Associative connections of the cat parietal cortex

Interneuronal connections of area 7 of the cat parietal cortex with projection areas of the visual, auditory, and somatosensory cortex were analyzed by orthograde degeneration and retrograde transport of horseradish peroxidase methods. By combined investigation the cortico-cortical sources of afferentation of parietal area 7 could be precisely identified and concentration sites of neurons sending their axons into this area identified, and the morphological characteristics of these neurons could also be determined.A. A. Ukhtomskii Physiological Institute, A. A. Zhdanov Leningrad State University. Donetsk Medical Institute. Translated from Neirofiziologiya, Vol. 12, No. 1, pp. 13–17, January–February, 1980.     

Associative learning and memory in Drosophila: beyond olfactory conditioning

The associative learning abilities of the fruit fly, Drosophila melanogaster, have been demonstrated in both classical and operant conditioning paradigms. Efforts to identify the neural pathways and cellular mechanisms of learning have focused largely on olfactory classical conditioning. Results derived from various genetic and molecular manipulations provide considerable evidence that this form of associative learning depends critically on neural activity and cAMP signaling in brain neuropil structures called mushroom bodies. Three other behavioral learning paradigms in Drosophila serve as the main subject of this review. These are (1) visual and motor learning of flies tethered in a flight simulator, (2) a form of spatial learning that is independent of visual and olfactory cues, and (3) experience-dependent changes in male courtship behavior. The present evidence suggests that at least some of these modes of learning are independent of mushroom bodies. Applying targeted genetic manipulations to these behavioral paradigms should allow for a more comprehensive understanding of neural mechanisms responsible for diverse forms of associative learning and memory.     

State-dependent sensory gating in olfactory cortex

Sensory systems show behavioral state-dependent gating of information flow that largely depends on the thalamus. Here we examined whether the state-dependent gating occurs in the central olfactory pathway that lacks a thalamic relay. In urethane-anesthetized rats, neocortical EEG showed a periodical alternation between two states: a slow-wave state (SWS) characterized by large and slow waves and a fast-wave state (FWS) characterized by faster waves. Single-unit recordings from olfactory cortex neurons showed robust spike responses to adequate odorants during FWS, whereas they showed only weak responses during SWS. The state-dependent change in odorant-evoked responses was observed in a majority of olfactory cortex neurons, but in only a small percentage of olfactory bulb neurons. These findings demonstrate a powerful state-dependent gating of odor information in the olfactory cortex that works in synchrony with the gating of other sensory systems. They suggest a state-dependent switchover of signal processing modes in the olfactory cortex.     

Associative evoked responses of the frontal areas of the cortex

The associative responses (AR) of the frontal areas of the cat cerebral cortex were investigated. It is suggested that they are the result of dispersed heterochronous activation of cortical dendrites. The first, positive, component of the AR reflects postsynaptic hyperpolarization of dendrites, which is accompanied by moderate depolarization of the body of deep pyramidal cells. The latter, responding to a second afferent volley leading to a negative phase throughout the cortex, generates impulses forming a complex heterogeneous efferent volley along descending pathways. These centrifugal influences give rise to action potentials of the skeleton muscles. Repetitive rhythmic stimuli produce habituation of AR and muscle responses, which was not noted for primary responses (PR). The characteristics of AR and muscle responses reflect the main properties of the orientational reflex. It is suggested in this connection that the AR of the frontal area are an electrical expression of activation of the functional system of the orientational reflex. Unlike the PR, the AR do not reflect physical or spatial characteristics of the stimulus but display a dependence on its "novelty." Apparently the informational significance of the AR is determined primarily by the novelty of the stimulus.A. A. Ukhtomskii Physiological Institute, Leningrad State University. Translated from Neirofiziologiya, Vol. 2, No. 4, pp. 373–383, July–August, 1970.     

Calcium-binding proteins: differential expression in the rat olfactory cortex after neonatal olfactory bulbectomy

Calbindin, parvalbumin, and calretinin, members of EF-hand calcium-binding proteins, play important roles in buffering intracellular calcium ions. These proteins are localized in distinct populations of cells in the olfactory bulb (the primary sensory relay in the olfactory system) and its major synaptic target, the primary olfactory cortex (POC). In the present study, the postnatal expression of these calcium-binding proteins in layer III of POC was quantitatively examined 30 days after neonatal bulbectomy, a manipulation known to cause cell death and neurotransmitter changes. The numbers of both calbindin and parvalbumin-immunoreactive profiles showed significant increases (68% and 163%, respectively), while calretinin-immunoreactive profiles exhibited a 46% reduction. The data demonstrate that the expression of these calcium-binding proteins is regulated in part by the afferent input from the olfactory bulb. Furthermore, the resultant increase in calbindin and parvalbumin expression may provide neuroprotective support necessitated by possible alterations in intracellular calcium ions and other neurochemical factors that accompany neonatal bulb removal.     

Analysis of the Lynch-Granger model for olfactory cortex

The behavior of the Lynch-Granger model for layer-II piriform cortex is reviewed, and a simple neural model with similar properties is introduced. This model allows us to understand the observed functionality of the Lynch-Granger model intuitively, and suggests which of the many biological facts introduced into the original model are relevant to this particular behavior.     

The rules of formation of the olfactory representations found in the orbitofrontal cortex olfactory areas in primates.

Approximately 35% of neurons in the orbitofrontal cortex taste and olfactory areas with olfactory responses provide a representation of odour that depends on the taste with which the odour has been associated previously. This representation is produced by a slowly acting learning mechanism that learns associations between odour and taste. Other neurons in the orbitofrontal cortex respond to both the odour and to the mouth feel of fat. The representation of odour thus moves for at least some neurons in the orbitofrontal cortex beyond the domain of physico-chemical properties of the odours to a domain where the ingestion-related significance of the odour determines the representation provided. Olfactory neurons in the primate orbitofrontal cortex decrease their responses to a food eaten to satiety, but remain responsive to other foods, thus contributing to a mechanism for olfactory sensory-specific satiety. It has been shown in neuroimaging studies that the human orbitofrontal cortex provides a representation of the pleasantness of odour, in that the activation produced by the odour of a food eaten to satiety decreases relative to another food-related odour not eaten in the meal. In the same general area there is a representation of the pleasantness of the smell, taste and texture of a whole food, in that activation in this area decreases to a food eaten to satiety, but not to a food that has not been eaten in the meal.     

Associative fear learning enhances sparse network coding in primary sensory cortex

Several models of associative learning predict that stimulus processing changes during association formation. How associative learning reconfigures neural circuits in primary sensory cortex to "learn" associative attributes of a stimulus remains unknown. Using 2-photon in vivo calcium imaging to measure responses of networks of neurons in primary somatosensory cortex, we discovered that associative fear learning, in which whisker stimulation is paired with foot shock, enhances sparse population coding and robustness of the conditional stimulus, yet decreases total network activity. Fewer cortical neurons responded to stimulation of the trained whisker than in controls, yet their response strength was enhanced. These responses were not observed in mice exposed to a nonassociative learning procedure. Our results define how the cortical representation of a sensory stimulus is shaped by associative fear learning. These changes are proposed to enhance efficient sensory processing after associative learning.     

Calcium‐binding proteins: Differential expression in the rat olfactory cortex after neonatal olfactory bulbectomy

Calbindin, parvalbumin, and calretinin, members of EF‐hand calcium‐binding proteins, play important roles in buffering intracellular calcium ions. These proteins are localized in distinct populations of cells in the olfactory bulb (the primary sensory relay in the olfactory system) and its major synaptic target, the primary olfactory cortex (POC). In the present study, the postnatal expression of these calcium‐binding proteins in layer III of POC was quantitatively examined 30 days after neonatal bulbectomy, a manipulation known to cause cell death and neurotransmitter changes. The numbers of both calbindin and parvalbumin‐immunoreactive profiles showed significant increases (68% and 163%, respectively), while calretinin‐immunoreactive profiles exhibited a 46% reduction. The data demonstrate that the expression of these calcium‐binding proteins is regulated in part by the afferent input from the olfactory bulb. Furthermore, the resultant increase in calbindin and parvalbumin expression may provide neuroprotective support necessitated by possible alterations in intracellular calcium ions and other neurochemical factors that accompany neonatal bulb removal. © 1999 John Wiley & Sons, Inc. J Neurobiol 39: 207–217, 1999     

Respiratory modulation of olfactory neurons in the rodent brain

In this review we report data from freely breathing animals in an attempt to show how respiratory dynamics can influence bulbar and cortical activity. Relying on in vivo data as well as in vitro observations, we try to emphasize the multiple mechanisms that underlie this modulation, its multiple origins, and its possible functional role.     

Thalamic relay of somatic and visceral signals to the orbital cortex

We investigated the role of different thalamic nuclei in the relaying of afferent signals into the anterior section of the coronary gyrus and into the orbital gyrus, using the evoked-potentials method, in delicate experiments on cats under Nembutal or Nembutal-chloralose narcosis, and also in experiments on cats not anesthetized but immobilized by injection of succinyl choline. Specific projection zones of the lingual, vagus, and glosso-pharyngeal nerves have been charted in the anterior coronary gyrus. The thalamic relay for that region is the medial pole of the ventral posterior nucleus. The orbital gyrus contains associative projections of both somatic and visceral nature. The relay for signal transmission in this region is also located in the ventral posterior nucleus. Relaying takes place, however, not in the central parts of the nucleus, where projections of the corresponding receptor zones have been charted, but nearer its lower medial surface. There is also an indirect route for associative projections, passing through the medial center and the intralaminar nuclei. That route emerges into the cortex through the ventral anterior and reticular nuclei. A feature of the projections of the vagus nerve in the orbital cortex is the existence of a supplementary region that exhibits responses, lying along the sulcus rhinalis. It was found that relaying for that region takes place in the ventral medial and submedial nuclei of the thalamus.N. I. Pirogov Vinnitsa Medical Institute. Translated from Neirofiziologiya, Vol. 1, No. 1, pp. 65–72, July–August, 1969.