Selective temporal shift in the somatosensory evoked potential produced by chronic stimulation of the human index finger
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Summary
The present study determined whether the cortical potential from the human index finger changed with chronic nerve stimulation. Cerebral potentials were repeatedly recorded to stimulation of the ulnar nerve and the digital nerves of thumb, index and middle fingers, before and during a 7-day period in which the index was electrically stimulated (80 Hz) for 8–10 h daily. Cerebral potentials were recorded at three scalp sites over the contralateral “hand” area. Chronic stimulation produced no significant changes in the amplitudes or distribution of the cerebral potentials from the individual digits or the ulnar nerve. However, for the stimulated index finger there was a significant, progressive increase in latency of N20 and P25 without a detectable change in conduction velocity of distal peripheral axons. Timing in human central somatosensory pathways may be altered by the previous pattern of peripheral nerve inputs.
Key words
Cutaneous afferents Plasticity Hand functionPreview
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References
- Applegate C, Burke D (1989) Changes in excitability of human cutaneous afferents following prolonged high-frequency stimulation. Brain 112:147–164PubMedGoogle Scholar
- Calford MB, Tweedale R (1988) Immediate and chronic changes in responses of somatosensory cortex in adult flying-fox after digit amputation. Nature 332:446–448PubMedGoogle Scholar
- Debecker J, Desmedt JE (1964) Les potentiels évokées cérébraux et les potentials de nerf sensible chez l'homme. Acta Neurol Psychiat 64:1212–1248Google Scholar
- Desmedt JE, Cheron G (1981) Non-cephalic reference recording of early somatosensory potentials to finger stimulation in adult or aging normal man: differentiation of widespread N18 and contralateral N20 from the prerolandic P22 and N30 components. Electroencephalogr Clin Neurophysiol 52:553–570PubMedGoogle Scholar
- Donoghue JP, Sanes JN (1988) Organization of adult motor cortex representation patterns following neonatal forelimb nerve injury in rats. J Neurosci 8:3221–3232PubMedGoogle Scholar
- Dowman R, Wolpaw JR (1989) Diurnal rhythms in primate spinal reflexes and accompanying cortical somatosensory evoked potentials. Electroencephalogr Clin Neurophysiol 72:69–80CrossRefPubMedGoogle Scholar
- Eisen A, Purves S, Hoirch M (1982) Central nervous system amplification: its potential in the diagnosis of early multiple sclerosis. Neurology 32:359–364PubMedGoogle Scholar
- Emerson RG, Sgro JA, Pedley TA, Hauser WA (1988) State-dependent changes in the N20 component of the median nerve somatosensory evoked potential. Neurology 38:64–68PubMedGoogle Scholar
- Gandevia SC, Burke D (1984) Saturation in human somatosensory pathways. J Neurophysiol 54:582–585Google Scholar
- Gandevia SC, Burke D, McKeon B (1982) The relationship between the size of a muscle afferent volley and the cerebral potential it produces. J Neurol Neurosurg Psychiat 45:705–710PubMedGoogle Scholar
- Gandevia SC, Burke D, McKeon BB (1983) Convergence in the somatosensory pathway between cutaneous afferents from the index and middle fingers in man. Exp Brain Res 50:415–425CrossRefPubMedGoogle Scholar
- Gandevia SC, Macefield G, Burke D, McKenzie DK (1990) Voluntary activation of human motor axons in the absence of muscle afferent feedback: the control of the deafferented hand. Brain 113:1563–1581PubMedGoogle Scholar
- Jenkins WM, Merzenich MM (1987) Reorganization of neocortical representations after brain injury: a neurophysiological model of the bases of recovery from stroke. In: Seil FJ, Herbert E, Carlson BM (eds) Progress in brain research, Vol 71. Elsevier, North Holland, pp 249–266Google Scholar
- Johansson RS, Westling G (1984) Roles of glabrous skin receptors and sensorimotor memory in automatic control of precision grip when lifting rougher or slippery objects. Exp Brain Res 56:550–564CrossRefPubMedGoogle Scholar
- Kaas JH, Merzenich MM, Killackey HP (1983) The reorganization of somatosensory cortex following peripheral nerve damage in adult and developing mammals. Ann Rev Neurosci 6:325–356CrossRefPubMedGoogle Scholar
- Macefield G, Burke D (1991) Long-lasting depression of central synaptic transmission following prolonged high-frequency stimulation of cutaneous afferents: a mechanism for post-vibratory hypaesthesia. Electroencephalogr Clin Neurophysiol 78:150–158CrossRefPubMedGoogle Scholar
- Mauguière F, Desmedt JE, Courjon J (1983) Astereognosis and dissociated loss of frontal or pivotal components of somatosensory evoked potentials in hemispheric lesions: detailed correlations with clinical signs and computerized tomographic scanning. Brain 106:271–311PubMedGoogle Scholar
- Merzenich MM, Kaas JH, Wall JT, Sur M, Nelson RJ, Felleman DJ (1983) Progression of change following median nerve section in the cortical representation of the hand in areas 3b and 1 in adult owl and squirrel monkeys. Neurosci 10:639–665CrossRefGoogle Scholar
- Merzenich MM, Nelson RJ, Stryker MP, Cynader MD, Schoppmann A, Zook JM (1984) Somatosensory cortical map changes following digit amputation in adult monkeys. J Comp Neurol 224:591–605PubMedGoogle Scholar
- Ng A, Burke D, Al-Shehab A (1987) Hyperexcitability of cutaneous afferents during the supernormal period. Brain 110:1015–1031PubMedGoogle Scholar
- Rasmusson DD (1982) Reorganization of raccoon somatosensory cortex following removal of the fifth digit. J Comp Neurol 205:313–326PubMedGoogle Scholar
- Recanzone GH, Allard TT, Jenkins WM, Merzenich MM (1990) Receptive-field changes induced by peripheral nerve stimulation in SI of adult cats. J Neurophysiol 63:1213–1225PubMedGoogle Scholar
- Sica REP, Sanz OP, Cohen LG, Freyre JD, Panizza M (1984) Changes in the N1-P1 component of the somatosensory cortical evoked response in patients with partial limb amputation. Electromyogr Clin Neurophysiol 24:415–427PubMedGoogle Scholar
- Wall JT, Felleman DJ, Kaas JH (1983) Recovery of normal topography in the somatosensory cortex of monkeys after nerve crush and regeneration. Science 221:771–773PubMedGoogle Scholar
- Wall JT, Kaas JH, Sur M, Nelson RJ, Felleman DJ, Merzenich MM (1986) Functional reorganization in somatosensory cortical areas 3b and 1 of adult monkeys after median nerve repair: possible relationships to sensory recovery in humans. J Neurosci 6:218–233PubMedGoogle Scholar
- Zarzecki P, Wiggin DM (1982) Convergence of sensory inputs upon projection neurons of somatosensory cortex. Exp Brain Res 48:28–42CrossRefPubMedGoogle Scholar