Impedance across the cat's foot pad, the glands being at rest, has a high quite constant value in a given preparation. Stimulation of the sudomotor nerves causes a decrease to a low constant value. After cessation of stimulation impedance returns slowly over a course that is linear with respect to the logarithm of time. The resistive and capacitative components vary with each other. Sweat reabsorption during recovery progresses linearly with respect to time. Hence impedance varies as the logarithm of reabsorption, and therefore as the mean level of sweat columns in the ducts. This relation can be accommodated by supposing that the sweat duct epithelium resembles a core conductor. An electrical model constructed on this principle is shown to behave as does the foot pad. During stimulation at a fixed frequency impedance change varies as the logarithm of duration showing that the amount of sweat produced per impulse at a given frequency is a constant. With frequency of a fixed number of stimuli varied the impedance change varies with it in a manner consistent with the view that the amount of sweat produced per impulse is a constant regardless of frequency.

Animals↗

PubMed1959

Response of cholinergically innervated sweat glands to adrenaline and noradrenaline.

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Acetylcholine↗

PubMed1959

Functional organization in the terminal segments of the spinal cord with a consideration of central excitatory and inhibitory latencies in monosynaptic reflex systems.

Prominent monosynaptic and disynaptic reflex discharges characterize ipsilateral reflex transmission in the third sacral segment. Convergence upon the motoneurons from the two sides of the body is inhibitory, that through disynaptic paths excitatory. The relative latencies of excitation and inhibition of reflex responses, of excitatory and inhibitory synaptic potentials, and of various aspects of impulse discharge in motoneurons are considered. It is concluded: (1) that a direct (i.e. monosynaptic) action of primary afferent collaterals upon motoneurons is responsible for inhibition of monosynaptic reflex discharge of antagonist motoneurons within a myotatic unit; (2) that the inhibitory postsynaptic potential as described is not the primary agency for monosynaptic reflex inhibition of monosynaptic reflex discharge; (3) that, however, a common causal agent may be responsible for inhibition of reflex discharge and for generation of an inhibitory postsynaptic potential; and (4) that the inhibitory post-synaptic potential may be linked with, or be the agent for, inhibition of soma response.

Motor Neurons↗

PubMed1959

Early and late post-tetanic potentiation, and post-tetanic block in a monosynaptic reflex pathway.

Observations have been made upon the nature of early and late post-tetanic potentiation and upon post-tetanic block of presynaptic collaterals with particular reference to behavior in circumstances of varied duration and frequency of conditioning stimulation. Early potentiation is most conspicuous following brief tetani at high frequency, late potentiation following long tetani, much lower frequencies being all that are needed. The two phenomena thus are distinguishable and separate. Dorsal root electrotonus produced by stimulations of varying duration and frequency is described, and the similarity between behavior of the D.R.IV R. electronic potential and early potentiation demonstrated. It is shown how early potentiation and post-tetanic block are due to the same process (hyperpolarization) at different intensities. The view that the agency for potentiation is associated with augmented presynaptic action due to hyperpolarization is confirmed. A diagram is constructed to indicate the probable temporal courses of early and late potentiation.

Ganglia, Spinal↗

PubMed1958

The approach to unitary analysis of neuron response.

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Humans↗

PubMed1957

Input-output relation in a flexor reflex.

Observations have been made upon a typical flexor reflex with the aim of disclosing the changes in amount, latency, and temporal configuration of reflex discharge that take place as afferent input is varied from zero to maximal for the band of cutaneous myelinated afferent fibers that extends upward from approximately 6 micro in diameter (group II fibers). Reflex threshold is reached at 6 to 12 per cent maximal afferent input. From threshold to maximal input the relation between input and amount of output is essentially linear, latency on the average decreases, the shorter central paths in general gain preference, but the known minimum pathway, one of three neurons, does not transmit unless aided by convergent activity. Flexor reflex discharge may occur in several bursts suggesting the existence of closed chain connections in the internuncial pools of the spinal cord. At any given input there is, in successively elicited reflexes, little correlation between latency and amount of discharge, at first sight a surprising result for each variable can be taken as a measure of excitability status of the motoneuron population. However, latency of discharge indicates excitability at the beginning of the reflex event whereas amount of discharge is an expression of excitability over the entire period of discharge. Given a constantly and rapidly fluctuating excitability absence of correlation between these variables would be an anticipated result.

Motor Neurons↗

PubMed1957

Reflex depression in rhythmically active monosynaptic reflex pathways.

A study has been made of the depression that occurs when a monosynaptic reflex pathway is subjected to repetitive stimulation. Reflex depression has a dual origin. High frequency or early depression is postsynaptic in origin and results from subnormality in the motoneurons. Low frequency, late, or enduring depression is presynaptic in origin. The conditioning volley-test volley technique and the frequency-mean monosynaptic reflex amplitude relation yield similar information concerning reflex depression. Each method has its advantages and for some purposes one or the other of the methods necessarily must be employed. The results of a variety of experiments are consistent with the proposition that reflex depression in the monosynaptic reflex pathway originates by action in the group IA afferent fibers of muscle origin that are responsible for monosynaptic reflex transmission. Depression is present at a frequency of 0.1 per second (6 per minute) and absent at a frequency of 0.05 per second (3 per minute). Thus it is impractical for most purposes to employ repetition rates that satisfy the requirement for designation as "single shock" stimulations. The temporal course of enduring depression has been determined. It is identical with that for a number of other phenomena observable in monosynaptic reflex pathways, which suggests a common origin. The mechanism of low frequency or enduring depression is discussed in the light of this suggestion.

Depression↗

PubMed1957

Temporal summation in rhythmically active monosynaptic reflex pathways.

Monosynaptic reflex responses elicited by repetitive stimulation in the frequency range between 60 and 100 per second yield evidence of temporal summation. The relation between stimulus interval and mean monosynaptic reflex response in the steady state at the frequencies studied is described adequately by an exponential decaying to 1/e in 4 msec. Since the temporal course of spatial summation is described adequately by the same exponential it is concluded that the two phenomena, temporal and spatial, are expressions of the same fundamental process intrinsic to the workings of the monosynaptic reflex pathway, to wit the synaptic potential-residual facilitation mechanism of prior descriptions. Some discussion of implications is appended.

Reflex↗

PubMed1957

Monosynaptic reflex response of individual motoneurons as a function of frequency.

An assemblage of individual motoneurons constituting a synthetic motoneuron pool has been studied from the standpoint of relating monosynaptic reflex responses to frequency of afferent stimulation. Intensity of low frequency depression is not a simple function of transmitter potentiality. As frequency of stimulation increases from 3 per minute to 10 per second, low frequency depression increases in magnitude. Between 10 and approximately 60 per second low frequency depression apparently diminishes and subnormality becomes a factor in causing depression. At frequencies above 60 per second temporal summation occurs, but subnormality limits the degree of response attainable by summation. At low stimulation frequencies rhythm is determined by stimulation frequency. Interruptions of rhythmic firing depend solely upon temporal fluctuation of excitability. At high frequency of stimulation rhythm is determined by subnormality rather than inherent rhythmicity, and excitability fluctuation leads to instability of response rhythm. In short, whatever the stimulation frequency, random excitability fluctuation is the factor disrupting rhythmic response. Monosynaptic reflex response latency is stable during high frequency stimulation as it is in low frequency stimulation provided a significant extrinsic source of random bombardment is not present. In the presence of powerful random bombardment discharge may become random with respect to monosynaptic afferent excitation provided the latter is feeble. When this occurs it does so equally at low frequency and high frequency. Thus temporal summation is not a necessary factor. There is, then, no remaining evidence to suggest that the agency for temporal summation in the monosynaptic system becomes a transmitting agency in its own right.

Motor Neurons↗

PubMed1955

Mono-synaptic reflex responses of individual motoneurons.

Individual motoneuron responses to a variety of afferent inputs have been examined. At a given input some motoneurons respond to every trial, some to no trial, and some respond to a certain percentage of trials that is characteristic for the motoneuron at that input. The performance of a motoneuron is expressed by means of a firing index that relates the number of responses to the number of trials. In a representative assemblage of individual motoneurons some 20 to 30 per cent display intermediate firing indices. This number, comprising an "intermediate zone" remains fairly constant at different levels of input although the individuals within it may be entirely different at two different levels of input. Frequency distribution of individuals with respect to firing indices is U-shaped. Intermediacy of firing indices depends upon temporal fluctuation of excitability which, in the first approximation, is normal. The individual motoneurons are approximately equally frequently distributed with respect to transmitter potentiality of their monosynaptic reflex afferent connections. The distribution of motoneurons with respect to transmitter potentiality of their monosynaptic reflex connections is considered representative of a natural pool in that the sum of their individual post-tetanic response behaviors accurately reproduces the course of post-tetanic potentiation in a natural pool.

Humans↗

PubMed1955

Transmitter potentiality of homonymous and heteronymous monosynaptic reflex connections of individual motoneurons.

An assemblage of 110 individual tricipital motoneurons has been examined with the aim of determining those factors that predispose certain motoneurons to heteronymous response in post-tetanic potentiation. Motoneurons that respond most readily to homonymous volleys are not those that respond most readily to post-tetanically potentiated heteronymous volleys. Hence differences in presynaptic organization rather than differences in mean postsynaptic threshold determine differences in readiness for response. Every motoneuron exhibits a distinct asymmetry in transmitter potentiality of homonymous and heteronymous monosynaptic reflex connections. The range of transmitter potentialities is wide and that of heteronymous connections to some motoneurons is greater than that of homonymous connections to some other motoneurons.

Motor Neurons↗

PubMed1955

Transmission in fractionated monosynaptic spinal reflex systems.

A study has been made of conditions that support monosynaptic reflex transmission from afferent fibers of one part of a synergic muscle mass to motoneurons of another part. Heteronymous response so called can be brought on by prior tetanization of the afferent pathway and by asphyxiation to a critical stage. The response is facilitated by cooling and may appear in the cold preparation without need for prior tetanization. By appropriate asymmetrical subdivision of a monosynaptic reflex system an afferent inflow can be obtained that is sufficiently powerful to secure heteronymous transmission without the need for prior tetanization or cooling. Each junction between a monosynaptic afferent fiber and a motoneuron possesses some degree of potentiality for transmitting. Transmitter potentiality of an afferent fiber at its several junctions with motoneurons varies widely. Reasons are advanced for supposing the variation to be graded rather than stepwise, and quantitative rather than qualitative.

Motor Neurons↗