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PubMed1980

[Individual variability of sources of blood supply to the diencephalon].

As a result of investigations performed on 119 cerebral preparations of human corpses injected with roentgenopaque masses, variants of individual changeability have been determined in the cavernous and supraclinoid parts of the internal carotid artery, anterior and posterior cerebral, anterior and posterior connective, anterior villose arteries. As the criteria for determination the variants have been used: 1) degree of embryonic development; 2) source of origin; 3) twistity; 4) ratio of diameters of the interconnected arteries. The results obtained are of interest for anatomists, neurosurgeons, neuropathologists, roentgenologists.

Basilar Artery↗
PubMedDate not supplied

[Accessory groups of nonapeptidergic cells in the diencephalon of intact and hypophysectomized rats].

Accessory groups (AG) of oxytocin (OT)--and vasopressin (VP)--ergic cells (circular, perifornical, ventro- and dorsolateral groups and periventricularly localized nonapeptidergic cells) were studied morphometrically in intact and hypophysectomized rats. Additionally, the AG of medulla stria thalamus was demonstrated and investigated. The total number of nonapeptidergic cells in the AG is about 600 cells. The AG consist of OT-ergic cells predominantly (58%) except the perifornical group (68%) VP-ergic cells) and ventrolateral group (equal propotion). 7 days after hypophysectomy the size of perikaryon, nucleus and nucleolus of the cells in AG decreased, though, in contrast to the supraoptic and paraventricular hypothalamic centres, no degeneration of cell occured. That is why it is possible to suggest, that axons of the AG cells do not project to the posterior pituitary. The absence of hypertrophy of the AG cells in compensatory function of degenerating cells in the supraoptic and paraventricular nuclei indicates a functional diversity of these nonapeptidergic cells.

Animals↗
PubMed1976

[Quantitative growth analysis of limbic nuclei areas fresh volume in diencephalon and mesencephalon of an albino mouse ontogenic series. I. Nucleus habenulare].

The fresh volumes of the Nucl. mediales et laterales habenulae of 52 male white mice aged between 17 and 60 days of ontogenesis have been determined. The data of both nuclei have been fitted by a sum of logistic functions. There is an increasing component and a decreasing component. The degree of maturity and its differential quotient have been discussed. The Nucl. medialis habenulae belongs to those structures of the central nervous system developing extremely early, the Nucl. lateralis habenulae belongs to those structures of the central nervous system developing extremely early, the Nucl. lateralis habenulae belongs to those structures developing early. It has been pointed out, that there is a complex heterochrony of regional development in the brain. There have to be more quantitative analyses.

Age Factors↗
PubMed1975

Olfactory relationships of the telencephalon and diencephalon in the rabbit. I. An autoradiographic study of the efferent connections of the main and accessory olfactory bulbs.

The efferent connections of the main and accessory olfactory bulbs in the female albino rabbit have been studied using the autoradiographic method for tracing axonal pathways. Following unilateral injections of 3H-proline or 3H-leucine into the main olfactory bulb, radioactively labeled material transported intraaxonally by axoplasmic flow in an anterograde direction from soma to axon terminal is present ipsilaterally in the superficial half of the plexiform layer (IA) of: the entire circumference of the olfactory peduncle, the tenia tecta, the full mediolateral extent of the olfactory tubercle, the entire length of the prepyriform cortex, a transition area between the prepyriform cortex and the horizontal limb of the nucleus of the diagonal band, the nucleus of the lateral olfactory tract, the anterior cortical and posterolateral cortical amygdaloid nuclei (periamygdaloid areas 1, rostral half of 2, 5 of Rose, '31), and the ventrolateral entorhinal cortex (entorhinal areas 1, 2, 4, 5, 7 of Rose, '31). No subcortical or contralateral projection of main bulb efferents was found. After a unilateral injection of 3H-leucine into the accessory olfactory bulb, transported material could be followed caudally along the dorsal surface of the ipsilateral lateral olfactory tract. This heavily labeled projection is distinct from the unlabeled lateral olfactory tract and has been termed the accessory olfactory tract. Beginning at the level of the caudal third of the olfactory tubercle and extending caudally to the nucleus of the lateral olfactory tract is a group of small neurons intimately associated with the accessory olfactory tract. This cell group is referred to as the bed nucleus of the accessory olfactory tract. Projection sites of the accessory bulb include the bed nucleus of the accessory olfactory tract and layer IA of the medial nucleus and the posteromedial cortical nucleus of the amygdala (periamygdaloid areas 3, 4, PAM, caudal half of 2, 6 of Rose, '31). An additional accessory bulb efferent projection was found to enter the stria terminalis at the level of the medial amygdaloid nucleus and could be traced to a posterior segment of the bed nucleus of the stria terminalis. The autoradiographic findings indicate that the accessory olfactory bulb connects with portions of the amygdala that do not receive afferent input from the main olfactory bulb and provide evidence for the existence of two distinct and separate olfactory systems.

Amygdala↗
PubMed1975

Olfactory relationships of the telencephalon and diencephalon in the rabbit. II. An autoradiographic and horseradish peroxidase study of the efferent connections of the anterior olfactory nucleus.

The efferent connections of the anterior olfactory nucleus in the female albino rabbit have been studied using the autoradiographic and horseradish peroxidase methods for tracing axonal pathways. Following a unilateral injection of 3H-leucine into the olfactory peduncle, radioactively labeled efferent projections from the anterior olfactory nucleus were traced into all layers of the ipsilateral main olfactory bulb beneath the olfactory nerve layer and through the ipsilateral anterior limb of the anterior commissure and plexiform layer of the medial side of the cerebral hemisphere to the deep half of the plexiform (IB) and pyramidal cell (II) layers of the prepyriform cortex, the tenia tecta, and the entire surface of the olfactory tubercle. Labeled projections crossing the midline within the anterior commissure were followed to the layers IB and II of the contralateral anterior prepyriform cortex and pars externa, pars lateralis, and pars dorsalis of the anterior olfactory nucleus, and through the periventricular layer of the olfactory peduncle to all layers of the main olfactory bulb beneath the olfactory nerve layer. No well-defined labeled projection was traced to the contralateral accessory olfactory bulb. Evidence for possible anterior olfactory nucleus and/or prepyriform cortical projections to the ipsilateral paleocortical half of the claustrum, horizontal limb of the nucleus of the diagonal band, the posterior lateral hypothalamus at the level of the mammillary complex, and to the bed nucleus of the stria terminalis is discussed. Intra-axonal retrograde transport of horseradish peroxidase from axon terminals to parent cell bodies after unilateral injection of the protein into the main olfactory bulb or anterior olfactory nucleus revealed that anterior olfactory nucleus projections to the olfactory bulbs and the contralateral anterior olfactory nucleus arise predominately from the pars externa. The autoradiographic data indicate that the anterior olfactory nucleus projects to olfactory cortical structures which also receive afferent input from the olfactory bulb and that the termination of these projections is complementary to those from the olfactory bulb.

Animals↗
PubMed1978

Development of the diencephalon in the rat. I. Autoradiographic study of the time of origin and settling patterns of neurons of the hypothalamus.

Groups of pregnant rats were injected with two successive daily doses of 3H-thymidine from gestational day 13 (E13 + 14) until the day before birth (E21 + 22). This double labelling procedure was combined with an injection schedule of a single day delay between groups (E13 + 14; E14 + 15; E15 + 16 . .). The two injections assured the comprehensive labelling of practically all neurons of a given structure prior to the onset of their differentiation (comprehensive labelling), whereas the progressive daily delay in injections made it possible to estimate the proportion of neurons formed in various regions of the hypothalamus on a single day. Hypothalamic areas or nuclei were assigned into four classes on the basis of their cytogenetic isochronicity. Structures composed of the earliest arising (class 1) neurons constitute a lateral tier that includes the lateral preoptic and lateral hypothalamic areas, and the lateral mammillary nucleus. Structures composed of early arising (class 2) neurons form a heterogeneous collection of nuclear systems, including the paraventricular, internuclear and supraoptic magnocellular neurons, and several intermediate tier nuclei of the anterior and posterior hypothalamus. The late arising (class 3) and latest arising (class 4) nuclei constitute a periventricular system anteriorly and a more extensive region posteriorly. The latter two nuclear systems may constitute the hypophysiotropic area of the hypothalamus. The nuclei of the mammillary system, which are produced sequentially, are distinguished from other hypothalamic structures by their more rapid generation time. Internuclear labelling gradients were used to infer the neuroepithelial site of origin and settling pattern of neurons. Common sites of origin were indicated for the following structures: the magnocellular neurohypophysial neurons; the neurons of the dorsomedial and ventromedial nuclei; and the neurons of the tubermammillary and arcuate nuclei. The sites of origin of these groups of nuclei were related to specialized ventricular linings in the mature hypothalamus.

Animals↗
PubMed1978

Development of the diencephalon in the rat. III. Ontogeny of the specialized ventricular linings of the hypothalamic third ventricle.

The development of the specialized linings of the hypothalamic third ventricle was examined autoradiographically in mature rats that were labelled with 3H-thymidine during the developmental period, and in a closely spaced series of embryonic and infant rats. We distinguished in mature rats, apart from the typical ependymal wall, three specialized linings: the convoluted ependyma, the laminated epithelium, and the tanycytic epithelium. The ventricular wall of most of the anterior hypothalamus, and of the dorsal portion of the posterior hypothalamus, is composed of ciliated ependymal cells and most of them are generated several days before birth, soon after the cessation of neurogenesis in the adjacent hypothalamic nuclei. The cells of the rostral convoluted ependyma adjacent to the paraventricular nucleus are produced at about the same time as the neighboring cells of the smooth ependyma. Its cells come from the same germinal region that we have assumed to generate the neurons of the magnocellular neurohypophysial secretory system. The structural differentiation of the convoluted ependyma starts after birth and is completed by the beginning of the second week. Many of the ependymal cells of the laminated epithelium are produced postnatally, and the production of the specialized cells that form a parallel subependymal row extends into the third week. These cells appear to arise from the same matrix that generates earlier the neurons of the dorsomedial and ventromedial hypothalamic nuclei; their structural differentiation begins during the second week. Also the cells of the tanycytic epithelium are produced mostly postnatally, predominantly during the first week. They appear to arise from the same matrix that generated earlier the neurons of the hypophysiotropic tuberomammillary and arcuate nuclei. It is postulated that these three specialized ventricular linings are specifically related to the three cpmponents of the endocrine hypothalamus with which they have shared neuroepithelial sites of origin.

Animals↗
PubMed1979

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.

Animals↗
PubMed1979

Development of the diencephalon in the rat. VI. Re-evaluation of the embryonic development of the thalamus on the basis of thymidine-radiographic datings.

The development of the thalamus was examined in normal and X-irradiated embryos from day 13 (E13) to the day before birth (E22). The differentiating, radioresistant neurons of the lateral habenular nucleus, derived from a portion of the superior neuroepithelial lobule (SL1), were settling by day E15 and by this time the habenulopeduncular tract was forming. The neurons of the reticular nucleus, derived from the middle neuroepithelial lobe, began to settle on day E15 but a massive migration was still evident on day E16. Adjacent to the reticular nucleus the internal capsule appeared on day E16; this fiber bundle seemed to be continuous with fibers embedded in the first transitory zone of cells issuing from the dorsal neuroepithelial lobe. Because of the immaturity of the neocortex at this time, it was postulated that thalamocortical fibers of the dorsal thalamus are the earliest components of the internal capsule. By day E17 all the sensory relay nuclei of the thalamus were recognizable and it was assumed that the second transitory zone issuing from the receding dorsal neuroepithelial lobe contained the neurons of the later forming intralaminar nuclei. Suggestive evidence was obtained that the late arising neurons of the medial thalamus (the anterior nuclei, the mediodorsal nucleus, and some or all of the midline nuclei) originate in a portion of the superior neuroepithelial lobule designated as SL2. Our present and previous studies showed that the major divisions of the hypothalamus and thalamus are derived embryonically from distinguishable parts of the third ventricle neuroepithelium. This implies the te third ventricle neuroepithelium has a "mosaic" organization and suggests that the fate of hypothalamic and thalamic neurons may be determined to some extent while their precursors are still proliferating.

Animals↗
PubMed1983

Spatial relationships between the terminations of somatic sensory motor pathways in the rostral brainstem of cats and monkeys. II. Cerebellar projections compared with those of the ascending somatic sensory pathways in lateral diencephalon.

Previous studies have shown that ascending somatic sensory pathways arising from the dorsal column nuclei, lateral cervical nucleus and spinothalamic tract terminate in parts of the thalamus adjacent to those which receive cerebellar terminations. This termination pattern creates a border between the ventroposterolateral nucleus (VPL) and the ventrolateral nucleus (VL) in the cat and between the caudal and oral parts of VPL (VPLc and VPLo, respectively) in the monkey. Since it is not clear how sharp these borders are, a double orthograde labeling strategy was used in the present study to make direct comparisons of the projections to the thalamus from these sources of input. It was found that there was a change in the sources of afferent input to the different target areas that paralleled changes in cytoarchitecture. Moving caudally to rostrally, VPL in the cat and VPLc in the monkey received projections predominantly from the middle, dorsal (clusters) portion of the dorsal column nuclei. These projections were gradually replaced near the VPL-VL border in the cat and VPLc-VPLo border in the monkey first by input from the lateral cervical nucleus (cat only) and the rostral and ventral portions of the dorsal column nuclei and then by spinothalamic projections. Towards VL in the cat and the rostral parts of VPLo in the monkey (referred to as Vim by Hassler, '59 and Mehler, '71), these projections were in turn replaced by those from the cerebellum. This sequence resulted in a complex pattern (summarized in Fig. 10) where some thalamic territories received input predominantly from one source and others received converging input from several sources. The major region receiving converging ascending somatic sensory and cerebellar terminations was located at the border between VPL and VL in the cat and in the caudal parts of Olszewski's ('52) VPLo in the monkey (that is, between VPLc and Vim). In general, the results in the cat were similar to those in the monkey. One notable difference was that the domain containing terminals from the cerebellum and the rostral-ventral parts of the dorsal column nuclei was located medially between VPLc and Vim in the monkey, whereas it extended across the entire mediolateral border between VPL and VL in the cat. In both species, thalamic neurons received input predominantly from one afferent source and only minor input, if any, from other sources.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1987

Distribution of neurotensin-like immunoreactivity in the diencephalon of the Japanese monkey (Macaca fuscata).

The distribution of neurotensin-like immunoreactive (NT-LI) neurons was examined in the thalamus and hypothalamus of the Japanese monkey (Macaca fuscata) by using the peroxidase-antiperoxidase immunocytochemistry technique. In the thalamus, NT-LI neuronal perikarya were distributed mainly in the midline nuclear group and the dorsomedial nucleus, and partially in the intralaminar nucleus: Immunoreactive fibers were mainly distributed in the midline nucleus, particularly in the nucleus rhomboidalis. Numerous immunoreactive fibers were also detected in the regions that contain the pathways to extrathalamic areas such as the stratum zonale and inferior thalamic peduncle. In the hypothalamus, many immunoreactive neuronal perikarya were distributed in the lateral hypothalamic area and in the arcuate nucleus. Immunoreactive fibers were disseminated throughout the hypothalamus, but they were dense in the preoptic area and sparse in the ventromedial nucleus. An accumulation of dense immunoreactive endings was also observed in the external layer of the median eminence. NT-LI fibers in the external layer of the median eminence were considered to represent nerve endings near portal vessels. Functional roles of neurotensin in the thalamus and hypothalamus are discussed from the anatomical point of view.

Animals↗
PubMed1976

Modulation of reward and aversion processes in the rat diencephalon by neuroleptics: differential effects of clozapine and haloperidol.

The effects of clozapine and haloperidol on self-stimulation in rats were investigated in a shuttle-box that provides concurrent rate-independent indexes of the rewarding and aversive components of intracranial stimulation. The use of two concurrent measures of performance permits the differentiation of specific reward modulation effects from the variety of nonspecific performance decrements that these drugs may produce. Clozapine produced a dose-dependent reduction in reward that could be clearly dissociated from its nonspecific effects. In contrast, the apparent reduction in reward produced by haloperidol could not be dissociated from a nonspecific performance decrement. Consequently, the attenuation of self-stimulation produced by haloperidol does not indicate a direct role for dopamine in modulating reward. It is suggested that the attenuation of reward produced by neuroleptics reflects a reduction in noradrenergic transmission, whereas their nonspecific effects reflect their blockade of dopamine receptors.

Animals↗