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  • Cell buffer capacity  (1)
  • Isolated proximal tubule Metabolic substrates Norepinephrine Tissue culture media Tubular bicarbonate absorption  (1)
  • 1
    ISSN: 1432-2013
    Keywords: Rabbit renal proximal tubule ; S3 segment ; Basolateral cell membrane-Cl−/HCO3 − exchange ; Cell buffer capacity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Isolated microperfused S3 segments of rabbit renal proximal tubule were investigated with pH-sensitive double-barrelled intracellular microelectrodes to determine whether the Cl−/base exchanger, which we have previously identified in the basolateral cell membrane of this segment requires HCO3 − or can also work in CO2/HCO3 − free conditions. Cell pH (pHi) was measured in response to sudden substitution of bath Cl− by gluconate. In control solutions containing 25 mmol/l HCO3 pHi increased initially by 5.0±0.3 × 10−3 unit/s but after perfusion with CO2/HCO3 −-free solutions pHi of the same cells increased only by 1.3±0.2 × 10−3 unit/s in response to Cl− substitution. From measurements of the cellular buffering power it was calculated that the control base flux had fallen drastically from 3.7±0.3 to 0.3±0.1 × 10−12 mols/s·cm tubule length. To test whether the remaining flux might have resulted from metabolic CO2, oxidative metabolism was poisoned with cyanide (5 mmol/l). This abolished the pH change (ΔpHi) in CO2/HCO3 −-free solutions, but did not affect the pH shift in the presence of HCO3 −. The data indicate that basolateral Cl−/base exchange in S3 segment requires HCO3 − to operate. A model in which HCO3 − absorption proceeds in form of OH− and CO2 can be largely excluded.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Isolated proximal tubule Metabolic substrates Norepinephrine Tissue culture media Tubular bicarbonate absorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Using a new stop-flow perfusion technique with microspectrofluorometric determination of luminal fluid pH, we have studied which substrates or incubation conditions allow isolated rabbit proximal tubules to attain in-vivo-like rates of HCO3 – absorption (J HCO3) and maximal responses of J HCO3 to norepinephrine (NE). Essentially three incubation media were tested: plasma-like HCO3 –-Ringer solution containing 5 mmol/l d-glucose (G-Ringer sol.), the same solution also containing 10 mmol/l lactate and 5 mmol/l l-alanine, (LAG-Ringer sol.), and two tissue culture media (DMEM and RPMI 1640). Compared to G-Ringer sol., application of LAG-Ringer sol. in the bath and/or lumen, or application of DMEM or RPMI 1640 in the bath either slightly increased or decreased J HCO3 with borderline significance. However, RPMI 1640 plus 1 mmol/l pyruvate stimulated J HCO3 by 55%. While NE (10–5 mol/l), if applied in G-Ringer sol., had no effect, in the presence of LAG-Ringer sol. it increased J HCO3 by ≅40%, and in the presence of DMEM or RPMI 1640 it increased J HCO3 by ≅100%. This stimulation by NE followed Michaelis–Menten kinetics with an EC50 value of 0.25 µmol/l and was probably mediated by α1-adrenergic receptors. Additional cell pH measurements suggest that NE stimulates the basolateral Na+-HCO3 – cotransporter which then becomes susceptible to inhibition by cAMP. We conclude that incubation in tissue culture media allows isolated proximal tubules to maintain a better functional state than the commonly used solutions with unphysiologically high substrate concentrations.
    Type of Medium: Electronic Resource
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