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  • 1
    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.
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  • 2
    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.
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  • 3
    ISSN: 1432-2013
    Keywords: Key words ATP ; DIDS ; Intracellular and extracellular Na+ ; Renal Na+-HCO3 ; cotransporter ; Transport stoichiometry ; Xenopus laevis oocytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The rat kidney Na+-HCO3 – cotransporter (rkNBC) was expressed in Xenopus laevis oocytes and transport via rkNBC was studied with the patch-clamp technique in giant inside/out (i/o) or outside/out (o/o) membrane patches. The current/voltage (I/V) relation(s) of individual patches was(were) determined in solutions containing only Na+ and HCO3 – as permeable ions. The current carried by rkNBC (I NBC) was identified by its response to changing bath Na+ concentration(s) and quantified as the current blocked by 4,4’-diisothiocyanatostilbene disulfonate (DIDS). The stoichiometric ratio (q) of HCO3 – to Na+ transport was determined from zero-current (reversal) potentials. The results and conclusions are as follows. First, DIDS (250 µmol/l) blocks I NBC irreversibly from both the extracellular and the intracellular surface. Second, in the presence of Na+ and HCO3 – concentration gradients similar to those which rkNBC usually encounters in tubular cells, q was close to 2. The same value was also observed when the HCO3 – concentration was 25 mmol/l throughout, but the Na+ concentration was either high (100 mmol/l) or low (10 mmol/l) on the extracellular or intracellular surface of the patch. These data demonstrate that in the oocyte cell membrane rkNBC works with q=2 as previously observed in a study of isolated microperfused tubules (Seki et al., Pflügers Arch 425:409, 1993), however, they do not exclude the possibility that in a different membrane and cytoplasmic environment rkNBC may operate with a different stoichiometry. Third, in most experiments bath application of up to 2 mmol/l ATP increased the DIDS-inhibitable conductance of i/o patches by up to twofold with a half saturation constant near 0.5 mmol/l. This increase was not associated with a change in q, nor with a shift in the I/V relationship which would suggest induction of active transport (pump current). Since the effect persisted after ATP removal and was not observed with the non-hydrolysable ATP analogue AMP-PNP, it is possible that rkNBC is activated by phosphorylation via protein kinases that might adhere to the cytoplasmic surface of the membrane patch.
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  • 4
    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.
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  • 5
    ISSN: 1432-2013
    Keywords: Key words Isolated proximal tubule ; Na-HCO3 cotransport ; Acetazolamide ; Norepinephrine ; Cellular substrate supply ; CO32 ; /pH disequilibrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  In the preceding publication we reported that some transport properties of proximal tubules perfused in vitro differ from those of tubules perfused in vivo, and that the in vivo function can be largely recuperated by improved metabolic substrate supply and stimulation with norepinephrine (NE). Since we have previously observed that the basolateral Na-HCO3-cotransporter operates with an overall stoichiometric ratio of q ≈3 HCO3 – :1 Na+ in vivo, but with q ≈2 HCO3 –:1 Na+ in vitro and that it responds differently in both cases to acetazolamide (ACZ), we have now tested whether the cotransporter can regain its in vivo function in vitro if the incubation conditions are improved. Cell membrane potentials (V b) and cell pH (pHi) were measured with microelectrodes and microfluorimetric techniques on isolated S2 segments of rabbit proximal tubule and the instantaneous V b response to a 2:1 reduction of bath HCO3 –or Na+ concentration was determinded. (ΔV b)HCO3 and (ΔV b)Na averaged 13.1 ± 0.9 mV (SEM) and 6.9 ± 0.5 mV in D-glucose-containing control HCO3-Ringer solution and decreased respectively to 10.1 ± 0.5 mV and 3.8 ± 0.2 mV (n = 8) after incubation in tissue culture medium and NE (10–5 mmol/l). These data imply that q increased from 1.9 to 2.7. Concomitantly the tubules became susceptible to ACZ (1 mmol/l), which reduced (ΔV b)HCO3 in control conditions only to 94.6 ± 1.2% but under improved incubation conditions to 64.5 ± 2.4%. As verified in voltage divider measurements the latter reduction was not caused by activation of a basolateral K+ conductance. The results indicate that improved incubation conditions can at least partially revert cotransport function towards that of the in vivo state. The effect of ACZ may be explained if in the improved state 1 CO3 2–+ 1 HCO3 –+ 1 Na+ are cotransported, in which case inhibition of carbonic anhydrase (CA) may cause a CO3 2–/pH disequilibrium to develop in the basal labyrinth which impedes the cotransport. Under conventional incubation conditions, however, when only 2 HCO3 –+ 1 Na+ are cotransported no such disequilibrium should develop irrespective of whether CA is active or inhibited.
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