Literature DB >> 2611682

Physiological and morphological characteristics of periodontal mesencephalic trigeminal neurons in the cat--intra-axonal staining with HRP.

Y Shigenaga1, K Doe, S Suemune, Y Mitsuhiro, K Tsuru, K Otani, Y Shirana, M Hosoi, A Yoshida, K Kagawa.   

Abstract

Intra-axonal recording and horseradish peroxidase (HRP) injection techniques were employed to define the response properties of periodontal mechanoreceptive afferents originating from the trigeminal mesencephalic nucleus (Vmes) and their morphological characteristics. The periodontal Vmes neurons were classified into two types: slowly adapting (SA) and fast adapting (FA) types. The central terminals of 7 SA and 4 FA afferents were recovered for detailed analyses. The whole profile of SA and FA neurons were unipolar in shape and their cell bodies were located in the dorsomedial parts of the Vmes. The united (U) fiber traveled caudally from the soma to the dorsolateral aspect of the trigeminal motor nucleus (Vmo), where it split into the peripheral (P) and C fibers with a T- or Y-shaped appearance. The P fiber joined the trigeminal sensory or motor tract. The C fiber descended caudally within Probst's tract. All 3 stem fibers issued main collaterals. The main collaterals of all neurons examined formed terminal arbors in the supratrigeminal nucleus (Vsup) and all but two SA neurons projected to the intertrigeminal region (Vint), while the projections to other nuclei of the trigeminal motor nucleus (Vmo), juxtatrigeminal region (Vjux), main sensory nucleus (Vp) and oral nucleus (Vo.r) differed between SA and FA afferents and between neurons of the same type. The SA and FA neurons were classified into three and two subgroups, respectively. The major differences in central projections between the two types were that all the FA neurons projected to the Vp or Vo.r but none of SA type and this relation was reversed in the projection to the Vjux, and that more than half of SA neurons projected to Vmo but only one FA neuron to the Vmo. The Vmes neurons which sent their collaterals into the Vmo had the P fiber passing through the tract of the trigeminal motor nerve. The average size of somata and mean diameters of U fibers and main collaterals from C fiber were significantly larger in SA neurons than FA neurons. The average size of fiber varicosities became smaller in the following nuclei, Vmo, Vsup, Vp, Vint and Vo.r, but not significant between the two functional types. The functional role of the periodontal Vmes afferents to jaw reflexes was discussed particularly with respect to their central projection sites in the brainstem nuclei.

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Year:  1989        PMID: 2611682     DOI: 10.1016/0006-8993(89)90119-4

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  16 in total

1.  Quantitative analysis of the dendritic architectures of single jaw-closing and jaw-opening motoneurons in cats.

Authors:  Masayuki Moritani; Hideki Kida; Yoshitaka Nagase; Hideyuki Fukami; Shiho Honma; Motohide Takemura; Yuji Masuda; Yong Chul Bae; Yoshio Shigenaga; Atsushi Yoshida
Journal:  Exp Brain Res       Date:  2003-04-18       Impact factor: 1.972

2.  Involvement of histaminergic inputs in the jaw-closing reflex arc.

Authors:  Chikako Gemba; Kiyomi Nakayama; Shiro Nakamura; Ayako Mochizuki; Mitsuko Inoue; Tomio Inoue
Journal:  J Neurophysiol       Date:  2015-04-22       Impact factor: 2.714

3.  The recurrent case for the Renshaw cell.

Authors:  Gardave S Bhumbra; B Anne Bannatyne; Masahiko Watanabe; Andrew J Todd; David J Maxwell; Marco Beato
Journal:  J Neurosci       Date:  2014-09-17       Impact factor: 6.167

4.  Integration in trigeminal premotor interneurones in the cat. 3. Input characteristics and synaptic actions of neurones in subnucleus-gamma of the oral nucleus of the spinal trigeminal tract with a projection to the masseteric motoneurone subnucleus.

Authors:  K G Westberg; G Sandström; K A Olsson
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

5.  Creation of a novel trigeminal tractography atlas for automated trigeminal nerve identification.

Authors:  Fan Zhang; Guoqiang Xie; Laura Leung; Michael A Mooney; Lorenz Epprecht; Isaiah Norton; Yogesh Rathi; Ron Kikinis; Ossama Al-Mefty; Nikos Makris; Alexandra J Golby; Lauren J O'Donnell
Journal:  Neuroimage       Date:  2020-06-20       Impact factor: 6.556

6.  Quantitative analysis of synaptic contacts made between functionally identified oralis neurons and trigeminal motoneurons in cats.

Authors:  A Yoshida; H Fukami; Y Nagase; K Appenteng; S Honma; L F Zhang; Y C Bae; Y Shigenaga
Journal:  J Neurosci       Date:  2001-08-15       Impact factor: 6.167

7.  Role of the trigeminal mesencephalic nucleus in rat whisker pad proprioception.

Authors:  Ombretta Mameli; Stefania Stanzani; Gabriele Mulliri; Rosalia Pellitteri; Marcello A Caria; Antonella Russo; Pierluigi De Riu
Journal:  Behav Brain Funct       Date:  2010-11-15       Impact factor: 3.759

8.  Evidence for a trigeminal mesencephalic-hypoglossal nuclei loop involved in controlling vibrissae movements in the rat.

Authors:  Ombretta Mameli; Marcello Alessandro Caria; Rosalia Pellitteri; Antonella Russo; Salvatore Saccone; Stefania Stanzani
Journal:  Exp Brain Res       Date:  2015-12-08       Impact factor: 1.972

9.  Peripheral muscle targets and central projections of the mesencephalic trigeminal nucleus in macaque monkeys.

Authors:  Niping Wang; Paul J May
Journal:  Anat Rec (Hoboken)       Date:  2008-08       Impact factor: 2.064

10.  Synaptic Connectivity between Renshaw Cells and Motoneurons in the Recurrent Inhibitory Circuit of the Spinal Cord.

Authors:  Niall J Moore; Gardave S Bhumbra; Joshua D Foster; Marco Beato
Journal:  J Neurosci       Date:  2015-10-07       Impact factor: 6.167

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