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  • 1
    ISSN: 1432-2013
    Keywords: BCECF H+ secretion HCO3– absorption Isolated renal proximal tubule Luminal pH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. In the present experiments on microdissected tubules of rabbit kidney we present a refined stop-flow method for determining the rate of HCO3 – absorption (J HCO3) or H+ secretion (J H) that can be applied to isolated microperfused tubules. Using the pH-sensitive indicator dye BCECF (2',7'-bis [2-carboxyethyl]-5[6]-carboxyfluorescein) the luminal perfusate pH is continuously measured with a microspectrofluorometric set-up, and the pH change following a sudden stop of perfusion is analysed. Because the tubules partially collapse after stop-flow the calculation of fluxes requires a correction for volume loss. This is achieved by referring all fluxes to the remaining luminal volume, which can be estimated from the decay of the 440 nm reference fluorescence. During perfusion of the lumen with pure HCO3 – Ringer solution, and of the bath with the same solution but containing 5.5 mmol/l d-glucose as metabolic substrate, J HCO3 averaged 4.4±0.2 pmol cm–1·s–1 (n=40) and 13.4±0.8 pmol·cm–1·s–1 (n=5) in proximal straight tubules (PST) and in proximal convoluted tubules respectively. These values agree very well with data obtained in other laboratories with the picapnotherm technique. The present method has the advantage of requiring fewer micromanipulations and a shorter measuring time, thus allowing regulatory changes in J HCO3 to be analysed. Moreover it does not involve measurements of radioactivity, and it also allows J H to be measured in HCO3 –-free solutions which in PST averaged 0.9 pmol·cm–1·s–1 (n=8) in the present experiments.
    Type of Medium: Electronic Resource
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  • 2
    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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