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  • 1
    ISSN: 0014-5793
    Keywords: Messenger RNA ; Nephron ; Polymerase chain reaction ; Receptor ; β-Adrenergic
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    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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  • 3
    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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  • 4
    ISSN: 1432-2013
    Keywords: BCECF Cell pH Corneal endothelial cells Na+-HCO3– cotransporter RT-PCR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Although bicarbonate transport in corneal endothelium has been suggested to be coupled to Na+, the underlying molecular mechanism has not been clarified. In the present study we investigated whether a recently cloned Na+-HCO3 – cotransporter (NBC-1) is responsible for this process, and, if so, whether the endothelium expresses a separate isoform or one of the other two isoforms that have recently been identified (kNBC-1 from kidney and pNBC-1 from pancreas). Using primers designed for specific and common regions we demonstrated by reverse transcriptase polymerase chain reaction (RT-PCR) that both kNBC-1 and pNBC-1 are expressed in cultured human corneal endothelial cells. In addition functional studies with a pH-sensitive fluorescence probe were performed. In the presence of HCO3 –/CO2 a pH regulatory process was demonstrated which depends on the presence of Na+ and membrane potential, but is independent of Cl– and is inhibited by the disulfonic stilbene DIDS. These results support the presence of NBC-1 as the major bicarbonate transport system in corneal endothelium.
    Type of Medium: Electronic Resource
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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 422 (1992), S. 55-59 
    ISSN: 1432-2013
    Keywords: Renal proximal tubule ; S3 segment ; Cl−/HCO 3 − exchange ; Carbonic anhydrase inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Cell pH (pHi) and cell membrane potential (V b) were measured in isolated S3 segments of rabbit renal proximal tubule with double-barrelled microelectrodes to search for a possible effect of the carbonic anhydrase inhibitor, acetazolamide (ACZ), on Cl−/HCO 3 − exchange in the basolateral cell membrane. ACZ was found to retard and reduce the pHi response to bath Cl− removal reversibly with half-maximal inhibition at 0.42 mmol/l and a rather flat concentration dependence (Hill coefficient ≈ 0.36). To determine whether the retardation resulted from inhibition of cytoplasmic carbonic anhydrase, which might have delayed the attainment of HCO 3 − /CO2 equilibrium, we have measured the response of pHi to step changes in PCO2 in the presence and absence of ACZ. ACZ greatly retarded the pHi response to CO2 steps; however, the concentration dependence differed (half-maximal inhibition at 18 μmol/l) and even at maximal ACZ concentrations the response to CO2 steps was more than twice as fast as the response to Cl− replacement. Since, in addition, the ACZ inhibition of Cl−/HCO 3 − exchange could not be overcome by increasing PCO2 we conclude that the ACZ effect on Cl−/HCO 3 − exchange in rabbit proximal tubule S3 segments does not result from inhibition of cytosolic or membrane-bound carbonic anhydrase, but from a direct interaction with the exchanger molecule.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 422 (1992), S. 60-65 
    ISSN: 1432-2013
    Keywords: Renal proximal tubule ; S2 segment ; Rheogenic Na+-HCO 3 − cotransport ; Cl−/HCO 3 − exchange ; Carbonic anhydrase inhibitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The influence of the carbonic anhydrase inhibitor acetazolamide (ACZ) was investigated on HCO 3 − transport mechanisms in the basolateral cell membrane of rabbit renal proximal tubule. Experiments were performed on isolated S2 segments using double-barrelled microelectrodes to measure cell membrane potential (V b) and cell pH (pHi) during step changes in bath perfusate ion concentrations. Peritubular application of ACZ (1 mmol/l) reduced the initial V b response to 10∶1 reduction of bath HCO 3 − concentration only slightly, from +53.8±4.2 mV to+49.1±0.3 mV (n=5), but caused an intermittent overshooting repolarization in the secondary V b response. In conjunction with these effects it left the initial pHi response virtually unchanged but induced a secondary slow acidification. These observation indicate that — under the present experimental conditions — ACZ does not block the Na+-HCO 3 − cotransporter but acts via inhibition of cytosolic carbonic anhydrase. This was confirmed by studying the effect of elevated intracellular HCO 3 − concentrations under reduced flux conditions and by comparing the concentration dependence of the V b response with the inhibition kinetics of cytosolic carbonic anhydrase. In contrast, peritubular ACZ inhibited Na+-independent Cl−/HCO 3 − exchange in the basolateral cell membrane of S2 segments directly in a similar way to that described in the preceding publication for S3 segments.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2013
    Keywords: Isolated renal proximal tubule ; Na+-HCO3 − cotransport ; Coupling stoichiometry ; Rheogenicity ; Super-Nernst slope
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract All the relevant literature reports indicate that net rates of salt and water absorption and cell membrane potentials (V b) are lower, but intracellular Na+ concentration is higher in rabbit renal proximal tubule in vitro than in rat proximal tubule in vivo. Since the different driving forces should influence basolateral Na+-HCO3 − cotransport we have studied the operation of the cotransporter in isolated rabbit renal proximal tubule in vitro with special emphasis on the stoichiometry of flux coupling (q). Using conventional and ion-selective intracellular microelectrodes three series of experiments were performed: (a) we determined the V b response to a 2∶1 reduction of bath HCO3 − or Na+ concentration, (b) we determined initial efflux rates of HCO3 − or Na+ ions in response to a sudden 10∶1 reduction of bath HCO3 − concentration, and (c) we collapsed the tubules and determined electrochemical driving forces of Na+ and HCO3 − across the basolateral cell membrane under conditions approaching zero net flux in the control state in the presence of Ba2+- and in Cl−-free solutions. All measurements concurrently yielded a coupling ratio of approximately two HCO3 − ions to one Na+ ion (q=2). This result contrasts with the ratio q=3, which we have previously observed in similar experiments on rat renal proximal tubule in vivo [Yoshitomi et al. (1985) Pflügers Arch 405:360] and which was also observed on rabbit renal basolateral cell membrane vesicles in vitro [Soleimani et al. (1987) J Clin Invest 79:1276]. This indicates that — depending on the functional state of the cell — the Na+-HCO3 − cotransporter can operate with variable stoichiometry and suggests that it transports either 1 Na+ + 1 HCO3 − + 1 CO3 2− ion [Soleimani and Aronson (1989) J Biol Chem 264:18 302] or 1 Na+ + 2 HCO3 − ions.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2013
    Keywords: Key words Isolated renal proximal tubule ; Metabolic substrates ; Na/K pump ; Amiloride-inhibitable K+ conductance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Isolated microperfused rabbit renal proximal tubule S2 segments, if incubated in conventional substrate containing HCO3 –Ringer solution, exhibit lower cell membrane potentials (V b) and elevated intracellular Na+ concentrations ([Na]i) compared to rat tubules in vivo. Assuming that these and other differences reflect insufficient metabolic and/or hormonal stimulation of the cells, we have used microelectrode techniques to test whether improving substrate supply and applying norepinephrine (NE, to compensate for the missing nerve supply) reverts V b and [Na]i to values observed in vivo. Application of D-glucose (5.5 mmol/l) and additional application of pyruvate, lactate, or L-alanine (each 10 mmol/l), or bathing the tubules in Dulbecco’s modified Eagle’s tissue culture medium (DMEM) significantly increased V b and, whenever tested, reduced [Na]i as compared to substrate-free or D-glucose-containing control solution and these effects could be prevented – as tested in the case of pyruvate – by inhibition of the Na/K pump with ouabain. However, high concentrations of acetate, β-hydroxybutyrate, or L-glutamine had no significant effect. The largest effect was obtained with joint application of DMEM and NE (10 μmol/l) which increased V b from –42.8 ± 1.3 mV (SEM) to –55.3 ± 2.5 mV (n = 11). Interestingly we noticed that under the latter conditions the V b response to bath application of 1 mmol/l amiloride virtually disappeared, i.e. it changed from a depolarization of +14.6 ± 1.4 mV (in D-glucose Ringer solution) to +0.6 ± 0.7 mV (in DMEM plus NE) (n = 8), with some tubules showing even a small hyperpolarization. The latter implies partial restoration of the in vivo behaviour, since in experiments on rat proximal tubules in vivo amiloride regularly hyperpolarized the cells (by –3.4 ± 0.76 mV, n = 5). Obviously under conventional in vitro conditions an amiloride-inhibitable K+ conductance is activated which is inactive in vivo and also inactivates under improved conditions in vitro. In agreement with observations reported in the subsequent publication our results demonstrate that isolated proximal tubules undergo functional alterations which may be largely prevented by improved metabolic and stimulatory incubation conditions.
    Type of Medium: Electronic Resource
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