Ivan N. Pigarev

Neurons with radial receptive fields in monkey area V4A: evidence of a subdivision of prelunate gyrus based on neuronal response properties

In recordings from two awake, behaving macaque monkeys we found that neurons in the crown of the prelunate gyrus differed in their responsiveness to simple visual stimuli. Neurons in the posterior part of the gyrus (area V4) responded strongly to stationary or moving bars, while neurons in the anterior part (area V4A) responded only weakly to such stimuli. Most receptive fields in area V4A were elongated with long axes oriented radially towards the fovea. These neurons were sensitive to radial movements, especially to sudden shifts of real 3D objects. The border between areas V4 and V4A coincided with the representation of the horizontal meridian. Area V4A extended into the posterior bank of the superior temporal sulcus, where its border corresponded to the representation of the vertical meridian. The sequence of the representations of the horizontal and vertical meridians over the prelunate gyrus suggests the existence of another area between V4A and V4t.

Visually triggered K-complexes: a study in New Zealand rabbits

K-complexes are the EEG elements recorded during the state of developing sleep and during slow wave sleep. They are the only EEG components which can be elicited by sensory stimulation during sleep. The peculiarity of New Zealand rabbits to sleep with their eyes open allows the use of visual stimuli to elicit K-complexes. Experiments were performed with three rabbits. For visual stimulation, an elongated screen illuminated by LED flashes was attached to an implant on the animal’s skull. The screen covered 20–120° of the visual field of one eye, and moved with the head during animal motion. One-millisecond flashes (15-s interval) were used during daytime in an illuminated room. Flashes elicited evoked responses, which, during the first stages of sleep, were often accompanied by K-complexes. The induced K-complexes were recorded from electrodes located both above visual and somatosensory areas. Evoked responses to visual stimuli were also recorded from both pairs of electrodes, although they were generated exclusively in the visual cortex. Correlation analysis showed that visual evoked responses and K-complexes induced by this stimulation were generated in visual cortex, and passively spread to the electrodes above the somatosensory area. Investigation of the latencies of induced K-complexes revealed two time windows when these complexes could be seen. Within each window there was no correlation between latency and amplitude of K-complexes. There was also no correlation between amplitudes of the visual evoked responses and K-complexes elicited by these responses. We propose that visual stimulation in light sleep temporarily opens a gate for some independent external signals, which evoke activation of the visual cortex, reflected in K-complexes.

Cortical visual areas process intestinal information during slow‐wave sleep

Background  Previously we have shown that, during sleep, electrical and magnetic stimulation of areas of the stomach and small intestine evoked neuronal and EEG responses in various cortical areas. In this study we wanted to correlate natural myoelectrical activity of the duodenum with cortical neuronal activity, and to investigate whether there is a causal link between them during periods of slow‐wave sleep.

Partial sleep in the context of augmentation of brain function.

Inability to solve complex problems or errors in decision making is often attributed to poor brain processing, and raises the issue of brain augmentation. Investigation of neuronal activity in the cerebral cortex in the sleep-wake cycle offers insights into the mechanisms underlying the reduction in mental abilities for complex problem solving. Some cortical areas may transit into a sleep state while an organism is still awake. Such local sleep would reduce behavioral ability in the tasks for which the sleeping areas are crucial. The studies of this phenomenon have indicated that local sleep develops in high order cortical areas. This is why complex problem solving is mostly affected by local sleep, and prevention of local sleep might be a potential way of augmentation of brain function. For this approach to brain augmentation not to entail negative consequences for the organism, it is necessary to understand the functional role of sleep. Our studies have given an unexpected answer to this question. It was shown that cortical areas that process signals from extero- and proprioreceptors during wakefulness, switch to the processing of interoceptive information during sleep. It became clear that during sleep all “computational power” of the brain is directed to the restoration of the vital functions of internal organs. These results explain the logic behind the initiation of total and local sleep. Indeed, a mismatch between the current parameters of any visceral system and the genetically determined normal range would provide the feeling of tiredness, or sleep pressure. If an environmental situation allows falling asleep, the organism would transit to a normal total sleep in all cortical areas. However, if it is impossible to go to sleep immediately, partial sleep may develop in some cortical areas in the still behaviorally awake organism. This local sleep may reduce both the “intellectual power” and the restorative function of sleep for visceral organs.

The state of sleep and the current brain paradigm.

Up to the present time cerebral cortex was considered as substrate for realization of the highest psychical functions including consciousness. Cortical sensory areas were regarded as structures specialized for processing of information coming from one particular modality (visual, auditory, somatosensory, and so on). However, studies of cortical activity in sleep-wake cycle demonstrated that during sleep the same neurons in the same cortical areas switch to processing of signals coming from the various visceral systems. After awakening these visceral responses disappear and the neurons return to processing of the information coming from the exteroreceptors. These observations indicate that most likely cortical areas are universal processors, which perform particular operations with incoming information independent of its origin. During wakefulness, results of the information processing on the cortical level should be directed to structures connected with organization of behavior and consciousness, while during sleep cortical outputs should be redirected to structures performing integration of the visceral information. Thus, results of sleep studies indicate that current brain paradigm should be changed.

Whether radial receptive field organization of the fourth extrastriate crescent (area V4A) gives special advantage for analysis of the optic flow. Comparison with the first crescent (area V2)

Recently, elongated comet-shaped receptive fields were discovered in the fourth extrastriate crescent (area V4A) of cats and monkeys. It was shown that the long axes of these receptive fields were oriented radially toward the centre of the retina. Such unusual “radial” organization of this extrastriate area led to the assumption that these neurons may contribute to the analysis of optic flow. To investigate this assumption we recorded activity of neurons in the V4A of cats during real motion in depth toward or away from a stationary visual scene. Responses of neurons in area V4A were compared with activity of neurons in area V2 under similar conditions of stimulation. Area V2 is known to be sensitive to motion but does not have radial organization. It was found that a substantial number of visual neurons in both areas did not fire at all when cats were exposed to motion in depth. Nevertheless, neurons with selective activation to direction of motion in depth were identified, but comparable numbers were found in both areas studied. We conclude that radial organization of the fourth extrastriate crescent does not provide any special advantage for the analysis of optic flow information.

Association of sleep impairments and gastrointestinal disorders in the context of the visceral theory of sleep

It was noticed long ago that sleep disorders or interruptions to the normal sleep pattern were associated with various gastrointestinal disorders. We review the studies which established the causal link between these disorders and sleep impairment. However, the mechanism of interactions between the quality of sleep and gastrointestinal pathophysiology remained unclear. Recently, the visceral theory of sleep was formulated. This theory proposes that the same brain structures, and particularly the same cortical sensory areas, which in wakefulness are involved in processing of the exteroceptive information, switch during sleep to the processing of information coming from various visceral systems. We review the studies which demonstrated that neurons of the various cortical areas (occipital, parietal, frontal) during sleep began to fire in response to activation coming from the stomach and small intestine. These data demonstrate that, during sleep, the computational power of the central nervous system, including all cortical areas, is engaged in restoration of visceral systems. Thus, the general mechanism of the interaction between quality of sleep and health became clear.

Absolute Depth Sensitivity in Cat Primary Visual Cortex under Natural Viewing Conditions

Mechanisms of 3D perception, investigated in many laboratories, have defined depth either relative to the fixation plane or to other objects in the visual scene. It is obvious that for efficient perception of the 3D world, additional mechanisms of depth constancy could operate in the visual system to provide information about absolute distance. Neurons with properties reflecting some features of depth constancy have been described in the parietal and extrastriate occipital cortical areas. It has also been shown that, for some neurons in the visual area V1, responses to stimuli of constant angular size differ at close and remote distances. The present study was designed to investigate whether, in natural free gaze viewing conditions, neurons tuned to absolute depths can be found in the primary visual cortex (area V1). Single-unit extracellular activity was recorded from the visual cortex of waking cats sitting on a trolley in front of a large screen. The trolley was slowly approaching the visual scene, which consisted of stationary sinusoidal gratings of optimal orientation rear-projected over the whole surface of the screen. Each neuron was tested with two gratings, with spatial frequency of one grating being twice as high as that of the other. Assuming that a cell is tuned to a spatial frequency, its maximum response to the grating with a spatial frequency twice as high should be shifted to a distance half way closer to the screen in order to attain the same size of retinal projection. For hypothetical neurons selective to absolute depth, location of the maximum response should remain at the same distance irrespective of the type of stimulus. It was found that about 20% of neurons in our experimental paradigm demonstrated sensitivity to particular distances independently of the spatial frequencies of the gratings. We interpret these findings as an indication of the use of absolute depth information in the primary visual cortex.