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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric nephrology 2 (1988), S. 477-484 
    ISSN: 1432-198X
    Keywords: Proximal tubule ; Sodium-cotransport systems ; Organic anion transport ; l-glutamate transport ; Electrogenicity ; Parsrecta ; Pars convoluta
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This contribution first reviews the distribution of transport systems within the plasma membrane of the proximal tubule cell (polarity), with particular emphasis on transport systems located in the basal-lateral plasma membranes and on the role of cascade coupling in tubular transport. Then, the differences between transport systems in the pars convoluta and the pars recta of the proximal tubule are discussed (diversity). Finally, evidence is presented that changes in the microenvironment of sodium cotransport systems can alter the mode of operation of the transporter (plasticity). The two examples mainly addressed are the sodium-d-glucose and the sodium-glutamate cotransport system.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 417 (1990), S. 324-328 
    ISSN: 1432-2013
    Keywords: Choline ; Inner medullary collecting duct ; Organic osmolytes ; Osmoregulation ; Glycerophosphorylcholine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: 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.
    Type of Medium: Electronic Resource
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