Literature DB >> 10100891

Physiologic and morphologic properties of motoneurons and spindle afferents innervating the temporal muscle in the cat.

A Yoshida1, N Mukai, M Moritani, Y Nagase, Y Hirose, S Honma, H Fukami, K Takagi, T Matsuya, Y Shigenaga.   

Abstract

Little is known about physiology and morphology of motoneurons and spindle afferents innervating the temporalis and on synaptic connections made between the two. The present study was aimed at investigating the above issues at the light microscopic level by using the intracellular recording and horseradish peroxidase or biotinamide labeling techniques and by the use of succinylcholine (SCh) for the classification of spindle afferents in the cat. Temporalis motoneurons had dendritic trees that ranged from a spherical form to an egg-shaped form. The shape deformation was more prominent for the dendritic trees made by motoneurons located closer to the nuclear border. No axon collaterals of the motoneurons were detected. On the basis of the values for the dynamic index after SCh infusion, temporalis spindle afferents were classified into two populations: presumptive groups Ia and II. The spindle afferents terminated mainly in the supratrigeminal nucleus (Vsup), region h, and the dorsolateral subdivision (Vmo.dl) of the trigeminal motor nucleus (Vmo). The proportion of group Ia afferent terminals was lower in the Vsup than that of group II afferents. In the Vmo.dl, the proportion of group Ia afferent terminals was nearly even throughout the nucleus, but that of group II afferent terminals increased in the more outlying regions. The proportion of terminal distribution in the central region of Vmo.dl was higher for group Ia than group II. The frequency of contacts (presumptive synapses) made by a single spindle afferent on a motoneuron was higher for group Ia than group II. The present study provided evidence that the central organization of spindle afferent neurons is different between groups Ia and II.

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Year:  1999        PMID: 10100891

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


  6 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.  Masseteric nerve injury increases expression of brain-derived neurotrophic factor in microglia within the rat mesencephalic trigeminal tract nucleus.

Authors:  Hiroyuki Ichikawa; Tadasu Sato; Mitsuhiro Kano; Toshihiko Suzuki; Saburo Matsuo; Hiroyasu Kanetaka; Yoshinaka Shimizu
Journal:  Cell Mol Neurobiol       Date:  2011-01-12       Impact factor: 5.046

3.  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

4.  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

5.  A trigeminoreticular pathway: implications in pain.

Authors:  W Michael Panneton; Qi Gan; Robert S Livergood
Journal:  PLoS One       Date:  2011-09-21       Impact factor: 3.240

Review 6.  Synaptic Plasticity on Motoneurons After Axotomy: A Necessary Change in Paradigm.

Authors:  Francisco J Alvarez; Travis M Rotterman; Erica T Akhter; Alicia R Lane; Arthur W English; Timothy C Cope
Journal:  Front Mol Neurosci       Date:  2020-04-30       Impact factor: 5.639

  6 in total

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