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At least 19 recordsLinked to original sources
PubMed1991

Induction of a mesencephalic phenotype in the 2-day-old chick prosencephalon is preceded by the early expression of the homeobox gene en.

The homeobox gene en, homologous to the gene en-grailed of Drosophila, is expressed in the metencephalic-mesencephalic segment of the vertebrate neural tube. Using quail-chick chimeras, an antibody against en proteins, and cytoarchitectonic techniques, we demonstrate that metencephalon transplanted to prosencephalon, at E2, maintains a high level of en proteins and its presumptive cerebellar fate. The ectopic metencephalon induces in the contiguous host prosencephalon the expression of en and, subsequently, a mesencephalic phenotype. These related genetic and phenotypic expressions indicate that the transcriptional regulatory en gene is involved in cerebellar and mesencephalic cyto-differentiation. The expression of en can also be induced in chick prosencephalon by a mammalian metencephalic graft, indicating that the factors regulating the transcription of en are phylogenetically well conserved.

Animals↗
PubMed1976

Effect of stagnant hypoxia on acid ribonuclease activity in the rat prosencephalon during ontogenesis.

In the rat prosencephalon it proved possible to differentiate lysosomal ribonuclease from alkaline ribonuclease activity, which could be detected only in the presence of p-chlormercuribenzoate. Acid RNase activity related to the amount of protein in the prosencephalon fell during ontogenesis. It was not significantly affected by four hours' stagnant hypoxia induced by ligation of both carotids. Its release from the lysosomes rose, however (when isotonic homogenates were spun at 20,000 g, acid ribonuclease activity in the supernatants was elevated). The absence of correlation between this activation and the degree of maturity of the nervous tissue refutes the hypothesis that regulation of this enzyme is per se responsible for the known changes induced by hypoxia in the RNA content of the prosencephalon of rats of different ages. On the contrary, the results indirectly support studies which demonstrate changes in the extent of RNA synthesis after hypoxia.

Age Factors↗
PubMed1986

[Morphological characteristics of the changes in the prosencephalon of guinea pigs exposed to general vibrations].

After 7 or 30 days of exposure to general vibration (frequency: 40 Hz, amplitude: 1 mm) for 3 hours per day, the prosencephalon of guinea pigs exhibited a wide range of morphological changes, including congestion, haemorrhages, the presence of the heterochromic neurons and perivascular spaces as well as diffuse spongiosis. In contrast, after 14 days' exposure to general vibration of the same parameters, diffuse spongiosis of the prosencephalon was found in all the animals under examination. Hypothalamus, cerebral cortex and periventricular gray matter were unaffected by spongiosis in most of the animals. The nerve fibre sheats were unchanged in all cases.

Animals↗
PubMed1991

Projection of the retinal ganglion cells to the tectum differentiated from the prosencephalon.

The alar plate of the prosencephalon differentiates into a tectum-like structure when transplanted into the mesencephalon around the 10-somite stage. Here, we report on the projection pattern of the retinal ganglion cells to the transplants. Optic nerve fibers were labeled with horseradish peroxidase (HRP) and 3H-proline, and the innervation of the optic nerve fibers to the chimeric tectum was analyzed by HRP histochemistry on whole-mounted specimens, by autoradiography and by electron microscopy on embryonic day 16. In the chimeric tectum, the transplant was distinguished from the host by difference in nuclear structure between the quail and the chick cells. It was shown that the transplant had the laminar pattern of the optic tectum when the transplant was integrated into the host mesencephalon. The whole-mount HRP histochemistry showed that the optic nerve fibers extend to the transplants. Autoradiography showed that the distribution pattern of silver grains was similar in both the host and the transplant. These results may indicate that the optic nerve fibers turn to the transplant and terminate on the transplant. Electron microscopy further confirmed that optic nerve fibers ended by making synaptic contacts with the dendrites in the transplant region of the tectum. These results indicate that the transplant with the laminar pattern of the optic tectum is a true tectum receiving input from the eye.

Animals↗
PubMed1990

Distribution of neuropeptide Y in the prosencephalon of man and cotton-head tamarin (Saguinus oedipus): colocalization with somatostatin in neurons of striatum and amygdala.

The presence, chromatographic properties and localization of neuropeptide Y was demonstrated in postmortem human brain areas of neurologically and neuropsychiatrically normative controls using immunocytochemistry and high performance liquid chromatography combined with radioimmunoassay. NPY-immunoreactivity was found in many regions of the prosencephalon. Numerous perikarya and fibers were present in the neocortex, basal ganglia and limbic-hypothalamic areas. A moderate number of neurons and fibers was observed in the basal forebrain, including the septal complex. A comparative immunohistochemical investigation in perfusion-fixed brains of the old-world ape Saguinus oedipus revealed an almost identical distribution of NPY-immunoreactivity with only minor differences. Colocalization experiments on 1-2 microns thin consecutive paraffin sections revealed a large number of NPY neurons throughout the human neostriatum and amygdaloid complex that were also positive for somatostatin. Our findings indicate that detection of neuropeptides in fresh or fixed post-mortem human tissue by different immunochemical methods may actually reflect the in vivo conditions. In addition, the wide distribution of NPY throughout the human brain and its colocalization with other neurotransmitters suggests a physiological role as neuroactive substance, i.e. neuromodulator in the primate central nervous system.

Amygdala↗
PubMed1986

[Vascularization of the tela choroidea of the prosencephalon of the sheep (Ovis aries)].

The tela choroidea of the prosencephalon in sheep is vascularized by an anterior choroidal artery arising from the rostral branch of the carotid cerebral artery and by a posterior choroidal artery, arising from the caudal cerebral artery, branch of the carotidobasilar system. These two choroidal arteries give off choroidal branches which nourish the capillary networks of the tela. The latter consist of a velar capillary network and of a choroidal capillary network. Together, they drain into choroidal veinules and veins which are tributary of the superficial and of the deep venous systems of the brain.

Animals↗
PubMed1985

[Vascularization of the tela choroidea of the prosencephalon in the cat (Felis domestica)].

The tela choroidea of the prosencephalon in cat is vascularized by an anterior choroidal artery arising from the carotid system and by a posterior choroidal artery arising from the vertebral basilar system. The first essentially supplies the tela and the choroid plexus of the lateral ventricle. The second above all supplies the tela choroidea of the third ventricle. Both, the anterior and posterior choroidal arteries anastomose with their terminal branches. The choroidal branches which arise from these arteries nourish the capillary networks of the tela. These vessels drain into venules and veins which are tributary of the venous circle of the base and of the internal cerebral veins.

Animals↗
PubMed1985

The cerebellar and vestibular nuclear complexes in the turtle. II. Projections to the prosencephalon.

Prosencephalic projections from the cerebellar and vestibular nuclear complexes in the turtle Pseudemys scripta elegans were investigated with anterograde tracing. Following injections of 35S-methionine at various locations within the cerebellar and vestibular nuclear complexes, labeled ascending fibers were found to arise from the lateral cerebellar and the rostral (superior and/or dorsolateral) vestibular nuclei. The great majority of these fibers coursed within the ipsilateral ascending periventricular tract. There were possible terminations in the hypothalamosuprapeduncular region, the ovalis-complex, and the nucleus commissuralis anterior, but scarcely any indication of terminal labeling within the dorsal thalamus. The labeled fibers, however, continued rostralward, entered the lateral forebrain bundle, and terminated in the anterior dorsal ventricular ridge--in all but one case, exclusively ipsilaterally. The terminal area within the lateral division (referred to as area L) of the anterior dorsal ventricular ridge was sharply delimited, being situated ventrolateral to the visually oriented area D of the anterior dorsal ventricular ridge (Balaban and Ulinski, '81), medial to the lateral cortex, and ventral to the pallial thickening (motor pallium of Johnston, '16). The findings are compared with related ones in mammals, particularly those pertaining to telencephalic somatosensorimotor regions and their interactions with the vestibular nuclear complex and the cerebellum.

Animals↗
PubMed1985

Mapping of the early neural primordium in quail-chick chimeras. I. Developmental relationships between placodes, facial ectoderm, and prosencephalon.

Defined fragments of the anterolateral neural ridge and of the associated region of the neural plate of presomitic to three-somite stage quail embryos were grafted isotopically and isochronically into chick hosts. This resulted in the development of apparently normal brain and facial structures to which the contribution of the grafted tissue could be observed by means of the quail nuclear marker. It was shown that the anterolateral neural ridge contains the progenitor cells of the adenohypophyseal and olfactory placodes and also of the superficial ectoderm lining the nasal cavity and conchae and the superficial ectoderm of the beak. When the appropriate region of the neural ridge was involved in the quail-chick substitution, the egg tooth was made up of graft-derived cells. Grafting of the neural plate area adjacent to the "ridge" territory containing the placodal ectoderm revealed that the presumptive region of the hypothalamus is in contiguity with that of the adenohypophyseal placode. The same observation was made for the olfactory placode and the floor of the telencephalon from which the olfactive bulb later develops.

Animals↗
PubMed1990

Do CNS anlagen have plasticity in differentiation? Analysis in quail-chick chimera.

Heterotopic transplantations of brain vesicles of a quail embryo into a chick embryo were carried out in order to elucidate if CNS anlagen have plasticity in differentiation at the 7-10 somite stage. Quail cells are distinguished from chick cells due to the difference in nuclear morphology. The prosencephalon did not differentiate into the cerebellum when transplanted into the metencephalon, although previous study showed that the prosencephalon has the capacity to differentiate into the optic tectum. The mesencephalon differentiated as an optic tectum when transplanted into the prosencephalon or into the rhombencephalon. The metencephalon differentiated as a cerebellum in the telencephalon. It is concluded that only the prosencephalon has limited plasticity, but the mesencephalon and rhombencephalon are determined by the 7-10 somite stage.

Animals↗
PubMed1985

Prosencephalic afferents to the mediodorsal thalamic nucleus.

The afferent projections from the prosencephalon to the mediodorsal thalamic nucleus (MD) were studied in the cat by use of the method of retrograde transport of horseradish peroxidase (HRP). Cortical and subcortical prosencephalic structures project bilaterally to the MD. The cortical afferents originate mainly in the ipsilateral prefrontal cortex. The premotor, prelimbic, anterior limbic, and insular agranular cortical areas are also origins of consistent projections to the MD. The motor cortex, insular granular area, and some other cortical association areas may be the source of cortical connections to the MD. The subcortical projections originate principally in the ipsilateral rostral part of the reticular thalamic nucleus and the rostral lateral hypothalamic area. Other parts of the hypothalamus, the most caudal parts of the thalamic reticular nucleus, the basal prosencephalic structures, the zona incerta, the claustrum, and the entopeduncular and subthalamic nuclei are also sources of projections to the MD. Distinct, but somewhat overlapping areas of the prosencephalon project to the three vertical subdivisions of MD (medial, intermediate, and lateral). The medial band of the MD receives a small number of prosencephalic projections; these arise mainly in the caudal and ventral parts of the prefrontal cortex. Cortical projections also arise in the infralimbic area, while subcortical projections originate in the medial part of the rostral reticular thalamic nucleus and lateral hypothalamic area. The intermediate band of the MD receives the largest number of fibers from the prosencephalon. These arise principally in the intermediate and dorsal part of the lateral and medial surface of the prefrontal cortex, the premotor cortex, and the prelimbic and agranular insular areas. Projections also originate in basal prosencephalic formations (preoptic area, Broca's diagonal band, substantia innominata, and olfactory tubercle), rostral reticular thalamic nucleus, and lateral hypothalamic area. A large number of prosencephalic structures also project to the lateral band of the MD. These are mainly the most dorsal and caudal parts of the lateral and medial surface of the prefrontal cortex, the premotor and motor cortices, and the prelimbic, anterior limbic, and insular areas. Projections arise also in the lateral rostral and caudal parts of the reticular thalamic nucleus, the zona incerta, the lateral and dorsal hypothalamic area, the claustrum, and the entopeduncular nucleus. These and previous results demonstrate a gradation in the afferent connections to the three subdivisions of the MD.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗