Literature DB >> 3179716

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

Y Shigenaga1, A Yoshida, K Tsuru, Y Mitsuhiro, K Otani, C Q Cao.   

Abstract

The physiology and morphology of masticatory motoneurons of adult cats were examined by the methods of intracellular recording and intracellular injection of horseradish peroxidase. Masseter and jaw-opening motoneurons were identified by intracellular recordings of the antidromic response following stimulation of the masseter and mylohyoid nerves, respectively. An excitatory postsynaptic potential (EPSP) was recorded from masseter neurons by stimulation of the masseter nerve with stimulus intensity below threshold for antidromic response. In contrast, the EPSP was not recorded from jaw-opening motoneurons by stimulation of the mylohyoid nerve with stimulus intensity below threshold for antidromic response. Patterns of postsynaptic potentials (PSPs) in the masseter motoneurons following stimulation of the tooth pulp or periodontal afferents were classified into 4 types: hyperpolarization (n = 40), depolarization-hyperpolarization (n = 9), hyperpolarization-depolarization (n = 5), and depolarization with spike potentials (n = 10). On the other hand, patterns of the PSPs in the jaw-opening motoneurons following stimulation of the same afferents were classified into two types: depolarization with spike potentials (n = 19), and hyperpolarization (n = 5). Twenty-five masseter and 7 jaw-opening motoneurons and an intranuclear neuron were reconstructed from serial sections in the transverse plane. On the basis of dendritic morphology, the masseter motoneurons could be classified into two major groups, type I (n = 15) and type II (n = 9), whereas two neurons were found to constitute a separate category of the masseter motoneuron. The dendritic distributions of all the jaw-opening motoneurons examined were generally similar and there was no indication of the existence of subtypes, whereas there were 2 or 3 subgroups in type I and type II masseter motoneurons. Type I masseter neurons had primary dendrites which extended radially in all directions, and the whole profile of their dendritic trees presented a spherical and an egg-shaped appearance. In type II masseter neurons, the origin of primary dendrites was bipolar or tripolar, and the whole profile of their dendritic trees presented a hemispherical and mirror-imaged, funnel-shaped appearance. The other two masseter motoneurons had a particular dendritic tree which was much simpler in configuration, with less tapering or branching than those of other neurons examined. In contrast, the dendritic profiles of all the jaw-opening motoneurons were similarly organized and showed vertically oriented dendritic trees which were more developed in the dorsomedial than in the ventrolateral direction.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1988        PMID: 3179716     DOI: 10.1016/0006-8993(88)90255-7

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


  13 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.  Synchronization of motor units in human masseter during a prolonged isometric contraction.

Authors:  M A Nordstrom; T S Miles; K S Türker
Journal:  J Physiol       Date:  1990-07       Impact factor: 5.182

3.  Dense transient receptor potential cation channel, vanilloid family, type 2 (TRPV2) immunoreactivity defines a subset of motoneurons in the dorsal lateral nucleus of the spinal cord, the nucleus ambiguus and the trigeminal motor nucleus in rat.

Authors:  R D Lewinter; G Scherrer; A I Basbaum
Journal:  Neuroscience       Date:  2007-10-11       Impact factor: 3.590

4.  H-reflexes in masseter and temporalis muscles in man.

Authors:  G M Macaluso; A De Laat
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

5.  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

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.  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

8.  Gamma-aminobutyric acid-immunoreactive neurons in the rat trigeminal nuclei.

Authors:  E Ginestal; C Matute
Journal:  Histochemistry       Date:  1993-01

9.  Projection of cat jaw muscle spindle afferents related to intrafusal fibre influence.

Authors:  A Taylor; R Durbaba; J F Rodgers
Journal:  J Physiol       Date:  1993-06       Impact factor: 5.182

10.  Integration in trigeminal premotor interneurones in the cat. 2. Functional characteristics of neurones in the subnucleus-gamma of the oral nucleus of the spinal trigeminal tract with a projection to the digastric motoneurone subnucleus.

Authors:  K A Olsson; K G Westberg
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

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