Connections of neurons of the cat somatosensory cortex with the thalamic relay nuclei

Of 103 neurons in the rostral part of the posterior sigmoid gyrus of the cat cortex 30 responded to stimulation of the ventro-posterolateral and ventrolateral nuclei of the thalamus (VPL and VL), 42 responded to stimulation of VL only, and 31 to stimulation of VPL only. It was shown by intracellular recording that stimulation of VPL induces a spike response with or without subsequent IPSPs in some neurons and an initial IPSP in others. The spike frequency of single neurons reached 60/sec, but the IPSP frequency never exceeded 10–20/sec. Stimulation of VL was accompanied by: a) antidromic spike responses; b) short-latency monosynaptic EPSPs and spikes capable of following a stimulation frequency of 100/sec; c) long-latency polysynaptic EPSPs and spikes appearing in response to stimulation at 4–8/sec; d) short-latency IPSPs; e) long-latency IPSPs increasing in intensity on repetition of infrequent stimuli. It is concluded that the afferent inputs from the relay nuclei to neurons of the somatosensory cortex are heterogeneous. An important role is postulated for recurrent inhibition in the genesis of the long-latency IPSPs arising in response to stimulation of VL, and for direct afferent inhibition during IPSPs evoked by stimulation of VPL. It is shown that the rostral part of the posterior sigmoid gyrus performs the role of somatic projection and motor cortex simultaneously.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 4, No. 3, pp. 245–255, May–June, 1972.     

Inhibitory synaptic potentials of the smooth muscle cells of guinea pig taenia coli

A single submaximal intramural application of rectangular stimuli (duration 0.2–0.5 msec) to an atropine-treated taenia coli muscle band evoked inhibitory postsynaptic potentials (IPSP) and a marked relaxation of the muscle band in the vast majority of muscle cells. The latency period of the IPSP was 122±16 msec; the times for a rise and fall of amplitude were 96±8 and 370±60 msec, respectively. The mean latency period of muscle relaxation was 800 msec. The latency period, and especially the amplitude of the IPSP depended on the intensity of the intramural stimulation. This indicates that one muscle cell is inhibited by several nerve fibers. IPSP evoked by threshold stimuli displayed a tendency toward summation, while the amplitude of the second and of subsequent IPSP evoked by low-frequency maximal stimuli was always less than that of the first IPSP. After periodic stimulation (frequency 10–60 impulses/min) was discontinued, a posttetanic decrease in IPSP amplitude was observed. Anodic polarization of the muscle band with a direct current raised the effectiveness of synaptic transmission, as was evidenced by the considerable increase in IPSP amplitude. When the muscle membrane was hyperpolarized with noradrenaline, IPSP inhibition was reversible. This is evidence that the unknown mediator and noradrenaline have a common ionic inhibitory mechanism.A. A. Bogomol'ts Institute of Physiology of the Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 2, No. 5, pp. 544–551, September–October, 1970.     

Neuronal and synaptic mechanisms of cortical inhibition

The latent periods, amplitude, and duration of IPSPs arising in neurons in different parts of the cat cortex in response to afferent stimuli, stimulation of thalamocortical fibers, and intracortical microstimulation are described. The duration of IPSPs evoked in cortical neurons in response to single afferent stimuli varied from 20 to 250 msec (most common frequency 30–60 msec). During intracortical microstimulation of the auditory cortex, IPSPs with a duration of 5–10 msec also appeared. Barbiturates and chloralose increased the duration of the IPSPs to 300–500 msec. The latent period of 73% of IPSPs arising in auditory cortical neurons in response to stimulation of thalamocortical fibers was 1.2 msec longer than the latent period of monosynaptic EPSPs evoked in the same way. It is concluded from these data that inhibition arising in most neurons of cortical projection areas as a result of the arrival of corresponding afferent impulsation is direct afferent inhibition involving the participation of cortical inhibitory interneurons. A mechanism of recurrent inhibition takes part in the development of inhibition in a certain proportion of neurons. IPSPs arise monosynaptically in 2% of cells. A study of responses of cortical neurons to intracortical microstimulation showed that synaptic delay of IPSPs in these cells is 0.3–0.4 msec. The length of axons of inhibitory neurons in layer IV of the auditory cortex reaches 1.5 mm. The velocity of spread of excitation along these axons is 1.6–2.8 msec (mean 2.2 msec).A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 16, No. 3, pp. 394–403, May–June, 1984.     

Characteristics of cortical inhibitory neurons

Spikes were recorded extracellularly and IPSPs intracellularly from auditory cortical neurons of cats immobilized with D-tubocurarine in response to stimulation of geniculo-cortical fibers. Fibers whose stimulation induces IPSPs in auditory cortical neurons mainly have low thresholds. When two stimuli, each of which separately evoked an IPSP of maximal amplitude, were applied to them the shortest interval at which the second stimulus evoked an effect was 2.5–3 msec. This effect consisted of an increase in the duration of the integral IPSP, the amplitude of which either remained unchanged or increased under these circumstances by only 5–10%. The interval at which a separate IPSP appeared in response to the second stimulus depended on the duration of the ascending phase of the IPSP and varied from 4 to 22 msec for different neurons. The amplitude of the second IPSP in this case depended on the interval between stimuli. Under moderately deep pentobarbital anesthesia the number of neurons responding to stimulation of the geniculo-cortical fibers by spikes fell sharply but the number of neurons responding by primary IPSPs remained almost unchanged. Under very deep pentobarbital anesthesia, when spike responses of the cortical neurons completely disappeared, the IPSPs also were completely suppressed. It is concluded that inhibitory neurons of the auditory cortex are excited by thick low-threshold fibers, they have a short refractory period, and they are resistant to the narcotic action of pentobarbital.     

Unit responses in the cat auditory cortex to medial geniculate body stimulation

Responses of 98 auditory cortical neurons to electrical stimulation of the medial geniculate body (MGB) were recorded (45 extracellulary, 53 intracellularly) in experiments on cats immobilized with tubocurarine. Responses of the same neurons to clicks were recorded for comparison. Of the total number of neurons, 75 (76%) responded both to MGB stimulation and to clicks, and 23 (24%) to MGB stimulation only. The latent period of extracellularly recorded action potentials of auditory cortical neurons in response to clicks varied from 7 to 28 msec (late responses were disregarded), and that to MGB stimulation varied from 1.5 to 12.5 msec. For EPSPs these values were 8–13 and 1–4 msec respectively. The latent period of IPSPs arising in response to MGB stimulation varied from 2.2 to 6.5 msec; for 34% of neurons it did not exceed 3 msec. The difference between the latent periods of responses to clicks and to MGB stimulation varied for different neurons from 6 to 21 msec. Responses of 11% of neurons to MGB stimulation, recorded intracellularly, consisted of sub-threshold EPSPs, while responses of 23% of neurons began with an EPSP which was either followed by an action potential and subsequent IPSP or was at once cut off by an IPSP; 66% of neurons responded with primary IPSPs. Neurons responding to MGB stimulation by primary IPSPs are distributed irregularly in the depth of the cortex: there are very few in layers III and IV and many more at a depth of 1.6–2 mm. Conversely, excited neurons are predominant in layer III and IV, and they are few in number at a depth of 1.6–2 mm. It is concluded that the afferent volley reaching the auditory cortex induces excitation of some neurons therein and, at the same time, by the principle of reciprocity, induces inhibition of others. This afferent inhibition takes place with the participation of inhibitory interneurons, and in some cells the inhibition is recurrent. The existence of reciprocal relationships between neurons in different layers of the auditory cortex is postulated.A. A. Bogomolets' Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 4, No. 1, pp. 23–31, January–February, 1972.     

Effect of pentobarbital on neuronal inhibitory response evoked in an isolated slab of cat auditory cortex by intracortical stimulation

Neuronal responses of an acutely isolated slab of auditory cortex (area AI) to intracortical electrical stimulation were studied intracellularly in cats anesthetized with pentobarbital. It was found that 77% of responses were primary IPSPs, and allowing for secondary inhibitory responses, an inhibitory response was observed in 92% of neurons. All types of neuronal responses in the slab were short-latency. The maximal response latency did not exceed 5 msec. Neurons responding to stimulation by IPSPs were found at all depths in the slab, with a maximum in layers II–III. Nearly all primary IPSPswere mono- and disynaptic. Pentobarbital increased the duration of individual neuronal inhibitory responses in the isolated slab of auditory cortex without affecting maximal duration of the IPSP. The mechanisms of the effect of pentobarbital on the amplitude and duration of IPSPs are discussed.I. I. Mechnikov Odessa State University. Translated from Neirofiziologiya, Vol. 16, No. 2, pp. 147–152, March–April, 1984.     

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.     

Neuronal inhibitory responses to intracortical stimulation of an isolated slab of cat auditory cortex

Neuronal responses of an isolated slab of cortex to intracortical stimulation were studied intracellularly. The predominant responses were primary IPSPs. Their latent periods did not exceed 10 msec. Within the volume of cortex studied, neurons inhibited in response to stimulation were most numerous in the upper layers (II, III). Predominance of disynaptic IPSPs is evidence of the important role of cortical interneurons in their genesis. It is concluded from the results that primary IPSPs limit the spread of excitation primarily in the activated area of cortex. Since involvement of neurons of the isolated slab in the inhibition process takes place for only 10 msec after stimulation, neurons giving spike responses to intracortical stimulation with a longer latent period can transmit information into other brain zones. The role of duration of IPSP in the dynamics of interneuronal interaction in the cerebral cortex is discussed.I. I. Mechnikov Odessa State University. Translated from Neirofiziologiya, Vol. 16, No. 1. pp. 42–49, January–February, 1984.     

Inhibitory Synapses on Pacemaker Neurons in the Heart Ganglion of a Stomatopod, Squilla oratoria

The pacemaker neurons of the Squilla heart ganglion are innervated from the CNS through three pairs of extrinsic nerves. One of them, the α-nerve, is inhibitory to the heart beat. The effect of α-nerve stimulation on the pacemaker potential was examined with intracellular electrodes. Without extrinsic nerve stimulation the membrane potential of the pacemaker cell fluctuated spontaneously. On application of a tetanic train of stimuli to the α-nerve the membrane potential was shifted and fixed to a steady level, which with K₂SO₄-filled electrodes was near the peak of hyperpolarization after a spontaneous burst, but was less negative with KCl-filled electrodes. The shift of the membrane potential was due to the summated IPSP's. By changing the level of the membrane potential with injection of the polarizing current the IPSP could be reversed in sign, and the size of the IPSP was linearly correlated with the membrane potential level. During inhibition the membrane conductance increased. The increase depended on divalent cation concentrations in the outside medium. In Ca-rich saline the IPSP was greatly enhanced. In Mg-rich saline it was suppressed. The amplitude of antidromic spikes was reduced during inhibition especially when the spike frequency was high.     

Synaptic events during specific and nonspecific inhibition of visual cortical neurons

Intracellular and quasi-intracellular recordings were made of changes in membrane potential in visual cortical neurons of the waking rabbit during specific (to flashes) and nonspecific (to nonvisual stimuli) inhibition. As a rule, specific inhibition was accompanied by some degree of hyperpolarization of the cell membrane while nonspecific was unaccompanied by any appreciable degree of membrane hyperpolarization. It is postulated that this difference is caused by differences in the arrangement of the inhibitory synapses on the body and dendrites of the neurons. Long-latency prolonged IPSPs arising in response to photic stimulation can be suppressed by the action of various nonvisual stimuli and by stimulation of the mesencephalic reticular formation. A decrease in amplitude of the IPSPs may lead to filling of the inhibitory pauses with spikes. These phenomena are evidently based either on inhibition of inhibitory neurons or on a disturbance of the synchronization of their discharges, leading to weakening of the integral IPSPs.Brain Institute, Academy of Medical Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 4, No. 4, pp. 349–357, July–August, 1972.     

Characteristics of inhibition in the kitten sensory-motor cortex

Responses of 340 neurons of the sensory-motor cortex to electric shocks applied to the limbs were investigated in kittens aged 3–30 days. In 9.4% of cells of kittens aged 3–10 days and in 17.1% of cells in kittens aged 21–30 days pauses were observed immediately after the excitatory component of the extracellular response. Intra- and quasiintracellular recording showed that postsynaptic inhibition participates in the genesis of these pauses. The IPSPs which, as a rule, followed the excitatory component of the response were of much longer duration (up to 250–380 msec) than the analogous IPSPs in the sensory-motor cortex of adult cats. Usually the amplitude of the IPSP in kittens did not exceed 5 mV.A. A. Zhdanov Leningrad State University. Translated from Neirofiziologiya, Vol. 9, No. 3, pp. 227–231, May–June, 1977.     

Aspects of excitation and inhibition produced in parietal association cortex neurons by stimulating thalamic association nuclei

Neuronal response to single stimuli applied to the thalamic dorsolateral and posterolateral nuclei (DLN and PLN resepctively) was investigated in the parietal association cortex. Primary IPSP following DLN and PLN stimulation was noted in 62.5% and 79.6% of instances respectively. Latencies of EPSP and IPSP when stimulating the two nuclei were longer for the DLN. The amplitude of EPSP evoked by stimulating association nuclei rose and declined smoothly, while that of IPSP showed a fast rise and a more steady decline. The EPSP appearing during the evolution of IPSP were of higher amplitude than control level of resting potential. Both amplitude and duration of IPSP induced in a single unit by stimulating different association nuclei were extremely similar, thus confirming the involvement in this operation of the same inhibitory cortical interneurons. Duration of IPSP was shorter than that of inhibitory background spike activity. It is postulated that the discrepancy in duration can largely be ascribed to properties of the neurons themselves.State University, Odessa. Translated from Neirofiziologiya, Vol. 23, No. 5, pp. 529–536, September–October, 1991.     

Unit responses in the anterior zone of the suprasylvian gyrus to peripheral stimuli of different modalities

Unit responses in the anterior zone of the suprasylvian gyrus to visual, electrodermal, and acoustic stimulation were investigated in experiments on unanesthetized cats immobilized with tubocurarine. Electrical activity was recorded from 131 units, 121 of which were spontaneously active. In 65.5% of cells responses consisted of a short or long increase or a decrease in intensity of spike activity. Most cells (58.2%) were monosensory. Responses to visual stimulation were given by 72% of neurons, to electrodermal by 61.6%, and to acoustic by 9.3%. The corresponding latent periods were 20–40, 20–30, and 15–20 msec. Responses of the same neurons to different peripheral stimuli were uniform or they differed in their dynamics. Intracellular recording gave responses in the form of EPSPs (amplitude 4–5 mV, duration 60–80 msec) or, rarely, IPSPs (amplitude 2–3 mV, duration 160–200 msec). The functional organization of the associative cortex and mechanisms of analysis of incoming afferent information are discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 4, No. 4, pp. 368–374, July–August, 1972.     

Synaptic mechanisms controlling receptor unit activity in the stretch receptor—Abdominal ganglionic chain system of the crayfish

Inhibitory control over activity of the receptor neuron was investigated in a preparation of the stretch receptor and abdominal ganglionic chain in crayfishes. Potentials were recorded intracellularly from receptor neurons and neurons of the abdominal ganglion, and extracellularly from the dorsal roots. IPSPs appeared in the receptor neuron in response to stimulation of that same neuron or of the abdominal ganglionic chain. The relationship between spikes at the input and output of the inhibitory neuron varied over a wide range depending on the functional state of the neuron. A linear relationship was established between the time before appearance of the IPSP and the duration of the interspike interval of the slowly adapting neuron (SAN) and also between the firing rate of this and the inhibitory neurons during recurrent inhibition. Factors influencing the length of the interspike interval of the SAN on the appearance of an IPSP in it were investigated. It is postulated that summation of potentials evoked by spikes of the SAN and also of potentials evoked by spikes of that neuron, together with local processes evidently of endogenous nature takes place in the inhibitory neuron. IPSPs were recorded from two neurons resistant to strychnine and blocked by picrotoxin on the receptor neuron. The structural and functional organization of the individual elements in the chain of recurrent inhibition and inhibition evoked by stimulation of the abdominal ganglionic chain is discussed.Institute of Higher Nervous Activity and Neurophysiology, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 5, No. 3, pp. 323–332, May–June, 1973.     

Monosynaptic inhibitory postsynaptic potentials of cortical neurons

Monopolar intracortical stimulation of the auditory cortex was carried out in cats immobilized with D-tubocurarine. A macroelectrode (tip diameter 100 µ) or a microelectrode (tip diameter 10–15 µ) was used for stimulation. In both cases, besides excitatory responses, primary IPSPs with latent periods of 0.4–1.2 and 1.4–6.0 msec were recorded in cortical neurons close to the point of stimulation. The first group of IPSPs are considered to be generated in response to direct stimulation of bodies or axons of inhibitory cortical neurons, i.e., monosynaptically. The amplitude of these IPSPs varied in different neurons from 3 to 15 mV, and their duration from 4 to 150 msec. Additional later inhibitory responses were superposed on many of them. Of the IPSPs generated in auditory cortical neurons in response to stimulation of geniculocortical fibers 1.5% had a latency of 0.8–1.3 msec. They also are assumed to be monosynaptic. It is concluded that the duration of synaptic delay of IPSPs in cortical neurons and spinal motoneurons is the same, namely 0.3–0.4 msec. Axons of auditory cortical inhibitory neurons may be 1.5 mm long. The velocity of impulse conduction along these axons is 1.6–2.8 m/sec. The genesis of some special features of IPSPs of cortical neurons is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 7, No. 5, pp. 458–467, September–October, 1975.     

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.     

Habituation of postsynaptic unit responses of the cat motor cortex to stimuli of different modalities

Habituation (extinction) of postsynaptic unit responses of the cat motor cortex to repetitive electrodermal, photic, acoustic, and combined bimodal stimulation was investigated by intracellular recording. Habituation was shown by a decrease in the number of spikes per grouped discharge and a decrease in the amplitude and duration of the EPSPs, and sometimes IPSPs, on repetition of the stimulus. The way in which the course of habituation depends on the modality and duration of stimulation (at a constant frequency of 1/sec) is examined. Habituation of postsynaptic responses to sensory stimuli is observed with neurons of different functional groups, namely identified neurons of pyramidal tract and unidentified neurons, some of which were evidently pyramidal neurons and interneurons. The hypothesis is put forward that the habituation of PSPs of the cortical neurons is based on processes taking place mainly at the subcortical level.A. A. Zhdanov Leningrad State University. Translated from Neirofiziologiya, Vol. 4, No. 5, pp. 545–553, September–October, 1972.     

Suppression of "fast" IPSP,superposed on "slow", as a possible cause of priming in murine hippocampus

Intra- and extracellular response in area CA1 to stimulation of two independent afferent inputs, one a priming or conditioned and the other a test or primed input (C1 and C2, respectively) were recorded in surviving murine hippocampal slices. Duration and amplitude of test field potentials (FP) and of excitatory postsynaptic potentials (EPSP), were measured, as well as amplitude of "fast" and "slow" components of inhibitory postsynaptic potentials or stimulation varying between 0 and 1 sec. Conditioning brought about an increase in the duration of FP, in duration and amplitude of EPSP, and suppression of IPSP at intervals of between 50 and 500 msec peaking at 200 msec (i.e., priming effect). These changes correlated with level of IPSP_b in response to conditioned stimuli. The most pronounced effect could be seen in neurons manifesting hyperpolarizing IPSP in response to test stimuli. Suppression of test IPSP_a after superposition on IPSP_b is thought to bring about the increase in test FP and EPSP seen during priming.Institute for Brain Research, All-Union Mental Health Research Center, Academy of Medical Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 22, No. 6, pp. 730–739, November–December, 1990.     

Postsynaptic inhibition in the general cortex of the turtle forebrain

Postsynaptic inhibition in the general cortex of the turtle forebrain was investigated by recording unit activity intracellularly. Depending on the type of IPSPs recorded in response to electrical stimulation of the contralateral optic nerve and cortical surface the neurons were subdivided into three groups: 1) with long direct IPSPs, 2) with long and short direct, and also recurrent IPSPs, 3) with short direct and recurrent IPSPs. It is concluded that inhibitory pathways of the short direct and recurrent IPSPs have a common final component, a stellate interneuron. Compared with the recurrent collaterals of the principal neurons, the direct afferents make contact with more distal portions of the dendrites of this cell. Synapses formed on dendrites of the principal neurons by axons of the stellate cells are nearer to the soma than synapses responsible for generation of the long direct IPSP.M. V. Lomonosov Moscow State University. Translated from Neirofiziologiya, Vol. 5, No. 4, pp. 375–383, July–August, 1973.     

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.