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  • 1975-1979  (2)
  • Microperfusion  (1)
  • Proximal tubule  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 374 (1978), S. 243-248 
    ISSN: 1432-2013
    Keywords: Oxalate ; Wistar rat ; Microperfusion ; Microinfusion ; Organic acid secretion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Renal transport of14C-oxalate was studied in the rat by clearance and micropuncture techniques. The ultrafilterability of oxalate was 0.98±0.02 (n=7). Fractional clearance of oxalate was significantly above unity in antidiuresis and volume expansion: mean 1.24 ±0.04 (n=115). Pyrazinamide (1.1·10−3 mol/kg BW) and probenecid (0.35·10−3 mol/kg BW) had no significant effect on oxalate clearance. P-aminohippurate (1.45·10−3 mol/kg BW) and urate (0.48 ·10−3 mol/kg BW) depressed the fractional clearance of oxalate significantly from 116 to 91 and from 125 to 90%, respectively. Excess excretion of14C-oxalate over3H-inulin was invariably demonstrable in peritubular microperfusion experiments (n=5) and in microinfusions underneath the kidney capsule (n=4). Together with the first 50% of3H-inulin 58±2% of the total14C-oxalate were excreted in the peritubular microperfusions, and 64±3% in the subcapsular microinfusions. In tubular microinfusion experiments (n=36) urinary14C-oxalate recovery was almost complete after early proximal microinfusion (93±4%) and complete after late proximal microinfusion (102±4%). In continuous microperfusion experiments of proximal tubules (n=42) a small but highly significant outflux of14C-oxalate of 7% per mm perfusion distance was found. The data suggest that oxalate is freely filterable at the glomerular site. A small but significant amount of oxalate is reabsorbed in the proximal nephron. Most likely at the same site and in the pars recta oxalate is secreted and tubular load increased to 124% of filtered load. This amount is excreted in final urine. The secretion of oxalate is inhibited by organic acids which are known to be secreted by the proximal tubule and the pars recta.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Proximal tubule ; Micropuncture ; Carbonic anhydrase ; Benzolamide ; Acidification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Luminal pH in early and late proximal tubules was recorded continuously with antimony microelectrodes before and during carbonic anhydrase inhibition. Following i.v. application of benzolamide (25 μmol/kg BW), luminal pH decreased almost immediately in early proximal tubules (ΔpH −0.42±0.06 SEM), but increased in late proximal tubules (ΔpH +0.27±0.06). Urinary pH increased (ΔpH +1.6±0.16) after a delay of some 30 s. Similar results, i.e. decrease of pH in early and increase of pH in late proximal tubules, were obtained, when benzolamide containing solutions were microinfused into early proximal tubules or superfused on the nephron surface. In contrast, luminal pH decreased in late proximal tubules, when benzolamide was microinfused into the same nephron segment. The decrease of luminal pH indicates inhibition of luminally active carbonic anhydrase, leading to delayed buffering of secreted hydrogen ions. The increase of luminal pH in late proximal tubules may be attributed to several factors including increased delivery of bicarbonate, impaired bicarbonate exit at the antiluminal membrane and decreased hydrogen ion formation in the tubular cell due to inhibition of cellular carbonic anhydrase.
    Type of Medium: Electronic Resource
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