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A Urano

Publications and source records attributed to A Urano.

At least 55 records · Page 3Linked to original sources

Cloning and sequence analyses of cDNAs encoding vasotocin and isotocin precursors of chum salmon, Oncorhynchus keta: evolutionary relationships of neurohypophysial hormone precursors.

The nucleotide sequences of cloned cDNAs were used to determine the primary structures of the precursors of vasotocin (sVT) and isotocin (sIT) from the hypothalamus of the chum salmon, Oncorhynchus keta. Two different cDNAs were obtained for each of sVT and sIT precursors (sVT-I and sVT-II; sIT-I and sIT-II). Both sVT and sIT precursors were found to contain a signal peptide and hormone that is connected to a neurophysin by a Gly-Lys-Arg sequence. Northern and Southern blot analyses showed that the sVT and sIT genes are expressed by the same chum salmon hypothalamus, but not by the liver and kidney. Microheterogeneity was found in the nucleotide and amino acid sequences of sVT precursors between our results and the previously reported data (Heierhorst et al. 1990). The conspicuous difference is the occurrence of a stop codon in the middle of sVT-II cDNA. The carboxyl termini of both sVT and sIT neurophysins are about 30 amino acids longer than neurophysins of toad and mammalian neurohypophysial hormone precursors. Although these extended regions do not contain a glycosylation site, they show striking similarity with the glycopeptide moiety (copeptin) of toad vasotocin and mammalian vasopressin precursors. The central portion of the neurophysins shows highest homology among corresponding regions of sVT and sIT precursors. Moreover, calculation of nucleotide substitution rates suggests that a recent gene conversion may have occurred which encompasses the exon that encodes the central segment of the sVT and sIT precursors. A possible pathway for the evolution of precursor molecules of neurohypophysial hormones is discussed.

Amino Acid Sequence↗

Growth hormone and prolactin gene expression and release in the pituitary of rainbow trout in serum-free culture.

The trout pituitary continuously released a large amount of GH for over a week in serum-free culture, but PRL secretion declined by day 2 in culture. The total amount of GH released during the 8 days exceeded the initial content. The pituitary content of PRL remained unchanged after 8 days of culture. The number of weakly stained GH-immunoreactive (ir) cells was increased by day 4 in culture. The GH mRNA levels in individual cells as revealed by in situ hybridization were maintained at around the same level throughout culture. In contrast, the stainability of PRL-ir cells remained unchanged during culture, although the levels of PRL mRNA decreased by day 8. Electron microscopic immunocytochemistry showed a decrease in the numbers of secretory granules and dilation of rough endoplasmic reticulum in GH-ir cells. GH synthesis, measured by incorporated [3H]leucine after GH immunoprecipitation, was elevated 120% on day 8 over day 0. The dominant control of GH and PRL secretion in rainbow trout seems to be the converse of those seen in mammals; inhibition for GH and stimulation for PRL.

Animals↗

Effects of castration on volumes of the preoptic nucleus and the amygdala and on immunoreactivity of LH-RH fibers in the brain of the toad, Bufo japonicus.

We examined the influence of castration on the volumes of sexually dimorphic nuclei, the amygdala pars medialis (Am) and lateralis (Al), and the anterior part of the preoptic nucleus, and on the immunoreactivity of luteinizing hormone-releasing hormone (LH-RH) in brains of Japanese toads captured in spring and autumn. Animals were castrated (GnX) and half were implanted with testosterone (T) (GnX + T) and then killed and dissected after 1 month. Compared with sham-operated (Sham) toads, plasma androgen levels in autumn toads were significantly decreased by the castration, and those in both spring and autumn GnX toads were significantly elevated by the T implantation. The volume of Am in autumn toads was significantly reduced by GnX. Although not significant, changes in the volumes of the other nuclei, except for Al in spring toads, showed the following tendency 30 days after the operation: GnX + T greater than Sham greater than GnX. GnX did not alter LH-RH immunoreactivity in the median eminence. However, dense immunoreactive LH-RH fibers were found in the mesencephalic tegmental region in spring GnX toads but not in the other operation groups in both spring and autumn. LH-RH immunoreactivity was not altered in autumn toads. In spring GnX toads, thumb pads degenerated and evoked release calling was infrequent. These results suggest that (i) the volumes of sexually dimorphic nuclei, especially Am in the autumn toad, are androgen-dependent, and (ii) castration can modulate activity of the extrahypothalamic LH-RH-ergic projection in toad brain.

Amygdala↗

Cloning and sequence analysis of cDNAs for neurohypophysial hormones vasotocin and mesotocin for the hypothalamus of toad, Bufo japonicus.

The primary structures of the precursors of neurohypophysial hormones vasotocin (VT) and mesotocin (MT) in the hypothalamus of the toad Bufo japonicus were determined by analyzing the nucleotide sequences of the cloned cDNAs encoding them. The MT precursor consists of 125 amino acid residues containing a signal peptide followed directly by MT, which in turn is connected to the MT neurophysin by Gly-Lys-Arg, a processing and carboxyl-terminal amidation signal. In contrast, the VT precursor includes a glycoprotein of 36 amino acids following the VT neurophysin. Except for glycoprotein, the structures of MT and VT precursors are quite similar. RNA transfer blotting analysis showed that both MT and VT mRNAs are present in the brain but not in the liver, ovaries, and testes of the toad. The sequences and the structural organizations of the MT and VT precursors are highly homologous to those of their mammalian counterparts, oxytocin and arginine vasopressin precursors, respectively. This fact suggests that, in the evolutionary pathway of neurohypophysial hormones, VT is the ancestor molecule of vasopressin, while MT is that of oxytocin.

Amino Acid Sequence↗

Extrahypothalamic projection of luteinizing hormone-releasing hormone fibers in the brain of the toad, Bufo japonicus.

Extrahypothalamic projection of luteinizing hormone-releasing hormone (LHRH) fibers in the brain of the toad (Bufo japonicus) was examined immunohistochemically by the avidin-biotin-peroxidase complex (ABC) method. Immunoreactive LHRH perikarya are localized in the nuclei medialis septi and of the diagonal band of Broca. A part of the LHRH fibers are sent anteriad to the medial and dorsal pallia. Some fibers reach the olfactory bulb. Dorsocaudally, LHRH neurons in the medial septum project their fibers to the deep layers of the optic tectum and the posterior mesencephalon including the nucleus pretrigeminalis, which is considered to be a generator of mate calling behavior, via the habenular and posterior thalamic regions. In addition, LHRH fibers which run caudad through the dorsal infundibular region and then the mesencephalic reticular formation were widely distributed in both the gray and the white matter of the medulla oblongata. These findings suggest that LHRH acts as a neurotransmitter or a neuromodulator in the various neuronal circuitries for reproductive behavior in the central nervous system, because LHRH has been considered to be related to amphibian seasonal breeding, and many regions where the immunoreactive LHRH fibers were observed are the loci concerned with mating behavior.

Animals↗

In situ hybridization of the vasopressin mRNA in the rat hypothalamus by use of a synthetic oligonucleotide probe.

A 22mer oligonucleotide complementary to the rat vasopressin (AVP) mRNA was synthesized, radioactively labeled with 32P, and was applied to in situ hybridization with the mRNA on paraffin sections of the rat hypothalamus. The AVP mRNA in magnocellular neurosecretory neurons of the paraventricular and the supraoptic nuclei was demonstrated by use of this synthetic probe. Specificity of the autoradiographic signals was confirmed by a competition test using an excess amount of unlabeled probe and an absorption test using a synthetic template of the probe. Further, the mRNA of vasotocin, the ancestral molecule of AVP, was hybridized weakly with the probe, showing that the present probe can discriminate a few base substitutions. Autoradiographic signals representing hybrids of the probe and the AVP mRNA were rarely found in the region rich in oxytocin neurons whose mRNA is homologous to the AVP mRNA. These results show that the in situ hybridization method using synthetic oligonucleotide probes can be a powerful and specific tool for the study of gene expression in the central nervous system.

Animals↗

Projections of luteinizing hormone-releasing hormone and vasotocin fibers to the anterior part of the preoptic nucleus in the toad, Bufo japonicus.

The anterior part of the preoptic nucleus (APON) is a crucial locus for triggering male mate calling behavior in anuran amphibia. The projections to this locus of luteinizing hormone-releasing hormone and vasotocin fibers were immunohistochemically demonstrated in the brain of the toad (Bufo japonicus) using the avidin-biotin-peroxidase complex method. Immunoreactive (ir)-LH-RH perikarya are localized in the nucleus medialis septi and the nucleus of the diagonal band of Broca. A part of ir-LH-RH fibers arising from these nuclei project to the lateral part of the APON, where the APON neurons form their dendritic field, and often protrude into its medial neuronal cell mass. Meanwhile, a considerable number of vasotocin fibers arising from the ventral magnocellular part of the preoptic nucleus project anterior to these loci. These observations indicate that the LH-RH and vasotocin fibers may form ordinary and/or en passant synapses with the APON neurons to transmit peptidergic neuronal signals which are concerned with initiation of seasonal reproductive behavior.

Animals↗

An immunohistochemical study of seasonal changes in luteinizing hormone-releasing hormone and vasotocin in the forebrain and the neurohypophysis of the toad, Bufo japonicus.

Seasonal changes in luteinizing hormone-releasing hormone (LH-RH) and arginine vasotocin (AVT) were examined immunohistochemically in the toad forebrains and neurohypophyses. Strongly immunoreactive (ir-) LH-RH perikarya, from which dense ir-LH-RH fibers project to the median eminence, were localized in the medial septal nucleus and the nucleus of the diagonal band of Broca in the animals captured in the spring and the autumn. While, in the animals collected in the summer, ir-LH-RH perikarya and fibers were sparse, and immunoreactivity in the median eminences was weak. Artificially induced hibernation decreased the density of ir-LH-RH in the median eminence, in contrast with strong immunoreactivity in the control animals kept at room temperature. The amounts of ir-LH-RH in the median eminences of hibernating toads which were captured shortly before the breeding period varied conspicuously among individuals. The median eminences in migrating toads showed relatively weak LH-RH immunoreactivity. After the breeding, the immunoreactivity returned to the strong level that was observed in the spring and the autumn. These seasonal changes in ir-LH-RH seem to correspond to seasonal reproductive activity in this species. However, significant seasonal variations were not found in ir-AVT.

Acclimatization↗

The volume of the toad medial amygdala-anterior preoptic complex is sexually dimorphic and seasonally variable.

The anterior part of the preoptic nucleus (APON) in anurans is considered to be a center for mate calling. This locus makes an anatomical complex with the amygdala pars medialis (Am). The nuclear volumes of the Am and APON in the male toad are significantly larger than those in the female. In addition, the nuclear volumes of these loci in the hibernating male are larger than those in the post-breeding animal. These results suggest that the Am-APON complex has an important role in male sexual behavior, and this complex can be activated during the breeding season in the spring.

Amygdala↗

A stereotaxic atlas for diencephalic nuclei of the frog, Rana pipiens.

A stereotaxic apparatus was devised for frogs (Rana pipiens pipiens) by adaptation of a commercially available apparatus. An atlas of orienting illustrations emphasizing detailed structure and distribution of forebrain nuclei was prepared from celloidin sections and paraffin sections. Nomenclature of nuclei is discussed and an attempt made to reconcile various interpretations in the published literature.

Animals↗

Effects of the eye enucleation on the activity of monoamine oxidase and acetylcholinesterase in the superior colliculus of the rat.

Changes in the activity of monoamine oxidase (MAO) and acetylcholinesterase (AChE) following unilateral eye enucleation were measured for the superior colliculus (SC), lateral geniculate body (LGB), and nucleus suprachiasmaticus (NSC) in the rat by means of microspectrophotometry. The most conspicuous change of high significance was the decrease of MAO activity in the superficial strata of the SC contralateral to the enucleated eye. The other layers of SC, such as the stratum opticum, the intermediate strata, the deep strata and the central gray did not show significant postoperative changes in MAO acitivity. MAO activity of the LGB and the NSC was also not affected to a significant degree. The site of decrease of MAO activity in the superficial strata of the SC sould be degenerating optic nerve terminals. The strong AChE activity in the superficial strata may be derived from the horizontal cells. AChE activity in the SC showed only slight postoperative changes. The possible roles of the monoaminergic and cholinergic systems in the process of visual information are discussed.

Acetylcholinesterase↗