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  • 1
    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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  • 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.
    Type of Medium: Electronic Resource
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