Literature DB >> 3512624

Anatomical studies on the nucleus reticularis tegmenti pontis in the pigmented rat. I. Cytoarchitecture, topography, and cerebral cortical afferents.

Y Torigoe, R H Blanks, W Precht.   

Abstract

The nucleus reticularis tegmenti pontis (NRTP) is a precerebellar reticular nucleus that has been found to be related to cerebropontocerebellar pathways and, more recently, to eye movements. The present study investigates the cytoarchitecture, the topography, and the cerebral cortical projections to the NRTP in the pigmented rat. The cytoarchitecture and topography of the NRTP was determined by examination of Nissl-stained material sectioned in the transverse and sagittal planes. Two cytoarchitectonically distinct portions of the NRTP are apparent; a central subdivision (NRTPc) composed of large multipolar, small spherical, and fusiform neurons, and a pericentral subdivision (NRTPp) composed of loosely packed small fusiform and spherical neurons. The NRTPc is located dorsal to the medial lemniscus and pyramidal tracts over the caudal two-thirds of the pons. It extends caudodorsally to the region just rostral and ventral to the abducens nucleus. The NRTPp is adjacent to the lateral margins of the NRTPc, rostrally, and lies ventral to the caudal portions of the NRTPc. Large injections of horseradish peroxidase (HRP) were made into the cerebellum in order to determine the degree to which each subdivision of the NRTP contributes to the cerebellar projection. A high percentage of NRTPc neurons and a lower percentage of NRTPp neurons were labeled. These differences in labeling density and neuronal morphology noted above confirm the appropriateness of subdividing the NRTP into central and pericentral subdivisions. The cerebral cortical afferents to the NRTP were examined by placing small iontophoretic injections of HRP into the NRTPc and NRTPp. A systematic examination of all cortical areas revealed that the HRP-labeled neurons are entirely localized within pyramidal layer V of three major cortical areas: the ipsilateral prefrontal cortex (Brodmann areas 8, 8a, 11, and 32); the ipsilateral motor and somatosensory cortices (Brodmann areas 2, 4, 6, and 10), and the bilateral cingular cortex (Brodmann areas 24a, 24b, 29c, and 29d). By far, the heaviest cortical labeling with HRP injections into the medial NRTPc is within the cingular cortex that may, in the rat, be homologous to the frontal eye field of the cat and monkey. In contrast, injections involving the lateral NRTPc or the NRTPp produced labeling within wide regions of the cortex with the greatest number in the somatomotor cortex.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3512624     DOI: 10.1002/cne.902430107

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


  5 in total

1.  Descending projections from the superior colliculus in rat: a study using orthograde transport of wheatgerm-agglutinin conjugated horseradish peroxidase.

Authors:  P Redgrave; I J Mitchell; P Dean
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

2.  The Cerebellar Cortex Receives Orofacial Proprioceptive Signals from the Supratrigeminal Nucleus via the Mossy Fiber Pathway in Rats.

Authors:  Yumi Tsutsumi; Fumihiko Sato; Takahiro Furuta; Katsuro Uchino; Masayuki Moritani; Yong Chul Bae; Takafumi Kato; Yoshihisa Tachibana; Atsushi Yoshida
Journal:  Cerebellum       Date:  2022-07-04       Impact factor: 3.847

3.  Neurons in the rat subiculum with transient postmamillary collaterals during development maintain projections to the mamillary complex.

Authors:  B B Stanfield; D D O'Leary
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

4.  Effects of kainic acid lesions of the nucleus reticularis tegmenti pontis on fast and slow phases of vestibulo-ocular and optokinetic reflexes in the pigmented rat.

Authors:  B J Hess; R H Blanks; J Lannou; W Precht
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

5.  Anatomical pathways involved in generating and sensing rhythmic whisker movements.

Authors:  Laurens W J Bosman; Arthur R Houweling; Cullen B Owens; Nouk Tanke; Olesya T Shevchouk; Negah Rahmati; Wouter H T Teunissen; Chiheng Ju; Wei Gong; Sebastiaan K E Koekkoek; Chris I De Zeeuw
Journal:  Front Integr Neurosci       Date:  2011-10-04
  5 in total

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