Literature DB >> 35781609

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

Yumi Tsutsumi1, Fumihiko Sato1, Takahiro Furuta1, Katsuro Uchino2, Masayuki Moritani3, Yong Chul Bae4, Takafumi Kato5, Yoshihisa Tachibana6, Atsushi Yoshida7,8.   

Abstract

Proprioceptive sensory information from muscle spindles is essential for the regulation of motor functions. However, little is known about the motor control regions in the cerebellar cortex that receive proprioceptive signals from muscle spindles distributed throughout the body, including the orofacial muscles. Therefore, in this study, we investigated the pattern of projections in the rat cerebellar cortex derived from the supratrigeminal nucleus (Su5), which conveys orofacial proprioceptive information from jaw-closing muscle spindles (JCMSs). Injections of an anterograde tracer into the Su5 revealed that many bilateral axon terminals (rosettes) were distributed in the granular layer of the cerebellar cortex (including the simple lobule B, crus II and flocculus) in a various sized, multiple patchy pattern. We could also detect JCMS proprioceptive signals in these cerebellar cortical regions, revealing for the first time that they receive muscle proprioceptive inputs in rats. Retrograde tracer injections confirmed that the Su5 directly sends outputs to the cerebellar cortical areas. Furthermore, we injected an anterograde tracer into the external cuneate nucleus (ECu), which receives proprioceptive signals from the forelimb and neck muscle spindles, to distinguish between the Su5- and ECu-derived projections in the cerebellar cortex. The labeled terminals from the ECu were distributed predominantly in the vermis of the cerebellar cortex. Almost no overlap was seen in the terminal distributions of the Su5 and ECu projections. Our findings demonstrate that the rat cerebellar cortex receives orofacial proprioceptive input that is processed differently from the proprioceptive signals from the other regions of the body.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Deep sensation; Muscle spindle; Precerebellar neurons; Tract tracing; Trigeminal

Year:  2022        PMID: 35781609     DOI: 10.1007/s12311-022-01434-z

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  65 in total

1.  Projection patterns of single mossy fiber axons originating from the dorsal column nuclei mapped on the aldolase C compartments in the rat cerebellar cortex.

Authors:  Pham Nguyen Quy; Hirofumi Fujita; Yukiyo Sakamoto; Jie Na; Izumi Sugihara
Journal:  J Comp Neurol       Date:  2011-04-01       Impact factor: 3.215

2.  Primary- and secondary-like jaw-muscle spindle afferents have characteristic topographic distributions.

Authors:  D Dessem; R Donga; P Luo
Journal:  J Neurophysiol       Date:  1997-06       Impact factor: 2.714

3.  Morphology of masticatory motoneurons stained intracellularly with horseradish peroxidase.

Authors:  A Yoshida; K Tsuru; Y Mitsuhiro; K Otani; Y Shigenaga
Journal:  Brain Res       Date:  1987-07-28       Impact factor: 3.252

4.  An unrelayed projection of jaw-muscle spindle afferents to the cerebellum.

Authors:  R Donga; D Dessem
Journal:  Brain Res       Date:  1993-10-29       Impact factor: 3.252

5.  Differential distribution of cell bodies and central axons of mesencephalic trigeminal nucleus neurons supplying the jaw-closing muscles and periodontal tissue: a transganglionic tracer study in the cat.

Authors:  S Nomura; N Mizuno
Journal:  Brain Res       Date:  1985-12-16       Impact factor: 3.252

6.  The cells of origin of the trigeminothalamic, trigeminospinal and trigeminocerebellar projections in the cat.

Authors:  M Matsushita; M Ikeda; N Okado
Journal:  Neuroscience       Date:  1982-06       Impact factor: 3.590

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

Authors:  A Yoshida; N Mukai; M Moritani; Y Nagase; Y Hirose; S Honma; H Fukami; K Takagi; T Matsuya; Y Shigenaga
Journal:  J Comp Neurol       Date:  1999-03-29       Impact factor: 3.215

8.  Sensory neurons and motoneurons of the jaw-closing reflex pathway in rats: a combined morphological and physiological study using the intracellular horseradish peroxidase technique.

Authors:  K Lingenhöhl; E Friauf
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

9.  Central distribution of synaptic contacts of primary and secondary jaw muscle spindle afferents in the trigeminal motor nucleus of the cat.

Authors:  H Kishimoto; Y C Bae; A Yoshida; M Moritani; M Takemura; S Nakagawa; Y Nagase; T Wada; B J Sessle; Y Shigenaga
Journal:  J Comp Neurol       Date:  1998-02-02       Impact factor: 3.215

10.  Physiological and morphological characteristics of cat masticatory motoneurons--intracellular injection of HRP.

Authors:  Y Shigenaga; A Yoshida; K Tsuru; Y Mitsuhiro; K Otani; C Q Cao
Journal:  Brain Res       Date:  1988-10-04       Impact factor: 3.252

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