Phelps
Journal:  Eur J Neurosci       Date:  2017-02-10       Impact factor: 3.386

4.  Effects of electrical stimulation of the thoracic spinal cord on bladder and external urethral sphincter activity in the decerebrate cat.

Authors:  B Fedirchuk; S J Shefchyk
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

5.  Localization of substance P-like immunoreactive fibers in the thoracic spinal cord of guinea pig.

Authors:  M S Davidoff; P G Galabov; P Kaufmann
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

6.  Distinct distribution of opioid receptor types in rat lumbar spinal cord.

Authors:  B J Morris; A Herz
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1987-08       Impact factor: 3.000

7.  Projections from the rat cuneiform nucleus to the A7, A6 (locus coeruleus), and A5 pontine noradrenergic cell groups.

Authors:  Dusica Bajic; Herbert K Proudfit
Journal:  J Chem Neuroanat       Date:  2013-03-20       Impact factor: 3.052

8.  Collateral projections of neurons in laminae I, III, and IV of rat spinal cord to thalamus, periaqueductal gray matter, and lateral parabrachial area.

Authors:  Khulood M Al-Khater; Andrew J Todd
Journal:  J Comp Neurol       Date:  2009-08-20       Impact factor: 3.215

9.  Soma size distinguishes projection neurons from neurokinin 1 receptor-expressing interneurons in lamina I of the rat lumbar spinal dorsal horn.

Authors:  K S Al Ghamdi; E Polgár; A J Todd
Journal:  Neuroscience       Date:  2009-10-01       Impact factor: 3.590

10.  A quantitative study of brainstem projections from lamina I neurons in the cervical and lumbar enlargement of the rat.

Authors:  Erika Polgár; Lorna L Wright; Andrew J Todd
Journal:  Brain Res       Date:  2009-10-23       Impact factor: 3.252

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