Evoked potentials in the frog medulla to electrical stimulation of the glossopharyngeal nerve

Evoked potentials in the frog medulla to stimulation of the glossopharyngeal nerve appear on the ipsilateral side in a zone of limited area. They are recorded at depths not exceeding 2000 µ. Depending on their form the surface evoked potentials are divided into two groups, negative and positive—negative, differing from each other in their parameters and properties. During insertion of the microelectrode the phase of the negative potential is changed. The principal slow components of the responses reflect postsynaptic processes. The first fast wave of the evoked potential is regarded as the presynaptic component. Differences in the properties of the evoked potential recorded at different points are determined by the neuromorphological heterogeneity of the structures of the primary center.     

Evoked potentials to electrical stimulation of the facial nerve in the carp tectum mesencephali

Tectal evoked potentials to stimulation of the facial nerve, containing afferent fibers of nonolfactory chemoreception, in the carp are positive evoked potentials with a latent period of 5 to 25 msec which show no phase shift as the microelectrode is advanced to a depth of 600 µ. Depending on the amplitude and latency of evoked potentials seven active zones differing in one or both parameters were distinguished in the ipsilateral tectum mesencephali. The role of impulses from the medulla in the mechanism of tectal evoked potentials to facial nerve stimulation is proved by differences in latent periods and disappearance of the tectal response (although it is preserved in the primary center) after severance of connections between the two parts of the brain. Descending influences from the tectum on the primary center were found: its extirpation disturbs evoked potential generation in several parts of the medullla, so that they either disappear completely or their parameters are modified.A. A. Zhdanov State University, Leningrad. Translated from Neirofiziologiya, Vol. 8, No. 1, pp. 39–46, January–February, 1976.     

Loss of information on central summation of local postsynaptic potentials

The spatio-temporal pattern of spikes converging on a neuron and variations in the combined depolarizing potential in the trigger zone are regarded as information carriers. In both cases the quantity of information is calculated; it is assumed that the depolarizing potential is formed as the weighted sum of the local PSPs. It is concluded from a comparison of the results that "algebraic" summation of PSPs is accompained by loss of essential information, and information carried by variation in the combined PSP is generated only by unessential input information. The investigation confirms the important role of a high spatial damping constant of electrotonic potentials in the dendrites. The damping prevents annihilation of much of the information. Electrical action of "effective" synapses on the trigger zone must evidently be regarded as sensitivity control, with no effect on the information content of the process but capable of weakening or interrupting the transmission of information from dendrites to the trigger zone. It is concluded that the combined PSP cannot serve as an information carrier and that this function may perhaps be performed by signals of a different physical nature which do not undergo damping in the dendrites.M. I. Kalinin Leningrad Polytechnical Institute. Translated from Neirofiziologiya, Vol. 5, No. 2, pp. 186–192, March–April, 1973.     

Electrical potentials from the eye and optic nerve of Strombus: effects of electrical stimulation of the optic nerve.

1. Photic stimulation of the mature eye of Strombus can evoke in the optic nerve 'on' activity in numerous small afferent fibres and repetitive 'off' bursts of afferent impulses in a smaller number of larger fibres. 2. Synchronous invasion of the eye by electrically evoked impulses in small optic nerve fibres (apparently the 'on' afferents, antidromically activated) can evoke a burst of impulses in the larger 'off' fibres which propagate away from the eye. Invasion of the eye via one branch of optic nerve can evoke an answering burst in another branch. 3. Such electrically evoked bursts are similar to light-evoked 'off' bursts with respect to their impulse composition, their ability to be inhibited by illumination of the eye, and their susceptibility to MgCl2 anaesthesia. 4. Invasion of the eye by a train of repetitive electrically evoked impulses in the absence of photic stimulation can give rise to repetitive 'off' bursts as well as concomitant oscillatory potentials in the eye which are similar to those normally evoked by cessation of a photic stimulus. 5. The electrically evoked 'off' bursts appear to be caused by an excitatory rebound following the cessation of inhibitory synaptic input from photoreceptors which can be antidromically activated by electrical stimulation of the optic nerve. 6. The experimental results suggest that the rhythmic discharge of the 'off' fibres evoked by the cessation of a photic stimulus is mediated by the abrupt decrease of inhibitory synaptic input from the receptors.     

A model of motor and sensory axon activation in the median nerve using surface electrical stimulation

Surface electrical stimulation has the potential to be a powerful and non-invasive treatment for a variety of medical conditions but currently it is difficult to obtain consistent evoked responses. A viable clinical system must be able to adapt to variations in individuals to produce repeatable results. To more fully study the effect of these variations without performing exhaustive testing on human subjects, a system of computer models was created to predict motor and sensory axon activation in the median nerve due to surface electrical stimulation at the elbow. An anatomically-based finite element model of the arm was built to accurately predict voltages resulting from surface electrical stimulation. In addition, two axon models were developed based on previously published models to incorporate physiological differences between sensory and motor axons. This resulted in axon models that could reproduce experimental results for conduction velocity, strength-duration curves and activation threshold. Differences in experimentally obtained action potential shape between the motor and sensory axons were reflected in the models. The models predicted a lower threshold for sensory axons than motor axons of the same diameter, allowing a range of sensory axons to be activated before any motor axons. This system of models will be a useful tool for development of surface electrical stimulation as a method to target specific neural functions.     

Mechanisms controlling choline transport and acetylcholine synthesis in motor nerve terminals during electrical stimulation

Electrical stimulation of the chick ciliary nerve leads to a frequency-dependent increase in the Na+-dependent high affinity uptake of [3H]choline (SDHACU) and its conversion to acetylcholine (ACh) in the nerve terminals innervating the iris muscle. The forces that drive this choline (Ch) uptake across the presynaptic membrane were evaluated. Depolarization with increased [K+] out or veratridine decreases Ch accumulation. In addition to the electrical driving force, energy is provided by the Na+ gradient. Inhibition of the Na,K-ATPase decreased the Ch taken up. Thus, changes in the rate of Ch transport are dependent on the electrochemical gradients for both Ch and Na+. Ch uptake and ACh synthesis were increased after a conditioning preincubation with high [K+] out or veratridine. As is the case for electrical stimulation, this acceleration of Ch uptake and ACh synthesis was strongly dependent on the presence of Ca++ in the incubation medium. Na+ influx through a TTX-sensitive channel also contributed to this acceleration. Inasmuch as membrane depolarization reduces the initial velocity of Ch uptake and ACh synthesis, their increases during electrical stimulation therefore cannot be the direct effect of the depolarization phase of the action potential. Instead they are the result of the ionic fluxes accompanying the presynaptic spike. It is concluded that stimulation of Ch uptake and ACh synthesis by nerve activity depends first, on the ACh release elicited by Ca++ influx after depolarization and second, on the activation of the Na,K-ATPase due to Na+ entry. Furthermore, it is suggested that the release of ACh after stimulation drives translocation of cytoplasmic ACh into a protected compartment (probably vesicular). This recompartmentation of intraterminal ACh stimulates ACh synthesis by mass action, allowing further accumulation of Ch.     

Effect of dimedrol on the function of the neuromuscular synapse and the generation of action potentials by motor nerve fibers

Microelectrode registration of synaptic potentials in the frog cutaneous-pectoris muscle has shown dimedrol (7.9 X 10(-5) M) to act on synaptic transmission decreasing the quantal content, estimated by mean EPP amplitude to mean miniature EPP amplitude ratio, the quantal content calculated by variation coefficient of EPP amplitude being unaffected. The data suggest possible transmitter release and depletion of mediator stock. The experiments on isolated motor nerve fibers have demonstrated dimedrol to cause the increase in transmitter release probability by widening the action potentials in the terminals and thus enhancing Ca2+ influx.     

电刺激大鼠腓肠神经引起Aδ、 C类传入神经纤维的背根反射

在距脊髓约 15mm处切断大鼠L5背根 ,将中枢端分成 4～ 5条细束 ,电刺激腓肠神经在背根细束上记录背根反射 (dorsalrootreflex ,DRR)。共记录到DRR 5 1例 ,根据引起DRR所兴奋的腓肠神经纤维类别和DRR在背根逆向传出的纤维类别将DRR分为 5类 :Aαβ Aαβ·DRR、Aβδ Aδ·DRR、Aβδ C·DRR、Aαβδδ C·DRR和C C·DRR。结果证明 ,电刺激外周神经激活各类纤维不但能引起A类 (包括Aδ)纤维的DRR ,而且也能引起C类纤维的DRR。记录的Aδ·DRR和C·DRR为细纤维传入终末产生突触前抑制提供了客观指标 ,为DRR逆向传出冲动到达外周组织 ,释放神经肽类递质 ,调节外周效应器的功能提供了证据