Ascending projections of the locus coeruleus in the rat. II. Autoradiographic study.

The ascending projections of the locus coeruleus were studied using an autoradiographic method. The major projection of locus coeruleus neurons ascends in a dorsal pathway traversing the midbrain tegmentum in a position ventrolateral to the periaqueductal gray. At the caudal diencephalon the locus coeruleus axons descend to enter the medial forebrain bundle at a caudal tuberal hypothalamic level. They are jointed in the medial forebrain bundle by a much smaller locus coeruleus projection which takes a ventral course through the midbrain tegmentum and enters the medial forebrain bundle via the mammillary peduncle and ventral tegmental area. Terminal projections are evident in the midbrain to the periaqueductal gray, tegmentum and raphe nuclei. There are widespread projections to the dorsal thalamus. The heaviest of these are to the intralaminar nuclei, the anteroventral and anteromedial nuclei, the dorsal lateral geniculate and the paraventricular nucleus. In the hypothalamus the largest projections are to the lateral hypothalamic area, periventricular nucleus, supraoptic nucleus and paraventricular nucleus. As the locus coeruleus projection ascends in the medial forebrain bundle, fibers leave it to traverse the lateral hypothalamus and zona incerta and enter the internal capsule, the ventral amygdaloid bundle and ansa peduncularis. These appear to terminate in the amygdaloid complex and, via the external capsule, in the lateral and dorsal neocortex. At the level of the septum 4 projections are evident. One group of fibers enters the stria medullaris to terminate in the paraventricular nucleus and habenular nuclei. A second group joins the stria terminalis to terminate in the anygdaloid complex. The third group turns into the diagonal band and medial septum; some fibers terminate in the septal nuclei and others continue into the fornix to termimate in hippocampus. A large component continues around the corpus callosum into the cingulum to terminate in the cingulate and adjacent neocortex, the subiculum and hippocampus. The remaining fibers continue rostrally in the medial forebrain bundle to terminate in olfactory forebrain and frontal neocortex. Commissural projections arise at 4 locations. The first decussation occurs in the dorsal tegmentum just below the central gray rostral to the locus coeruleus. The crossing fibers enter the contralateral dorsal bundle. A second group of fibers leaves the ipsilateral dorsal pathway, crosses in the posterior commissure and enters the contralateral dorsal pathway at the level. The third commissural projection arises more rostrally and crosses in the dorsal supraoptic commissure to enter the contralateral medial forebrain bundle. The fourth commissural projection is through the anterior commissure. The termination of the contralateral projection appears similar to that of the ipsilateral projection.     

Gustatory pathways in the bullhead catfish. 1. Connections of the anterior ganglion.

The central projections of the external gustatory system in bullhead catfish were examined using orthograde degeneration and retrograde transport of horseradish peroxidase (HRP) techniques. Both large and small cells were observed in the anterior ganglion which contains a mixture of elements from the trigeminal, facial and anterior lateral line nerves. Some of the large cells on the lateral margin of the ganglion were found to belong to the lateral line system. No separation of trigeminal and facial nerve connections could be made. Using HRP, the relation between the barbels and specific ganglion regions was determined. The dorsalmost portion of the ganglion received recurrens nerve inputs (from taste buds on the trunk); the rostromedial portion of the ganglion, from the maxillary and mandibular barbel nerves. The facial lobe (similar to part of the n. solitarius) was found to be divided into lobules by fascicles of nerve fibers. The lateral lobule received input only from the dorsal-most part of the ganglion (recurrens nerve: trunk receptors); the intermediate lobule from the rostro-lateral part of the ganglion (nasal barbel); and the medial lobule from the ventral areas of the ganglion (maxillary and mandibular barbels). Thus a topographical relationship exists between the different taste receptor groups and their locus of representation in the facial lobe. The trunk receptors connect to the lateral lobule; the nasal barbel receptors to the intermediate lobule, and the maxillo-mandibular receptors to the medial lobule.     

Development of the diencephalon in the rat. V. Thymidine-radiographic observations on internuclear and intranuclear gradients in the thalamus.

Groups of pregnant rats were injected with two successive daily doses of 3H-thymidine from gestational days 13 and 14 (E13 + 14) until the day before birth (E21 + 22). Internuclear and intranuclear cytogenetic gradients were examined in radiograms of the thalamus sectioned in the coronal, sagittal and horizontal planes. There was a precise and segregated lateral-to-medial gradient between and within the habenular nuclei. In the ventral thalamus the reticular nucleus had a lateral-to-medial gradient, the subthalamic nucleus a laterodorsal-to-medioventral gradient. There was a caudal-to-rostral gradient between the medial geniculate and dorsal lateral geniculate nuclei, and between the pars posterior and pars anterior of the lateral nucleus. A clear intranuclear gradient could not be detected in the sensory relay nuclei with the exception of the medial geniculate nucleus. A lateral-to-medial internuclear gradient was seen between the relay nuclei and the intralaminar nuclei, and between the latter and some of the midline nuclei. On the basis of a consideration of the time of origin and time span of production of neurons of various thalamic nuclei, and taking into account some of the recognizable internuclear and intranuclear gradients, the thalamus was divided into five principal cytogenetic components; the epithelamus, the ventral thalamus, the dorsal thalamus, the medial thalamus, and the posterior thalamus. The epithalamic nuclei form over a protracted period resembling the nuclei of the hypothalamus. The nuclei of the ventral thalamus are generated early and over a relatively long period. The dorsal thalamus consists of the relay nuclei and the intralaminar nuclei; they form rapidly and ahead of the medial thalamus. The medial thalamus was subdivided into the earlier-forming anteromedial nuclei and the latest-forming midline nuclei. The posterior thalamus was not examined in detail.     

Role of neocortex in binsural hearing in the cat. I. Contralateral masking.

Cats with earphones were trained with a shock avoidance procedure to detect the occurrence of 1 kHz tone pulses at one ear while continuous noise pulses were simultaneously presented to the opposite ear. For normal cats the presence of the noise produced a mean increase of 5.4 dB in the thresholds for detection of tones at the opposite ears. After large unilateral auditory cortex ablations the same cats exhibited an asymmetry between the ears in the size of the contralateral masking effect. There was a mean increase of 10.9 dB in the detection thresholds for tones at the ear contralateral to the damaged hemisphere when noise was presented to the ear opposite the intact hemisphere. Noise of the same physical intensity when presented to the ear contralateral to the damaged cortex produced no significant changes from the preoperative masking levels. Subsequent ablation of the auditory cortex of the opposite hemisphere resulted in a cancellation of the unilateral lesion effect; the cats exhibited interaurally symmetrical masking levels of the same magnitude as those observed prior to the first operation. Additional control tests indicate that the unilateral lesion effect is a central nervous system phenomenon and is specific to lesions of auditory cortex.     

Development of the diencephalon in the rat. IV. Quantitative study of the time of origin of neurons and the internuclear chronological gradients in the thalamus.

Groups of pregnant rats were injected with two successive daily doses of 3H-thymidine from gestational days 13 and 14 (E13 + 14) until the day before birth (E21 + 22). With this progressively delayed comprehensive labelling procedure we determined the time of origin of neurons in the nuclei of the epithalamus, thalamus, and ventral thalamus. The zona incerta, subthalamic nucleus, reticular nucleus, posterior nucleus, and ventral lateral geniculate nucleus are composed of the earliest arising neurons (E13, or before, to E15). The neurons of the lateral habenular nucleus are produced between days E13--16. The neurons of the medial geniculate and lateral geniculate nuclei, the ventrobasal and ventrolateral complexes, and the nucleus lateralis, pars posterior, arise rapidly on days E14--15; the medial geniculate nucleus with a peak on day E14, the others with a peak on day E15. Neurons of a group of nuclei, with ill-defined boundaries medial to the sensory relax nuclei, arise apparently on days E15--16, with a peak on day E15; these may represent the intralaminar nuclei. The next group is generated on days E15--16 but with peak formation time on day E16; this includes the anteroventral, anterodorsal, anteromedial and mediodorsal nuclei. The rhomboid, reuniens and paratenial nuclei, and the paraventricular nucleus, pars anterior, arise next (E16--17). The medial habenular nucleus forms last and over a protracted period (E15--19). With their lengthy generation time the lateral and medial habenular nuclei resemble more the nuclei of the hypothalamus than the nuclei of the dorsal thalamus.     

The fine structure of the inferior colliculus in the cat. II. Synaptic organization.

The synaptic organization of the central nucleus of the inferior colliculus (ICc) of the cat has been investigated by means of electron microscopy. On the basis of the following criteria: the size and the shape of the synaptic vesicles, the distribution and density of the vesicular population, the size and the shape of the synaptic boutons, their origin, and the characteristics of the active synaptic zones, several types of synaptic boutons in the ICc have been discriminated: LR1, LR2, SR, SSB, F1, F2, P, DCV-terminals, and "d"-profiles. The LR1, LR2, SR and SSB bouton types contain clear, round or slightly oval synaptic vesicles and form asymmetrical synapses mainly with middle sized and small dendrites and dendritic spines. LR2-terminals not rarely contact also the neuronal perikarya, whilst the SR-boutons form exclusively axodendritic and axospinous synapses. The P, F1 and F2-boutons contain a pleomorphic vesicular population (P-boutons), with an increased degree of vesicle flattening (F1 and F2-boutons) and form symmetrical axosomatic, axodendritic and axospinous contacts. Especially often the F1-boutons form axosomatic synapses, whilst the F2-terminals end mainly on dendrites. The DCV-boutons contain a mixed population of clear round synaptic vesicles and large dense core vesicles. The DCV-boutons terminate mainly on spines and small distal dendrites by means of asymmetrical synaptic specializations. The "d"-profiles originate from dendrites, and are identical to the thalamic "d"-profiles but are far more rarely observed in the ICc. The "d"-profiles are postsynaptic mainly to the LR-types, and are presynaptic to conventional dendrites, thus participating in synaptic triads. The axonal hillocks and the initial axonal segments of the larger perikarya in the ICc are substantially innervated mainly by LR and P-boutons. Glomerulus-like formations are fairly often, especially around the LR1-terminals, contacting several small postsynaptic targets. True synaptic glomeruli are only rarely observed. Branching myelinated axons are found mainly within the fibrodendritic laminae, whilst unmyelinated collaterals, emitted by myelinated axons are especially often encountered outside the laminae. Various types of myelinated axons form nodal synapses.     

Laminar thermocoagulation of the visual cortex in the rat. II. Visual pattern discrimination.

Hooded rats were trained on a series of four visual discrimination tasks in a Y-maze, and subjected to a variety of posterior cortical lesions. In 17 animals this consisted of an extensive aspiration lesion contralateral to a more superficial lesion made by laminar thermocoagulation and centered over the striate area. After operation the animals were tested on the same problem series. The behavioral deficit in this group varied with the extent and depth of the thermal lesion, and six animals with very superficial thermal lesions displayed an isolated difficulty in solving an encircled triangle problem. This deficit seemed to be referable to widespread involvement of supragranular cortex, and specifically of layer I of area striata which receives an input from the nonspecific thalamocortical afferents. The possible influence of various interlaminar projections upon underlying vertically-oriented cell columns as a mechanism for the mediation of 'selective attention' was discussed.     

Grey matter degeneration of the C.N.S. in carcinosis

Summary Two cases of grey matter degeneration of the C. N. S. due to carcinosis are described.In the first besides elements of the cerebellum other grey complexes also were affected, in the second manifestations of deficiency-encephalopathy were found. It was emphasized that systematic diseases mostly are not so systematic as generally accepted, that many grey matter degenerations are not systematic at all, and that the carcinogenous affections do not differ essentially from the latter.C. N. S. affections in carcinosis are to be considered as unspecific, unsystematic, as only one of many etiologically different ganglion cell degenerations in which the cerebellar cortex relatively frequently partakes, as unpredictable with respect to both their occurrence at all and to the distribution and the intensity of the degeneration.

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Zusammenfassung Zwei Fälle von Degeneration der grauen Substanz des Zentralnervensystems bei Carcinose werden beschrieben. Im ersten Falle sind außer den Elementen des Kleinhirns auch andere graue Gebiete betroffen, im zweiten Fall finden sich Zeichen von Mangel-Encephalopathie. Es wird betont, daß System-Krankheiten meistens nicht so systematisch, wie allgemein angenommen, sind, daß viele Degenerationen der grauen Substanz überhaupt nicht systematisch sind und daß die carcinogenen Affektionen sich von den letzteren nicht wesentlich unterscheiden.Die Affektion des zentralen Nervensystems bei Carcinose muß man als unspezifisch und unsystematisch betrachten, als eine der ätiologisch verschiedenen Formen von Ganglienzell-Degenerationen, bei denen die Kleinhirnrinde relativ häufig beteiligt ist, sowie als nicht vorausbestimmbar sowohl hinsichtlich ihres Auftretens überhaupt als hinsichtlich der Verteilung und der Stärke der Degeneration.

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With 2 Figures in the Text     

Epidemiological study of mental illness in the U.S.S.R.

Summary Recent developments in psychiatric epidemiology in the Soviet Union are discussed. Some results of a survey of schizophrenic patients living in one particular district of Moscow are used to illustrate the value of the new techniques.

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Zusammenfassung Es werden die jüngsten Entwicklungen der psychiatrischen Epidemiologie der Sowjetunion diskutiert. Einige Ergebnisse einer Begutachtung schizophrener Patienten, die in einem besonderen Viertel von Moskau leben, wurden benutzt, um den Wert neuer Techniken zu illustrieren.

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Résumé L'auteur discute les progrès récents de l'épidémiologie en Union soviétique. Il se sert de quelques résultats d'une revue de malades schizophrènes vivant dans un district particulier de Moscou pour illustrer la valeur des nouvelles techniques.

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Based on a paper given at the Séminaire interrégional de l'Organisation Mondiale de la Santé sur l'hygiène mentale, Moscow, 1967.     

Preparation for movement in the cat. I. Unit activity in the cerebral cortex.

Single unit activity was recorded from the 'motor' cortex of cats during performance of a forelimb flexion movement. Two classes of cortical neurons were defined with respect to the onset of electrographic activity associated with this movement. 'Early' unit, first showing changes in firing rates more than 0.5 sec prior to the movement, were found almost exclusively in the medial precruciate cortex. The lateral cortex appears to be made up almost uniformly of 'late' unit, that is, neurons whose activities are more closely related with the actual movement. The medial cortex, on the other hand, contains both 'early' and 'late' units and thus may have the additional function of participating in the neural system which is the substrate for response set.     

Connections of the parahippocampal cortex in the cat. II. Subcortical afferents

The organization of subcortical inputs to the parahippocampal cortex, which in the present study in the cat is considered to comprise the entorhinal and perirhinal cortices, was studied by using retrograde and anterograde tracing techniques. The results of the retrograde tracer horseradish peroxidase (HRP), HRP conjugated with wheat germ agglutinine (WGA-HRP), Fast Blue (FB) or Nuclear Yellow (NY] injections indicate that the entorhinal and perirhinal cortices receive inputs from the magnocellular basal forebrain and from distinct portions of the amygdaloid complex, the claustrum, and the thalamus. The two cortices are further projected upon by fibers from the supramamillary region of the hypothalamus, the ventral tegmental area of the mesencephalon, the dorsal raphe nucleus, the nucleus centralis superior, and the locus coeruleus. The entorhinal cortex, in addition, receives projections from the medial septum. As regards the projections from the amygdaloid complex, it was observed that the entorhinal cortex receives its heaviest input from the basolateral amygdaloid nucleus, whereas the perirhinal cortex receives a strong projection from the lateral nucleus and a weaker projection from the basomedial nucleus of the amygdala. Of the thalamic nuclei that project to the parahippocampal cortex, the nucleus reuniens is only connected with the entorhinal cortex, while fibers from the medial geniculate nucleus and the lateral posterior nucleus terminate in the perirhinal cortex. Injections of tritiated amino acid (3H-leucine) were placed in the medial septum, the dorsal and ventral claustrum, the basolateral and basomedial amygdaloid nuclei, and the nucleus reuniens of the thalamus. The results of these experiments demonstrate that, with the exception of the claustrum, these subcortical areas project mainly to the superficial layers I-III and the lamina dissecans of the parahippocampal cortex, and to a lesser degree to the deep layers V and VI.     

Connections of the pretectum in the cat.

The connections of the pretectal complex in the cat have been examined by anatomical methods which utilize the anterograde axonal transport of tritiated proteins or the retrograde axonal transport of the enzyme horseradish peroxidase. Following injections of tritiated amino acids into the eye, label can be seen in the contralateral and ipsilateral nucleus of the optic tract and olivary nucleus where it appears as two or three finger-like strips. Following large injections of tritiated amino acids into the pretectal complex transported label accumulates ipsilaterally in a region dorsolateral to the red nucleus, the central and pericentral divisions of the tegmental reticular nucleus, the intermediate layers of the superior colliculus, the nucleus of Darkschewitch, the thalamic reticular nucleus, zona incerta and fields of Forel, the central lateral nucleus, the pulvinar nucleus and the ventral lateral geniculate nucleus. Contralaterally label accumulates in the nucleus of the posterior commissure, the interstitial nucleus of Cajal, the anterior, posterior and medial pretectal nuclei, and the ventral lateral geniculate nucleus From smaller injections, more or less well confined to single nuclei, the following patterns of connections are demonstrated. The nucleus of the optic tract projects to the ipsilateral ventral lateral geniculate nucleus and pulvinar nucleus and to the contralateral nucleus of the posterior commissure. The anterior pretectal nucleus projects to the ipsilateral central lateral nucleus, the reticular nucleus, zona incerta, fields of Forel, the region dorsolateral to the red nucleus and to the contralateral anterior pretectal nucleus. The posterior pretectal nucleus seems to project only to the ipsilateral reticular nucleus and zona incerta. The central tegmental fields deep to the pretectum project to the tegmental reticular nucleus of the brainstem. When the injection involves the nucleus of the posterior commissure label is seen in the ipsilateral nucleus of Darkschewitch, and in the contralateral nucleus of the posterior commissure and interstitial nucleus of Cajal but no nucleus of the pretectum could be positively identified as projecting to any of the motor nuclei of cranial nerves III, IV, and VI. Following large injections of horseradish peroxidase into the pretectal complex, labeled cells are seen in the superficial layers of the ipsilateral superior colliculus, in the ipsilateral ventral lateral geniculate nucleus, reticular nucleus and zona incerta and in the contralateral anterior, medial and posterior pretectal nuclei, nucleus of the optic tract and ventral lateral geniculate nucleus.