Inhibition in hippocampal pyramidal neurons during peripheral stimulation

Responses of hippocampal pyramidal neurons were investigated intracellularly in unanesthetized rabbits immobilized with tubocurarine. A single stimulus, applied to the sciatic nerve, evoked prolonged (up to 2.5 sec) hyperpolarization of the cell membrane, accompanied by inhibition of action potentials. The latent period of the evoked hyperpolarization was 48±16.4 msec, and its amplitude 2.5±1.9 mV. In some neurons the development of hyperpolarization potentials was preceded by excitation. The suggestion is made that hyperpolarization of the membrane of pyramidal cells during peripheral stimulation is manifested as an inhibitory postsynaptic potential (IPSP), generated with the participation of hippocampal interneurons. The possibility of prolonged tonic action of interneurons from outside as a cause of prolonged inhibition of the pyramidal neurons is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 1, No. 3, pp. 278–284, November–December, 1969.     

EPSPs of masseter motoneurons evoked by stimulation of low-threshold infraorbital nerve afferents in cat

Stimulation of the infraorbital nerve at strengths 1.4–2.5 times higer than the threshold of excitation of A fibers in cats anesthetized with chloralose and pentobarbital evoked EPSPs with an amplitude up to 3.0 mV and a duration of 9–15 msec in 69% of masseter motoneurons after 1.5–3.0 msec. These EPSPs were complex and formed by summation of simpler short-latency and long-latency EPSPs. The short-latency EPSPs appeared in response to infraorbital nerve stimulation at 1.1–1.5 thresholds and had a slow rate of rise (2.5–4.5 msec, mean 3.7±0.4 msec), low amplitude (under 2.0 mV), and short duration (5–6 msec). Their latent period varied from 1.5 to 3.0 msec (mean 2.1±0.2 msec). The shortness of the latent period and its constancy during stimulation of the nerve at increasing strength, and also the character of development of facilitation and inhibition of the EPSP during high-frequency stimulation suggests that these EPSPs are monosynaptic. The slow rate of rise suggested that these EPSPs arise on distal dendrites of the motoneurons. Long-latency EPSPs appeared 7–9 msec after stimulation of the infraorbital nerve at 1.1–1.5 thresholds. Their amplitude reached 1.5–2.0 mV and their duration 7–9 msec. The long duration of the latent period combined with low ability to reproduce high-frequency stimulation (up to 30/sec) points to the polysynaptic origin of these EPSPs.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 9, No. 6, pp. 583–591, November–December, 1977.     

Electrophysiological investigation of the cat ciliary ganglion

Electrical responses of some nerves of the ciliary ganglion to stimulation of its other nerves were recorded, and intracellular recordings were also made from neurons of the ganglion (in situ). The overwhelming majority of preganglionic fibers terminate synaptically on neurons of the ganglion. Postganglionic fibers leave in the lateral and medial ciliary nerves, in which the velocity of conduction of excitation ranges from 1.9 to 9.0 m/sec. A few preganglionic fibers pass through the ciliary ganglion into the lateral ciliary nerve, giving off collaterals to neurons of the ganglion, so that stimulation of the lateral ciliary nerve evokes a response in the medial ciliary nerve (preganglionic axon reflex). The resting potential of neurons of the ciliary ganglion is 57±2.8 mV, and their action potential 68±3.6 mV. Single orthodromic stimulation usually evokes a single action potential in a neuron. The amplitude of the EPSP is increased during hyperpolarization of the postsynaptic membrane, confirming the chemical nature of synaptic transmission in the ganglion. The antidromic response consists of an IS-component and spike. The spike is followed by after-hyperpolarization, with a mean amplitude equal to 31% of the spike amplitude, and the time taken for it to fall to one–third of its initial amplitude is 75–135 msec.A. A. Bogomolets' Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 1, No. 1, pp. 101–108, July–August, 1969.     

Postsynaptic potentials of neurons of the cat auditory cortex

The electrical reactions of 294 neurons of the auditory cortex to a click were recorded in experiments on cats immobilized with tubocurarine (174 intra- and 120 extracellularly). The value of the membrane potential varied from 30 to 70 mV with intracellular leads. The following types of reactions were obtained (the number of neurons is given in parentheses): a peak without slow oscillations in the membrane potential (4), EPSP (3), EPSP-peak (6), EPSP-peak-IPSP (17), EPSP-IPSP (9), primary IPSP (114, including 23 with an after-discharge). Twenty one neurons did not react to a click. The amplitude of the sub-threshold EPSP was 1–1.5 mV, the duration of the ascending part was about 10 and of the descending part 20–30 msec. The peak potential on the ascending part of the EPSP developed at the critical level of 3–4 mV. The amplitude of the peaks varied from several millivolts to 50–60. In 17 neurons prolonged hyperpolarization having all the properties of an IPSP, developed after the peak. The amplitude of these IPSP varied in different neurons from 1 to 10 mV and the duration varied from 20 to 80 msec. IPSP without preceding excitation of the given neuron were the predominant types of reaction. The latent period of these primary IPSP varied from 7 to 20 msec and the amplitude from 1 to 15 msec with a duration of 30–200, more frequently 80–100 msec. It is suggested that two types of inhibition develop in neurons of the auditory cortex in response to a click: recurrent and afferent. The functional significance of the first consists in limiting the duration of the discharge in the reacting neurons, the second prevents the development of excitation in adjacent neurons, thereby limiting the area of neuronal activity.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSSR, Kiev. Translated from Neirofiziologiya, Vol. 3, No. 4, pp. 339–349, July–August, 1971.     

Mechanism of inhibition following reflex discharge in spinal cord interneurons

Using the method of microelectrode (intracellular and extracellular) recording, the mechanism of inhibition following reflex discharge in interneurons of the lumbosacral section of the spinal cord of cats on activation of cutaneous and high-threshold muscle afferents was studied. It was shown that the postdischarge depression of the reflex responses 10–20 msec after the moment of activation of the neuron is due to afterprocesses in the same neuron and presynaptic pathways. The depression of spike potentials from the 20th to the 100th msec is produced by inhibitory postsynaptic potentials (IPSP). During the development of IPSP the inhibition of spike potentials can be due to both a decrease of the depolarization of the postsynaptic membrane below the critical threshold and a decrease of sensitivity of the cell membrane to the depolarizing action of the excitatory postsynaptic potential (EPSP). At intervals between the stimuli of 30–100 msec the duration of EPSP after the first stimulus does not differ from that after the second stimulus. Hence, it is suggested that the presynaptic mechanisms do not play an essential part in this type of inhibition of interneurons. The inhibition following the excitation favors the formation of a discrete message to the neurons of higher orders.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 2, No. 1, pp. 3–9, January–February, 1970.     

Self-sustained rhythmic spike and wave activity and response of glial and nerve cells in the cat sensorimotor cortex

During acute experiments on unanesthetized cats, immobilized with myorelaxants, it was found that during rhythmic stimulation (8–14 Hz, duration: 10 sec) of the ventroposterolateral thalamic nucleus brief hyperpolarization is succeeded by depolarization in the pyramidal neurons of the sensorimotor cortex. Following this depolarization, rhythmic (approximately 3 Hz) paroxysmal depolarizing shifts in membrane potential are produced by ending stimulation, succeeded by protracted hyperpolarization and termination of rhythmic wave activity. Depolarization only is observed in glial cells, however, while hyperpolarization sets in after hyperpolarization is completed in the neurons. It is suggested that long-term changes in the membrane potential of cortical cells could make some contribution to the setting up and termination of rhythmic spike and wave activity.I. S. Beritashvili Institute of Physiology, Academy of Sciences of the Georgian SSR, Tbilisi. Translated from Neirofiziologiya, Vol. 18, No. 3, pp. 319–325, May–June, 1986.     

Posthyperpolarization rebound: Gradualness of intensity and duration effects

Rebound was recorded in the latent pacemaker neuron ofLimnaea stagnalis as an off-response to incoming pulses of constant duration (50 msec) and different strengths (0.17–16.1 nA) or of different duration (10 msec-360 sec) and constant strength (5 nA). To pulses of short duration and weak strength this response consists of a single depolarization wave. With an increase in these parameters the wave gradually grows and is followed by a hyperpolarization wave. At an intensity of 10–12 nA or duration of about 200 msec the rebound response becomes spike-shaped, but the spike is completely formed only at 15.2 nA or 4–5 sec. The last stage of its formation is characterized by "constriction" of the depolarization component. A further increase in pulse intensity of the same duration does not change the rebound response. On the other hand, with a further increase in pulse duration in the corresponding series of experiments fresh spikes were continually added to the first, and depending on the choice of durations, this process could be followed step by step. At a duration of about 190 sec the rebound response reached saturation when it consisted of 8 spikes with a total response duration of about 5 sec. These results are used as the basis for a hypothesis of the possible organization of excitation of the somatic membrane of mollusk pacemaker neurons. Some aspects of the possible mechanism of rebound formation are discussed.Institute of Physiology and Pathology of the Cardiovascular System, Kaunas Medical Institute, Kaunas, Lithuania. Translated from Neirofiziologiya, Vol. 5, No. 5, pp. 451–459, September–October, 1973.     

Synaptic responses of medullary neurons of turtles to stimulation of the locomotor region

Responses of medullary neurons to microstimulation of the locomotor region by a current of up to 30 µA were studied by intracellular recording in turtles. The resting potential recorded in these neurons was from 22 to 42 mV. Depolarization PSPs (EPSPs) were recorded in 43 neurons, hyperpolarization PSPs (IPSPs) in 12, and mixed in 36. Synaptic discharges were observed in 29 neurons. Of these cells 11 generated action potentials without visible PSPs. The latent period of the PSPs was most frequently between 2 and 8 msec. The time from the beginning of the EPSP to the beginning of the action potential was 1–3 msec if the response index was high, but in the case of weaker stimulation, it began to fluctuate strongly and lengthened. Unitary EPSPs were recorded in 15 neurons and IPSPs in three. Their amplitude was 0.6–0.8 mV, from 2 to 12 times less than the depolarization threshold (1–7 mV). These results, together with those obtained previously by extracellular recording of medullary unit activity in turtles and cats, are used to discuss the possible mechanism of spread of locomotor activity.Institute for Problems in Information Transmission, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 14, No. 2, pp. 122–129, March–April, 1982.     

Electrophysiological properties of neurons and neuronal organization of the crayfish somatogastric ganglion

Experiments with intracellular recording from neurons of the isolated crayfish somatogastric ganglion established that the membrane potential of the neurons is 53±3 mV. Single stimulation of the central branches of the ganglion evoked EPSP and a spike in the neurons. The spike amplitude was 7.5±0.6 mV. The small amplitude of the spike is explained by the fact that it arises at some distance from the body of the neuron and propagates electrotonically in it. Summation of several EPSP is necessary in most cases for initiation of the spike. When the orthodromic stimulus was strong enough, and IPSP occurred in some cells in addition to the EPSP and spike. Stimulation of the peripheral nerves of the ganglion induced in most neurons antidromic excitation and in some neurons orthodromic excitation. Some neurons spontaneously discharged rhythmically with an unstable frequency (11–27 impulses/sec). An investigation of the effect on neurons of chemical agents [acetylcholine, adrenalin, noradrenalin, gamma-aminobutyric acid (GABA), glutamic acid, and dopamine] showed that acetylcholine has the strongest and most stable depolarizing action and apparently is a synaptic transmitter in the ganglion. The other agents excited some neurons — depolarized them and evoked rhythmic discharges — and, coversely, hyperpolarized and suppressed the rhythmic activity of other neurons. A scheme of neuronal organization of the somatogastric ganglion of the crayfish is proposed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 2, No. 3, pp. 307–313, May–June, 1970.     

Possible interaction between synaptic and pacemaker mechanisms of electrical activity in bursting neurons of Helix pomatia

Membrane hyperpolarization induced by short pulses of inward current, by stimulation of the anal nerve, which leads to the appearance of a long IPSP in the neuron, and developing during the appearance of spontaneous IPSPs in the neuron was investigated in neuron RPa1 ofHelix pomatia. Short-term hyperpolarization of the neuron membrane by an inward current (10 msec) led to the development of self-maintained (regenerative) membrane hyperpolarization lasting several seconds. The amplitude and duration of regenerative hyperpolarization increased with an increase in amplitude and duration of the pulse of inward current. The time course of IPSPs arising spontaneously in the neuron and in response to stimulation of the anal nerve was similar to that of regenerative hyperpolarization evoked by a pulse of inward current. It is suggested that regenerative hyperpolarization associated with activation of endogenous mechanisms of regulation of the bursting activity of the neuron may be due not only to short-term membrane hyperpolarization of the test neuron by the electric current, but also to hyperpolarization occurring during IPSP generation.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 13, No. 1, pp. 67–74, January–February, 1981.     

Postsynaptic mechanisms initiating bursting activity in theHelix pomatia RPal neuron under the influence of an interneuron

Postsynaptic mechanisms of the connection between the interneuron in the visceral ganglion initiating bursting activity in RPal and B7 neurons and these neurons themselves were investigated in the snail (Helix pomatia). Using voltage clamping at the membrane of these cells, stimulation of the interneuron gave rise to a slow inward current with a 2 sec latency; it rose in amplitude as stimulation increased in duration. Reducing the temperature from 25 to 5°C diminished the rise and decay rate of this current with a temperature coefficient of about 10. The current-voltage relationship of the slow inward current was nonlinear, with a maximum of –65 mV. Reducing the concentration of sodium ions in the extracellular fluid increased the amplitude of the current. While hyperpolarization of the burster neuron membrane produced a burst of inward current prior to stimulation, this same hyperpolarization induced a pulse of outward current at the peak of the slow inward current. Stimulating the interneuron is thus thought to activate at least two types of ionic channel in the cell body of the burster neurons: a steady sodium and a voltage- and time-dependent channel for outward current. This process could well be mediated by a biochemical cytoplasmic chain reaction.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 19, No. 1, pp. 28–36, January–February, 1987.     

Inhibition in the fish olfactory bulb

Inhibition in the olfactory bulb of the carp was studied by recording potentials from secondary neurons intracellularly. Three types of inhibition — trace, early, and late — can arise in neurons of the olfactory bulb. Trace inhibition corresponds to hyperpolarization about 20 msec in duration, which is closely connected with the spike, but it is not after-hyperpolarization but an IPSP. Early and late inhibition correspond to IPSPs of different parameters. The first has a latency of 0–50 msec (relative to the spike) and a duration of 60–400 msec; the corresponding values for the second are 100–400 msec and 0.5–3 sec. The possible mechanisms of these types of inhibition are discussed.M. V. Lomonosov Moscow State University. Translated from Neirofiziologiya, Vol. 3, No. 6, pp. 650–656, November–December, 1971.     

Monosynaptic excitation of motoneurons of the accessory nerve nucleus by reticulofugal impulses

Acute experiments on cats anesthetized with chloralose and pentobarbital showed that excitation of fast-conducting (130 m/sec) reticulospinal fibers, arising during stimulation of the ipsilateral medullary reticular gigantocellular nucleus evoked monosynaptic EPSPs in motoneurons of the accessory nerve nucleus. The EPSPs had latent periods of between 0.6 and 1.0 msec (mean 0.7 msec), they reached their maximal amplitude (4.0 mV) after 2.0–2.5 msec, and lasted about 10 msec. The EPSPs underwent only weak potentiation through the different types of stimulation of the gigantocellular nucleus and were not transformed into action potentials.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 12, No. 1, pp. 62–66, January–February, 1980.     

Effect of direct and transcallosal stimulation on inhibition of unit activity in the cat association cortex

Inhibition of association cortical neurons (in the form of inhibition of spontaneous activity or of IPSPs) during direct and transcallosal stimulation was studied in cats immobilized with muscle relaxants. The duration of inhibition of stimulation and the number of stimuli. With an increase in the strength of stimulation inhibition deepened to a certain level for a particular neuron, after which it could be further lengthened with an increase in the number of stimuli. In the case of repeated stimulation by volleys of stimuli, very prolonged inhibition developed gradually in the neurons, during which spontaneous activity was inhibited for 2–5 sec. The duration of the IPSP depended on the intensity of stimulation and number of stimuli and its amplitude depended on the intensity and frequency of stimulation and on the number of stimuli. In some cases the amplitude of the IPSP continued to rise after a short volley of stimuli, even after the end of stimulation. An increase in the number of stimuli in the volley lengthened the IPSPs, but their amplitude remained constant throughout the period of stimulation. Prolonged inhibition (up to a few seconds) was connected with the development of a hyperpolarization postsynaptic potential in the neurons. It is suggested that neurons exerting a monosynaptic inhibitory influence on cells of the association cortex may be located in the opposite hemisphere.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 13, No. 2, pp. 133–141, March–April, 1981.     

A model of oscillation generation by molluscan neurons

A model describing slow oscillations of membrane potential in molluscan neurons is suggested. It is based on the view that the depolarization phase is due to the slow calcium current, whereas the hyperpolarization phase is due to the potassium current activated by intracellular Ca ions. It is shown that depending on values of the parameters of the model there are three possible types of electrical activity of the neurons: stable membrane hyperpolarization up to the resting potential which is between ?49 and ?53 mV; slow oscillations of membrane potential from ?30 to ?60 mV, with a period of 12–17 sec, and stable membrane depolarization to between ?40 and ?30 mV, which may lead to the onset of stable rhythmic activity of these neurons. Dependence of the amplitude of the oscillations of potential on the extracellular concentration of Ca, K, and Na ions was calculated and agrees qualitatively with the experimental data of Barker and Gainer [4].     

Voltage-activated ionic channels and conductances in embryonic chick osteoblast cultures

Summary Patch-clamp measurements were made on osteoblast-like cells isolated from embryonic chick calvaria. Cell-attachedpatch measurements revealed two types of high conductance (100–250 pS) channels, which rapidly activated upon 50–100 mV depolarization. One type showed sustained and the other transient activation over a 10-sec period of depolarization. The single-channel conductances of these channel types were about 100 or 250 pS, depending on whether the pipettes were filled with a low K⁺ (3mm) or high K⁺ (143mm) saline, respectively. The different reversal potentials under these conditions were consistent with at least K⁺ conduction. Whole-cell measurements revealed the existence of two types of outward rectifying conductances. The first type conducts K⁺ ions and activates within 20–200 msec (depending on the stimulus) upon depolarizing voltage steps from <–60 mV to >–30 mV. It inactivates almost completely with a time constant of 2–3 sec. Recovery from inactivation is biphasic with an initial rapid phase (1–2 sec) followed by a slow phase (>20 sec). The second whole-cell conductance activates at positive membrane potentials of >+50 mV. It also rapidly turns on upon depolarizing voltage steps. Activation may partly disappear at the higher voltages. Its single channels of 140 pS conductance were identified in the whole cell and did conduct K⁺ ions but were not highly Cl^– or Na⁺ selective. The results show that osteoblasts may express various types of voltage controlled ionic channels. We predict a role for such channels in mineral metabolism of bone tissue and its control by osteoblasts.     

Effects of applying electrical stimulation to the locus coeruleus on neuronal activity in the parietal association cortex

It was shown during experiments on cats undergoing surgery under ketamine-induced anesthesia and immobilized with myorelaxin that applying trains of stimuli to the locus coeruleus (LC) produces an effect on 79% of parietal cortex neurons. This manifests as inhibition lasting 300–700 msec or a 16–32% decline in the activity rate of neurons with background activity. Hyperpolarization of 5–7 mV lasting 120–500 msec preceded by a latency of 30–90 msec was noted in such neurons as well as "silent" cells during intracellular recording. Duration of the inhibitory pause in neuronal background activity induced by transcallosal stimulation (TCS) increased by 50–200 msec under the effects of conditioned stimuli applied to the LC. Duration of the IPSP triggered by TCS likewise increased (by 50–100 msec) under the effects of LC stimulation. It was concluded that the effects of stimulating the LC on neuronal activity in the parietal cortex may manifest either directly, as inhibition of background activity and hyperpolarization, or else as modulation of influences exerted by other neurotransmitters.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 22, No. 4, pp. 486–494, July–August, 1990.     

The slow negative wave of the evoked potential of the frog midbrain tectum

A surface-negative slow wave (SW) with a latent period of 50–60 ms, an amplitude of up to 3 mV, and a duration of 0.5–1.5 sec follows the postsynaptic components in the potential of the midbrain tectum (MBT) of a curarized frog (Rana temporaria L.) evoked by electrical stimulation of the optic nerve. The SW develops as a result of the arrival of a synchronous afferent volley along amyelinic fibers; it is generated as a result of depolarization of radially oriented cellular elements; the periventricularly located parts of these structures serve as the source of the current. In the case of rhythmical stimulation, the SW is summed to a value exceeding 10 mV, while at the beginning of stimulation with a frequency of 10–40/sec, the SW is facilitated. After the injection of picrotoxin, selective sensitivity of the SW to this substance was not found. An SW also develops from direct stimulation of the MBT. Comparison of the results of recording neuronal activity shows that the SW is connected with direct afferent inhibition. It is assumed that the SW is generated by elements of the ependymoglia.A. N. Severtsov Institute of Evolutionary Animal Morphology and Ecology, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 3, No. 2, pp. 145–153, March–April, 1971.     

Inhibition of spinal reflex responses in the last period of embryogenesis

Some characteristics of spinal reflex reaction inhibition were studied in cat fetuses during the last three weeks of antenatal development. The experiments were conducted on fetuses with intact placental circulation. Restoration of the excitability of the spinal reflex arcs was very slow after stimulation of the dorsal root by a single stimulus. In embryos studied 20 days before birth the full inhibition of reflex responses lasted about 500 msec. Even 2–3 sec after a single stimulation of the afferent fibers the amplitude of the reflex response to the second stimulus was only 30–40% of the control value. It was determined that such long postactivation depression is unrelated to refractoriness or antidromic inhibition. The presence of a prolonged intense depolarization of afferent terminal fibers at these stages suggests a presynaptic inhibition as one of the most probable reasons for the prolonged postactivation depression. Another important factor in the appearance of postactivation depression is probably the morphologic and functional immaturity of synaptic structures. A reciprocal inhibition was observed in cat fetuses on the 10–12th antenatal day. On the basis of these data it is suggested that in embryogenesis presynaptic inhibition considerably precedes that of postsynaptic fibers.Institute of Higher Nervous Activity and Neurophysiology, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 3, No. 1, pp. 68–75, January–February, 1971.     

Cortical and subcortical spreading depression in rats produced by focused ultrasound

Steady potential shifts produced by focused ultrasond were recorded in the cerebral cortex, hippocampus, thalamus, and caudate nucleus. Impulses of 50–100 msec duration were presented at a frequency of 5 and 10 Hz. Negative steady potential shifts were produced in each of the structures investigated, which gradually increased during rhythmic electrical reaction to reach –3 to –7 mV within 10–30 sec, often succeeded by a wave of spreading depression (SD). In each structure analyzed amplitude of SD waves measured 20–30 mV, lasting 30–40 sec in the cortex, the caudate nucleus and the thalamus, and 80–120 sec in the hippocampus. In unanesthetized and lightly anesthetized animals SD waves were on occasions the precursors of convulsive discharges forming under the action of focused ultrasound. Ultrasound at threshold doses proved ineffective for 5–7 min after the occurrence of an SD wave, but again evoked repeated SD waves once the refractory period had ended. Accordingly, local effects produced by focused ultrasound can result in functional blockage of the brain structures due to cortical and subcortical spreading depression.Institute of Higher Nervous Activity and Neurophysiology, Academy of Sciences of the USSR, Moscow. Institute of Brain Research, All-Union Research Center of Mental Health, Academy of Medical Sciences of the USSR, Moscow. N. N. Andreev Acoustic Institute, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 18, No. 1, pp. 55–61, January–February, 1986.