Central representation of the anterior lateral line nerve in dwarf catfish]

The central distribution of the anterior lateral line nerve (ramus) (NLLa) were studied in the pygmean sheat-fish (Ictalurus nebulosus) by means of the method of Nauta--Gygax. NLLa, as well as posterior lateral line nerve (NLLp), projects topographically on the nucleus medialis of the acoustic-lateral area. Within the nucleus medialis NLLa can be traces in the rostro-lateral parts. A majority of NLLa fibres can be followed ipsilaterally, although a definite contralateral contribution also exists. It is concluded that NLLa, representing the electro- and mechanoreceptors of the head region, distributes predominantly within the rostral part of the medial nucleus, while NLLp, representing the trunk receptors, distributes in the caudal half of the medial nucleus. There is some overlapping within the middle part of the nucleus.     

Connections of the corticospinal and rubrospinal tracts with neurons of the cervical spinal cord in cats

The distribution of focal potentials over the cross section of the 7th cervical segment of the spinal cord was studied during stimulation of the pyramids, the red nucleus, and a peripheral nerve (ulnar) in adult cats anesthetized with chloralose and Nembutal. The earliest focal potentials in the fasciculus dorsolateralis were recorded 1.4–1.5 msec after stimulation of the pyramids and 0.8–0.9 msec after stimulation of the red nucleus. These times correspond to maximal condution velocities of 56–68 and 105–124 m/sec respectively. The earliest post-synaptic activity in response to pyramidal stimulation was found in the lateral areas of laminae V and VI, and in response to stimulation of the red nucleus in laminae VI and VII in Rexed's classification. The pyramidal wave also evoked considerable postsynaptic activity in medial areas of the dorsal horn. In response to stimulation of peripheral afferents activity was evoked in neurons in the central and medial parts of laminae V and VI. It is postulated on the basis of these results that corticospinal and rubrospinal fibers may be connected monosynaptically with specialized interneurons, free from peripheral influences, in the lateral areas of laminae V and VII respectively; in the lateral part of lamina VI convergence of both types of influences on the same cells is possible. Interaction between descending and afferent influences possibly takes place on more medially located neurons.A.A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 4, No. 2, pp. 158–167, March–April, 1972.     

The neurohypophysis of the crested newt

Summary In the median eminence of the newt a medial region and two lateral regions are described.In cross section, the medial region appears to be made up of 1) an outer or glandular zone (Zone I) containing aldehyde-thionine-positive and negative nerve fibres and blood capillaries. Nerve fibres appear aligned in palisade array along the capillaries. 2) An inner zone (Zone II) made up of a) a layer of aldehyde-thionine-positive nerve fibres (fibrous layer) belonging to the preoptic hypophyseal tract and b) a layer of ependymal cells lining the infundibular lumen and reaching the blood vessels with their long processes.The lateral regions display a less pronounced stratification and aldehyde-thionine positive nerve fibres are nearly absent.A slender lamina (ependymal border) containing mainly aldehyde-thionine-positive nerve fibres and ependymal cells connects the median eminence to the pars nervosa.At the ultrastructural level, in the outer zone of the medial region at least 4 types of nerve fibres and nerve endings are identified:Type I nerve fibres containing granular vesicles of 700–1000 Å and clear vesicles (250–400 Å).Type II nerve fibres containing granular vesicles and polymorphous granules of 900–1300 Å and clear vesicles (250–400 Å).Type III nerve fibres containing dense granules of 1200–2000 Å and clear vesicles of 250–400 Å.Type IV nerve fibres containing only clear vesicles of 250–400 Å. In the inner zone too, all these nerve fiber types are found among ependymal cells, while the fibrous layer consists of nerve fibres containing granules of 1200–2000 Å in diameter.In the lateral regions Type I, Type II and Type IV nerve fibres and their respective perivascular terminals are found; axons containing dense granules (1200–2000 Å) are scanty. In these regions typical synapses between Type I nerve fibres and processes rich in microtubules are visible.The classification and functional significance of nerve fibres in the median eminence are still unsolved, but it may be assumed that nerve fibres of the medial region belong to both the preoptic hypophyseal and tubero hypophyseal tract, while the lateral regions are characterized by nerve fibres of the tubero hypophyseal tract. Peculiar specializations of the ependymal cells in the median eminence of the newt are also discussed.Work supported by a grant from the Consiglio Nazionale delle Ricerche.The authors are indebted to Mr. G. Gendusa and P. Balbi for technical assistance.     

Electrophysiological investigation of cortico-hypothalamic relations in cats

Projections of different parts of the orbito-frontal cortex, the basal temporal cortex, and the hippocampus on hypothalamic nuclei were studied by recording focal responses in acute experiments on cats anesthetized with pentobarbital and chloralose. The proreal gyrus was shown to have local projections in the latero-dorsal zones of the preoptic region, in the rostral parts of the medial forebrain bundle, and also in the region of the lateral and posterior hypothalamus with the mammillary bodies. The orbital gyrus projects mainly to the latero-dorsal portions of the forebrain bundle, the latero-ventral part of the preoptic region, and the region of the lateral and latero-dorsal hypothalamic nuclei; projections from the orbital gyrus are relatively diffuse in character. The basal temporal cortex has diffuse projections in the central part of the preoptic region, in the latero-ventral parts of the medial forebrain bundle, and in the lateral mammillary body. No marked foci of activity were found in the hypothalamic structures during hippocampal stimulation. Diffuse projections of the hippocampus were traced in the ventral part of the preoptic region and the ventral regions of the medial forebrain bundle, and also in the lateral hypothalamus and in the lateral mammillary nucleus.A. M. Gor'kii Donetsk Medical Institute. Translated from Neirofiziologiya, Vol. 8, No. 4, pp. 358–365, July–August, 1976.     

Spatial organization of direct connections of the sensomotor cortex with the rhombencephalon and spinal cord in the cat

The distribution and ultrastructure of terminals of corticofugal fibers in the rhombencephalon and spinal cord of the cat were studied by light and electron microscopy at various times (4–6 days) of experimental degeneration after extensive or local (about 3 mm in diameter) destruction of the sensomotor cortex. Definite topographical organization of corticofugal projections in the nuclei of the dorsal columns and in the spinal cord was detected by the Fink — Heimer method. After local destruction of the lateral zones of the sensomotor cortex, maximal foci of degeneration were found in the nucleus of Burdach and the lateral basilar region of the cervical segments; after local destruction of the medial zones of the sensomotor cortex maximal foci of degeneration of corticofugal fibers were observed in Goll's nucleus and the lateral basilar region of the lumbar segments. The results show that even an extremely localized area of the cat sensomotor cortex forms two separate systems of descending corticospinal fibers. The first projects into the dorsolateral and dorsomedial parts of the intermediate zone, chiefly contralaterally, whereas the second projects bilaterally into both dorsolateral and ventromedial parts of the intermediate zone. The possible physiological significance of this duality of projections is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 8, No. 2, pp. 126–133, March–April, 1976.     

Activation of various areas of the ventral horn of lumbar segments during stimulation of the motor cortex

Focal potentials (FP) in segments L₆–L₇ of the ventral horn, evoked by stimulation of the motor cortex with series of stimuli of threshold magnitude for the flexor nerve response, were studied in acute experiments on cats. Appreciable differences were found to exist between the FP arising in the medial zone (layer VIII of Rexed) and those in the inner and outer parts of the lateral zone (layer IX). The FP of the medial zone appear earlier than in other zones (with a latency of 5–12 msec); they are multiphasic, negative components predominating over the positive ones. The FP from the inner part of layer IX possess the largest amplitude (up to 500 µV), a latency of 7–13 msec, a large first negative phase, and marked late positivity. Positive — negative FP (latency 9–15 msec) of small amplitude are recorded from the outermost portion of the ventral horn. The FP of the three zones mentioned above differ also with respect to other functional criteria. The FP of the medial zone are assumed to reflect the realization at the segmental level of the extrapyramidal component of descending cortical activity, the FP of both lateral zones reflecting reciprocal interrelations between postsynaptic processes in the motoneurons of flexor and extensor nuclei during implementation of a cortical motor reaction.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 3, No. 2, pp. 175–184, March–April, 1971.     

Laminar ultrastructure of the dorsal cochlear nucleus in rats

The laminar ultrastructure of the dorsal cochlear nucleus was studied in ultrathin wide frontal sections, passing through all layers of the nucleus, placed on blinds with a Formvar film. The ultrastructural characteristics of cells corresponding to the cell types distinguished previously by light microscopy are described. The laminar distribution of the axon terminals was studied. In the surface and middle layers of the neuropil, by contrast with the deep layer, large branching terminals measuring 6–8 µ with spherical synaptic vesicles 40–50 nm in diameter, small terminals measuring 1–3 µ with spherical synaptic vesicles 45–60 nm in diameter, and thin unmyelinated fibers running perpendicularly to the plane of the section were predominant. On transition from the middle to the deep layer there was a corresponding increase in the number of myelinated axons and large oval-shaped terminals measuring 4–6 µ, with central mitochondria and neurofilaments, and also with spherical synaptic vesicles 50–60 nm in diameter, in the neuropil. In the surface and middle layers granular cells also were more numerous than in the deep layer. The functional significance of terminals of each type is discussed.N. A. Semashko Moscow Medical Stomatologic Institute. Translated from Neirofiziologiya, Vol. 10, No. 4, pp. 368–374, July–August, 1978.     

The area octavo-lateralis in Xenopus laevis

Summary Central projections of afferents from the lateral line nerves and from the individual branches of the VIIIth cranial nerve in Xenopus laevis and Xenopus mülleri were studied by the application of HRP to the cut end of the nerves.Upon entering the rhombencephalon, the lateral line afferents form a longitudinal fascicle of ascending and descending branches in the ventro-lateral part of the lateral line neuropile. The fascicle exhibits a topographic organization, that is not reflected in the terminal field of the side branches. The terminal field can be subdivided into a rostral, a medial and a caudal part, each of which shows specific branching and terminal pattern of the lateral line afferents. These different patterns within the terminal field are interpreted as the reflection of functional subdivisions of the lateral line area. The study did not reveal a simple topographic relationship between peripheral neuromasts and their central projections.Two nuclei of the alar plate with significant lateral line input were delineated: the lateral line nucleus (LLN) and the medial part of the anterior nucleus (AN). An additional cell group, the intermediate nucleus (IN), is a zone of lateral line and eighth nerve overlap, although such zones also exist within the ventral part of the LLN and the dorsal part of the caudal nucleus (CN). Six nuclei which receive significant VIIIth nerve input are recognized: the cerebellar nucleus (CbN), the lateral part of the anterior nucleus, the dorsal medullary nucleus (DMN), the lateral octavus nucleus (LON), the medial vestibular nucleus (MVN) and the caudal nucleus (CN).All inner ear organs have more than one projection field. All organs project to the dorsal part of the LON and the lateral part of the AN. Lagena, amphibian papilla and basilar papilla project to separate regions of the dorsal medullary nucleus (DMN). There is evidence for a topographic relation between the hair cells of the amphibian papilla (AP) and the central projections of AP fibers. The sacculus projects extensively to a region between the DMN and the LON. Fibers from the sacculus and the lagena project directly to the superior olive. Fibers from the utriculus and the three crista organs terminate predominantly in the medial vestibular nucleus (MVN) and in the adjacent parts of the reticular formation, and their terminal structures appear to be organotopically organised. Octavus fiber projections to the cerebellum and to the spinal cord are also described.     

Vestibular efferent neurons forming projections to the saccule in the guinea pig

A comparative analysis was made of the distribution of vestibular efferent neurons projecting to the saccule and efferent cells sending out axons to the auditory nerve ("cochlear efferent neurons") in the guinea pig, using retrograde horseradish peroxidase axonal transport techniques. Saccular efferent neurons were discovered bilaterally in the subependymal granular layer at the base of the fourth cerebral ventricle and laterally to the facial nerve genu ispsilaterally in the parvocellular reticular nucleus, as well as nuclei of the superior olivary complex: the lateral olivary nucleus and lateral nucleus of the trapezoid body. Cochlear efferent neurons are located ipsilaterally in the pontine reticular caudal nucleus, in the anteroventral cochlear nucleus, and in the lateral and medial olivary nuclei. Neurons were found contralaterally in the medial nucleus of the trapezoid body. It thus emerged that location zones of vestibular saccular efferent neurons and those of cochlear efferent units partially overlapped. The possible involvement of saccular vestibular efferent neurons in the mechanisms of auditory perception is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 22, No. 5, pp. 657–665, September–October, 1990.     

Experimental morphological study of primary afferent terminals at the base of the dorsal horn of the cat spinal cord

The distribution and ultrastructure of primary afferent terminals in the gray matter of the cervical and lumbar regions of the cat spinal cord were studied by the experimental degeneration method of Fink and Heimer. Most preterminals of primary afferents were shown to be concentrated in the region of the intermediate nucleus of Cajal (central part of Rexed's laminae VI–VII), in the substantial gelatinosa (laminae II–III), and in the nucleus proprius of the dorsal horn (central and medial parts of lamina IV). Fewer are found in the region of the motor nuclei. The number of degenerating axon terminals in the lateral parts of laminae IV and V differed: 31.5 and 0.4% respectively of all axon terminals. Many terminals of primary afferents in lamina IV contribute to the formation of glomerular structures in which they exist as terminals of S-type forming axo-axonal connections with other terminals. These results are in agreement with electrophysiological data to show that interneurons in different parts of the base of the dorsal horn differ significantly in the relative numbers of synaptic inputs formed by peripheral afferents and descending systems.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 5, No. 4, pp. 406–414, July–August, 1973.     

Neurulation in the anterior trunk region of the zebrafish Brachydanio rerio

We have studied the process of neurulation within the anterior trunk region of the zebrafish by means of serial sectioning of staged embryos and labelling cells by applications of the dye Dil and intracellular injections of fluoresceine dextran amine. The first morphological manifestation of the prospective neural plate is a dorsomedial ectodermal thickening which becomes visible immediately after gastrulation. Within 1–2 h, by the time somatogenesis begins, two bilaterally symmetrical thickenings have appeared more laterally, which eventually fuse with the medial thickening to form the neural keel. The central canal forms next by separation of the cells on either side of the midline of the neural keel, beginning ventrally at the 17-somite stage and progressing towards dorsal levels. By means of fluorescent dye labelling in the late gastrula, we found that both the medial and lateral thickenings contribute to the nerve cord. The medial thickening was found to contain, exclusively, neural progenitor cells from the 90–100% epiboly stage on, whereas the adjacent regions contained a mixture of neural and epidermal progenitor cells, as well as prospective neural crest cells. Between the 90–100% epiboly and 2-somite stages, this heterogeneity of developmental capabilities is resolved into territories, with epidermogenic and neurogenic cells clearly separated from each other. To achieve this segregation into neural and epidermal anlagen, cells from the lateral thickenings have to move over a distance of roughly 400 m within 1–2 h. Epidermal overgrowth of the nerve cord occurs during the morphogenetic movements that accompany nerve cord formation. Correspondence to: J.A. Campos-Ortega     

Correlation between morphology and function in the rat hippocampus and hypothalamus

Correlation between morphology and function in the hippocampus and hypothalamus was studied by electrophysiological and morphological techniques. Single unit responses were recorded extracellularly in the arcuate and medial preoptic nuclei of the hypothalamus to application of single stimuli to the hippocampus. Phasic responses and primary inhibition predominated in the arcuate nucleus, whereas both phasic and tonic responses were observed in the medial preoptic nucleus. In the morphological experiments horseradish peroxidase was injected into the same region of the hippocampus. Stained cells were found in the nuclei of the mammillary body, mediobasal hypothalamus, and medial preoptic nucleus. Groups of stained neurons were discovered at the periphery of the ventro- and dorsomedial and also in the lateral and mammillary nuclei of the hypothalamus. Besides fusiform and triangular neurons, reticular neurons also were found in all structures except the medial mammillary nucleus. The results are discussed from the standpoint of interaction between hypothalamus and hippocampus.A. A. Zhdanov State University, Leningrad. Translated from Neirofiziologiya, Vol. 11, No. 5, pp. 427–434, September–October, 1979.     

Axonal composition of the marginal and basal optic tracts in frogs

An electron-microscopic investigation was made of the medial and lateral branches of the marginal and basal optic tracts. The ultrastructure and composition of the branches of the marginal tract are similar. The basal tract has a relatively loose structure and contains a high proportion of myelinated fibers of large diamter. On average these structures contain 3900 (4.7%), 4700 (4.9%), and 700 (28%) of myelinated and 79,800 (95.3%), 91,500 (95.1%), and 1800 (72%) unmyelinated fibers respectively. The myelinated fibers in the branches of the marginal tract have a diameter of 0.4–2.6 (main maximum 1.0, additional maximum 1.6 µ), those in the basal tract from 0.4 to 4.0 µ (main maximum 1.8, small additional maximum at 3.2 µ). The diameters of the unmyelinated fibers in all three tracts are 0.1–0.5 µ; the diameter of 60% of these fibers is approximately 0.2 µ. Degeneration of 99% of myelinated fibers of the optic nerve and 100% of fibers of the basal tract was found 85 days after enucleation and keeping at 18–20°C. Many nondegenerated myelinated fibers were found in the medial and lateral branches of the marginal tract (33 and 13%, ranges of diameters 0.6–1.4 and 0.6–1.0 µ respectively). These fibers perhaps participate in the organization of ipsilateral visual projection of the tectum. The nonmyelinated fibers were unchanged in all the tracts.A. N. Severtsov Institute of Evolutionary Morphology and Ecology of Animals, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 8, No. 1, pp. 54–61, January–February, 1976.     

Afferent connections of the cat lateral vestibular nucleus

Location within the brain of HP-labeled neurons (origins of projections to the lateral vestibular nucleus) was investigated by iontophoretic injection of this enzyme. Bilateral projections to the following midbrain structures were revealed: the field of Forel, interstitial nuclei of Cajal, oculomotor nerve nuclei, and the red nucleus — to all parts of the lateral vestibular nucleus. Bilateral projections were also shown from more caudally located structures, viz. the superior, medial and inferior (descending) vestibular nuclei, Y groups of the vestibular nuclear complex, facial nucleus and hypoglossi, nucleus prepositus nervi hypoglossi and caudal nuclei of the trigeminal tract; ipsilateral projections from crus IIa of lobulus ansiformus of the cerebellar hemisphere; contralateral projections from the bulbar lateral reticular nucleus and Deiter's nucleus. A tonic organization pattern of afferent inputs from a number of brainstem formations to the dorsal and ventral lateral vestibular nucleus is revealed and trajectories of HP-labeled fiber systems projecting to Deiter's nucleus described.L. A. Orbeli Institute of Physiology, Academy of Sciences of the Armenian SSR, Erevan. Translated from Neirofiziologiya, Vol. 20, No. 4, pp. 494–503, July–August, 1988.     

Projections from neurons of the medial terminal nucleus of the accessory optic tract to the caudate nucleus in the cat revealed by combining techniques of retrograde axonal transport and experimentally induced degeneration

Neurons of the medial terminal nucleus of the accessory optic tract receiving direct retinal inputs were shown to project to the heat and body of the caudate nucleus in the cat using techniques of retrograde horseradish peroxidase axonal transport and experimentally induced degeneration. These primarily ipsilateral projections are evenly distributed throughout the aforementioned areas of the nucleus. Neurons of the medial terminal nucleus forming synaptic connections with caudate nucleus cells are distinguished by their varied shapes and sizes, ranging from 20 × 10 to 37.5 × 18 µm and are located in both the ventral and dorsal subdivisions of the nucleus. The supposed functional significance of these projections for the regulation of muscle tonus tension is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 18, No. 2, pp. 214–219, March–April, 1986.     

The rhombencephalic "locomotor region" in turtles

Electrical stimulation (10–20 µA, 20–30 Hz) of the rhombencephalon in decerebrate turtles can induce cyclic coordinated limb movemnts. The "locomotor region" is a strip, oriented in the rostro-caudal direction, which coincides in its location with the lateral reticular formation. Both in the medial and in the lateral reticular formation extracellular ipsilateral and contralateral synaptic responses of single neurons evoked by stimulation of the "locomotor region," (10–30 µA, 2 Hz), were recorded. Usually these responses had latent periods of between 3 and 12 msec (mode 5–6 msec). Excitation of the "locomotor region" thus leads to extensive spread of activity in the rhombencephalon. The possible mechanisms of this spread are discussed.Institute of Problems in Information Transmission, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 12, No. 4, pp. 382–390, July–August, 1980.     

Sources of thalamic afferents projecting to the suprasylvian gyrus of the black sea porpoise

Neurons sending fibers to different loci of the suprasylvian gyrus (SSG) of the porpoise(Phocaena phocaena) cortex were located in the thalamus by retrograde horseradish peroxidase transport and fluorescent tracing techniques. Horseradish peroxidase injection into the anterior section of the suprasylvian gyrus led to retrograde labelling of neurons in the lateral portion of the ventrobasal complex of nuclei and the ventroposteroinferior nucleus. A group of labelled cells was found in the ventral section of the main medial geniculate nucleus. Injecting bisbenzimide into different loci of the medial suprasylvian gyrus also led to retrograde labelling of neurons belonging to the ventral division of the main medial geniculate nucleus. Somewhat lower numbers of labelled cells were found in the inferior nucleus of the pulvinar. Small groups of labelled neurons were also found in the lateral nucleus of the pulvinar, the medioventral nucleus of the medial geniculate body, and the posterior complex of nuclei. A similar distribution of labelled cells was also observed after injecting bisbenzimide into the more caudal portion of the gyrus, although the location of labelled cells in the ventral division of the main medial geniculate nucleus and the lower pulvinar nucleus were shifted in a lateral direction.A. N. Severtsov Institute of Animal Evolutionary Moprhology and Ecology, Academy of Sciences of the USSR, Moscow. National University, Singapore. Translated from Neirofiziologiya, Vol. 21, No. 4, pp. 529–539, July–August, 1989.     

Unit responses in area 5b of the suprasylvian gyrus to stimulation of the posterior lateral thalmamic nucleus

In response to stimulation of the posterior lateral nucleus in unanesthetized cats immobilized with D-tubocurarine an evoked potential consisting of three components with a latent period of 3–5 msec appeared in area 5b of the suprasylvian gyrus. All three components were reversed at about the same depth in the cortex (1500–1600 µ). Reversal of the potential shows that it is generated in that area by neurons evidently located in deeper layers of the cortex and is not conducted to it physically from other regions. Responses of 53 spontaneously active neurons in the same area of the cortex to stimulation of the posterior lateral nucleus were investigated. A characteristic feature of these reponses was that inhibition occurred nearly all of them. In 22 neurons the responses began with inhibition, which lasted from 30 to 400 msec. In 30 neurons inhibition appeared immediately after excitation while one neuron responded by excitation alone. The latent periods of the excitatory responses varied from 3 to 28 msec. The short latent period of the evoked potentials and of some single units responses (3–6 msec) confirms morphological evidence of direct connections between the posterior lateral nucleus and area 5b of the suprasylvian gyrus. Repetitive stimulation of that nucleus led to strengthening of both excitation and inhibition. Influences of the posterior lateral nucleus were opposite to those of the specific nuclei: the posterior ventrolateral nucleus and the lateral and medial geniculate bodies. Stimulation of the nonspecific reticular nucleus, however, evoked discharges from neurons like those produced by stimulation of the posterior lateral nucleus.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 5, No. 5, pp. 502–509, September–October, 1973.     

The amygdala of the cat: A golgi study

Summary The amygdaloid complex in the cat was studied in a series of Golgi preparations. Both the lateral and the basal nucleus are composed of the same two cell types, one of which (type P) resembles the pyramidal and the other (type S) the stellate neuron of the cortex. The cortical nucleus can be divided into three layers (I, II, and III–IV) which are made up of cells similar to those in the periamygdaloid cortex. In addition, there are sufficient differences in the organization of these layers to justify a subdivision of the cortical nucleus into lateral and medial parts. The dendrites of neurons in the medial part of the central nucleus, the medial nucleus and the anterior amygdaloid area undergo less branching and carry fewer spines than those of the type P cell. The neurons in the nucleus of the lateral olfactory tract are all of the pyramidal or modified pyramidal type. These findings are discussed in relation to those of previous investigators who employed the Nissl and Golgi methods.This investigation was supported by the Medical Research Council of Canada, Grant M.T. 870. The author wishes to thank Miss Elizabeth Korzeniowski for her technical assistance.     

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.