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  • Calcium channel  (1)
  • Electronic books.  (1)
  • Glycerophosphorylcholine  (1)
  • 1990-1994  (2)
  • 1985-1989  (1)
Publikationsart
Sprache
Erscheinungszeitraum
  • 1990-1994  (2)
  • 1985-1989  (1)
Jahr
  • 1
    Online-Ressource
    Online-Ressource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Schlagwort(e): Liver-Physiology-Congresses. ; Electronic books.
    Beschreibung / Inhaltsverzeichnis: Proceedings of a Symposium, held May 8-11, 1988 at Schloß Ringberg, Rottach Egern.
    Materialart: Online-Ressource
    Seiten: 1 online resource (440 pages)
    Ausgabe: 1st ed.
    ISBN: 9783642742477
    Serie: Proceedings in Life Sciences Series
    Sprache: Englisch
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    ISSN: 1432-2013
    Schlagwort(e): Intracellular calcium ; Volume regulation ; Calcium channel ; Inner medullary collecting duct
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract There is ample evidence of calcium being an intracellular second messenger during volume regulatory processes in various cells including inner medullary collecting duct (IMCD) cells. Therefore, we measured intracellular calcium concentrations (Cai under anisotonic conditions in primary cultures of IMCD cells using the Fura-2 technique. Basal steady-state calcium at 600 mosmol/l was found to be 110±4 nmol/l; n=119. Exposure to hypotonic medium (300 mosmol/l, reduction of sucrose) resulted, within 1 min, in a strong increase in calcium to 563±87 nmol/l (n=7; P〈0.01), followed by a decrease over 4–6 min to twice the initial values. The calcium increase was smaller (260±14 nmol/l; n=5; P〈0.05) when the osmotic pressure was decreased by reducing NaCl instead of sucrose. Stepwise reduction of osmolarity to either 500 or 400 mosmol/l increased calcium by a significantly smaller extent, suggesting a threshold for calcium influx between 400 and 300 mosmol/l. In hypotonic calcium-free solutions no significant increase in calcium was observed. Verapamil (40 μmol/l), D-600 (40 μmol/l), diltiazem (40 μmol/l), and nifedipine (40 μmol/l) inhibited the hypotonically induced calcium influx in decreasing order of potency. Lanthanum (La3+) and gadolinium (Gd3+) had no effect. Membrane depolarization by incubation in potassium-rich solution diminished calcium influx. Preincubation with cytochalasin B (50 μmol/l for 30 min) resulted in a lower basal calcium level and attenuated the calcium increase during hypotonic shock. These results demonstrate an increased calcium influx during hypotonic shock in IMCD cells in culture mediated by channels whose nature (stretch activated and/ or voltage dependent) remains to be determined. The transient increase in Cai in turn may trigger inorganic and organic osmolyte fluxes observed previously.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Pflügers Archiv 417 (1990), S. 324-328 
    ISSN: 1432-2013
    Schlagwort(e): Choline ; Inner medullary collecting duct ; Organic osmolytes ; Osmoregulation ; Glycerophosphorylcholine
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Glycerophosphorylcholine (GPC) plays an important role in the osmoregulation of the renal inner medulla. Under hyperosmotic conditions, a striking increase in cellular GPC content is observed. In order to characterize the cellular events involved in GPC metabolism, we have studied the uptake of choline, a precursor of GPC, by freshly isolated rat inner medullary collecting duct (IMCD) cells at 300 mosmol/l. Choline uptake occurred by a single transport system with an apparent affinity (K m) of 80 μM and a maximal velocity (V max) of 120 pmol/μl cell water/min. Hemicholinium-3, ethanolamine and N,N-dimethylethanolamine were potent inhibitors, but betaine had no effect. Choline uptake was not altered by the replacement of Na+ with N-methylglucamine+, suggesting a sodium-independent process. Addition of 50 mM KCl to the incubation medium to reduce the cell membrane potential inhibited choline uptake by 19±4% after 10 min. Increasing the extracellular osmolarity to 600 or 900 mosmol/l had no effect on the kinetic parameters of choline uptake. These results suggest that choline uptake into IMCD cells occurs by a sodium-independent transport system driven by the inside negative cell membrane potential. Furthermore, the increase in the GPC content under hyperosmotic conditions is not associated with increased activity of the transport systems of biosynthetic precursors.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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