Literature DB >> 2821084

The organization of trigeminotectal and trigeminothalamic neurons in rodents: a double-labeling study with fluorescent dyes.

L L Bruce1, J G McHaffie, B E Stein.   

Abstract

Retrogradely transported fluorescent dyes (fast blue and diamidino-dihydrochloride yellow) were used to compare the distributions of trigeminofugal neurons that project to the superior colliculus and/or the thalamus in three rodent species. The objective was to determine what the projection and collateralization patterns of these trigeminofugal pathways are and whether they are similar among different species. In each anesthetized animal, one dye was injected into the superior colliculus and the other into the topographically congruent area of the thalamus. Counts of the numbers of yellow, blue, and double-labeled neurons were made throughout the trigeminal complex: principalis, pars oralis, pars interpolaris, and pars caudalis. Trigeminothalamic projections were similar in each of the rodent species studied. The densest concentration of retrogradely labeled neurons was in principalis, with substantially fewer neurons in pars interpolaris, and fewer still in pars oralis and pars caudalis. These neurons were generally small and tended to have round or fusiform somata. A common pattern was also noted among the three species for trigeminotectal neurons. Most trigeminotectal projections originated from neurons in pars interpolaris, somewhat fewer from pars oralis, and the fewest from principalis and pars caudalis. These neurons tended to be the largest in each subdivision and were often multipolar. Following paired injections of the tracers, double-labeled neurons were scattered throughout the sensory trigeminal complex and had morphologies characteristic of single-labeled trigeminotectal neurons. Although comparatively few double-labeled neurons were observed in any species, most of those seen were restricted to the ventrolateral portion of pars interpolaris, a position that corresponds to the representation of the vibrissae. These data indicate that, regardless of the rodent species, the vast majority of labeled trigeminal neurons project either to the superior colliculus or the thalamus, but not to both targets. This might be expected on the basis of the very different behavioral roles these structures play. On the other hand, a subpopulation of trigeminal neurons exists (mainly in pars interpolaris) that does project to both the superior colliculus and the thalamus, perhaps because both structures require some of the same somatosensory information to perform their behavioral functions.

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Year:  1987        PMID: 2821084     DOI: 10.1002/cne.902620302

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


  16 in total

1.  Single- and multi-whisker channels in the ascending projections from the principal trigeminal nucleus in the rat.

Authors:  P Veinante; M Deschênes
Journal:  J Neurosci       Date:  1999-06-15       Impact factor: 6.167

2.  Consistency of angular tuning in the rat vibrissa system.

Authors:  Marie E Hemelt; Ernest E Kwegyir-Afful; Randy M Bruno; Daniel J Simons; Asaf Keller
Journal:  J Neurophysiol       Date:  2010-07-28       Impact factor: 2.714

3.  Sensory responses of intralaminar thalamic neurons activated by the superior colliculus.

Authors:  B S Grunwerg; G M Krauthamer
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

4.  Early sensory pathways for detection of fearful conditioned stimuli: tectal and thalamic relays.

Authors:  Jeremy D Cohen; Manuel A Castro-Alamancos
Journal:  J Neurosci       Date:  2007-07-18       Impact factor: 6.167

5.  Feedforward inhibition determines the angular tuning of vibrissal responses in the principal trigeminal nucleus.

Authors:  Marie-Andrée Bellavance; Maxime Demers; Martin Deschênes
Journal:  J Neurosci       Date:  2010-01-20       Impact factor: 6.167

6.  Responses of neurones in the ventrobasal complex of the thalamus to orofacial noxious stimulation after large trigeminal tractotomy.

Authors:  P Raboisson; R Dallel; A Woda
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

7.  Detection of low salience whisker stimuli requires synergy of tectal and thalamic sensory relays.

Authors:  Jeremy D Cohen; Manuel A Castro-Alamancos
Journal:  J Neurosci       Date:  2010-02-10       Impact factor: 6.167

Review 8.  Peripheral neural circuits regulating IOP? A review of its anatomical backbone.

Authors:  M P ten Tusscher; H J Beckers; G F Vrensen; J Klooster
Journal:  Doc Ophthalmol       Date:  1994       Impact factor: 2.379

9.  C-Fos expression in trigeminal nucleus neurons after chemical irritation of the cornea: reduction by selective blockade of nociceptor chemosensitivity.

Authors:  S Martinez; C Belmonte
Journal:  Exp Brain Res       Date:  1996-04       Impact factor: 1.972

10.  Collateralization of the tectonigral projection with other major output pathways of superior colliculus in the rat.

Authors:  Véronique Coizet; Paul G Overton; Peter Redgrave
Journal:  J Comp Neurol       Date:  2007-02-20       Impact factor: 3.215

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