Neuronal responses are differentially affected by the polarity of tectal DC stimulation in the toad Bufo bufo

Male toads were tested behaviourally for their prey catching responses to worm-like stimuli before being prepared for visual unit and slow potential shift (SPS) recording from the optic tectum. The neuronal responses of toads to a prey-like visual stimulus reflected their motivational tendency prior to operations. One second of DC stimulation to the tectum was followed by an SPS of reversed polarity during which time a visual prey-like stimulus was presented. A negative SPS following positive DC stimulation was associated with enhanced neuronal responses to a visual stimulus. The positive SPS that followed negative stimulation was associated with a decline in neural responses below background when a visual stimulus was additionally given. The SPS was largely a result of DC stimulation that interacted with the motivational tendency to produce enhanced neuronal responses, while the potential was negative and vice versa.     

Visual Stimuli Evoked Action Potentials Trigger Rapidly Propagating Dendritic Calcium Transients in the Frog Optic Tectum Layer 6 Neurons

The superior colliculus in mammals or the optic tectum in amphibians is a major visual information processing center responsible for generation of orientating responses such as saccades in monkeys or prey catching avoidance behavior in frogs. The conserved structure function of the superior colliculus the optic tectum across distant species such as frogs, birds monkeys permits to draw rather general conclusions after studying a single species. We chose the frog optic tectum because we are able to perform whole-cell voltage-clamp recordings fluorescence imaging of tectal neurons while they respond to a visual stimulus. In the optic tectum of amphibians most visual information is processed by pear-shaped neurons possessing long dendritic branches, which receive the majority of synapses originating from the retinal ganglion cells. Since the first step of the retinal input integration is performed on these dendrites, it is important to know whether this integration is enhanced by active dendritic properties. We demonstrate that rapid calcium transients coinciding with the visual stimulus evoked action potentials in the somatic recordings can be readily detected up to the fine branches of these dendrites. These transients were blocked by calcium channel blockers nifedipine CdCl₂ indicating that calcium entered dendrites via voltage-activated L-type calcium channels. The high speed of calcium transient propagation, >300 μm in <10 ms, is consistent with the notion that action potentials, actively propagating along dendrites, open voltage-gated L-type calcium channels causing rapid calcium concentration transients in the dendrites. We conclude that such activation by somatic action potentials of the dendritic voltage gated calcium channels in the close vicinity to the synapses formed by axons of the retinal ganglion cells may facilitate visual information processing in the principal neurons of the frog optic tectum.     

How does the toad's visual system discriminate different worm-like stimuli?

Behavioral experiments show that toads exhibit stimulus- and locus-specific habituation. Different worm-like stimuli that toads can discriminate at a certain visual location form a dishabituation hierarchy. What is the neural mechanism which underlies these behaviors? This paper proposes that the toad discriminates visual objects based on temporal responses, and that discrimination is reflected in different average neuronal firing rates at some higher visual center, hypothetically anterior thalamus. This theory is developed through a large-scale neural simulation which includes retina, tectum and anterior thalamus. The neural model based on this theory predicts that retinal R2 cells play a primary role in the discrimination via tectal small pear cells (SP) and R3 cells refine the feature analysis by inhibition. The simulation demonstrates that the retinal response to the trailing edge of a stimulus is as crucial for pattern discrimination as the response to the leading edge. The new dishabituation hierarchies predicted by this model by reversing contrast and shrinking stimulus size need to be tested experimentally.     

Massed and spaced stimulus sequences in dimensional discrimination

In two experiments, pigeons' responding to a visual flicker-rate continuum was established by a maintained generalization procedure. For both experiments, variable-interval reinforcement was available for responses during stimuli from one half of the stimulus continuum while responses during other stimuli were extinguished. The first experiment compared gradients of dimensional stimulus control produced by randomly presented positive and negative stimuli with gradients produced by massed positive and negative stimuli. The second experiment alternated the order of massed stimulus sequences. In both cases, massing of stimulus sequences diminished positive dimensional contrast effects, without seriously disturbing discrimination between positive and negative stimuli. The results indicate that stimulus sequences can have an important role in the production of dimensional contrast effects.     

DC electrical stimulation of the pretectal thalamus and its effects on the feeding behavior of the toad (Bufo bufo)

The feeding motivation of the common European common toad (Bufo bufo) can be quantified by the feeding sequence of arousal-orientation-approach-fixate-snap. Previous work has found that the optic tectum is an important structure responsible for the mediation of feeding behaviors, and combined electrical and visual stimulation of the optic tectum was found to increase the animals feeding behaviors. However, the pretectal thalamus has an inhibitory influence upon the optic tectum and its lesion results in disinhibited feeding behaviors. This suggests that feeding behavior of anurans is also subject to influence from the pretectal thalamus. Previous studies involving the application of DC stimulation to brain tissue has generated slow potential shifts and these shifts have been implicated in the modulation of the neural mechanisms associated with behavior. The current study investigated the application of DC stimulation to the diencephalon surface dorsal to the lateral posterodorsal pretectal thalamic nucleus in Bufo bufo, in order to assess effects on feeding motivation. The application of DC stimulation increased the incidence of avoidance behaviors to a visual prey stimulus while reducing the prey catching behavior component of approach, suggesting that the DC current applied to the pretectum increased the inhibition upon the feeding elements of the optic tectum. This can be explained by the generation of slow potential shifts.     

Medullary reticular neurons in the Japanese toad: morphologies and excitatory inputs from the optic tectum

1. To elucidate the neural mechanisms that mediate visual responses of optic tectum (OT) to medullary and spinal motor systems, we analyzed medullary reticular neurons in paralyzed Japanese toads (Bufo japonicus). We examined their responses to electrical stimulation of OT, and stained some neurons intracellularly. Responses to stimulation of the glossopharyngeal nerve (IX) were also analyzed. 2. Extracellular single unit recording revealed excitatory responses of medullary neurons to OT and IX stimulation. Among 92 units encountered, 79 responded to OT stimuli, 10 to IX stimuli, and 3 to both. Some units responded to successive stimuli of short intervals with relatively stable lags. 3. Intracellular recording and staining experiments revealed morphologies of reticular neurons that received excitatory inputs from OT. Thirteen units were identified after complete reconstruction of somata and dendrites. Neurons in the nucleus reticularis medius received excitatory inputs from bilateral OT. They had wide dendrites in ventral, ventrolateral and lateral funiculi, and single axons descending in the ipsilateral ventral funiculus as far caudally as the cervical spinal cord. Some collaterals of these axons projected directly to the hypoglossal and spinal motor nuclei. Some neurons in other medullary nuclei (nuc. reticularis superior, pretrigeminal nucleus, nuc. reticularis inferior, and nuc. tractus spinalis nervi trigemini) also responded to the OT stimulation. 4. Activities in bilateral OT converge onto medullary reticular neurons, which may directly control medullary and spinal motor systems.     

Changes in receptive field of tectal neurons evoked by vestibular and acoustic stimulation in pigeons

Responses to visual, acoustic, and vestibular stimuli were studied in neurons of the middle and deep layers of the tectum in the pigeon. Changes in the receptive field (RF) were assessed from comparison of unit responses to isolated movement of a shaped visual stimulus with responses to movement of a stimulus during simultaneous action of a vestibular or acoustic stimulus. Changes in RF of the neuron could be observed during the action of both a vestibular and an acoustic stimulus. These changes affected the identification of the predominant direction of movement of the stimulus, the position of the maximum in the response histogram, and the duration and number of spikes in the response. The direction of change in RF of the neuron was found not necessarily to coincide with the sign of the response to the same neuron to isolated presentation of a vestibular or acoustic stimulus. It is postulated on the basis of the results and data in the literature that the tectum transforms the flow of impulses arriving from the retina depending on the nature of the information received by it from other sensory systems.     

Temporal discharge patterns of tectal and medullary neurons chronically recorded during snapping toward prey in toads Bufo bufo spinosus

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.

     

A neural model of interactions subserving prey-predator discrimination and size preference in anuran amphibia

The model described is an extension of a previous model of the optic tectum (Arbib & Lara, 1982; Lara, Arbib & Cromarty, 1982; Lara & Arbib, 1982) and takes into consideration anatomical, physiological and behavioral studies in anurans, as well as earlier modelling efforts (Ewert & Von Seelen, 1974; Didday, 1976). Computer simulations were conducted to analyze how interactions among retina, optic tectum and pretectum may give frogs and toads the ability to discriminate between prey and predator stimuli. Results from simulations have allowed us to reproduce empirical observations, to suggest new experiments, and to postulate what neural mechanisms might be involved in some phenomena related to prey-catching orienting behavior, with direction invariance of prey-predator recognition being a consequence of tectal architecture, and size preference and response latency depending on the motivational state of the animal.     

A model of the visual localization of prey by frog and toad

In this paper we demonstrate how prey localization can be acheived rapidly and accurately by coupling prey-selection and lens-accommodation processes within a feedback loop. Information derived from prey selection supplies a setpoint for accomodation. In turn, adjustment of the lens modifies the visual input and can alter the prey selection process. The natural feedback of this goal-seeking system automatically corrects for the problem of ambiguity in binocular matching.Although it is of general interest as a depth algorithm, we tie the model to the known anatomy, physiology and behavior of frogs and toads. Instead of building a global depth-map we propose that the goal of catching a prey leads a frog or toad to select a particular region of its visual world for special scrutiny. We suggest that the first step of the prey-catching sequence is to adjust the accommodative state of the lenses and thus lock the visual apparatus on to a stimulus. We identify brain regions that could provide the neural substrates necessary to support the model's various functional stages and present experiments, with a computer simulation, that compare its functioning to animal behavior.     

Experimental analysis of the prey catching behavior ofHydromantes italicus Dunn (Amphibia,Plethodontidae)

Summary 1. The Italian bolitoglossine salamanderHydromantes italicus shows a periodic cave life. In spring and in the fall it leaves the caves after which it lives under stones, in leaves and crevices. Inside the limestone caves,H. i. can be found both in the zone of dim light near the entrance and in total darkness. 2. Corresponding to these two environments there are two guidance systems of the prey catching behavior: one visual and one olfactory. 3. The visually guided prey catching behavior is determined by the stimulus parameters: velocity, size, contrast, and ambient illumination. Continuously moving objects are effective within a velocity range of 0.05 to 6 cm/s with an optimum at 1.25 cm/s (Fig. 2). Stimuli moving stepwise elicit fixation of the prey and complete approach more frequently than continuously moving stimuli. The prey size which elicits prey catching ranges from 0.5 to 10 mm² with an optimum size between 2.5–5.0 mm² (Fig. 3). The prey catching behavior is hardly impaired by a decrease in ambient illumination down to 0.03 cd/m². Beyond 0.03 cd/m², the prey catching activity decreases sharply, but there are still responses at an illumination level of 0.003 cd/m² (Fig. 4). 4.H.i. also responds to stationary non-smelling visual stimuli following stimulation by smell or movement.H.i. is able to detect prey by smell only both in total darkness and in the light (Fig. 5 A). In the light, the prey catching behavior with regard to smelling objects is inhibited by the absence of visual contrast (Fig. 5B).I would like to thank Prof. Dr. R. Altevogt, University of Münster (Germany) for his generous help and constant encouragement. Furthermore, I want to express my gratitude to Prof. Dr. D.B. Wake, University of California, Berkeley (USA), Prof. Dr. P. Mancino, University of Pisa (Italy), and Prof. Dr. J.-P. Ewert, University (GH) of Kassel (Germany) for stimulating discussions and helpful comments.     

Spatiotemporal organization of unit activity in the frog tectum and its modification by visual stimuli

Unit activity was recorded in the tectum of curarized frogs during presentation of various visual stimuli (on- and off-responses to diffuse illumination and movement of an object of recognizable shape). It was shown that different types of stimulation lead to the organization of a different distribution of unit activity in the tectum, in the form of excitatory-inhibitory neuronal mosaics; inhibitory responses, limiting and exacerbating the excitatory responses of other neurons, predominate. The differences observed in the spatiotemporal characteristics of the neuronal mosaics under the influence of different stimuli may be evidence of specificity of coding of visual impulses carrying different information from the retina in the tectum.     

Vision and electroreception: Integration of sensory information in the optic tectum of the weakly electric fishApteronotus albifrons

Summary The responses of single neurons to visual and electrosensory stimulation were studied in the optic tectum of the weakly electric fishApteronotus albifrons. Most of the cells recorded in the region of the tectum studied, the anterior medial quadrant, were poorly responsive or completely insensitive to flashes of light or to bursts of AC electrical stimuli applied to the entire fish. However, these cells gave vigorous responses to moving visual or electrosensory stimuli. Most cells showed differences in their response contingent upon the direction of the stimulus movement and most received input from both the visual and electrosensory systems. Electrosensory responses to moving stimuli were depressed by jamming stimuli, 4 Hz amplitude modulation of the animal's electric organ discharge, presented simultaneously with the moving stimulus. However, the jamming signal presented alone typically evoked no response. Moving visual stimuli, presented simultaneously with the electrosensory, were usually able to restore the magnitude of a response toward its value in the unjammed situation. For most of the cells studied the receptive fields for vision and electroreception were in register. In some cases the visual and electrosensory components could be separated by presenting the two types of stimuli separately, or by presenting both simultaneously but with some amount of spatial separation, which causes the two to be misaligned relative to the fish. In other cases the individual responses could not be separated by spatial manipulations of the two stimuli and in these cases differences in the alignment of the two types of stimuli could cause changes in the intensity of the cells' responses.Abbreviations AM amplitude modulation - EOD electric organ discharge - PLLL posterior lateral line lobe     

Behavior and Approximate Entropy of Right-eye Lateralization During Predation in the Music Frog

Brain asymmetry for processing visual information is widespread in animals. However, it is still unknown how the complexity of the underlying neural network activities represents this asymmetrical pattern in the brain. In the present study, we investigated this complexity using the approximate entropy(ApEn)protocol for electroencephalogram(EEG) recordings from the forebrain and midbrain while the music frogs(Nidirana daunchina) attacked prey stimulus. The results showed that(1) more significant prey responses were evoked by the prey stimulus presented in the right visual field than that in the left visual field,consistent with the idea that right-eye preferences for predatory behaviors exist in animals including anurans;(2) in general, the ApEn value of the left hemisphere(especially the left mesencephalon) was greatest under various stimulus conditions, suggesting that visual lateralization could be reflected by the dynamics of underlying neural network activities and that the stable left-hemisphere dominance of EEG ApEn may play an important role in maintaining this brain asymmetry.     

Visual Sensation of an Ethological Stimulus, the Agonistic Display of Betta splendens, Revealed using Multi-Unit Recordings from Optic Tectum

We made multi-unit recordings from the optic tectum of Betta splendens while they viewed the agonistic display of conspecifics. Movement of displaying animals evoked brisk, arrhythmic bursting in tectal units. Particularly high frequency spike bursts coincided with the onset of full display, a behavioral element known to be of ethological significance. These results show that it is possible to obtain informative electrophysiological recordings from optic tectum using behaving conspecifics as stimuli. More frequent use of natural stimuli can be expected to contribute to a greater understanding of the link between the neural substrates of vision and visually guided behavior.     

Signaling without the risk of illegitimate receivers: do predators respond to the acoustic signals of <Emphasis Type="Italic">Cyprinella</Emphasis> (Cyprinidae)?

Acoustic and visual signals are commonly used by fishes for communication. A significant drawback to both types of signals is that both sounds and visual stimuli are easily detected by illegitimate receivers, such as predators. Although predator attraction to visual stimuli has been well-studied in other animals, predator response to acoustic stimuli has received virtually no research attention among fishes and snakes. This study assessed whether the calls of male tricolor shiner (Cyprinella trichroistia) made during the breeding season would attract potential predators. We also examined the effect of visual stimulus of tricolor shiners on predators. Predators used were red eye bass (Micropterus coosae) and midland water snakes (Nerodia sipedon pleuralis). Neither predator was attracted to tricolor sounds when presented alone. Micropterus coosae responded significantly more to a visual stimulus, and to a combination of visual and acoustic stimuli, but with no greater intensity in the latter. Nerodia sipedon pleuralis did not responded to visual stimulus presented alone, but did respond to visual and acoustic stimuli presented simultaneously, and with greater intensity to the latter, indicating that acoustic signals may play a role in prey detection by N. sipedon pleuralis.     

On the problem of cooperation of the reactions of hands: III. Cooperation of hand reactions to auditory and visual stimuli in patients with focal lesions of the brainstem and diencephalon

The response time (simple mental reaction time) cooperation was estimated in 53 patients with focal lesions of the brainstem and diencephalon (thalamus). The cooperation between the left-and right-hand simple mental reactions to auditory and visual stimuli presented after a warning stimulus was analyzed to determine the morphological structures responsible for the cooperation of responses. The cooperation of the simple mental reaction remained normal in some of the subjects and was disturbed in others. In the latter case, the correlation coefficient between the left-and right-hand simple mental reactions to an auditory or visual stimulus or both stimuli simultaneously was changed. The disturbances were detected in patients with lesions of the tectum at the boundary between the medulla and the pons and in those with affected lateral regions of the thalamus.     

A shift in prey color preference in the green toad Bufo viridis Laur. after food satiation]

In the behavioural experiments when showing simultaneously coloured stimuli (food targets) and also in choosing between two stimuli, red and blue, it had been shown with a high level of reliability that the hungry Bufo viridis which had not been fed for at least a week, in the overwhelming majority of cases chose the red-coloured food targets. Within 1-3 days after an abundant feeding, in the same animals the changes occurred in their preferences of the prey colour. The percentage of choosing the blue targets by the satiated toads significantly increases. In a separate series of experiments had been demonstrated that the changing motivation is conditioned by colour, since hungry and satiated Bufo viridis under conditions of simultaneous demonstration of four stimuli, black and three different grey stimuli, chose exclusively the black stimulus.     

Properties of neurons of the tectal portion of the visual system of the axolotl Ambystoma mexicanum]

In the tectum opticum of the adult neotenic A. mexicanum, responses of single neuronal units to diffuse illumination and moving visual stimuli have been investigated. Of 111 unites investigated, 27 are presented by tectal neurons, their maximum distribution being observed at a depth of 500-600 mu. In superficial layers 9 ipsi-elements were found; their receptive fields are located in the antero-dorsal part of the visual field, at both sides of the body axis. Among the units identified as the terminals of visual fibers, 70% have receptive fields of 5-10 degrees, being localized in general more close to the surface as compared to the units with the receptive field diameter of 40 and more degrees (11%). Visual neurons and ganglionic retinal cells with axons terminating in the tectum, exhibit poor specificity to the size of a stimulus within 5-30 degrees and do not react to stimuli of 2 degrees.     

Functional aspects of evoked alpha and theta responses in humans and cats

A systems theoretical approach was used to compare possible functional roles of theta (4--7 Hz) and alpha (8--15 Hz) response components of brain evoked potentials. These response components were described earlier by Ba\c sar (1980). We recorded EEG and evoked potentials (EPs) from occipital scalp locations in 11 subjects. We used auditory and visual stimuli as inadequate and adequate stimuli, respectively (``cross-modality' measurements). The combined EEG-EP epochs were analysed in frequency domain with fast Fourier transform and adaptive digital filters. Alpha (8--15 Hz) response components turned out to be dependent on whether the stimulus was adequate or not (median amplitude with inadequate vs. adequate stimulation: vs. ). Theta (4--7 Hz) response components were less dependent on stimulus modality (inadequate vs. adequate stimulation: vs. ). In EP recordings the occipital alpha response almost disappeared in the first 250 ms following auditory stimulation. Comparable behaviour was observed in similar experiments with recordings from the cat visual cortex (area 17) and with occipital magnetoencephalographic recordings. Taking into account the above-mentioned previous reports on intracranial recordings in primary sensory areas of the cat brain and preliminary results of magnetoencephalographic measurements, we propose the following hypothesis: alpha responses in a time window of about 250 ms after stimulation might predominantly reflect primary sensory processing whereas the theta responses in the first 250 ms after stimulation might be more involved in supra-modality -- or cross-modality -- associative-cognitive processing. Received: 25 February 1994 / Accepted in revised form: 5 August 1994