Literature DB >> 3171650

Synaptic organization of the tectal-facial pathways in the cat. I. Synaptic potentials following collicular stimulation.

P P Vidal1, P J May, R Baker.   

Abstract

1. The synaptic pathways underlying tectal influence over pinna movements were studied using an acute electrophysiological approach. Under pentobarbital anesthesia, postsynaptic potentials were recorded intracellularly in antidromically identified, cat facial motoneurons following electrical stimulation of the superior colliculus. How collicular topography is reflected in these synaptic potentials was examined using multiple stimulation sites. The pathways responsible for tectally evoked synaptic potentials were studied by making acute brain stem lesions and by intra-axonal horseradish peroxidase (HRP) staining. 2. Monosynaptic excitatory potentials (EPSPs) with latencies ranging from 0.7 to 1.1 ms and amplitudes that were always less than 1 mV were recorded in motoneurons following stimulation of the contralateral superior colliculus. Larger disynaptic EPSPs ranging in latency from 1.2 to 2.0 ms were recorded both in isolation and in association with monosynaptic EPSPs. In addition, disynaptic inhibitory synaptic potentials (IPSPs) with latencies ranging from 1.5 to 2.5 ms were observed, often in combination with monosynaptic EPSPs. Both disynaptic EPSPs and IPSPs were graded, augmented by multiple stimuli and found in all categories of motoneurons. 3. Stimulation of the ipsilateral superior colliculus produced nearly the same spectrum of potentials and latencies as did contralateral tectal stimulation. Occlusion between ipsi- and contralaterally evoked IPSPs suggests there might be a common element in the inhibitory disynaptic pathways. 4. More discrete populations of facial motoneurons were investigated. Specifically, motoneurons innervating the platysma and orbicularis oculi muscles, the intrinsic ear muscles, and muscles that move the vibrissae all displayed tectally elicited mono- and di-synaptic potentials. Collicular input was not restricted to motoneurons involved in orienting the pinnae. 5. The presence, polarity, and amplitude of the synaptic potentials evoked in individual facial motoneurons exhibited variations that were related to the site of stimulation in either the ipsi- or contralateral colliculus. These variations are compatible with the idea that the collicular input to facial motoneurons is topographically organized. 6. Acute lesions at the level of the superior olive indicated that the pathway producing the contralateral monosynaptic EPSPs runs, near the midline, ipsilateral to the target facial nucleus, whereas the contralateral disynaptic and the ipsilateral mono- and disynaptic pathways lie further lateral.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1988        PMID: 3171650     DOI: 10.1152/jn.1988.60.2.769

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  13 in total

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Authors:  M A Meredith; M T Wallace; B E Stein
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2.  Descending brainstem projections of the pedunculopontine tegmental nucleus in the rat.

Authors:  I Grofova; S Keane
Journal:  Anat Embryol (Berl)       Date:  1991

3.  Visual and vestibular signals in the lateral mesencephalic tegmental region of the cat.

Authors:  I Gerlach; P Thier; W Koehler
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4.  Anatomical evidence that the superior colliculus controls saccades through central mesencephalic reticular formation gating of omnipause neuron activity.

Authors:  Niping Wang; Eddie Perkins; Lan Zhou; Susan Warren; Paul J May
Journal:  J Neurosci       Date:  2013-10-09       Impact factor: 6.167

Review 5.  Circuits for Action and Cognition: A View from the Superior Colliculus.

Authors:  Michele A Basso; Paul J May
Journal:  Annu Rev Vis Sci       Date:  2017-06-15       Impact factor: 6.422

6.  Superior colliculus control of vibrissa movements.

Authors:  Marie E Hemelt; Asaf Keller
Journal:  J Neurophysiol       Date:  2008-06-18       Impact factor: 2.714

7.  An explanation for reflex blink hyperexcitability in Parkinson's disease. II. Nucleus raphe magnus.

Authors:  M A Basso; C Evinger
Journal:  J Neurosci       Date:  1996-11-15       Impact factor: 6.167

8.  Not looking while leaping: the linkage of blinking and saccadic gaze shifts.

Authors:  C Evinger; K A Manning; J J Pellegrini; M A Basso; A S Powers; P A Sibony
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9.  Neuronal premotor networks involved in eyelid responses: retrograde transneuronal tracing with rabies virus from the orbicularis oculi muscle in the rat.

Authors:  Sara Morcuende; José-Maria Delgado-Garcia; Gabriella Ugolini
Journal:  J Neurosci       Date:  2002-10-15       Impact factor: 6.167

10.  Connectivity of the goldfish optic tectum with the mesencephalic and rhombencephalic reticular formation.

Authors:  M P Pérez-Pérez; M A Luque; L Herrero; P A Nunez-Abades; B Torres
Journal:  Exp Brain Res       Date:  2003-05-14       Impact factor: 1.972

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