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  • 1
    Online Resource
    Online Resource
    Wiley ; 2000
    In:  Physiologia Plantarum Vol. 110, No. 2 ( 2000-10), p. 151-151
    In: Physiologia Plantarum, Wiley, Vol. 110, No. 2 ( 2000-10), p. 151-151
    Type of Medium: Online Resource
    ISSN: 0031-9317
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2000
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    detail.hit.zdb_id: 2020837-6
    SSG: 12
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  • 2
    In: Nephron Experimental Nephrology, S. Karger AG, Vol. 97, No. 1 ( 2004-11-17), p. e1-e16
    Abstract: 〈 i 〉 Background/Aim: 〈 /i 〉 In a rat model, lithium treatment is associated with polyuria and severe downregulation of aquaporin-2 (AQP2) protein in the inner medulla (IM) or in the whole kidney. However, it is not known (1) to what extent this downregulation occurs at the mRNA level; (2) whether the main sodium transporter of the nephron, Na,K-ATPase, is regulated in parallel at the mRNA level, and (3) whether lithium treatment induces zonal or segmental differences in AQP2 and Na,K-ATPase mRNA levels. 〈 i 〉 Method: 〈 /i 〉 We examined the changes in mRNA expression levels for AQP2 and Na,K-ATPase in kidney cortex, inner stripe of the outer medulla (ISOM), and IM of rats treated with lithium orally using semiquantitative Northern blot analyses and in situ hybridization at the light and electron microscopic levels. 〈 i 〉 Results: 〈 /i 〉 The AQP2 mRNA levels decreased significantly (p 〈 0.01) in lithium-treated rats to 37 ± 4% in the cortex, to 17 ± 4% in the ISOM, and to 23 ± 5% in the IM, while the Na,K-ATPase mRNA levels were not altered in the cortex, but were significantly (p 〈 0.05) altered in the ISOM (144 ± 15% after 10 days, but 68 ± 4% after 4 weeks) and in the IM (63 ± 8% after 10 days, but normalized after 4 weeks). In situ hybridization showed reduced levels of AQP2 mRNA in all zones of the kidney, but the Na,K-ATPase mRNA expressions were slightly decreased only in IM collecting ducts. At the ultrastructural level, principal cells in the IM collecting ducts showed slight hypertrophy, but no cell damage after 4 weeks of lithium treatment. The results demonstrate substantial downregulation of AQP2 at the mRNA level throughout the collecting duct in experimental lithium-induced nephrogenic dabetes insipidus and moderately decreased Na,K-ATPase mRNA levels in the ISOM and in the IM. 〈 i 〉 Conclusion: 〈 /i 〉 The results suggest that decreased mRNA expressions of AQP2 and Na,K-ATPase contribute to the development of lithium-induced nephrogenic diabetes insipidus.
    Type of Medium: Online Resource
    ISSN: 1660-2129
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2004
    detail.hit.zdb_id: 2098337-2
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  • 3
    In: Physiologia Plantarum, Wiley, Vol. 112, No. 3 ( 2001-07), p. 359-371
    Type of Medium: Online Resource
    ISSN: 0031-9317
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2001
    detail.hit.zdb_id: 208872-1
    detail.hit.zdb_id: 2020837-6
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Elsevier BV ; 2005
    In:  Journal of Biological Chemistry Vol. 280, No. 45 ( 2005-11), p. 37717-37724
    In: Journal of Biological Chemistry, Elsevier BV, Vol. 280, No. 45 ( 2005-11), p. 37717-37724
    Type of Medium: Online Resource
    ISSN: 0021-9258
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2005
    detail.hit.zdb_id: 2141744-1
    detail.hit.zdb_id: 1474604-9
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  • 5
    In: Nephron Physiology, S. Karger AG, Vol. 109, No. 1 ( 2008-5-5), p. p1-p10
    Abstract: 〈 i 〉 Background: 〈 /i 〉 The genomic response to adaptation of IMCD3 cells to hypertonicity results in both upregulation and downregulation of a variety of genes. 〈 i 〉 Method: 〈 /i 〉 The present study was undertaken to assess the metabonomic and proteomic response of IMCD3 cells that have been chronically adapted to hypertonicity (600 and 900 mosm/kg H 〈 sub 〉 2 〈 /sub 〉 O) as compared to cells under isotonic conditions. 〈 i 〉 Results: 〈 /i 〉 Adaptation of IMCD3 cells to hypertonic conditions resulted in a change of a wide range of organic osmolytes, including sorbitol (+8,291%), betaine (+1,099%), myo-inositol (+669%), taurine (+113%) and glycerophosphorylcholine (+61%). Evaluation of the polyol pathway for sorbitol production revealed a reduction in sorbitol dehydrogenase and an increase in aldose reductase mRNA in adapted cells. Proteome analysis revealed increased expression of six glycolytic proteins, including malic enzyme and pyruvate carboxylase, indicating the activation of the pyruvate shunt and changes in glucose metabolism. This study showed that the observed reduction in cell replication could possibly reflect a redirection of cellular energy from cell growth and replication to maintenance of intracellular ion levels in chronically adapted cells. 〈 i 〉 Conclusion: 〈 /i 〉 The combined metabonomic and proteomic analysis was shown to be a very helpful tool for the analysis of the effects caused by chronic adaptation to hypertonicity. It made it possible to better evaluate the importance of certain changes that occur in the process of adaptation.
    Type of Medium: Online Resource
    ISSN: 1660-2137
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2008
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  • 6
    Online Resource
    Online Resource
    American Physiological Society ; 2006
    In:  American Journal of Physiology-Renal Physiology Vol. 291, No. 5 ( 2006-11), p. F1033-F1044
    In: American Journal of Physiology-Renal Physiology, American Physiological Society, Vol. 291, No. 5 ( 2006-11), p. F1033-F1044
    Abstract: The γ-subunit of Na-K-ATPase (FXYD2) and corticosteroid hormone-induced factor (CHIF; FXYD4) are considered pump regulators in kidney tubules. The aim of this study was to expand the information about their locations in the kidney medulla and to evaluate their importance for electrolyte excretion in an animal model. The cellular and subcellular locations and abundances of γ and CHIF in the medulla of control and sodium-depleted rats were analyzed by immunofluorescence and immunoelectron microscopy and semiquantitative Western blotting. The results showed that antibodies against the γ-subunit COOH terminus and splice variant γ a , but not splice variant γ b , labeled intercalated cells, but not principal cells, in the initial part of the inner medullary collecting duct (IMCD1). In subsequent segments (IMCD2 and IMCD3), all principal cells exhibited distinct basolateral labeling for both the γ-subunit COOH terminus, splice variant γ a , and CHIF. Splice variant γ b was abundant in the inner stripe of the outer medulla but absent in the inner medulla (IM). Double labeling by high-resolution immunoelectron microscopy showed close structural association between CHIF and the Na-K-ATPase α 1 -subunit in basolateral membranes. The present observations provide new information about the cellular and subcellular locations of γ and CHIF in the renal medulla and show a new γ variant in the IM. Extensive NaCl depletion did not induce significant changes in the locations or abundances of the γ-subunit COOH terminus and CHIF in different kidney zones. We conclude that the unchanged levels of these two FXYD proteins suggest that they are not primary determinants for urine electrolyte composition during NaCl depletion.
    Type of Medium: Online Resource
    ISSN: 1931-857X , 1522-1466
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2006
    detail.hit.zdb_id: 1477287-5
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  • 7
    Online Resource
    Online Resource
    American Physiological Society ; 2007
    In:  American Journal of Physiology-Renal Physiology Vol. 293, No. 3 ( 2007-09), p. F662-F669
    In: American Journal of Physiology-Renal Physiology, American Physiological Society, Vol. 293, No. 3 ( 2007-09), p. F662-F669
    Abstract: The distal convoluted tubule (DCT) Na + -Cl − cotransporter (NCC), the target of thiazide diuretics, is responsible for the reabsorption of 5–10% of filtered NaCl. The aim of this study was to test the hypothesis that acute infusion of the angiotensin-converting enzyme (ACE) inhibitor captopril (at 12 μg/min) for 20 min provokes trafficking of NCC from apical plasma membranes (APM) to subapical cytoplasmic vesicles (SCV), which is reversed by acute ANG II infusion (ANG II at 20 ng·kg −1 ·min −1 along with 12 μg/min captopril) for 20 min in male Sprague-Dawley rats (250–350 g). By immuno-electron microscopy using an anti-NCC (D. Ellison) 71.5 ± SD 4.9% of the NCC gold labeling was associated with the APM in control, sham operated, and infused rats, while captopril infusion reduced NCC in APM to 54.9 ± 6.9% ( P 〈 0.001) and markedly increased immunogold labeling of SCV. Subsequent infusion of ANG II with captopril restored NCC immunogold labeling of APM to 72.4 ± 4.2%, that is, 20% of the total NCC trafficked between APM and SCV. Likewise, on density gradients of cortex, captopril provoked redistribution of 27.3% of total NCC from low-density APM-enriched membranes to higher-density membranes and ANG II+captopril restored 20.3% of the NCC to APM-enriched fractions. Redistribution occurred independent of a change in NCC total abundance. In conclusion, this study demonstrates that ACE inhibition provokes acute trafficking of NCC out of the plasma membrane, which likely decreases DCT Na + reabsorption, while ANG II provokes rapid trafficking of NCC from stores in subapical vesicles to the plasma membrane, which likely increases DCT Na + reabsorption.
    Type of Medium: Online Resource
    ISSN: 1931-857X , 1522-1466
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2007
    detail.hit.zdb_id: 1477287-5
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  • 8
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 986, No. 1 ( 2003-04), p. 401-409
    Abstract: A bstract : The γ subunit of Na,K‐ATPase and CHIF both belong to the FXYD single‐membrane‐spanning protein family and have been suggested to have regulatory functions in kidney tubules. CHIF is known to be present in the collecting duct, and γ has been demonstrated in several segments of the rat kidney tubule, but never clearly in the inner medullary collecting duct (IMCD). Here, we demonstrate the cellular and subcellular localization of the γ subunit and CHIF in the IMCD in inner medulla by using Western blotting, laser‐scanning confocal immunofluorescence, and immunoelectron microscopy. In the initial quarter of the IMCD (next to the outer medulla), antibodies against the C‐terminal of γ as well as splice variant γa labeled the basolateral surface of intercalated cells (ICs), while principal cells (PCs) remained unlabeled. In the middle segment of the IMCD, all PCs exhibited distinct basolateral staining for the γC‐terminal as well as γa and CHIF. Immunoelectron microscopy showed that the γC‐terminal and CHIF were associated with the inner leaflet of the basolateral plasma membrane in the labeled cells. Immunoblotting demonstrated the presence of both the γC‐terminal and γa in inner medullary tissue. However, splice variant γb was not detected in inner medulla by immunocytochemistry or immunoblotting. The present observations demonstrate that the Na,K‐ATPase γ subunit and CHIF are strategically located in the inner medulla to participate in the fine‐tuning of urine ion composition through the regulation of the Na,K‐ATPase activity in the IMCD.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2003
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    detail.hit.zdb_id: 211003-9
    detail.hit.zdb_id: 2071584-5
    SSG: 11
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  • 9
    Online Resource
    Online Resource
    American Physiological Society ; 2005
    In:  American Journal of Physiology-Renal Physiology Vol. 288, No. 4 ( 2005-04), p. F650-F657
    In: American Journal of Physiology-Renal Physiology, American Physiological Society, Vol. 288, No. 4 ( 2005-04), p. F650-F657
    Abstract: Hypertonicity mediated by chloride upregulates the expression of the γ-subunit of Na-K-ATPase in cultured cells derived from the murine inner medullary collecting duct (IMCD3; Capasso JM, Rivard CJ, Enomoto LM, and Berl T. Proc Natl Acad Sci USA 100: 6428–6433, 2003). The purpose of this study was to examine the cellular locations and the time course of γ-subunit expression after long-term adaptation and acute hypertonic challenges induced with different salts. Cells were analyzed by confocal immunofluorescence and immunoelectron microscopy with antibodies against the COOH terminus of the Na-K-ATPase γ-subunit or the γ b splice variant. Cells grown in 300 mosmol/kgH 2 O showed no immunoreactivity for the γ-subunit, whereas cells adapted to 600 or 900 mosmol/kgH 2 O demonstrated distinct reactivity located at the plasma membrane of all cells. IMCD3 cell cultures acutely challenged to 550 mosmol/kgH 2 O with sodium chloride or choline chloride showed incorporation of γ into plasma membrane 12 h after osmotic challenge and distinct membrane staining in ∼40% of the cells 48 h after osmotic shock. In contrast, challenging the IMCD3 cells to 550 mosmol/kgH 2 O by addition of sodium acetate did not result in expression of the γ-subunit in the membranes of surviving cells after 48 h. The present results demonstrate that the Na-K-ATPase γ-subunit becomes incorporated into the basolateral membrane of IMCD3 cells after both acute hyperosmotic challenge and hyperosmotic adaptation. We conclude that the γ-subunit has an important role in the function of Na-K-ATPase to sustain the cellular cation balance over the plasma membrane in a hypertonic environment.
    Type of Medium: Online Resource
    ISSN: 1931-857X , 1522-1466
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2005
    detail.hit.zdb_id: 1477287-5
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  • 10
    In: Journal of Biological Chemistry, Elsevier BV, Vol. 282, No. 9 ( 2007-03), p. 6644-6652
    Type of Medium: Online Resource
    ISSN: 0021-9258
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2007
    detail.hit.zdb_id: 2141744-1
    detail.hit.zdb_id: 1474604-9
    SSG: 12
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