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1.
P. A. Gusev 《Neurophysiology》1994,26(1):50-54
Repetitive applications of L-glutamate (Gl) to single neurons of the sensorimotor cortex in unanesthetized rats, if associated with the applications of acetylcholine (ACh), are followed by significant rearrangements in the dynamics of their cholinoreactivity and background activity, compared with those observed when only ACh or only Gl are applied repetitively. The excitatory components of the responses to ACh are reduced, and the probability of appearance and the frequency of background spikes decrease if compared with those observed at the ACh applications without Gl. The decrease in the ACh reactivity resulting from the applications of ACh only is observed mostly in the cells with inhibitory-excitatory responses to ACh, rather than in the cells with pure excitatory responses. The dynamics of cholinoreactivity were found to depends on the temporal structure of the cortical neuronal responses to ACh, as well as on its modulation with Gl.Neirofiziologiya/Neurophysiology, Vol. 26, No. 1, pp. 61–67, January–February, 1994. 相似文献
2.
V. A. Dyatlov 《Neurophysiology》1991,23(1):28-35
The response was investigated of neurons composing the cerebral ganglia inAchatina fulica (the Giant African snail) to application of acetylcholine (ACh), gamma-aminobutyric acid (GABA), and glycine (Gly). Chloride-dependent currents induced by these transmitters in 1 1/2-month old siblings were inhibited by dibutyryl-cAMP and strychnine. Inhibition of ACh response produced 10–8 M GABA was mimicked by application of dibutyryl-cAMP and isobutylmethylxanthine. Complete cross-desensitization was characteristic of both GABA- and Bly-induced response, but this effect did not occur when ACh and GABA (or Gly) were applied. A conclusion was reached on the basis of the pharmacological relationship between GABA- and Gly-induced response that these amino acids act on a single receptor — channel complex in the neurons of infant snails, whereas ACh-, GABA-, and Gly-induced chloride currents were not so related in cells of 4 year-oldAchatina.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 23, No. 1, pp. 35–43, January–February, 1991. 相似文献
3.
N. A. Otmakhov 《Neurophysiology》1988,20(1):52-60
Investigations were performed on the effects of acetylcholine (ACh), norepinephrine (NE), 5-hydroxytryptamine (5-HT), and -aminobutyric acid (GABA) on the background firing of the three following groups of field CA3 neurons in guinea pig hippocampal slices: nonpyramidal neurons of the stratum radiatum moleculare (NSR), stratum pyramidale cells with single spike discharges (SD units), and those with complex discharge patterns (CD units) within the same layer. The action of ACh and NE on presumed interneurons of the pyramidal layer (IPL) was also investigated; CD units were found to differ from the remaining groups, which reacted similarly to the transmitters tested. It was shown that NE, 5-HT, and GABA inhibited the activity of CD cells, while ACh produced inhibitory-activating response in 50% of these units. Both NE and ACh exerted a monophasic activating effect on NSR, ISP, and SD, however, while 5-HT and GABA induced activation in a proportion of NSR and SD cells, as well as inhibitory response. The excitatory effects produced by ACh, NE, and 5-HT on NSR persisted during blockade of synaptic transmission, indicating that associated afferent fibers may be acting directly on these cells.Institute of Biological Physics, Academy of Sciences of the USSR, Pushchino-on-Oka. Translated from Neirofiziologiya, Vol. 20, No. 1, pp. 64–74, January–February, 1988. 相似文献
4.
Membrane currents elicited by iontophoretic applications of acetylcholine (ACh currents) were recorded from neurons of the guinea pig submucous plexus using a whole-cell patch-clamp recording technique. The ACh currents declined to 5–20% of their peak amplitude during about 2 sec-long application of ACh. After the end of ACh application, a transient increase of the ACh current (the aftercurrent, AC) was observed. The most probable mechanisms responsible for the ACh current decline and for the appearance of the AC are transitions of nicotinic ACh receptors first to a desensitized state, and then to the state with an open ionic channel, respectively.Neirofiziologiya/Neurophysiology, Vol. 25, No. 4, pp. 291–296, July–August, 1993 相似文献
5.
Electrophysiological and biochemical studies suggest that VIP may exert a facilitating action in the neocortical local circuitry. In the present study, we examined the actions of VIP and VIP + norepinephrine (NE) on somatosensory cortical neuron responses to direct application of the putative transmitters acetylcholine (ACh) and gamma-aminobutyric acid (GABA). Spontaneous and transmitter-induced discharges of cortical neurons from halothane-anesthetized rats were monitored before, during and after VIP, NE and VIP + NE iontophoresis. In 57 VIP-sensitive cells tested, VIP application (5-70 nA) increased (n = 18), decreased (n = 36) or had biphasic actions (n = 3) on background firing rate. In a group of 20 neurons tested for NE + VIP, the combined effect of both peptide and bioamine was predominantly (70%) inhibitory. On the other hand, inhibitory and excitatory responses of cortical neurons to GABA (11 of 15 cases) and ACh (10 of 18 cases), respectively, were enhanced during VIP iontophoresis. Concomitant application of VIP and NE produced additive (n = 2) or more than additive (n = 3) enhancing effects on GABA inhibition. NE administration reversed or enhanced further VIP modulatory actions on ACh-induced excitation. These findings provide electrophysiological evidence that NE and VIP afferents may exert convergent influences on cortical neuronal responses to afferent synaptic inputs such that modulatory actions are anatomically focused within the cortex. 相似文献
6.
The effects of tubocurarine (TC) on current induced by acetylcholine (ACh) in neurons of rat upper cervical ganglia were investigated using techniques for voltage-clamping at the membrane. Reinforcement of TC-induced blockade was achieved by paired application of ACh following prior activation of nicotinic cholinoreceptors, indicating that TC blocked the channels opened by ACh. On average, the TC-open channel complex persisted for 9.8±0.5 sec (n=7) at –50 mV and 20–24°C. It was found that increases exponentially with hyperpolarization at the membrane (a shift in membrane potential of 61 mV corresponds to an e-fold change). Suppression of ACh-induced current (ACh current) was eliminated completely under the effects of 3–30 M with depolarization of up to 80–100 mV at the membrane. Suppression of ACh current produced by membrane potential at negative levels is intensified with increasing doses of ACh. Findings would indicate that blockade of ionic channels opened by ACh is the only mechanism of TC action on nicotinic cholinoreceptors in rat sympathetic ganglia.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 5, pp. 672–680, September–October, 1988. 相似文献
7.
In an analysis of the postsynaptic mechanism of heterosynaptic facilitation, changes in the amplitude of the excitatory postsynaptic current (EPSC) and the current evoked by application of acetylcholine (ACh current), acting on the adenylate cyclase system of the LC-1 and RC-1 neurons of the molluskPlanorbis corneus, were compared. Both responses are n-cholinergic and depend on the membrane conductivity for Na+ and K+. Application of serotonin led to a 100–300% increase in the amplitude of the EPSC and (in most cases) the ACh current. However, in 30% of the cases, the increase in the EPSC was accompanied by a decrease in the ACh current. This is probably due to the different contributions of Na+ and K+ to the mechanism of activation of the conductivity of th channel-receptor complex of the nonsynaptic cell membrane. The influence of serotonin on the EPSC and ACh current was simulated by the action of phosphodiesterase blockers and adenylate cyclase activators. Phosphodiesterase activators and protein kinase blockers reversibly inhibited the EPSC and ACh current. Thus, activation of the adenylate cyclase system, mediated by the action of serotonin, promotes the development of a postsynaptic mechanism of formation of heterosynaptic facilitation of the EPSC in the command neurons of the mollusk.A. A. Bogomolets Institute of Physiology, Ukrainian Academy of Sciences, Kiev. Translated from Neirofiziologiya, Vol. 23, No. 6, pp. 676–683, November–December, 1991. 相似文献
8.
The importance of parasympathetic excitatory and inhibitory neural control of airway smooth muscles has been demonstrated. It is concluded that excitatory (acetylcholine, ACh) and inhibitory (NO- and VIP-related) neurotransmitters co-exist and are co-released from vagus nerve terminals. The latter transmitters can directly relax airway smooth muscles and, at the same time, inhibit ACh release, playing the role of the braking system against bronchoconstriction.Neirofiziologiya/Neurophysiology, Vol. 37, No. 1, pp. 80–81, January–February, 2005. 相似文献
9.
I. N. Antonov 《Neurophysiology》1993,25(3):191-199
This review is focused on the analysis of research data obtained in one of the models of conditioned reflex, heterosynaptic facilitation (HSF), in the molluscan nervous system. Our experiments were performed on identified giant command neurons LS1 and PS1 of the freshwater snail Planorbarius corneus. HSF was elicited during the electrical stimulation of two nerves: pallial (the analog of unconditioned stimulation — US) and one of the cerebral nerves (the analog of the conditioned stimulation — CS). The degree of HSF manifestation depended not on the intensity of the synaptic response of the giant neuron to US, but the efficacy of the connection between the pallial nerve and neurosecretory neurons surrounding the command neuron of the mesocerebrum. It is demonstrated that HSF develops due to the diffuse neurohumoral action of serotonin (5-hydroxytryptamine — 5-HT) on the postsynaptic structures, but not as a result of local synaptic action on the presynaptic mechanism. Approximately 70% of US cases of 5-HT application induced a four- to six-fold increase in amplitude of the excitatory postsynaptic potential (EPSP) and acetylcholine (ACh) response. Both responses are N-cholinergic and depend on the membrane permeability to Na+ and K+. In 30% of the cases, ACh response diminished simultaneously with EPSP increase. The 5-HT effect on EPSP and ACh responses were mimicked by the action of phosphodiersterase blockers and adenylate cyclase activators. Thus, the activation of the adenylate cyclase system following 5-HT action facilitates the postsynaptic mechanism underlying HSF formation in command neurons of Planorbarius corneus. Dopamine (DA) and noradrenaline (NA) blocked EPSP and simultaneously increased the amplitude of ACh response. These monoamines were also blocked HSF. The wash-out of catecholamines following HSF blockade enhanced the restoration and subsequent prolongation of synaptic facilitation. It is thus concluded that DA or NA may control the HSF intensity and duration under natural conditions of the nervous system in the molluscs.Neirofiziologiya/Neurophysiology, Vol. 25, No. 3, pp. 224–232, May–June, 1993. 相似文献
10.
Physiology and pharmacology of acetylcholinergic responses of interneurons in the antennal lobes of the mothManduca sexta 总被引:1,自引:0,他引:1
Brian Waldrop John G. Hildebrand 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1989,164(4):433-441
1. Neurons in the antennal lobe (AL) of the moth Manduca sexta respond to the application, via pressure injection into the neuropil, of acetylcholine (ACh). When synaptic transmission is not blocked, both excitatory (Fig. 2) and inhibitory (Fig. 3) responses are seen. 2. Responses to ACh appear to be receptor-mediated, as they are associated with an increase in input conductance (Figs. 2B and 3B) and are dose-dependent (Fig. 2 C). 3. All neurons responsive to ACh are also excited by nicotine. Responses to nicotine are stronger and more prolonged than responses to ACh (Fig. 4C). No responses are observed to the muscarinic agonist, oxotremorine (Fig. 4 B). 4. Curare blocks responses of AL neurons to applied ACh, while atropine and dexetimide are only weakly effective at reducing ACh responses (Figs. 5 and 6). 5. Curare is also more effective than atropine or dexetimide at reducing synaptically-mediated responses of AL neurons (Fig. 7). 6. In one AL neuron, bicuculline methiodide (BMI) blocked the IPSP produced by electrical stimulation of the antennal nerve, but it did not reduce the inhibitory response to application of ACh (Fig. 8). 相似文献
11.
The role of calcium ions in modulating serotonin action on acetylcholine (ACh) response in nonidentified and identified (LPa3 and RPa3) neurons ofHelix
pomatia was investigated using voltage-clamping at the neuronal membrane. Exposure for 1 min to serotonin prior to ACh application reduced response to ACh in neuron LPa3 and raised it in RPa3. The same two patterns of modulating ACh-induced response were produced by extracellular application of theophylline and dibutyryl c-AMP. Injecting calcium ions into neuron LPa3 led to reinforcement of ACh-induced current in the presence of serotonin, thus changing the pattern of serotonin-induced modulation of ACh response in this unit. In neuron RPa3, the same process enhanced the serotonin-induced modulating effect on ACh response but without changing the pattern of modulation, while injected EDTA produced the reverse effects. Increased intracellular concentration of calcium ions brought about a reduction in the degree of serotonin-induced modulation of ACh response in neuron RPa3. Possible reasons are discussed for changes in serotonin-induced bimodal modulation of ACh response in test neurons produced by altering the extracellular concentration of calcium ions.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 5, pp. 666–671, September–October, 1988. 相似文献
12.
Ionic mechanisms of EPSP generation and depolarization induced by iontophoretic application of acetylcholine (ACh) and serotonin (5-hydroxytryptamine, 5-HT) — acetylcholine and serotonin potentials — were investigated in neurons of the isolated rabbit superior cervical ganglion by means of intracellular microelectrodes. The reversal potentials (Er) for EPSP and the ACh-potential were –14.4±1.6 and –16.5±1.2 mV respectively, and they were about the same for the 5-HT potential. In some neurons (about one-third) much more negative values for Er were obtained for EPSP and the ACh-potential by extrapolation, probably due to an increase in the resistance of their membrane during hyperpolarization. A decrease in the external sodium and potassium concentrations was shown to make Er for EPSP and the ACh-potential more negative, whereas an increase in the external potassium concentration made it more positive than in normal solution; a change in the external chloride concentration did not alter Er. It is suggested that the excitatory transmitter and exogenous ACh (and also, probably, 5-HT) share the same ionic mechanism of action of the membrane, which includes an increase in the permeability of the membrane to two ions — sodium and potassium — simultaneously.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 10, No. 6, pp. 637–644, November–December, 1978. 相似文献
13.
Alexandre Widmer Izabela Panek Ulli Höger Shannon Meisner Andrew S. French Päivi H. Torkkeli 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》2006,192(1):85-95
Peripherally located parts of spider mechanosensory neurons are modulated by several neurotransmitters released from apposed
efferent fibers. Activities of acetylcholine (ACh) synthesizing enzyme choline acetyltransferase (ChAT) and ACh degrading
enzyme acetylcholine esterase (AChE) were previously found in some efferent fibers. ChAT activity was also present in all
the mechanosensory neurons, while AChE activity was only found in some. We show that spider mechanosensory neurons and probably
some efferent neurons are immunoreactive to a monoclonal antibody against muscarinic ACh receptors (mAChRs). However, application
of muscarinic agonists did not change the physiological responses or membrane potentials of neurons in the lyriform organ
VS-3. Similarly, the sensitivities of the neurons of trichobothria (filiform hairs) remained unchanged after application of
these agonists. Therefore, activation of mAChRs may only modulate the function of spider mechanosensory neurons indirectly,
for example, by affecting the release of other transmitter(s). However, a subgroup of VS-3 neurons was inhibited by ACh, which
also depolarized the membrane similar to these neurons’ responses to GABA, suggesting that ACh activates anion channels in
these neurons. Interestingly, all of the neurons responding to ACh were the rapidly adapting Type A neurons that were previously
shown to express AChE activity. 相似文献
14.
ATP-induced membrane durrents in the submucous neurons of the guinea pig small intestine were studied using the whole-cell patch-clamp recording technique. Being applied at –50 mV. ATP activated an inward non-selective cationic current in 68.3% of the investigated neurons. An increase in ATP concentration within the 1–1,000 µM range resulted in the s-like increase in the amplitude of ATP-induced current. The EC50 was 150.0±18.5 µM, while the Hill number was 1.6. The current was selectively activated by ATP and was not blocked by P2 purinoreceptor antagonist suramin (50–300 µM).,-Methylene-ATP (100–200 µM) and,-methylene-ATP (100–200µM), which are P2-purinoreceptor agonists, as well as adenosine (100–300 µM), exerted no effects. Reactive blue 2, if applied up to 4 min, enhanced ATP-induced current, while its longer application partially suppressed this current. In most submucous neurons, acetylcholine (ACh) likewise activated an inward cationic current. The amplitude of ACh-induced current was lower if ACh was applied during a long-lasting application of ATP than if ACh only was applied. Hexamethonium (50 µM), d-tubocurarine (20–40 µM), and trimethaphan (30 µM) completely and reversibly blocked ACh-induced currents, regardless of the presence of ATP, and did not affect ATP-induced currents. The results suggest that ATP-induced currents in submucous neurons are due to activation of a unique type of P2 purinoreceptors, which function in connection with nicotinic ACh receptors.Neirofiziologiya/Neurophysiology, Vol. 28, No. 2/3, pp. 100–110, March–June, 1996. 相似文献
15.
The effects of direct application of acetylcholine (ACh) and m- and n-cholinoreceptor blockers on test cells were investigated in waking cats having developed instrumental lever-pressing conditioned reflex. Changes were recorded in both spontaneous and invoked firing activity in a functionally homogeneous group of motor cortex cells, in which increased discharge rate usually preceded the start of conditioned reflex movements. It was found, however, that ACh increased spontaneous activity considerably in some of the neurons tested and reduced it moderately in others. Atropine sharply reduced background activity in cortical neurons while preserving spike response to presentation of a conditioned stimulus and n-cholino-blockers such as hexonium and (occasionally) tubocurarine inhibited spike response produced by conditioned stimuli; background activity was slightly inhibited by hexonium and reinforced by tubocurarine. It was concluded that ACh put out by cholinergic fibers helps to maintain background firing activity level in cortical neurons under naturally occurring conditions, acting via m-cholinoreceptors, whereas factors influencing generation of spike discharges associated with performance of conditioned reflex movements are mediated by n-cholinoreceptors.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 21, No. 5, pp. 579–589, September–October, 1989. 相似文献
16.
A. L. Byzov 《Neurophysiology》1969,1(2):160-166
We recorded by intracellular means responses of horizontal cells of the turtle retina to light increase and decrease of different values against the starting adapting level. In measuring these responses, curves reflecting the dependence of membrane potential deflection on light intensity (amplitude characteristics — ACh) were plotted. It is demonstrated that the ACh of transitional processes (on- and off-peaks) is considerably steeper than ACh of the plateau of the potential, but embraces a much smaller range of light intensities (slightly more than 1 log. un.). During a change in intensity of the adapting background (up to 3 log. un.), the ACh of transitional processes shifts along the scale of light intensities in such a way that its steep part remains in the zone of adapting light. We followed the dynamics in time of ACh shift after the transition from one adapting brightness to another. The ACh of total impulse response was plotted for ganglionic cells of the turtle at different intensities of adapting light. Comparison of these curves with the ACh of horizontal cells shows that its peripheral components are responsible for adaptive shifts of ACh of the visual system and that horizontal cells play an important role in the mechanism of adaptation. It is hypothesized that adaptive ACh shifts are the consequence of positive feedback between the horizontal cells and receptors.Institute of Problems of Information Transmission, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 1, No. 2, pp. 210–218, September–October, 1969. 相似文献
17.
Responses of rabbit visual cortical neurons to single and repetitive intracortical electrical stimulation were investigated. The stimulating electrode was located 0.7–1.2 mm away from the recording electrode. Response thresholds to single stimulation were as a rule 150–180 µA, whereas to series of stimuli they were 30–60 µA. The latent period to the first spike averaged 5–15 msec but the probability of the initial discharge was very low, namely 3–6%. With an increase in current intensity the duration of the initial inhibitory pause was increased in half of the neurons responding to it, whereas in the rest it was unchanged. After presentation of series of stimuli spontaneous activity was enhanced for a short time (4–6 sec). In about half of the cells the same kinds of discharge dynamics were observed in response to repetitive stimulation (frequency 0.25 Hz) as in responses to light, but more neurons with sensitization of discharge and fewer "habituating" neurons took part in responses to electrical stimulation. It is postulated that stimulation of a given point of the visual cortex evokes excitation of a local neuron hypercolumn and inhibition of neighboring cell columns.M. V. Lomonosov Moscow State University. Translated from Neirofiziologiya, Vol. 15, No. 4, pp. 412–419, July–August, 1983. 相似文献
18.
Effects of aspartate (2 · 10–5 M), substance P (10–7–10–8 M), and serotonin (5-hydroxytryptamine, 5-HT; 5 · 10–5 M) on the background activity of neurons in the central gray substance (CGS) were studied on slices of the rat midbrain. Aspartate and substance P (transmitters of nociceptive signals), and 5-HT (modulator of transmission of nociceptive influences) were found either to facilitate or to depress the activity of CGS neurons. The predominant effect of substance P or 5-HT applications to neurons of the dorsal CGS part was facilitation, and to neurons of the ventral CGS part, inhibition. The effects of aspartate application on studied CGS neurons were of varying nature, but inhibitory effects were found to prevail.The findings support our earlier hypothesis that assigned the studied neurons to spontaneously discharging inhibitory CGS interneurons, which control the activity of efferent CGS neurons. The role of tested substances in the regulation of CGS neuronal activity and the antinociceptive CGS effects is discussed.Neirofiziologiya/Neurophysiology, Vol. 25, No. 5, pp. 354–362, September–October, 1993. 相似文献
19.
Changes in spontaneous activity of 291 neurons in the rabbit amygdala were analyzed during microelectrophoretic application of somatostatin under pentobarbital anesthesia. Somatostatin was found both to enhance and to inhibit the spontaneous activity of these cells, by contrast with the exclusively inhibitory effect on spontaneous activity of hypothalamic neurons described previously. After partial chronic deafferentiation of the amygdala, 76% of 103 neurons responded to somatostatin application; 90% of the responding cells, in which the initial spontaneous firing rate was 6–20 spikes/sec, responded by more rapid firing, and only 10% of neurons (with an initial spontaneous discharge frequency of over 20 spikes/sec) showed a decrease in firing rate. Neuronal responses in the amygdala to somatostatin, glutamate, and noradrenalin are compared. Preliminary application of noradrenalin caused an increase in the number of inhibitory responses on subsequent application of somatostatin to the same cell.M. V. Lomonosov Moscow State University. Translated from Neirofiziologiya, Vol. 14, No. 6, pp. 601–607, November–December, 1982. 相似文献
20.
The effects of successive extracellular iontophoresis of acetylcholine (ACh) and atropine, and intracellular hyperpolarizing iontophoresis of cyclic GMP (cGMP) were studied in single neurons of the coronal-pericruciate cortex of awake cats. (a) Fifty-seven percent of the neurons that were tested responded to ACh with an increase in neuronal input resistance (Rm) and 50% responded to ACh with an increase in firing rate; 65% responded to cGMP with an increase in Rm and 60% responded to cGMP with an increase in firing rate. (b) After application of atropine, increases in Rm and firing rate associated with iontophoresis of ACh failed to recur. (c) Persistent increases in Rm following application of ACh accompanied by current-induced neuronal discharge were not diminished by subsequent application of atropine. (d) Atropine did not prevent increases in Rm and firing rate associated with intracellular iontophoresis of cGMP. (e) All cells tested with both ACh and cGMP that were shown initially to respond to extracellular ACh with increases in Rm were later shown to have comparable responses to cGMP. 相似文献