Population estimates for responses of cutaneous mechanoreceptors to a vertically indenting probe on the glabrous skin of monkeys
- 84 Downloads
- 13 Citations
Abstract
Recordings were obtained from low-threshold mechanoreceptive afferents during stimulation with a 0.5-mm-diameter probe at the receptive field (RF) center and at different distances from the point of maximal sensitivity. At each location, force-controlled stimuli of 0.5–4.0 g were ramped on to a plateau and then off at rates of 1, 10, and 100 g/s. The properties of rapidly adapting (RA) and slowly adapting type I (SAI) mechanoreceptors, when stimulated at the RF center, were similar in many respects to those reported in previous studies. Controlled stimulation away from the RF centers revealed that RF size for RAs was primarily dependent upon ramp rate, and for SAIs the size of the RF was primarily dependent upon load (force). The action potentials from individual afferents during stimulation at each location were binned in time and assigned to spatial segments of 1 mm. These responses were multiplied by: (A) an annular area of the receptive field and (B) the innervation density for the afferent type and skin region. The calculations provided estimates of overall rates of activity among the population of cutaneous afferents that respond to indentation by a small probe. Important differences were obtained between the responses of the population of afferents activated by the trapezoidal stimulus and the responses of afferents stimulated only at the RF center. Populations of tactile afferents provide more information for rate and intensity (force) discriminations than is available from units stimulated at the RF center. For RA afferents, the exponent of the power function describing relationships between stimulus rate and the population discharge (in impulses per second) was 0.3 times greater than the exponent for responses to on-center stimulation. For SAI mechanoreceptors, the exponent of the power functions for static responses to force was 0.22 times greater for the population responses than for on-center activation. Population functions for RA responses to the rate of force application and for SAI responses to static load saturated less than comparable responses to stimuation of the RF center. Thus, the coding capacity of the population extends the range of tactile discriminability. The slope and range of stimulus-response functions for populations was enhanced relative to responses to oncenter stimulation. This occurs because of recruitment of afferents with RF centers adjacent to and remote from the stimulus, depending upon thresholds and receptive field sizes for different stimulus parameters. With stimulation at increasing rates and forces, there is a progressive spatial recruitment of receptors. Over 90% of the activity elicited by suprathreshold punctate stimuli originated from mechanoreceptors with RF centers 1 mm or more away from the stimulus site. When the population response of SA afferents was calculated for different intensities of plateau stimulation, ranging from 1 to 4 g, the slope of the power function corresponded well to psychophysical estimates in the literature on the growth of touch intensity. Recruitment of afferents stimulated off the RF center shaped the temporal pattern of discharge. For RA afferents, the population response reached peak rates toward later portions of the onset and offset response than for on-center stimulation. For SAI afferents, the population discharge during slow onsets accelerated more positively than the responses to on-center stimulation. Variations in the rate, amplitude, and duration of stimulation were demonstrated to be useful in assessing the contribution of SAI and RA afferents to different tactile sensations. At very slow rates of stimulus application, the RA response was so minimal that the population response can be considered to arise from SAI afferents. At high stimulus rates, the population response was greatly accentuated during the onset (indentation) and offset (removal) of a trapezoidal ramp-and-hold stimulus, relative to firing rates during maintained indentation. Ratios of dynamic to static discharge were 3–4 times greater for the population than for on-center stimulation, reaching values as high as 60.2∶1. The ratios of dynamic to static population responses were greatest for stimuli presented to the palm and were least for stimuli presented to the base and middle phalanges of the fingers. Therefore, the relative magnitudes of onset, offset, and steadystate sensations elicited by stimulation at different rates and locations should vary systematically, according to the absolute and relative densities of each receptor type.
Key words
Cutaneous afferents Touch magnitude Somesthesis Skinsensitivity MonkeysPreview
Unable to display preview. Download preview PDF.
References
- Armett CJ, Hunsperger RW (1961) Excitation of receptors in the pad of the cat by single and double mechanical pulses. J Physiol (Lond) 158:15–38Google Scholar
- Åstrand K, Hämäläinen H, Aleksandrov YI, Järvilehto T (1986) Response characteristics of peripheral mechanoreceptive units in man: relation to the sensation magnitude and to the subject's task. Electroencephalogr Clin Neurophysiol 64:438–446Google Scholar
- Bliss JC (1978) Reading machines for the blind. In: Gordon G (ed) Active touch. Pergamon, Oxford, pp 243–248Google Scholar
- Burgess PR, Perl ER (1973) Cutaneous mechanoreceptors and nociceptors. In: Handbook of sensory physiology. Iggo A (ed) Springer, Berlin Heidelberg New York, pp 29–78Google Scholar
- Burgess PR, Howe JF, Lessler MJ, Whitehorn D (1974) Cutaneous receptors supplied by myelinated fibers in the cat. II. Number of mechanoreceptors excited by a local stimulus. J Neurophysiol 37:1373–1386Google Scholar
- Burgess PR, Mei J, Tuckett RP, Horch KW, Ballinger CM, Poulos DA (1983) The neural signal for skin indentation depth. I. tChanging indentations. J Neurosci 3:1572–1585Google Scholar
- Cohen RH, Vierck CJ Jr (1993) Relationships between touch sensations and estimated population responses of peripheral afferent mechanoreceptors. Exp Brain Res 94:120–130Google Scholar
- Darian-Smith I, Kenins P (1980) Innervation density of mechanoreceptive fibres supplying glabrous skin of the monkey's index finger. J Physiol (Lond) 309:147–155Google Scholar
- Dykes RW, Rasmussen DD, Hoeltzell P (1980) Organization of primary somatosensory cortex in the cat. J Neurophysiol 43:1527–1546Google Scholar
- Erickson RP (1968) Stimulus coding in topographic and non-topographic modalities: On the significance of the activity of individual sensory neurons. Psychol Rev 75:447–465Google Scholar
- Franzén O, Lindblom U (1976) Coding of velocity of skin indentation in man and monkey. A perceptual-neurophysiological correlation. In: Zotterman Y (ed) Sensory functions of the skin in primates. Pergamon, Oxford, pp 55–65Google Scholar
- Gardner EP, Palmer CI (1989) Simulation of motion on the skin. I. Receptive fields and temporal frequency coding by cutaneous mechanoreceptors of OPTACON pulses delivered to the hand. J Neurophysiol 62:1410–1436Google Scholar
- Gardner EP, Spencer WA (1972) Sensory funneling. II. Cortical neuronal representation of patterned cutaneous stimuli. J Neurophysiol 35:954–977Google Scholar
- Goodwin AW, Pierce ME (1981) Population of quickly adapting mechanoreceptive afferents innervating the glabrous skin: representation of two vibrating probes. J Neurophysiol 45:243–253Google Scholar
- Greenspan JD, Kenshalo DR Sr, Henderson R (1984) The influence of rate of skin indentation on threshold and suprathreshold tactile sensations. Somatosens Res 1:379–393Google Scholar
- Harrington T, Merzernich MM (1970) Neural coding in the sense of touch: human sensations of skin indentation compared with the responses of slowly adapting mechanoreceptive afferents innervating the hairy skin of monkeys. Exp Brain Res 10:251–264Google Scholar
- Jänig W (1971) Morphology of rapidly and slowly adapting mechanoreceptors in the hairless skin of the cat's hind foot. Brain Res 28:217–231Google Scholar
- Johansson R (1978) Tactile sensibility in the human hand: receptive field characteristics of mechanoreceptor units in the glabrous skin. J Physiol (Lond) 281:101–123Google Scholar
- Johansson R, Vallbo ÅB (1976) Skin mechanoreceptors in the human hand: an inference of some population properties. In: Zotterman Y (ed) Sensory functions of the skin in primates. Pergamon, Oxford, pp 171–184Google Scholar
- Johansson R, Vallbo ÅB (1979) Skin mechanoreceptors in the human hand: an inference of some population properties. In: Zotterman Y (ed) Sensory functions of the skin in primates. Pergamon, Oxford, pp 171–184Google Scholar
- Johansson RS, Vallbo ÅB (1980) Spatial properties of the population of mechanoreceptive units in the glabrous skin of the human hand. Brain Res 184:353–366Google Scholar
- Johnson KO (1974) Reconstruction of population response to a vibratory stimulus in quickly adapting mechanoreceptive afferent fiber population innervating glabrous skin of the monkey. J Neurophysiol 37:48–72Google Scholar
- Johnson KO, Lamb GD (1981) Neural mechanisms of spatial tactile discrimination: neural patterns evoked by braille-like dot patterns in the monkey. J Physiol (Lond) 310:117–144Google Scholar
- Jones MB, Vierck CJ Jr (1973) Length discrimination on the skin. Am J Psychol 86:49–60Google Scholar
- Jones MB, Vierck CJ Jr, Graham RB (1973) Line-gap discrimination on the skin. Percept Mot Skills 36:563–570Google Scholar
- Knibestöl M (1973) Stimulus-response functions of rapidly adapting mechanoreceptors in the human glabrous skin area. J Physiol (Lond) 232:427–452Google Scholar
- Knibestöl M (1975) Stimulus-response functions of slowly adapting mechanoreceptors in the human glabrous skin area. J Physiol (Lond) 245:63–80Google Scholar
- Knibestöl M, Vallbo ÅB (1980) Intensity of sensation related to activity of slowly adapting mechanoreceptive units in the human hand. J Physiol (Lond) 300:251–267Google Scholar
- Kruger L, Kenton B (1973) Quantitative neural and psychophysical data for cutaneous mechanoreceptor function. Brain Res 49:1–24Google Scholar
- Linblom U (1965) Properties of touch receptors in distal glabrous skin of monkey. J Neurophysiol 28:966–985Google Scholar
- Mei J, Tuckett RP, Poulos DA, Horch KW, Wei JY, Burgess PR (1983) The neural signal for skin indentation depth II. Steady indentations. J Neurosci 3:2652–2659Google Scholar
- Mountcastle VB (1967) The problem of sensing and the neural coding of sensory events. In: Quarton GC, Melnechuk T, Schmitt FO (eds) The neurosciences. Rockefeller University Press, New York, pp 393–408Google Scholar
- Mountcastle VB, Talbot WH, Sakata H, Hyvarinen J (1969) Cortical neuronal mechanisms in flutter-vibration studied in unanesthetized monkeys. Neuronal periodicity and frequency discrimination. J Neurophysiol 32:452–484Google Scholar
- Ochoa J, Torebjörk E (1983) Sensations evoked by intraneural microstimulation of single mechanoreceptor units innervating the human hand. J Physiol (Lond) 342:633–654Google Scholar
- Phillips JR (1976) Spatial response characteristics of slowly adapting mechanoreceptors in the palmar skin of the monkey. MS thesis. University of Melbourne, AustraliaGoogle Scholar
- Poulos DA, Mei J, Horch KW, Tuckett RP, Wei JY, Cornwell MC, Burgess PR (1984) The neural signal for intensity of a tactile stimulus. J Neurosci 4:2016–2024Google Scholar
- Pubols BH (1980) On- versus off-responses of raccoon glabrous skin rapidly adapting cutaneous mechanoreceptors. J Neurophysiol 43:1558–1570Google Scholar
- Pubols BH (1987) Effect of mechanical stimulus spread across glabrous skin of raccoon and squirrel monkey hand on tactile primary afferent fiber discharge. Somatosens Res 4:273–308Google Scholar
- Pubols BH (1988) Spread of skin deformation and mechanoreceptor discharge. Prog Brain Res 74:263–270Google Scholar
- Pubols BH, Pubols LM (1976) Coding of mechanical stimulus velocity and indentation depth by squirrel monkey and racoon glabrous skin mechanoreceptors. J Neurophysiol 39:773–787Google Scholar
- Pubols BH, Pubols LM (1987) Coding of mechanical stimulus velocity and indentation depth by squirrel monkey and racoon glabrous skin mechanoreceptors. J Neurophysiol 39:773–787Google Scholar
- Ray RH, Doetsch GS (1990a) Coding of stimulus location and intensity in populations of mechanosensitive nerve fibers of the raccoon. I. Single fiber response properties. Brain Res Bull 25:517–532Google Scholar
- Ray RH, Doetsch GS (1990b) Coding of stimulus location and intensity in populations of mechanosensitive nerve fibers of the raccoon. II. Across-fiber reponses patterns. Brain Res Bull 25:533–550Google Scholar
- Stevens JC, Mack JD (1959) Scales of apparent force. J Exp Psychol 58:405–413Google Scholar
- Sur M, Nelson RJ, Kaas JH (1982) Representations of the body surface in somatic koniocortex in the prosimian galago. J Comp Neurol 189:381–402Google Scholar
- Sur M, Wall JT, Kaas JT (1984) Modular distribution of neurons with slowly adapting and rapidly adapting responses in area 3b of somatosensory cortex in monkeys. J Neurophysiol 51:724–744Google Scholar
- Tuckett RP, Horch KW, Burgess PR (1978) Response of cutaneous hair and field mechanoreceptors in cat to threshold stimuli. J Neurophysiol 41:138–149Google Scholar
- Werner G, Mountcastle VB (1965) Neural activity in mechanoreceptive cutaneous afferents: stimulus-response relations, Weber functions, and information transmission. J Neurophysiol 28:359–397Google Scholar
- Werner G, Mountcastle VB (1968) Quantitative relations between mechanical stimuli to the skin and the neural responses evoked by them. In: Kenshalo DR (ed) The skin senses. Thomas, Springfield, Ill., pp 112–137Google Scholar