ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Keywords: mitochondrion-rich cell ; chloride cell ; euryhalinity ; stenohalinity ; diadromous migration ; Mozambique tilapia ; killifish ; chum salmon ; Japanese eel ; fugu ; Japanese dace ; ion transport
    Description / Table of Contents: 1. Introduction --- 2. Mitochondrion-rich (MR) cells --- 2-1. General characteristics of MR cells --- 2-2. Molecular mechanisms of ion-transporting functions of MR cells --- 3. Euryhalinity and stenohalinity of teleosts --- 4. Mozambique tilapia --- 4-1. MR cells in the yolk-sac membrane of tilapia embryos and larvae --- 4-2. FW- and SW-type MR cells in tilapia embryos and larvae --- 4-3. Functions of multicellular complexes of SW-type MR cells --- 4-4. Functional differentiation of MR cells in the yolk-sac membrane --- 4-5. Functional classification of MR cells in the yolk-sac membrane --- 4-6. "Yolk ball" incubation system --- 4-7. Salinity tolerance of adult tilapia --- 4-8. Possible osmoreception by MR cells --- 5. Killifish --- 5-1. Transitional processes of MR-cell distribution during early life stages --- 5-2. Distinct FW- and SW-type MR cells --- 5-3. Functional alteration and replacement of MR cells --- 5-4. Ion-absorbing mechanisms of MR cells --- 6. Chum salmon --- 6.1. Hypoosmoregulatory ability of chum salmon embryo --- 6-2. Seawater adaptability in chum salmon fry --- 6-3. MR-cell turnover in the gills of chum salmon fry --- 6-4. Loss of hypoosmoregulatory ability in mature chum salmon --- 7. Japanese eel --- 7-1. Epidermal MR cells in embryos and larvae --- 7-2. Ontogenic changes in MR cells during leptocephalus and glass eel stages --- 7-3. MR cells in glass eel acclimated to FW --- 7-4. Gill MR cells in eel cultured in FW and those acclimated to SW --- 7-5. MR cells in yellow and silver eel --- 8. Fugu --- 8-1. Low-salinity tolerance of fugu --- 8-2. Gill MR cells in fugu --- 8-3. Functional significance of prolactin in a marine teleost of fugu --- 8-4. Comparison of growth in fugu reared in 25 and 100% SW. --- 9. Japanese dace --- 9-1. Acid tolerance of Osorezan dace --- 9-2. Molecular mechanisms of acid adaptation --- 10. Conclusions and future perspectives
    Pages: Online-Ressource (62 Seiten)
    ISBN: 1882322X
    Language: English
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Keywords: perfused eel livers ; isolated eel hepatocytes ; cultured eel hepatocytes ; gluconeogenesis ; glycogen synthesis ; glucagon ; lipoprotein synthesis ; ganglioside GM4
    Description / Table of Contents: 1. Introduction --- 2. Eel as an experimental fish for studying liver functions --- 2-1. Availability of eel (Anguilla japonica) as an experimental fish --- 2-2. Perfusion of eel liver --- 2-3. Primary culture of eel hepatocytes --- 2-3A. Isolated eel hepatocytes --- 2-3B. Primary culture of eel hepatocytes --- 3. Glucose metabolisms in eel liver --- 3-1. Gluconeogenesis in rat liver --- 3-2. Gluconeogenesis in eel liver --- 3-2A. Gluconeogenesis by perfused eel liver --- 3-2B. Gluconeogenesis by isolated eel hepatocytes and cultured eel hepatocytes --- 3-3. Phosphoenolpyruvate synthesis pathway in eel liver --- 3-3A. Effects of inhibitors --- 3-3B. Subcellular distribution of enzymes --- 3-3C. Effects of leucine and other amino acids --- 3-3D. Effect of oleic acid --- 3-4. Comparison of PEP synthesis pathways between eel, rat, and pigeon liver --- 3-5. Glycogen metabolisms in eel liver --- 4. Lipoprotein metabolisms in eel liver --- 4-1. Characteristics of fish serum lipoproteins --- 4-2. Lipoproteins secreted by primary cultured eel hepatocytes --- 4-3. Effects of maturation on eel lipoprotein metabolism --- 4-3A. Comparison of body length, body weight, gonad-somatic index, and plasma thyroxine between silver and yellow eels --- 4-3B. Comparison of plasma lipoproteins between silver and yellow eels --- 4-3C. Comparison of lipoprotein synthesis by cultured hepatocytes of silver and yellow eels --- 4-3D. Effect of thyroxine on lipoprotein synthesis by cultured eel hepatocytes --- 4-4. HDL binding to primary cultured eel hepatocytes --- 4-4A. Stimulatory effect of HDL on VLDL-like lipoprotein synthesis and secretion --- 4-4B. ApoAI and apoAII of HDL do not function as a ligand for eel HDL receptor --- 4-4C. Ganglioside of HDL functions as a ligand for an HDL receptor of eel hepatocytes --- 4-4C-1. Ganglioside GM4 isolated from eel serum HDL --- 4-4C-2. GM4 as the ligand for eel HDL receptor --- 4-5. Vitellogenin induction by cultured eel hepatocytes --- 4-5A. Vitellogenin induction by estradiol-17β --- 4-5B. Vitellogenin induction by cultured eel hepatocytes --- 4-5C. Stimulatory effect of HDL on vitellogenin synthesis and secretion --- 5. Discussion --- 5-1. Integrity of a perfused eel liver, isolated and cultured hepatocytes --- 5-2. Gluconeogenesis and glycogen metabolisms in eel liver --- 5-2A. Gluconeogenesis --- 5-2B. Glycogen metabolisms --- 5-3. Lipoprotein metabolisms in eel liver --- 5-3A. Lipoprotein synthesized by cultured eel hepatocytes --- 5-3B. HDL metabolism --- 5-3C. Induction of vitellogenin synthesis by cultured eel hepatocytes. --- 5-4. General Discussion
    Pages: Online-Ressource (57 Seiten)
    ISBN: 1882322X
    Language: English
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: When a fresh specimen of yellowfin tuna Neothunnus albacora was analyzed, the cross-sectional area of ordinary (white) muscle fiber was 3.5 times larger than that of dark muscle. As heating temperature was raised, the shear force of dark muscle became progressively larger than that of ordinary muscle. Simultaneously, the A band in the ultrastructure of both muscles was stained more densely. While the Z line in I band of dark muscle still remained, that of ordinary muscle disappeared completely by heat treatment at 60°C for 30 min. Therefore, the differences in toughness change during heat treatment correlated well with that fiber sizes and ultrastructures of the two types of muscle.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1573-5168
    Keywords: somatolactin ; chum salmon ; spawning migration ; gonadal development ; calcium ; energy metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plasma somatolactin (SL) concentrations were examined in chum salmon in relation to gonadal maturation; immature salmon in the Bering Sea at various stages of maturation, and mature salmon during upstream migration caught at the ocean, bay and river. Plasma SL concentrations as well as plasma prolactin (PRL) and growth hormone (GH) levels in the immature fish caught in the Bering Sea were maintained essentially at similar levels. Plasma SL in mature salmon increased significantly from the fish in the ocean to the fish in the river in both sexes. Although all the fish had fully developed gonads, females completed ovulation while still in the bay, whereas final spermeation in males was achieved after entry into the river. Thus, no clear correlation was seen between plasma SL levels and final gonadal maturation. On the other hand, plasma PRL concentrations in both male and female fish were higher in the fish in the river than those in the ocean and bay, and plasma GH levels were higher in both sexes in the fish in the bay and river than those in the ocean. Plasma levels of triglycerides, glucose, free fatty acids and ionized sodium and calcium were also examined. Significant-negative correlations were seen between plasma SL and plasma ionized calcium in mature male salmon, and between plasma SL and plasma triglycerides in mature female salmon. Although our findings do not rule out the possibility of the involvement of SL in final maturation, the results indicate that SL seems to be involved at least in energy and/or calcium metabolism during the spawning migration.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Fish physiology and biochemistry 7 (1989), S. 337-342 
    ISSN: 1573-5168
    Keywords: parathyroid hormone (PTH) ; calcitonin ; calcitonin gene-related peptide (CGRP) ; hypocalcin ; radioimmunoassay ; immunocytochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Immunocytochemical localization of hypocalcin, a hypocalcemic factor in the corpuscles of Stannius (CS), in American eels was examined at the light (ABC method) and electron microscopic (protein A-gold technique) levels with the specific antiserum raised against purified rainbow trout hypocalcin. Only type 1 cells in the CS were immunoreactive in the light microscopic immunocytochemistry. At the electron microscopic level, however, hypocalcin immunoreactivity was observed in secretory granules of both type 1 and type 2 cells. Our findings may indicate that type 1 cells are the main source of hypocalcin, but that type 2 cells also produce it, suggesting that the presence of two cell types reflects different physiological conditions of a single cell type, rather than functionally different cell types. In addition, we summarize our recent data on the localization of other calcium regulatory, or putative calcium regulatory, hormones in fish: parathyroid hormone, calcitonin and calcitonin gene-related peptide.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1432-0878
    Keywords: Key words: Chloride cell ; Embryo ; Larva ; Yolk-sac membrane ; Seawater adaptation ; Na+ ; K+-ATPase ; Tilapia ; Oreochromis mossambicus (Teleostei)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Morphological changes in the chloride cells (CCs) in the yolk-sac membrane of euryhaline tilapia (Oreochromis mossambicus) embryos and larvae were examined in relation to environmental salinity. Half of a brood of embryos spawned in fresh water (FW) were transferred directly to seawater (SW) 1 day before hatching; the other half was maintained in FW. The embryos and larvae in both FW and SW contained a rich population of CCs in the yolk-sac membrane; the CCs were visualized by whole-mount immunocytochemistry with an antiserum specific for Na+,K+-ATPase. The sectional areas of CCs increased markedly following SW transfer, whereas they remained small in the embryos and larvae maintained in FW. Scanning electron microscopy showed that the apical opening of CCs was enlarged in the fish transferred to SW. Transmission electron microscopy revealed enhanced cellular activity in SW, as evidenced by well-developed mitochondria and tubular systems. The CCs in SW frequently formed a multicellular complex, consisting of a main CC and one or two accessory cells. Accessory cells interdigitated with the main cells and extended their cytoplasmic processes to the apex of the main cell. The three-dimensional arrangement of the cells participating in the complex was identified by confocal laser scanning microscopy. Such complexes were rarely observed in FW fish. The activated CCs in the yolk-sac membrane in the SW fish probably function as ion-extruding sites during embryonic and larval stages until gill CCs become functional.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1432-0878
    Keywords: Calcitonin gene-related peptide (CGRP) ; Small intestine ; Smooth muscle ; Mouse (ICR), rat (Sprague-Dawley), guinea pig, domestic fowl, Iguana iguana (Lacertilia), Rana catesbeiana (Anura), Salmo gairdneri (Teleostei)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Calcitonin gene-related peptide (CGRP) was found extensively in the small intestine of both non-mammalian and mammalian vertebrates using radioimmunoassay and immunocytochemistry. By radioimmunoassay, the levels of CGRP in rats, mice, chickens, bullfrogs and rainbow trout were found to range from 91.5 to 419.1 ng/g tissue. To localize CGRP in the small intestine, we used three different tissue preparations for immunocytochemistry: whole-mount preparations, and frozen and Paraplast sections. The combination of three tissue preparations made it easier to visualize the three-dimensional structure and reduced the possibility of missing the immunoreaction. Immunoreactive cell bodies were found in the plexi in the mammalian species. Dense and regular networks of CGRP fibers were observed in the smooth muscle layers, when examined in whole-mount preparations. In non-mammalian species, however, immunoreactive cell bodies could not be detected, although immunoreactive fibers were present, forming less dense and regular networks. Our results indicate that CGRP-immunoreactive fibers are present in the smooth muscle layers of the intestine from fish to mammals, suggesting that CGRP may be involved in regulating gastrointestinal smooth muscles in vertebrates.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 239 (1985), S. 337-342 
    ISSN: 1432-0878
    Keywords: Protein A-gold ; PAP ; Gonadotrophs ; Goldfish
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The immunocytochemical distribution of gonadotropin (GTH) in the goldfish pituitary gland was studied applying the peroxidase-antiperoxidase (PAP) method and the protein A-gold technique at lightand electron-microscopic levels, respectively, with an antiserum raised against silver carp GTH. In the light-microscopic immunocytochemistry, PAS-positive cells in the proximal pars distalis showed strong reaction with the antiserum. Gold particles were concentrated both on globules (large) and on granules (small) of the gonadotrophs (PAS-positive cells) in the electron-microscopic immunocytochemistry. Other cells in the pituitary gland, including thyrotrophs, displayed no immunoreactivity with the antiserum at the dilutions tested. These results indicate, not only immunocytochemical distribution of GTH both in globules and in granules in the gonadotrophs, but also the high purity of the antigen (silver carp GTH) and specificity of the antiserum.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1432-0878
    Keywords: Corpuscles of Stannius ; Hypocalcin ; Immunohistochemistry ; Carassius auratus ; Hippoglossoides elassodon ; Salmo gairdneri
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In order to identify the cell-type responsible for the production of hypocalcin (the recently isolated hypocalcemic hormone of teleost fish), the corpuscles of Stannius (CS) of trout, flounder and goldfish, were immunocytochemically stained with antisera raised against trout hypocalcin. The secretory granules of the type-1 cells of the CS, considered to be the hypocalcin-producing cells, showed intense immunoreactivity in all species examined. However, in trout and flounder, the secretory granules produced by the type-2 cells, which have been suggested to represent a functionally different cell-type, also showed an intense immunoreactivity. In goldfish, no type-2 cells were observed. We tentatively conclude that type-1 and type-2 cells represent structurally different forms of the same functional cell-type.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 161 (1991), S. 147-153 
    ISSN: 1432-136X
    Keywords: Prolactin ; Growth hormone ; Osmotic pressure ; Pituitary ; Eel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Effects of medium osmotic pressure on the release of prolactin (PRL) and growth hormone (GH) from the pituitary of the Japanese eel, Anguilla japonica, were examined during long-term organ culture in a defined medium. Prolactin and GH release, as measured by homologous radioimmunoassays, increased gradually for 7 days during incubation in isosmotic medium (295 mOsmolal). On day 7, 3 to 5 times more PRL and GH were released than on day 1. The amount of GH released was about 100 times greater than that of PRL. Electron microscopic observation revealed that both PRL and GH cells were in good condition after 7 days incubation. The reduction of medium osmotic pressure from 295 (isosmotic) to 235 or 260 mOsmolal significantly stimulated PRL release for 4 days. By contrast, an increase in medium osmolality from 295 to 360 mOsmolal was without effect. These treatments produced no significant alterations in GH release. The stimulatory effect of hyposmotic medium (235 mOsmolal) was no longer evident by 12 h after the pituitaries were returned to isosmotic medium. The isosmotic but low-sodium medium, prepared by adding mannitol to the hyposmotic medium, did not stimulate PRL release from the pituitary. These results indicate that plasma osmolality may be an important physiological factor controlling PRL release during freshwater adaptation of the eel.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...