Publications by authors named "Wolpaw J"

Monkeys can gradually change the amplitude of the wholly segmental, largely monosynaptic, spinal stretch reflex (SSR) when confronted by a task requiring such change (15-19). Change develops over months and may reverse and redevelop at similarly slow rates. We investigated the persistence of SSR amplitude change over nonperformance periods of up to 38 days.

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The study of the substrates of memory in higher vertebrates is one of the major problems of neurobiology. A simple and technically accessible experimental model is needed. Recent studies have demonstrated long-term adaptive plasticity, a form of memory, in the spinal stretch reflex (SSR).

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Monkeys can change the amplitude of the spinal stretch reflex (SSR), or M1, when reward is made contingent on amplitude. The present study demonstrates that reduced SSR day-to-day variation accompanies such adaptive SSR change. This finding supports the assumption that initial, phase I, SSR change results from contingency-appropriate stabilization of tonic activity in relevant descending spinal cord pathways.

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Monkeys can slowly increase or decrease the amplitude of the purely spinal, largely monosynaptic portion of the response to sudden muscle stretch, the spinal stretch reflex (SSR), when confronted by a task requiring such change (Wolpaw, J.R., V.

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Recent studies have revealed two phenomena producing considerable variation in amplitude of the initial, purely segmental, largely monosynaptic, response to sudden muscle stretch, the spinal stretch reflex (SSR), without change in background EMG activity or initial muscle length. The first is small and short-term, a modest diurnal rhythm in SSR amplitude. The second is large and long-term, marked adaptive change in SSR amplitude which occurs gradually over weeks and months when animals are rewarded for such change.

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The authors present psychoacoustic and electrophysiologic data concerning a patient with partial damage to the auditory nerve, presumably from a dilated arterial vessel. The lesion was described and documented during neurosurgery for vestibular nerve decompression. Pure tone thresholds, psychoacoustical tuning curves, speech reception ability for spondaic words, maximum word recognition performance for monosyllabic NU-6 word lists, and performance on the synthetic sentence identification test in the ipsilateral and contralateral competing message modalities were normal.

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Monkeys can gradually change the amplitude of the biceps spinal stretch reflex (SSR) without change in initial muscle length or biceps background electromyographic activity (EMG) (17). We investigated the concurrent behavior of synergist (brachialis and brachioradialis) and antagonist (triceps) muscles. Synergist background EMG remained stable while marked change occurred in biceps SSR amplitude.

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Description of the neuronal and synaptic bases of memory in the vertebrate central nervous system (CNS) requires a CNS stimulus-response pathway that is defined and accessible, has the capacity for adaptive change, and clearly contains the responsible substrates. This study was an attempt to determine whether the spinal stretch reflex (SSR), the initial, purely spinal, portion of the muscle stretch response, which satisfies the first requirement, also satisfies the second, capacity for adaptive change. Monkeys prepared with chronic fine-wire biceps electromyographic (EMG) electrodes were trained to maintain elbow position and a given level of biceps background EMG activity against constant extension torque.

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Monkeys can gradually increase or decrease the amplitude of the segmentally mediated spinal stretch reflex (SSR) without change in initial muscle length or background EMG activity. Both increase (under the SSR increases mode) and decrease (under the SSR decreases mode) occur slowly, progressing steadily over weeks. The present study investigated reversal and re-development of SSR amplitude change.

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The sequence of early, middle and late auditory evoked potentials is well known. However, it is unknown whether the late (60-250 msec) potentials can occur independently of the early, brain stem potentials. Therefore, in 6 subjects with markedly abnormal or absent brain stem potentials, we recorded two of the late potentials: the vertex potential and the T-complex.

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Monkeys can change the amplitude of the spinal stretch reflex without change in initial alpha motor neuron tone, as measured by EMG, or in initial muscle length. Change is apparent in 5-10 days, continues to develop over weeks, and persists during inactive periods. Spinal stretch reflex change may be a valuable system for studying the neuronal and synaptic bases of an adaptive change in primate CNS function.

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We studied primate spinal stretch reflex (SSR) amplitude as a function of time of day. SSR amplitude was greatest around midnight and smallest around noon. The diurnal rhythm was not simply a function of number of trials, or of the lighting cycle.

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The scalp distributions of human auditory evoked potentials (AEPs) between 20 and 250 msec were investigated using non-cephalic reference recordings. AEPs to binaural click stimuli were recorded simultaneously from 20 scalp locations over the right hemisphere in 11 subjects. Computer-generated isovoltage topographic maps at high temporal resolution were used to assess the stability of AEP scalp distributions over time and relate them to major peaks in the AEP wave forms.

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When a muscle is stretched in an awake, behaving primate the earliest electromyographic (EMG) responses of the muscle consists of several reflex components. The earliest, M1, is mediated entirely at the segmental level and is largely monosynaptic. The next M2, is at least in part the result of an oligosynaptic transcortical loop to control the M1 response remains to be established.

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1. Monkeys learned to maintain hand position against a range of background forces. Short-latency responses to passive wrist extension or flexion were recorded from units in areas 4, 3, 1, and 2.

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1. Monkeys were trained to maintain hand position against a range of constant forces. Short-latency responses to passive wrist extension or flexion, as well as short-latency responses to stretch of a single wrist muscle, were recorded from units in areas 4, 3, 1, and 2.

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The study investigated, in primary auditory cortex (AI) of awake cats, the relationship over a range of stimuli between the amplitude and latency of the initial positive deflection (P1) of the primary evoked potential and the intensity of concurrent underlying evoked single unit activity. Epidural evoked potentials and extracellular responses of 155 single units to monaural 100 musec clicks ranging from 45 to 110 dB were recorded. At low stimulus levels, considerable unit response could occur with a very small P1.

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Responses of single units in primary motor and sensory cortex of behaving primates to electromagnetic stretch of the muscle flexor carpi ulnaris are comparable in latency and intensity to responses to wrist extension. Thus, muscle stretch appears to be a major factor in cortical response to limb displacement during performance and probably has an important role in motor control at the cortical level.

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A previous paper (Wolpaw and Penry 1975) described separation of the 75-250 msec portion of the AER into N1P2, a product of large areas of cortex, and the T complex, probably a product of secondary auditory cortex. With monaural stimulation, the T complex is larger and earlier on the side contralateral to stimulation and on the right side. Thirty-one normal adults received 3 oz.

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The separation of the 80-250 msec portion of the AER to click stimulation into N1P2, produced by large areas of cortex, and the T complex, probably produced by secondary auditory cortex, was recently described (Wolpaw and Penry 1975). The present study investigated the ipsilateral vs. contralateral and right vs.

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