Literature DB >> 12713646

Cellular mechanisms of the trigeminally evoked startle response.

Susanne Schmid1, Nadine S Simons, Hans-Ulrich Schnitzler.   

Abstract

The startle response is an important mammalian model for studying the cellular mechanisms of emotions and of learning. It consists of contractions of facial and skeletal muscles in response to sudden acoustic, tactile or vestibular stimuli. Whereas the acoustic startle pathway is well described, only a few recent studies have investigated the tactile startle pathway. It was proposed that there is a direct projection from the principal sensory nucleus to the central sensorimotor interface of the startle response, which is formed by the giant neurons in the caudal pontine reticular formation. We explored this projection in greater detail in vitro. Anterograde tracing in rat brain slices confirmed projections with large axon terminals from the ventral part of the principal sensory nucleus to the lateral caudal pontine reticular formation. Electrophysiological studies revealed a monosynaptic glutamatergic connection between principal sensory nucleus neurons and caudal pontine reticular formation giant neurons. The synapses displayed paired-pulse facilitation at high-frequency stimulation, and homosynaptic depression at 1 Hz stimulation. The latter form of plasticity is thought to underlie habituation of the startle response. Furthermore, postsynaptic currents in caudal pontine reticular formation giant neurons evoked by principal sensory nucleus neuron stimulation summed in a linear way with signals evoked by stimulation of auditory afferents. Synaptic plasticity and summation of synaptic currents correspond well with in vivo data previously published by other groups. We thus presume that these synapses mediate trigeminal input to the startle pathway.

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Year:  2003        PMID: 12713646     DOI: 10.1046/j.1460-9568.2003.02565.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  7 in total

1.  A genome-wide screen identifies PAPP-AA-mediated IGFR signaling as a novel regulator of habituation learning.

Authors:  Marc A Wolman; Roshan A Jain; Kurt C Marsden; Hannah Bell; Julianne Skinner; Katharina E Hayer; John B Hogenesch; Michael Granato
Journal:  Neuron       Date:  2015-03-05       Impact factor: 17.173

Review 2.  Acoustic startle modification as a tool for evaluating auditory function of the mouse: Progress, pitfalls, and potential.

Authors:  Amanda M Lauer; Derik Behrens; Georg Klump
Journal:  Neurosci Biobehav Rev       Date:  2017-03-19       Impact factor: 8.989

3.  The Role of Cholinergic Midbrain Neurons in Startle and Prepulse Inhibition.

Authors:  Erin Azzopardi; Andrea G Louttit; Cleusa DeOliveira; Steven R Laviolette; Susanne Schmid
Journal:  J Neurosci       Date:  2018-08-31       Impact factor: 6.167

4.  Role of GluA4 in the acoustic and tactile startle responses.

Authors:  Sofía García-Hernández; María E Rubio
Journal:  Hear Res       Date:  2021-12-07       Impact factor: 3.208

Review 5.  Targeting Neuronal Networks with Combined Drug and Stimulation Paradigms Guided by Neuroimaging to Treat Brain Disorders.

Authors:  Carl L Faingold; Hal Blumenfeld
Journal:  Neuroscientist       Date:  2015-07-06       Impact factor: 7.519

6.  Synaptic depression and short-term habituation are located in the sensory part of the mammalian startle pathway.

Authors:  Nadine S Simons-Weidenmaier; Maruschka Weber; Claudia F Plappert; Peter K D Pilz; Susanne Schmid
Journal:  BMC Neurosci       Date:  2006-05-09       Impact factor: 3.288

Review 7.  Trigeminal, Visceral and Vestibular Inputs May Improve Cognitive Functions by Acting through the Locus Coeruleus and the Ascending Reticular Activating System: A New Hypothesis.

Authors:  Vincenzo De Cicco; Maria P Tramonti Fantozzi; Enrico Cataldo; Massimo Barresi; Luca Bruschini; Ugo Faraguna; Diego Manzoni
Journal:  Front Neuroanat       Date:  2018-01-08       Impact factor: 3.856

  7 in total

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