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W R LOEWENSTEIN

Publications and source records attributed to W R LOEWENSTEIN.

At least 37 records · Page 2Linked to original sources

Temperature and charge transfer in a receptor membrane.

The rate of rise and the amplitude of a mechanically elicited generator potential in a receptor membrane (Pacinian corpuscle) increases markedly with temperature. By contrast, the amplitude of the action potential of the Ranvier node adjacent to the receptor membrane remains practically unchanged over a wide range of temperature. The activation energy of the rate-limiting process in excitation of the receptor membrane is high; it indicates the existence of a high potential energy barrier for charge transfer.

Action Potentials↗

Effects of polarization of the receptor membrane and of the first Ranvier node in a sense organ.

It has previously been shown that the site of production of the generator potential in Pacinian corpuscles is the receptor membrane of the non-myelinated ending, and the site of initiation of the nerve impulse, the adjacent (first) Ranvier node. Effects of membrane polarization of these sites were studied in the present work. Nerve ending and first Ranvier node were isolated by dissection, electric activity was recorded from, and polarizing currents were passed through them. All observations were done at steady levels of polarization, seconds after onset of current flow. The following results were obtained: The amount of charge transferred through the excited receptor membrane is a function of the electrical gradients across the membrane. The generator potential in response to equal mechanical stimuli increases with resting potential of the receptor membrane. The refractory state of the generator potential is not affected by polarization. The electrical threshold for impulse firing at the first Ranvier node (measured by the minimal amplitude of generator potential which elicits a nodal impulse) is nearly minimal at normal resting potential of the node. Both, hyperpolarization and depolarization lead to a rise in nodal threshold. For any level of polarization of nodal and receptor membrane, the threshold for production of impulses by adequate (mechanical) stimulation appears determined by the generator potential-stimulus strength relation and by the electrical threshold of the node.

Nerve Endings↗

Electrical output of a receptor membrane.

The electrical output of the receptor membrane of the nonmyelinated ending of Pacinian corpuscles is a function of the electrical gradients across the receptor membrane. The generator potential of the receptor membrane in response to equal mechanical stimuli varies linearly with the intensity of polarizing currents passed through the membrane. The production of a generator potential leaves a refractory state in the receptor membrane which is independent of the amount of charge transferred across the membrane but is dependent on a factor related to the strength of the stimulus which produced the response.

Nerve Endings↗

After-effects of repetitive activity in a nerve ending.

REPETITIVE MECHANICAL STIMULATION CAUSES DEPRESSION OF EXCITABILITY IN ISOLATED PACINIAN CORPUSCLES: the mechanical threshold of the sense organ for producing nerve impulses increases progressively with time of repetitive stimulation. The effect is completely reversible; it can be elicited with repetitive stimuli of less than threshold strength. Within certain limits, the depression increases as a function of strength and frequency of the repetitive stimuli.

Nerve Endings↗

Post-tetanic potentiation and depression of generator potential in a single non-myelinated nerve ending.

Repetitive activity at the non-myelinated ending of Pacinian corpuscles leaves the following after-effects: (1) With certain parameters of repetitive mechanical stimulation of the ending a depression in generator potential is produced. The effect is fully reversible and has low energy requirements. The effect is a transient decrease in responsiveness of the receptor membrane which is unrelated to changes in resting membrane potential. It appears to reflect an inactivation process of the receptor membrane. Within certain limits, the depression increases as a function of strength, frequency, and train duration of repetitive stimuli. (2) With other, more critical parameters of repetitive stimulation a hyperpolarization of the ending and of the first intracorpuscular Ranvier node may be produced. This leads to respectively post-tetanic potentiation of generator potential and increase in nodal firing threshold. The balance of these after-effects determines the threshold for the production of nerve impulses by adequate (mechanical) stimulation of the sense organ. The after-effects of activity at the node can be elicited by dromic (mechanical) stimulation of the ending, as well as by antidromic (electric) stimulation of the axon; the after-effects at the ending can only be produced by dromic and not by antidromic stimulation.

Nerve Endings↗

The sites for mechano-electric conversion in a Pacinian corpuscle.

The sensory nerve ending in the Pacinian corpuscle is surrounded by a non-nervous capsular structure which occupies about 99.9 per cent of the corpuscle's entire mass. After extirpation of practically all of the non-nervous structure, the sense organ's remains continue to function as a mechano-receptor, namely to produce generator and all-or-nothing potentials in response to mechanical stimuli. Compression of the first intracorpuscular node of Ranvier abolishes the production of "all-or-nothing" potentials in the corpuscle. Graded generator potentials constitute then the only response to mechanical stimulation. This reveals that the first node is the site of origin of the all-or-nothing potential and that the non-myelinated ending is incapable of producing all-or-nothing responses in response to mechanical stimulation. Compression of the entire length of non-myelinated ending suppresses the production of generator potentials. Partial compression of the ending abolishes mechano-responsiveness only of the compressed part. The intact remains of the ending continue to give generator potentials upon mechanical stimulation. This suggests that the generator potential arises at functionally independent membrane parts distributed all over the non-myelinated nerve ending. 24 to 36 hours after denervation of the corpuscle by transection of its sensory axon, no sign of electric activity is detected. Failure of mechano-reception at the nerve ending precedes that of conduction at the degenerating myelinated axon.

Nerve Endings↗

The refractory state of the generator and propagated potentials in a pacinian corpuscle.

A propagated potential produced in the Pacinian corpuscle in response to mechanical stimuli leaves a refractory state of 7 to 10 msec. duration. The refractory state is presumably produced at the first intracorpuscular node of Ranvier. The recovery of receptor excitability for producing an all-or-none response to mechanical stimulation follows the same time course as that of the electrically excited axon. Upon progressive reduction of stimulus interval (mechanical), the propagated potential falls progressively to 75 per cent of its resting magnitude and becomes finally blocked within the corpuscle. A non-propagated all-or-none potential, presumably corresponding to activity of the first node, is then detected. The critical firing level for all-or-none potentials increases progressively during the relative refractory period of the all-or-none potential, as the stimulus interval is shortened. Thus generator potentials up to 85 per cent of a propagated potential can be produced in absence of all-or-none activity. Generator potentials show: gradual over-all increase in amplitude and rate of rise as a function of stimulus strength; constant latency; and spontaneous fluctuations in amplitude. A generator potential leaves a refractory state (presumably at the non-myelinated ending) so that the amplitude of a second generator response which falls on its refractory trail is directly related to the time elapsed after the first generator response and inversely to its amplitude. The generator potential develops independently of any refractory state left by a preceding all-or-none potential.

Nerve Endings↗

Generator processes of repetitive activity in a pacinian corpuscle.

Response patterns resulting from repetitive mechanical stimulation of the corpuscle depend on (1) the time course of recovery of the generator potential, on (2) the recovery of critical firing height, and on (3) the stimulus strength/generator potential function. By either augmenting stimulus frequency at constant strength, or by reducing strength at constant frequency, a sequence of propagated potentials is turned into a pattern of alternating regenerative and generator responses. In such a pattern an extra impulse can be set up whenever an extra stimulus produces a generator potential of enough amplitude to reach the firing height of the corresponding period. The new requirements of firing height introduced by the refractory trail of the extra impulse determine resetting of periodicity and appearance of a "compensatory pause." The decay time of the single generator potential is independent of stimulus duration. This is interpreted as a factor determining receptor adaptation. Upon repetitive stimulation at intervals above (1/2) decay time of the single generator potential, a compound generator potential is built up which shows no spontaneous decline. However, in spite of being considerably greater than the firing height for single impulses, the constant level of depolarization of the compound generator potential is unable to produce propagated potentials. A hypothesis is brought forward which considers the generator potential to arise from membrane units with fluctuating excitability scattered over the non-myelinated nerve ending.

Nerve Endings↗

Facilitation by previous activity in a pacinian corpuscle.

A period of supernormal excitability is left by a propagated impulse in a Pacinian corpuscle. The increase in excitability is found 6 to 10 msec. after an impulse occurs in the corpuscle. Supernormality is produced by either mechanically elicited dromic impulses, or by electrically excited antidromic impulses. Generator potentials do not cause supernormality. Local potentials discharged spontaneously by the corpuscle, and which fall on the supernormal trail left by an antidromic impulse, become enhanced in amplitude, an eventually are turned into propagated dromic potentials. The supernormal period is interpreted as caused by a negative after-potential left at the first intracorpuscular node of Ranvier which outlasts both the recovery time of the firing level and that of the generator potential during the corpuscle's relative refractory period.

Nerve Endings↗