Literature DB >> 823305

Coding of mechanical stimulus velocity and indentation depth by squirrel monkey and raccoon glabrous skin mechanoreceptors.

B H Pubols, L M Pubols.   

Abstract

1. A sample of 113 large, myelinated first-order afferent fibers innervating the glabrous skin of the squirrel monkey's hand proved to consist primarily of two basic types. In a sample where the only known source of sampling bias is a greater likelihood to record from larger diameter fibers, 40% of the fibers were rapidly adapting (RA) and 60% were very slowly adapting (VSA). Two units were moderately slowly adapting (MSA), and one had the properties of a Pacinian afferent (Pc). 2. The RA and VSA resemble those in the glabrous skin of other mammalian species in terms of thresholds, receptive-field areas, conduction velocities, and the coding of velocity of mechanical displacement of the skin. Mean instantaneous frequency during ramp stimulation is a power function of ramp velocity for both RA and VSA, with exponents generally less than 1.00. However, ramp discharge patterns differ for RA and VSA. 3. The VSA exhibit a wide range of coefficients of variation (CV) of their interspike-interval distributions, but form a continuous distribution with respect to this statistic. In other respects the VSA are more similar to slowly adapting type I than to slowly adapting type II. They lack spontaneous activity, have restricted receptive fields, and are relatively insensitive to skin stretch. 4. Effects of mechanical stimulus velocity and static indentation depth on static discharge rate were examined in 23 squirrel monkey and 22 raccoon SA units having receptive fields on glabrous skin of the hand. 5. Discharge rate during static indentation is a monotonic, increasing function of identation depth. However, the nature of the best-fitting function (highest r) varies from unit to unit. Using a set of standard conditions (milliseconds 100-500 of static displacements up to 960 mum, following a ramp velocity of 100 mum/ms, interstimulus interval of at least 10 s), the ratio of units for which linear, as opposed to logarithmic, functions provided the best fit was 4:3 for squirrel monkeys and 1:3 for raccoons. Few units had power functions as best fits in either species. Differences between fits for different functions within the same unit, however, were often trivial and insignificant. 6. Response rate during static skin displacement is also strongly influenced by prior stimulus ramp velocity. For at least the first 500 ms, discharge rate is positively related to onset velocity but, in many units, within the first 1 s of static displacement, this relationship reverses itself, and the inverse relationship may persist for at least 5 s.

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Year:  1976        PMID: 823305     DOI: 10.1152/jn.1976.39.4.773

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


  12 in total

1.  The activity of monkey thalamic and motor cortical neurones in a skilled, ballistic movement.

Authors:  E G Butler; M K Horne; N J Hawkins
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

2.  Velocity invariance of receptive field structure in somatosensory cortical area 3b of the alert monkey.

Authors:  J J DiCarlo; K O Johnson
Journal:  J Neurosci       Date:  1999-01-01       Impact factor: 6.167

3.  Neural Coding of Contact Events in Somatosensory Cortex.

Authors:  Thierri Callier; Aneesha K Suresh; Sliman J Bensmaia
Journal:  Cereb Cortex       Date:  2019-12-17       Impact factor: 5.357

4.  Tactile sensibility in the human hand: relative and absolute densities of four types of mechanoreceptive units in glabrous skin.

Authors:  R S Johansson; A B Vallbo
Journal:  J Physiol       Date:  1979-01       Impact factor: 5.182

5.  Contribution of tactile afferent information to the control of isometric finger forces.

Authors:  H Henningsen; B Ende-Henningsen; A M Gordon
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

6.  Population estimates for responses of cutaneous mechanoreceptors to a vertically indenting probe on the glabrous skin of monkeys.

Authors:  R H Cohen; C J Vierck
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

7.  Ascending spinal axons that signal the position of the hindlimbs under static conditions: location and receptor input.

Authors:  J Y Wei; J Simon; M Randić; P R Burgess
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

8.  Tactile sensibility in the human hand: receptive field characteristics of mechanoreceptive units in the glabrous skin area.

Authors:  R S Johansson
Journal:  J Physiol       Date:  1978-08       Impact factor: 5.182

9.  Statistical analysis of multipath neural systems.

Authors:  B N Segal; J S Outerbridge
Journal:  Biol Cybern       Date:  1980       Impact factor: 2.086

10.  Coding of information about tactile stimuli by neurones of the cuneate nucleus.

Authors:  P R Douglas; D G Ferrington; M Rowe
Journal:  J Physiol       Date:  1978-12       Impact factor: 5.182

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