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1.
  • 1.1. Recordings were made from primary afferent and secondary neurons in the electrosensory system of the thornback ray.
  • 2.2. The frequency response characteristics of these neurons were determined during sinusoidal modulation of uniform external fields.
  • 3.3. The form or the filter curves was similar in all primary and secondary cells, with a maximum amplitude of response occurring at a modulation frequency of 4 Hz.
  • 4.4. Secondary neurons showed an increased gain at low stimulus amplitude, and saturated at a much lower level than primary afferents.
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2.
  • 1.1. Exposure of isolated ventral nerve cords of the American cockroach to chlordimeform was followed by spontaneous and stimulus-induced hyperactivity which different from that induced by dieldrin in the distribution of spike amplitudes, the delay between stimulus and response and the stimulus threshold to induce hyperactivity.
  • 2.2. Calcium (20 mM) abolished the impulse-evoked hyper-response of the nerve to chlordimeform but not to dieldrin.
  • 3.3. Magnesium (40 mM) abolished the impulse-evoked hyper-responce of the nerve to dieldrin but not to chlordimeform.
  • 4.4. Treatment of the insects with reserpine prior to dissection had no effect on the subsequent hyper-response of the isolated nerve to chlordimeform.
  • 5.5. The observed action of chlordimeform is probably axonal, and is unrelated to its known aminergic effects.
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3.
  • 1.1. The stimulation sequence provoked by a luminous point moving in front of a column of ommatidia was simulated for the eye of Squilla mantis.
  • 2.2. The output from the ommatidia is transferred to one tangential, integrating fiber as graded potentials. These potentials follow a gaussian-shaped angular sensitivity function for each ommatidium.
  • 3.3. The tangential fiber sums the inputs as they arrive and generates a spike if the sum is above threshold at one instant of time and at one point of the fiber.
  • 4.4. The histograms of instantaneous frequencies of spike discharge resemble the input-pattern histograms.
  • 5.5. The discharge pattern changes with distance and speed of the moving spot as well for the simulations as in electrophysiological recordings, and is adapted to the size of the animal.
  • 6.6. The shape of the histograms (i.e. the pattern of spike discharge) is assumed to transmit the information on the position, speed and size of a moving target.
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4.
  • 1.1. The electric organ discharge (EOD) frequency modulations evoked by brief water vibration were analysed in the pulse-type fish Gymnotus carapo.
  • 2.2. The response consisted of a transient increase of the EOD frequency at short latency (30 msec). Response profiles were characteristic of the specimen and relatively independent on stimulus intensity.
  • 3.3. Conversely, they were dependent on stimulation sequence, showing a rapid decrement along successive stimuli and high temporal discrimination.
  • 4.4. The brief latencies indicate a relatively simple neural circuit.
  • 5.5. The response may be an electrolocation enhancement strategy for the detection of moving objects based on “sampling” the periphery at a higher frequency.
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5.
  • 1.1. Two kinds of neurons were identified in the body-wall longitudinal muscle layer of the earthworm, Amynthas hawayanus, by the simultaneous potential recording and Lucifer Yellow-CH injection method with a single microelectrode.
  • 2.2. Both kinds of neurons have their somata, neuntes and longitudinal processes imbedded in the longitudinal muscle layer. Those with two circular processes extending into the third segmental nerve trunk are tentatively named “intra-nerve-trunk” neurons and those with four circular processes extending into four setae shafts are tentatively named “intramural” neurons.
  • 3.3. Both kinds of neurons responded to electrical and mechanical stimuli applied in an afferent direction to them.
  • 4.4. The “intra-nerve-trunk” neuron decreased its response amplitudes to these stimuli after the third nerve trunk was sectioned in correlation to the response amplitude decrease recorded from the nerve trunk after it was sectioned.
  • 5.5. The response amplitude decrease due to denervation implies a nonlinear structure of the earthworm reflex circuits.
  • 6.6. The “intramural” neurons are believed to be primary sensory neurons connected to the mechanoreceptors in the setae.
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6.
  • 1.1. In crayfish, light stimulation of the retinular cells induces a depolarizing receptor potential.
  • 2.2. Experiments were designed to determine the role of Na+ and Ca2+ on receptor potential during dark And light states.
  • 3.3. Depolarization depends on Na+ and Ca2+ availability to the retinular cell.
  • 4.4. Repolarization velocity and response duration depend on extracellular Ca2+ availability.
  • 5.5. Light adaptation increases receptor potential dependence on calcium and sodium ions.
  • 6.6. We analyse these results with respect to other invertebrate photoreceptors.
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7.
  • 1.1. Goldfish (Carassius auratus) were fitted with ECG electrodes and intra-cranial stainless steel electrodes to monitor cardiac, EEG and SPS responses, during minimal restraint, to presentation of environmental stimuli (light-on, moving shadow, tap).
  • 2.2. All three stimuli evoked a bradycardia and increases in the EEG frequency; correlates of arousal responses in fish.
  • 3.3. EEG frequency changes were most evident in the fore- and midbrain regions; in the hindbrain smaller responses nevertheless showed discrimination between stimuli.
  • 4.4. EEG amplitude changes were more site- and stimulus-specific than frequency changes.
  • 5.5. SPSs occurred on stimulus presentations which were negative in polarity in the midbrain and positive in the forebrain and hindbrain, though the latter were smaller and less consistent.
  • 6.6. Principal components analyses and regression analyses were used to examine detailed associations between peripheral and central physiological changes.
  • 7.7. It was found that increases in the EEG frequency of fore- and midbrain regions were related to cardiac deceleration on early stimulus presentations.
  • 8.8. This was also shown for the negative SPS of the midbrain to the presentation of the tap stimulus.
  • 9.9. Positive SPSs of the forebrain were related to the bradycardia on later stimulus presentation i.e. during habituation of the arousal response.
  • 10.10. The results indicate that in fish, as in other vertebrates, negative SPSs in the midbrain are associated with arousal and implicate the forebrain in the modulation of arousal by its habituation.
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8.
  • 1.1. The recorcling sites of 68 acoustical (A), 86 visual (V) sensitive units and 36 bimodal units, predominantly encountered within the torus semicircularis, have been examined with respect to their response characteristics.
  • 2.2. Bimodal units are located more rostrally than A units, but no topographic preference has been found for the V units. The response signs of the three modality types (excitatory, inhibitory for the A modality; On, Off for the V modality) also show no topographic organization.
  • 3.3. The spontaneous spike rate of the V type is smaller than that of the A and bimodal type. Many bimodal cells showed spontaneous activity (76%). Non-spontaneous units are more numerous in the rostral torus.
  • 4.4. The frequency sensitivity of the A units can be divided into H (high frequency) and B (broadband) units.
  • 5.5. B units, which frequently show a more complex excitatory-inhibitory behaviour are located in the middle and caudal part, whereas the H units are mainly found in the rostral part of the torus.
  • 6.6. Phase-locking is restricted to spontaneous, monomodal B units.
  • 7.7. Clusters of neurons can be found in the torus, which contain either A or V units. In the dorso-ventral direction the A clusters are about half the size of the V clusters.
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9.
  • 1.1. Translocation of cytosol activity in phorbol-primed neutrophils was studied.
  • 2.2. Prior exposure of PMA or FMLP could potentiate the oxidative response by subsequent heterogeneous stimulus, FMLP or PMA.
  • 3.3. In FMLP-primed neutrophils, the cytosol had almost the same activity as resting one and cytosol activity was not eluted from the membrane.
  • 4.4. In PMA-primed neutrophils, however, the cytosol had less activity and cytosol activity was correspondingly eluted from the membrane.
  • 5.5. These observations suggested that cytosol activity was translocated in PMA-primed cells.
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10.
  • 1.1. The intestinal nerve of the fowl was studied in vitro.
  • 2.2. A significantly larger amplitude spike discharge was recorded in side branches of the nerve which innervate the gut when the aboral end of the main nerve trunk was stimulated than when the oral end was stimulated.
  • 3.3. Postganglionic autonomic neurones innervating the smooth muscle of the ileum are not located in the intestinal nerve. Evidence is presented, however, supporting the idea that such neurones innervating the rectum are located in the rectal position of the nerve.
  • 4.4. The increase in intraluminal pressure and circular muscle tension in the ileum was greater following aboral nerve stimulation than following oral nerve stimulation.
  • 5.5. It is suggested that excitatory efferent nerve fibres ascend the intestinal nerve to innervate the ileum.
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11.
  1. The significance of particular acoustic properties of advertisement calls for selective phonotaxis by the gray treefrog, Hyla versicolor (= HV), was studied behaviorally and neurophysiologically. Most stimuli were played back at 85 dB SPL, a level typically measured at 1–2 m from a calling male.
  2. Females preferred stimuli with conspecific pulse shapes at 20° and 24°C, but not at 16°C. Tests with normal and time-reversed pulses indicated the preferences were not influenced by the minor differences in the long-term spectra of pulses of different shape.
  3. Pulse shape and rate had synergistic or antagonistic effects on female preferences depending on whether the values of one or both of these properties in alternative stimuli were typical of those in HV or heterospecific (H. chrysoscelis = HC) calls.
  4. More auditory neurons in the torus semicircularis were temporally selective to synthetic calls (90%) than to sinusoidally AM tones and noise (< 70%).
  5. Band-pass neurons were tuned to AM rates of 15–60 Hz. Neurons were more likely to be tuned to HV AM rates ( < 40 Hz) when stimuli had pulses with HV rather than HC shapes.
  6. Sharp temporal tuning was uncommon and found only in neurons with band-pass or low-pass characteristics.
  7. Many neurons differed significantly in response to HV and HC stimulus sets. Maximum spike rate was more often elicited by an HV stimulus (74%) than by an HC stimulus (24%).
  8. Differences in spike rates elicited by HV and HC stimuli were attributable to combinations of differences in the rise times and shapes of the pulses.
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12.
  • 1.1. The afferent response recorded from single fibres innervating canal neuromasts on the head of the ruff shows phase shifts of 180°, depending on stimulus location.
  • 2.2. Based on these recordings it is shown, that in the flow field of a nearby moving object, the cupulae of adjacent neuromasts can be deflected in opposite directions.
  • 3.3. This information may, in addition to other cues, enable localization of the stimulus source.
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13.
  • 1.1. The medial (MGF), lateral (LGF) and motor (RMS-2) giant neurons were confirmed as neural components in the earthworm Amynthas hawayanus polysynaptic reflex circuit by simultaneous potential recording and dye injection.
  • 2.2. The reflex was initiated from the mechanoreceptors when evoked by mechanical stimulation but electrical stimulation also evoked an antidromic response in the motoneuron.
  • 3.3. The primary reflex response propagates decrementally along both giant axons but directly evoked action potentials conduct in an all-or-none fashion.
  • 4.4. The secondary reflex response continues to propagate after the primary response disappears.
  • 5.5. A rhythmically discharging neuron of uncertain function was also identified.
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14.
  • 1.1. Optical pooling is common in crustacean vision, both pooling in the single ommatidium and pooling inputs from many ommatidia by overlapping visual fields.
  • 2.2. Optical and neural pooling work together subdividing the eye into different surface regions with different tasks.
  • 3.3. Small-fiber and large-fiber systems with corresponding small and large dendritic branching provide a parallel processing system.
  • 4.4. Several parallel, integrating channels process that visual information which is needed for high-speed reactions.
  • 5.5. Visual fibers receive contributions from other modality inputs like vibration, olfaction or attention neurons. Inputs from mechanoreceptors transmitted over integrating fibers seem to join the signals in the intergrating visual fibers.
  • 6.6. The signal for a particular channel is expressed by the pattern of spikes (rather than changes in the mean frequency of spikes) which is modulated by any input variation.
  • 7.7. A particular discharge pattern may then be recognized by a command neuron or a muscle ensemble.
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15.
In freely moving toads, the temporal discharge patterns of tectal and medullary neurons were observed during prey-catching.
  1. Tectal T5.2 and T8.1 neurons displayed a premotor warming up firing that in the former was addressed specifically to prey orienting or snapping and in the latter generally to almost any kind of body movement.
  2. The temporal discharge patterns of T5.2 neurons during snapping were different from those during orienting toward prey. Snapping started in the peak phase of warming up; firing was immediately terminated during the snap; thereafter some rebound activity was observed. Orienting started after the premotor warming up in the declining phase whilst the neuron kept on firing during orienting and then settled when the orienting movement was completed.
  3. In toads which were not motivated to catch prey — comparabl to immobilized ones — the discharge frequency of T5.2 neurons toward a prey stimulus revealed no such warming up.
  4. Because it is known that prey-selective T5.2 neurons are controlled by pretectal inhibitory influences, the following experiment was conducted: during recording a T5.2 neuron a pretectal lesion was applied ipsilaterally to the recording site. After a few seconds, the neuron showed a strong premotor wanning up in response to any kind of moving object, followed by prey-catching.
  5. In the medulla oblongata, different H-type neurons of the hypoglossal nucleus displayed specific discharge patterns which resembled the tongue protractor and retractor muscle activities; a third type resembled the activity of the genio/sterno-hyoid muscle, which are suggested to stabilize the hyoid bone during snapping.
  6. There were medullary M8-type neurons with properties similar to T8.1.
  7. Snapping could be triggered by electrical stimulation of the optic tectum in the representation of the frontal visual field, but not by stimulation in the hypoglossal nucleus or the adjacent medial reticular formation.
  8. A concept of a neuronal circuit for the coordination of tongue muscle contractions in response to prey is proposed.
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16.
  • 1.1. Transduction and transmission in catfish ampullary electroreceptors is mediated by sensory cells bearing microvilli, chemically mediating synapses, nerve terminals and one axon. Although some aspects still remain to be clarified, a number of properties have been found.
  • 2.2. Spike generation per seand the modulation of spike frequency by electrical stimuli behave differently with respect to a number of experimental factors.
  • 3.3. Stimulus current enters presumably through non-voltage-sensitive or non-specific ion channels.
  • 4.4. Fluctuations of the spike frequency may be used as a measure for proper functioning of this sense organ.
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17.
  • 1.1.|Switching neurons, in the past referred to as a special scrotal afferent system, intergrate information not only from the scrotum, but from various body areas.
  • 2.2.|They are present in male and female rats, as well as in guinea-pigs.
  • 3.3.|They are present in midbrain, thalamus, hypothalamus and cortical areas.
  • 4.4.|Information processing from the scrotum, is not a special system, but part of the general thermo-and noci-afferent system.
  • 5.5.|Switching neurons seem to interact with behavioral, perhaps with autonomic thermoregulatory mechanisms, too.
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18.
  • 1.1. The axonal pathways of thirteen giant neurons identified in the right parietal and the visceral ganglia, found in the suboesophageal ganglia of an African giant snail (Achatina fulica Férussac), were investigated by intracellular injections of Lucifer Yellow, with regard to their axonal projections into the following six peripheral nerves: lap n (left anterior palliai nerve), lpp n (left posterior palliai nerve), int n (intestinal nerve), anal n (anal nerve), rpp n (right posterior palliai nerve) and rap n (right anterior palliai nerve).
  • 2.2. These projections were confirmed by the recording of the axonal responses from the nerves.
  • 3.3. On the dorsal surface of the right parietal ganglion, the following four giant neurons were identified: PON (periodically oscillating neuron), TAN (tonically autoactive neuron), RAPN (right anterior palliai neuron), and d-RPLN (dorsal-right parietal large neuron).
  • 4.4. The PON axonal pathways projected into int n; those of TAN into all of the nerves examined; those of RAPN into lap n, lpp n, int n, anal n and rap n.; and those of d-RPLN into pd nn (pedal nerves) through the pedal ganglia, lpp n, anal n, rap n and sometimes lap n.
  • 5.5. On the dorsal surface of the visceral ganglion, the following four giant neurons were also identified: VIN (visceral intermittently firing neuron), FAN (frequently autoactive neuron), INN (intestinal nerve neuron) and d-VLN (dorsal-visceral large neuron).
  • 6.6. The VIN axonal pathways, which had no branch into the six nerves examined, went to both the right and the left pedal ganglia, sending a branch into the cerebro-pleural connective; those of FAN projected into lap n, anal n and rap n, and sometimes into lpp n and rpp n; those of INN into int n; and those of d-VLN into pd nn, lap n, lpp n, anal n and rap n.
  • 7.7. On the ventral surface of the right parietal ganglion, v-RPLN (ventral-right parietal large neuron) was identified. The axonal pathways went to pd nn, lap n, lpp n, anal n and rap n.
  • 8.8. On the ventral surface of the visceral ganglion, the four giant neurons, v-VNAN (ventral-visceral noisy autoactive neuron), v-VLN (ventral-visceral large neuron), r-VMN (right-visceral multiple spike neuron) and 1-VMN (left-visceral multiple spike neuron) were identified.
  • 9.9. The axonal pathway of v-VNAN projected into rpp n and rap n; those of v-VLN into pd nn, lap n, anal n, rap n and sometimes to lpp n; those of r-VMN into int n and rpp n; and those of 1-VMN also into int n and rpp n.
  • 10.10. The present morphologial investigations of the giant neurons confirmed well the identifications of the neurons previously studied. The axon of the neurons examined here, except for VIN, projected into some of the peripheral nerves, while the VIN axon extended into the cerebro-pleural connective.
  • 11.11. The five neurons, PON, TAN, v-VNAN, r-VMN and 1-VMN, formed fine axonal arborizations terminating at the neuropile, while the arborizations of the other neurons were not clearly observed.
  • 12.12. Although the anatomical structures of the portion examined of the suboesophageal ganglia are asymmetrical, three pairs of symmetrically-situated neurons, d-RPLN and d-VLN, v-RPLN and v-VLN, and r-VMN and 1-VMN, were found, indicating the existence of symmetrical components in the ganglia.
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19.
  • 1.1. Synaptic short-term depression could be transferred into long term depression by repetition of series of stimuli.
  • 2.2. The transition from short-term depression to long-term depression was blocked by puromycin.
  • 3.3. The majority of the transition took place during resting periods between stimulus series.
  • 4.4. The initiation of the transition process was 83% completed after 5 min of stimulation.
  • 5.5. Short- and long-term depression were quantitatively separated into their two serial sites of origin: afferent axons and synaptic terminals.
  • 6.6. Long sequences evoked periods with increased and variable EPSPs not conforming to depression.
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20.
  • 1.1. The tissue specific patterns and ontogeny of lactate dehydrogenase (LDH) are reported.
  • 2.2. While all tissues (eye, brain, heart, intestine, liver, ovary and skeletal muscle) show isozymes of A and B subunit composition, only liver extracts possess isozymes resulting from C subunit synthesis.
  • 3.3. The A4 homopolymer appears simultaneously with initial muscle contractility and is correlated with the physiological function of muscular contraction.
  • 4.4. The activation of the Ldh-C locus is correlated with the first functioning of liver. It is suggested that the state of differentiation of liver cells may be the stimulus required for C locus expression.
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