Literature DB >> 3782507

A comparative light microscopic analysis of the sensory innervation of the mystacial pad. II. The common fur between the vibrissae.

F L Rice, B L Munger.   

Abstract

The innervation to the common fur between the vibrissae was examined in the hamster, mouse, rat, gerbil, rabbit, guinea pig, and cat. Samples were taken from central locations among the more caudal vibrissae in the mystacial pad and processed with Richardson's variant of the Bielschowsky silver technique or with Winkelmann's silver technique to selectively stain peripheral axons and terminals. Additional samples were taken among the rostral vibrissae in the rat. We found major unpredictable species-related variations in the distribution of receptor types, innervation density, and the quantity of innervation in the skin between neighboring vibrissae. The common fur is composed of numerous larger guard hairs and even more numerous smaller vellus hairs. The guard hairs usually are richly innervated with fully developed piloneural complexes composed primarily of a pallisade of lanceolate endings and a circumferential array of Ruffini and free nerve endings. The vellus hairs are usually innervated by individual or shared free nerve endings. The piloneural complexes in the cat, rat, and mouse are usually complete, whereas those in the other species were usually incomplete and lacked Ruffini endings. There is considerable interspecies variation in the relative quantity of innervation between homologous neighboring vibrissae. The quantity of innervation is related to a combination of receptor completeness, innervation density, and distance between vibrissae. The quantity of intervibrissal fur innervation is by far highest in the cat, relatively high in the rabbit, relatively low in the hamster and caudal mystacial pad of the rat, and lowest in the mouse, gerbil, guinea pig, and rostral mystacial pad of the rat. The differences in the innervation between the cat and the rabbit correlate well with published physiologic data on types of receptor units. Also, barrels are most prominent in species having relatively low quantities of intervibrissal innervation and are less prominent or absent in species having high quantities of intervibrissal innervation.

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Year:  1986        PMID: 3782507     DOI: 10.1002/cne.902520205

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  16 in total

1.  Imaging spatiotemporal dynamics of surround inhibition in the barrels somatosensory cortex.

Authors:  Dori Derdikman; Rina Hildesheim; Ehud Ahissar; Amos Arieli; Amiram Grinvald
Journal:  J Neurosci       Date:  2003-04-15       Impact factor: 6.167

2.  Loss of information concerning hair displacement and other somatic stimuli in the first somatic sensory cortex of unanesthetized Macaca mulatta monkeys following dorsal funiculus transections.

Authors:  R J Schneider
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

3.  Deflection of a vibrissa leads to a gradient of strain across mechanoreceptors in a mystacial follicle.

Authors:  Samuel J Whiteley; Per M Knutsen; David W Matthews; David Kleinfeld
Journal:  J Neurophysiol       Date:  2015-04-08       Impact factor: 2.714

4.  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

5.  A high concentration of Merkel cells in the bulge prior to the attachment of the arrector pili muscle and the formation of the perifollicular nerve plexus in human fetal skin.

Authors:  Y Narisawa; K Hashimoto; Y Nakamura; H Kohda
Journal:  Arch Dermatol Res       Date:  1993       Impact factor: 3.017

6.  Differential effects of NGF and NT-3 on embryonic trigeminal axon growth patterns.

Authors:  E Ulupinar; M F Jacquin; R S Erzurumlu
Journal:  J Comp Neurol       Date:  2000-09-18       Impact factor: 3.215

7.  Genetic Identification of an Expansive Mechanoreceptor Sensitive to Skin Stroking.

Authors:  Ling Bai; Brendan P Lehnert; Junwei Liu; Nicole L Neubarth; Travis L Dickendesher; Pann H Nwe; Colleen Cassidy; C Jeffery Woodbury; David D Ginty
Journal:  Cell       Date:  2015-12-17       Impact factor: 41.582

8.  The morphology and innervation of facial vibrissae in the tammar wallaby, Macropus eugenii.

Authors:  L R Marotte; F L Rice; P M Waite
Journal:  J Anat       Date:  1992-06       Impact factor: 2.610

9.  Postnatal development of autonomic and sensory innervation of thoracic hairy skin in the rat. A histochemical, immunocytochemical, and radioenzymatic study.

Authors:  R J Schotzinger; S C Landis
Journal:  Cell Tissue Res       Date:  1990-05       Impact factor: 5.249

10.  The innervation of the mystacial pad in the adult rat studied by anterograde transport of HRP conjugates.

Authors:  B T Fundin; F L Rice; K Pfaller; J Arvidsson
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

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