鲫鱼尾部神经分泌系统显微和亚显微结构的季节性变化

鲫鱼尾部神经分泌系统的神经分泌细胞和它的轴突中可观察到各种不同电子密度的颗粒。在性腺各个不同的发育阶段,该系统的分泌物具有累积、充满、释放和恢复这样一种周期性变化,由此说明鲫鱼的尾部神经分泌系统和它的生殖有关。     

A histoenzymological investigation of the caudal neurosecretory system in six species of freshwater teleosts: a comparative study

Enzymecytochemical features of the caudal neurosecretory system of 6 species of freshwater teleosts, Gudusia chapra, Gonialosa manmina (Clupeidae, Clupeiformes), Oxygaster bacaila (Cyprinidae, Cypriniformes), Mystus bleekeri (Bagridae, Cypriniformes), Sciaena coiter (Scienidae, Perciformes), and Mastacembelus pancalus (Mastacembelidae, Mastacembeliformes) have been investigated with the help of several specific histochemical techniques. No sex-dependent variation have been observed in the enzymecytochemical characteristics of the caudal neurosecretory system of the present species. The Dahlgren cells show intense RNA activity. Caudal neurosecretion lacks carbohydrate but seems to possess small amount of lipid. Acid-phosphatase is located in the Dahlgren cells and axons. Alkaline-phosphatase has been observed in the Dahlgren cells, axons, and urophysial blood-capillaries. Acetylcholine esterase is present in the Dahlgren cells, axons, and urophysis of Mystus, Mastacembelus, and Gonialosa, but lacking in the other 3 species. It is concluded that the caudal neurosecretory system of Mystus, Mastacembelus, and Gopialosa is innervated by cholinergic neurons. Despite their different taxonomic positions, caudal neurosecretory system of all 6 species produce similar responses to various enzymecytochemical tests, except for acetylcholine esterase.     

Sauvagine/urotensin I-like immunoreactivity in the caudal neurosecretory system of a seawater fish Diplodus sargus L. in normal and hyposmotic milieu

We report the presence of sauvagine/urotensin I-like immunoreactive (SV/UI-LI) elements in the caudal neurosecretory system of a teleost (Diplodus sargus L.) collected from aquaria tanks of the Aquaculture Center (Talassographic Institut of CNR) of Messina or maintained in an hyposmotic milieu for different periods. In normal specimens, SV/UI-LI material was recognizable in discrete or little amounts both in Dahlgren cell cytoplasm and in their axons that reach the urophysis. On the contrary, the specimens transferred in an hyposmotic milieu showed a fast and dramatic increase of immunoreactivity mainly in neurohemal endings of the urophysis. This suggests a physiological role of caudal neurosecretory products on osmoregulatory mechanisms.     

Caudal neurosecretory system of the zebrafish: ultrastructural organization and immunocytochemical detection of urotensins

The caudal neurosecretory system is described here for the first time in the zebrafish, one of the most important models used to study biological processes. Light- and electron-microscopical approaches have been employed to describe the structural organization of Dahlgren cells and the urophysis, together with the immunohistochemical localization of urotensin I and II (UI and UII) peptides. Two latero-ventral bands of neuronal perikarya in the caudal spinal cord project axons to the urophysis. The largest secretory neurons (~20 μm) are located rostrally. UII-immunoreactive perikarya are much more numerous than those immunoreactive for UI. A few neurons are immunopositive for both peptides. Axons contain 75-nm to 180-nm dense-core vesicles comprising two populations distributed in two axonal types (A and B). Large dense vesicles predominate in type A axons and smaller ones in type B. Immunogold double-labelling has revealed that some fibres contain both UI and UII, sometimes even within the same neurosecretory granule. UII is apparently the major peptide present and predominates in type A axons, with UI predominating in type B. A surprising finding, not previously reported in other fish, is the presence of dense-core vesicles, similar to those in neurons, in astrocytes including their end-feet around capillaries. Secretory type vesicles are also evident in ependymocytes and cerebrospinal-fluid-contacting neurons in the terminal spinal cord. Thus, in addition to the urophysis, this region may possess further secretory systems whose products and associated targets remain to be established. These results provide the basis for further experimental, genetic and developmental studies of the urophysial system in the zebrafish.     

Effect of electrical stimulation of the olfactory tract and the caudal spinal cord on the Dahlgren cells in Clarias batrachus L.

Electrical stimuli applied to the olfactory tract for one minute caused partial depletion, but for two to five minutes resulted in complete depletion of the neurosecretory material (NSM) from the Dahlgren cells as well as from the urophysis. However, if similar stimuli were directly applied to the caudal spinal cord for one minute, the NSM was completely depleted. The neurosecretory granules were reaccumulated in the neurons within fifteen minutes after the stimuli were cut of A rapid depletion of the NSM from the caudal neurons was correlated with their electrical properties and rapid transduction of nervous information into the hormonal message. The immediate response of the caudal neurons to the olfactory tract stimulation suggested that the former are synaptically controlled by a center in the brain.     

Liberation of urotensin II from the teleost urophysis: an historical overview

During the past 20 years, urotensin II (UII) has progressed from being a peptide synthesized only in the urophysis of the caudal neurosecretory system of teleost fish to being considered an important physiological regulator in mammals with implications for the pathogenesis of a range of human cardiovascular and renal diseases. The "liberation" of UII from the urophysis was a gradual process and involved the sequential realization that (a) UII is present not only in the urophysis but also in the central nervous systems (CNS) of teleosts, (b) UII peptides, similar in structure to the urophysial peptides, are present in the diffuse caudal neurosecretory systems and/or CNS of species less evolutionarily advanced than teleosts, including Agnatha, thereby showing that UII is a phylogenetically ancient peptide, (c) UII is present in the brain and spinal cord of a tetrapod, the green frog Rana ridibunda, and (d) the UII gene and its specific receptor (GPR14/UT) are expressed in the CNS and certain peripheral tissues of mammals, including the human. The discovery that the genomes of mammals contain an additional gene encoding a UII-related peptide (URP) and the availability of highly effective peptide and non-peptide antagonists to investigate the role of UII in human physiology and pathophysiology ensure that the peptide will remain "center stage" for several years to come.     

Ontogenetic Development of the Caudal Neurosecretory System in the Chum Salmon, Oncorhynchus keta, with Regard to Its Ultrastructural Changes and with Relation to Neuropeptide Y-immunoreactive Fibers

The ontogeny of the caudal neurosecretory cells (Dahlgren cells) in the caudal spinal cord of the chum salmon, Oncorhynchus keta, was examined by conventional electron microscopy and with immunohistochemistry for urotensins (U) and neuropeptide Y (NPY). The precursors of the Dahlgren cells first appeared as agranular ovoid cells in the caudal region of the neural tube of 40-day-old embryos about one week before hatching. The occurrence of cytoplasmic granules in the immature Dahlgren cells became evident by the 14th day after hatching. At this moment, the U-positive reaction was merely demonstrated in some of the granules. Close association of NPY-positive fibers with the caudal neurosecretory structures was recognizable in 1-month-old larvae. Thus, it is apparent that the salmon Dahlgren cells start their secretory activity (production of the secretory granules) in early larval stages and that, thereafter, NPYergic afferent innervation of the caudal neurosecretory system becomes evident.     

Development of the caudal neurosecretory system of the nile tilapia Oreochromis niloticus: an immunohistochemical and electron microscopic study

The development of the caudal neurosecretory system (CNSS) of the Nile tilapia, Oreochromis niloticus, has been investigated by means of UI/oCRF (urotensin I/ovine corticotropin-releasing factor) immunohistochemistry and transmission electron microscopy. UI-like immunoreactive perikarya and fibers are first detected in the caudal spinal cord of larval fish about 4 days after hatching (stage 21). In the region of the future urophysis two bundles of strongly immunoreactive neurosecretory fibers are observed. At this stage, neurosecretory axons terminate on the meninx sheath of the spinal cord with immature neurosecretory terminals. The histogenesis of the urophysis begins at stage 24. The future neurohemal organ consists of a small ventral swelling of the spinal cord, which is associated with dilated vessels. At this stage, neurosecretory axons terminate on the basal lamina of the ingrowing blood vessels. Further development occurs by means of progressive branching of vessels and the concomitant increase in the number of neurosecretory terminals. In the caudal spinal cord, immunoreactive neurons also increase in number and progressively differentiate morphologically. Typical features of the mature CNSS are recognizable in 4-month-old juveniles. Data suggest that in tilapia both the synthesis and the release of urophysial hormones begin before morphogenesis of the neurohemal organ takes place.     

Antidiuretic activity of teleost urophysial extracts in the rat

Summary Extracts of the carp urophysis elicit a marked decrease in urine flow in the anaesthetized hydrated rat. Reproducible dose-dependent responses are obtained within the range of 2 to 16 g of acetonedried carp urophysis per 100 gBW of the rat. The carp urophysial antidiuretic substance is peptidic, and is different from the neurohypophysial peptides. The bulk of antidiuretic activity is located in the electrondense granules in the carp urophysis. The antidiuretic substance, probably urotensin I, is found generally in teleost urophyses. The activity per mg of acetonedried urophysis is higher in freshwater teleost species than in seawater species.Abbreviations AVP arginine vasopressin - AVT arginine vasotocin - LVP lysine vasopressin - US carp urophysial standard preparation     

The fine structure of the caudal neurosecretory system in Raia batis

Summary The fine structure of the caudal neurosecretory system in Raia batis was studied. Far-reaching similarities with ultrastructural details of other vertebrate neurosecretory systems were noted. The secretion is present in all parts of the system in the form of elementary neurosecretory granules which seem to be formed in the Golgi complex of the cell body. The morphology of the terminal region is discussed in relation to the possible mode of secretion release and in connection with the routes of secretion to the vascular lumen.The Dahlgren cell is not considered to be a secretory neuron, but a specialized glandular cell type, which has, to some extent, the same properties as nerve cells.Aided by grants from the Swedish Natural Science Research Council.     

Ultrastructural changes in the urophysis of Mollienesia sphenops following adaptation to seawater

Summary The urophysis or neurohemal contact site of the caudal neurosecretory system of Mollienesia sphenops, the black molly, was studied in animals adapted to an artificial seawater environment. This species of fish was chosen for these studies because of its known ability to osmoregulate and its adaptability to the laboratory aquarium. The urophysis of freshwater acclimated mollys contained an abundance of neurosecretory granules. However, in fish subjected to a seawater environment for one week the number of neurosecretory granules was significantly decreased. In addition, there was an increase in blood cell infiltration of the urophysis.Supported by PHS 5429-16-19 (5-23311)The Author wishes to thank Drs. W. Young and J. Wells for their careful reading of this report and W. Boldosser for technical assistance     

A double sequential immunofluorescence method demonstrating the co-localization of urotensins I and II in the caudal neurosecretory system of the teleost,Gillichthys mirabilis

Summary A double immunofluorescence method was devised to localize simultaneously urotensin-I (UI) and -II (UII) immunoreactivities in the caudal neurosecretory system of the goby, Gillichthys mirabilis. In a sequential fashion, sections of the posterior spinal cord and urophysis were treated with antiserum to corticotropin-releasing factor (CRF) that cross-reacts with UI, fluorescein-conjugated sheep anti-rabbit IgG, biotinylated anti-UII and rhodamine-conjugated avidin. UI and UII immunoreactivities appeared to coexist in some neurons and in most fibers and urophysial tissue; the remainder of the fibers and urophysis and the majority of neurons were immunoreactive for CRF/ UI only. No convincing evidence of immunoreactivity for UII only was found. A few nonreactive cells were seen, but these may not be neurosecretory neurons. The two immunoreactive cell types were not segregated topographically, and the intensity of perikaryal immunofluorescence for CRF/UI was variable. To explain these results a hypothesis that all caudal neurosecretory cells may synthesize both UI and UII and that immunoreactive differences may reflect different states of cellular activity, is suggested. This sequential double immunofluorescence method offers several advantages over other techniques and is especially useful for co-localization studies when primary antisera from different species are not available.     

Ultrastructural Study of the Filum Terminate and Caudal Ampulla of the Spinal Cord of Amphioxus (Branchiostoma lanceolatum Pallas)

The filum terminale and caudal ampulla of amphioxus were studied by electron microscopy. The filum terminale consists of ependymal cells whose cilia are directed caudally. Remarkably, nerve fibres course through the filum terminale and caudal ampulla and end on the basal lamina forming neuro-connective structures. Moreover, these nerve boutons are divisible into several classes according to their vesicle content. Boutons containing large dense-cored vesicles are very similar in appearance to the neurosecretory terminals found in the caudal spinal cord of some vertebrates. These observations on nerve fibres suggest that a primitive neurosecretory system similar to the fish urophysis is present in the amphioxus.     

Immunocytochemical localization of urotensin I neurons in the caudal neurosecretory system of the white sucker (Catostomus commersoni)

Summary The localization of urotensin I has been investigated in the caudal neurosecretory system of the white sucker (Catostomus commersoni). The peptide is present in all the cells of the system both large and small, in the large axons passing to the urophysis, and in fine beaded fibres not only within the urophysis but also in a fine plexus lateral to the large cells in the spinal cord proper. The possibility that the caudal neurosecretory system is not a functionally uniform system but rather a collection of dissimilar cells of different synaptic inputs with a common entity, urotensin I, is discussed. Moreover, the feasibility of a urotensin I feedback loop is described.Financial support for this investigation was provided in part by MRC (Canada). K.L. is MRC career investigator; K.L.W, was in receipt of an Alberta Heritage Foundation for Medical Research Fellowship. It is a pleasure to record the valuable technical assistance of Mrs. W. Ho and the dedicated assistance in the collection of the experimental animals by Mrs. Helen Wilson of Nanton, Alberta.     

Immunohistochemical demonstration of urotensins I and II in the caudal neurosecretory system of the Japanese charr,Salvelinus leucomaenis,retained in sea water

This paper is concerned with part of the role and function of the caudal neurosecretory system of the charr,Salvelinus leucomaenis, studied by immunohistochemistry. In order to elucidate the different histologic changes, we examined the immunoreactivities of urotenisn I (UI) and urotensin II (UII) in 3 experimental groups: the feral (river) fish, the fresh-water aquarium-, and sea water aquarium-retained fish. Coexistence of UI and UII was demonstrated in most of the smaller and larger neurons distributed in and near the urophyseal system of all 3 groups. However, some of the larger neurons were immunoreactive only to a single hormone, UI or UII. Merely a few neurons indicated no reactivity for either UI or UII. No such clearcut differences were encountered immunohistochemically in the 3 groups. Neuronal and urophysial immuno-reactivity to UI of feral and fresh-water-retained fish was slightly stronger than that of sea water-retained fish. Moreover, in sea water-retained fish, the intensity of immunoreactivity for UI was variable, and the number of neurons positive for UII only was somewhat larger than that in feral and fresh-water-retained fish. A series of UII-positive cerebrospinal fluid (CSF)-contacting neurons were seen in the ependymal and subependymal layers ventral to the central canal of the spinal cord in every group. These CSF-contacting neurons might constitute another neurosecretory system aside from the ordinary caudal neurosecretory system equipped with urophysis. In contrast to the hypothalamohypophysial neurosecretory system, the caudal neurosecretory system did not show any significant changes among the 3 groups. This suggests that urotensins I and II have no essential role in osmoregulation of the charr.     

Hormone-Carrier-Neurosecretory Granule Association in the Urophysis of the Goby Gillichthys mirabilis*

Nishioka, R. S., Bern, H. A., Gunther, R. L. 1980. Hormone-carrier-neurosecretory granule association in the urophysis of the goby Gillichthys mirabilis. (Department of Zoology and Cancer Research Laboratory, University of California, Berkeley, California, N.S.A.) — Acta zool. (Stockh.) 61(1): 29–38. The caudal neurosecretory system of the mudsucker, Gillichthys mirabilis, was investigated using continuous sucrose density gradient centrifugation, electron microscopy, polyacrylamide gel electrophoresis, and bioassay. A strong light-scattering band near the 41 % sucrose concentration was shown to contain neurosecretory granules by electron microscopy and urotensin II activity by bioassay. Aliquots of this band were run in polyacrylamide gel electrophoresis and the selected regions of the gel containing those bands unique to urophysial tissue were cut out and eluted after the gel had been sliced longitudinally. The eluate from the region of the unique band (rf 0.46) gave the highest urotensin II bioassay activity when compared to adjacent areas. The remaining half of the gel was stained to confirm the localization of the unique bands. Gels made from regions adjacent to the 41 % sucrose concentration showed less stainability of the bands, and eluate of regions from its unique bands contained correspondingly less bioactivity.     

Light,fluorescence and electron microscopic studies on “neurosecretion” in tritonia diomedia bergh (Mollusca,Nudibranchia)

Summary Membrane-limited electron-dense inclusions designated as elementary neurosecretory granules have a characteristic distribution in cerebropleural ganglia of the nudibranch snail Tritonia diomedia. They occur in the neuropile and also in individual nerve fibres, connectives and commissures. These granules have been found neither in perikarya of nerve cells nor in proximal segments of their processes.Specific fluorescence obtained in Tritonia preparations with Sterba's pseudoisocyanin method for neurosecretory products has the same pattern of location.The distribution of stainable material in preparations prepared with ordinary neurosecretory procedures (chrome haematoxylin-phloxin after Gomori-Bargmann and paraldehydefuchsin after Gomori-Gabe) is similar to that described by different authors in other gastropods, but strongly differs from the locationof elementary neurosecretory granules and of pseudoisocyanin-positive material. The adequacy of different histological methods for studying neurosecretion in gastropods is discussed.     

The caudal neurosecretory system of the teleostean Clupea melanostoma

Summary The caudal neurosecretory system of Clupea melanostoma is described. The urophyseal area in this species is merely a spinal cord enlargement divided into two distinct zones: a ventral and ventrolateral vascular zone where neurosecretory material is concentrated, and a dorsal cell-rich area where the perikarya of the neurosecretory cells are found.The hypothesis is advanced that the first-named vascular area has developed into the more differentiated urophysis of the less primitive teleosts while the dorsal cell-rich area has become part of the filum terminale. Two main types of neurosecretory cells are described.This work was supported by grant L 96 Z from the Consejo Nacional de Investigaciones Cientificas y Técnicas.     

Terminal processes of serotonin neurons in the caudal spinal cord of the molly,Poecilia latipinna,project to the leptomeninges and urophysis

Summary The caudal neurosecretory complex of poeciliids has previously been shown to be innervated by extranuclear and intrinsic serotonergic projections. In the present study, immunohistochemical techniques were used to characterize fibers originating from serotonin neurons intrinsic to the caudal spinal cord. Bipolar and multipolar neurons were oriented ventromedially, and contained numerous large granular vesicles. Three types of serotonergic fibers were distinguished based on their distribution and morphology. Intrinsic Type-A fibers branched into varicose segments near the ventrolateral surface of the spinal cord and contacted the basal lamina beneath the leptomeninges. Type-B fibers coursed longitudinally to enter the urophysis, where they diverged and terminated around fenestrated capillaries. Labelled vesicles in Type-A and Type-B terminals were the same size as those in labelled cells and in unlabelled neurosecretory terminals in the urophysis. Type-C small varicose fibers branched within the neuropil of the caudal neurosecretory complex. Serotonin may be secreted into the submeningeal cerebrospinal fluid, the urophysis, and the caudal vein by Type-A and Type-B fibers, whereas, Type-C fibers may be processes of serotonergic interneurons in the neuroendocrine nucleus. The possibility that urotensins I and II or arginine vasotocin were colocalized in the processes of the intrinsic serotonin neurons was investigated immunohistochemically. The negative results of these experiments suggest that serotonin-containing neurons may represent a neurochemically distinct subpopulation in the caudal neurosecretory complex.