Literature DB >> 3973927

Facial morphology and vibrissal movement in the golden hamster.

L E Wineski.   

Abstract

The major cranial vibrissae in the golden hamster can be moved in complex ways that suggest they are served by a finely controlled motor system. Movements are hypothesized to be the products of differential blood flow and pressure regulation in the sinus surrounding each vibrissal follicle, contractions of the striated facial muscles, and elastic rebound in the connective tissues. The vasculature contributes hydrostatic forces that erect the vibrissae slightly and distort their connective tissue bedding, rigidify the vibrissal capsules, thus forming firm bases of attachment for certain facial muscles, and theoretically provide a pressure plate around the follicle, important in lowering the firing thresholds of receptor endings. The facial muscles supply the major forces in erection and protraction of the vibrissae by acting on both the capsules and the connective tissue bedding. The connective tissues are organized into capsular and extracapsular systems that serve to stabilize the vibrissae and return them to initial rest positions. The slight movements of the genal vibrissa are the effects of vascular and connective tissue dynamics, the musculature being uninvolved. Wide angle movements of the supraorbital vibrissae are products of the vasculature and connective tissues, plus contractions of the Mm. orbicularis oculi and frontalis. Mystacial vibrissal movement is quite complex. The vasculature supplies a small degree of capsular erection and mystacial pad distortion, but primarily rigidifies the capsules. The bulk of erection and protraction is produced by the M. nasolabialis profundus (NLP) and the vibrissal capsular muscles (VCM). The NLP distorts the mystacial pad; the VCM tilt the capsules relative to the pad. Retraction is mainly accomplished by elastic rebound in the pad, this being aided in its extreme degrees by the Mm. nasolabialis and maxillolabialis. The Mm. nasolabialis superficialis and buccinator pars orbicularis oris help to spread the vibrissae into a dorsoventral fan and stabilize the mystacial pad during whisking.

Entities:  

Mesh:

Year:  1985        PMID: 3973927     DOI: 10.1002/jmor.1051830208

Source DB:  PubMed          Journal:  J Morphol        ISSN: 0022-2887            Impact factor:   1.804


  29 in total

1.  Whisker deafferentation and rodent whisking patterns: behavioral evidence for a central pattern generator.

Authors:  P Gao; R Bermejo; H P Zeigler
Journal:  J Neurosci       Date:  2001-07-15       Impact factor: 6.167

2.  Transplantation of olfactory mucosa minimizes axonal branching and promotes the recovery of vibrissae motor performance after facial nerve repair in rats.

Authors:  Orlando Guntinas-Lichius; Konstantin Wewetzer; Toma L Tomov; Natalie Azzolin; Shohreh Kazemi; Michael Streppel; Wolfrum F Neiss; Doychin N Angelov
Journal:  J Neurosci       Date:  2002-08-15       Impact factor: 6.167

3.  Flow sensing by pinniped whiskers.

Authors:  L Miersch; W Hanke; S Wieskotten; F D Hanke; J Oeffner; A Leder; M Brede; M Witte; G Dehnhardt
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-11-12       Impact factor: 6.237

4.  Dorsorostral snout muscles in the rat subserve coordinated movement for whisking and sniffing.

Authors:  Sebastian Haidarliu; David Golomb; David Kleinfeld; Ehud Ahissar
Journal:  Anat Rec (Hoboken)       Date:  2012-05-29       Impact factor: 2.064

5.  Corticostriatal projections from rat barrel cortex have an anisotropic organization that correlates with vibrissal whisking behavior.

Authors:  K D Alloway; J Crist; J J Mutic; S A Roy
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

6.  The Brainstem Oscillator for Whisking and the Case for Breathing as the Master Clock for Orofacial Motor Actions.

Authors:  David Kleinfeld; Jeffrey D Moore; Fan Wang; Martin Deschênes
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2015-04-15

7.  Intercolumnar synchronization of neuronal activity in rat barrel cortex during patterned airjet stimulation: a laminar analysis.

Authors:  Mengliang Zhang; Kevin D Alloway
Journal:  Exp Brain Res       Date:  2005-11-12       Impact factor: 1.972

Review 8.  Whisking mechanics and active sensing.

Authors:  Nicholas E Bush; Sara A Solla; Mitra Jz Hartmann
Journal:  Curr Opin Neurobiol       Date:  2016-09-13       Impact factor: 6.627

9.  Haptic object localization in the vibrissal system: behavior and performance.

Authors:  Per Magne Knutsen; Maciej Pietr; Ehud Ahissar
Journal:  J Neurosci       Date:  2006-08-16       Impact factor: 6.167

10.  Active Touch and Self-Motion Encoding by Merkel Cell-Associated Afferents.

Authors:  Kyle S Severson; Duo Xu; Margaret Van de Loo; Ling Bai; David D Ginty; Daniel H O'Connor
Journal:  Neuron       Date:  2017-04-20       Impact factor: 17.173

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