Skip to main content
Erschienen in: Urolithiasis 3/2019

14.06.2018 | Original Paper

Oxalate transport by the mouse intestine in vitro is not affected by chronic challenges to systemic acid–base homeostasis

verfasst von: Jonathan M. Whittamore, Marguerite Hatch

Erschienen in: Urolithiasis | Ausgabe 3/2019

Einloggen, um Zugang zu erhalten

Abstract

In rats, we recently showed how a chronic metabolic acidosis simultaneously reduced urinary oxalate excretion and promoted oxalate secretion by the distal colon leading to the proposition that acid–base disturbances may trigger changes to renal and intestinal oxalate handling. The present study sought to reproduce and extend these observations using the mouse model, where the availability of targeted gene knockouts (KOs) would offer future opportunities to reveal some of the underlying transporters and mechanisms involved. Mice were provided with a sustained load of acid (NH4Cl), base (NaHCO3) or the carbonic anhydrase inhibitor acetazolamide (ATZ) for 7 days after which time the impacts on urinary oxalate excretion and its transport by the intestine were evaluated. Mice consuming NH4Cl developed a metabolic acidosis but urinary oxalate was only reduced 46% and not statistically different from the control group, while provision of NaHCO3 provoked a significant 2.6-fold increase in oxalate excretion. For mice receiving ATZ, the rate of urinary oxalate excretion did not change significantly. Critically, none of these treatments altered the fluxes of oxalate (or chloride) across the distal ileum, cecum or distal colon. Hence, we were unable to produce the same effects of a metabolic acidosis in mice that we had previously found in rats, failing to find any evidence of the ‘gut-kidney axis’ influencing oxalate handling in response to various acid–base challenges. Despite the potential advantages offered by KO mice, this model species is not suitable for exploring how acid–base status regulates oxalate handling between the kidney and intestine.
Literatur
4.
Zurück zum Zitat Costello JF, Smith M, Stolarski C, Sadovnic MJ (1992) Extrarenal clearance of oxalate increases with progression of renal-failure in the rat. J Am Soc Nephrol 3(5):1098–1104PubMed Costello JF, Smith M, Stolarski C, Sadovnic MJ (1992) Extrarenal clearance of oxalate increases with progression of renal-failure in the rat. J Am Soc Nephrol 3(5):1098–1104PubMed
5.
Zurück zum Zitat Hatch M, Freel RW, Vaziri ND (1994) Intestinal excretion of oxalate in chronic-renal-failure. J Am Soc Nephrol 5(6):1339–1343PubMed Hatch M, Freel RW, Vaziri ND (1994) Intestinal excretion of oxalate in chronic-renal-failure. J Am Soc Nephrol 5(6):1339–1343PubMed
11.
Zurück zum Zitat Charney AN, Goldfarb DS, Dagher PC (1995) Metabolic disorders associated with gastrointestinal disease. In: Arieff AI, DeFronzo RA (eds) Fluid, electrolyte, and acid–base disorders, 2nd edn. Churchill Livingstone, New York, pp 813–836 Charney AN, Goldfarb DS, Dagher PC (1995) Metabolic disorders associated with gastrointestinal disease. In: Arieff AI, DeFronzo RA (eds) Fluid, electrolyte, and acid–base disorders, 2nd edn. Churchill Livingstone, New York, pp 813–836
13.
Zurück zum Zitat Charney AN, Feldman GM (1984) Systemic acid–base-disorders and intestinal electrolyte transport. Am J Physiol Gastrointest Liver Physiol 247(1):G1–G12CrossRef Charney AN, Feldman GM (1984) Systemic acid–base-disorders and intestinal electrolyte transport. Am J Physiol Gastrointest Liver Physiol 247(1):G1–G12CrossRef
22.
Zurück zum Zitat Alesutan I, Daryadel A, Mohebbi N, Pelzl L, Leibrock C, Voelkl J, Bourgeois S, Dossena S, Nofziger C, Paulmichl M, Wagner CA, Lang F (2011) Impact of bicarbonate, ammonium chloride, and acetazolamide on hepatic and renal SLC26A4 expression. Cell Physiol Biochem 28(3):553–558. https://doi.org/10.1159/000335114 CrossRefPubMed Alesutan I, Daryadel A, Mohebbi N, Pelzl L, Leibrock C, Voelkl J, Bourgeois S, Dossena S, Nofziger C, Paulmichl M, Wagner CA, Lang F (2011) Impact of bicarbonate, ammonium chloride, and acetazolamide on hepatic and renal SLC26A4 expression. Cell Physiol Biochem 28(3):553–558. https://​doi.​org/​10.​1159/​000335114 CrossRefPubMed
26.
Zurück zum Zitat Ribayamercado JD, Gershoff SN (1984) Effects of sugars and vitamin-b-6 deficiency on oxalate synthesis in rats. J Nutr 114(8):1447–1453CrossRef Ribayamercado JD, Gershoff SN (1984) Effects of sugars and vitamin-b-6 deficiency on oxalate synthesis in rats. J Nutr 114(8):1447–1453CrossRef
29.
Zurück zum Zitat Freel RW, Hatch M, Earnest DL, Goldner AM (1980) Oxalate transport across the isolated rat colon. A re-examination. Biochem Biophys Acta 600(3):838–843CrossRefPubMed Freel RW, Hatch M, Earnest DL, Goldner AM (1980) Oxalate transport across the isolated rat colon. A re-examination. Biochem Biophys Acta 600(3):838–843CrossRefPubMed
32.
Zurück zum Zitat Wagner JD, Kurtin P, Charney AN (1985) Effect of systemic acid–base-disorders on colonic intracellular ph and ion-transport. Am J Physiol Gastrointest Liver Physiol 249(1):G39–G47CrossRef Wagner JD, Kurtin P, Charney AN (1985) Effect of systemic acid–base-disorders on colonic intracellular ph and ion-transport. Am J Physiol Gastrointest Liver Physiol 249(1):G39–G47CrossRef
33.
Zurück zum Zitat Feldman GM (1989) Effect of chronic metabolic-acidosis on net electrolyte transport in rat colon. Am J Physiol Gastrointest Liver Physiol 256(6):G1036–G1040CrossRef Feldman GM (1989) Effect of chronic metabolic-acidosis on net electrolyte transport in rat colon. Am J Physiol Gastrointest Liver Physiol 256(6):G1036–G1040CrossRef
34.
Zurück zum Zitat Goldfarb DS, Sly WS, Waheed A, Charney AN (2000) Acid–base effects on electrolyte transport in CA II-deficient mouse colon. Am J Physiol Gastrointest Liver Physiol 278(3):G409–G415CrossRefPubMed Goldfarb DS, Sly WS, Waheed A, Charney AN (2000) Acid–base effects on electrolyte transport in CA II-deficient mouse colon. Am J Physiol Gastrointest Liver Physiol 278(3):G409–G415CrossRefPubMed
36.
Zurück zum Zitat Brion LP, Cammer W, Satlin LM, Suarez C, Zavilowitz BJ, Schuster VL (1997) Expression of carbonic anhydrase IV in carbonic anhydrase II-deficient mice. Am J Physiol Renal Physiol 273(2):F234–F245CrossRef Brion LP, Cammer W, Satlin LM, Suarez C, Zavilowitz BJ, Schuster VL (1997) Expression of carbonic anhydrase IV in carbonic anhydrase II-deficient mice. Am J Physiol Renal Physiol 273(2):F234–F245CrossRef
37.
Zurück zum Zitat Lien YHH, Lai LW (1998) Respiratory acidosis in carbonic anhydrase II-deficient mice. Am J Physiol Lung Cell Mol Physiol 274(2):L301–L304CrossRef Lien YHH, Lai LW (1998) Respiratory acidosis in carbonic anhydrase II-deficient mice. Am J Physiol Lung Cell Mol Physiol 274(2):L301–L304CrossRef
38.
Zurück zum Zitat Packer RK, Curry CA, Brown KM (1995) Urinary organic anion excretion in response to dietary acid and base loading. J Am Soc Nephrol 5(8):1624–1629PubMed Packer RK, Curry CA, Brown KM (1995) Urinary organic anion excretion in response to dietary acid and base loading. J Am Soc Nephrol 5(8):1624–1629PubMed
41.
Zurück zum Zitat Lemann J, Hornick LJ, Pleuss JA, Gray RW (1989) Oxalate is overestimated in alkaline urines collected during administration of bicarbonate with no specimen pH adjustment. Clin Chem 35(10):2107–2110PubMed Lemann J, Hornick LJ, Pleuss JA, Gray RW (1989) Oxalate is overestimated in alkaline urines collected during administration of bicarbonate with no specimen pH adjustment. Clin Chem 35(10):2107–2110PubMed
42.
Zurück zum Zitat Mazzachi BC, Teubner JK, Ryall RL (1984) Factors affecting measurement of urinary oxalate. Clin Chem 30(8):1339–1343PubMed Mazzachi BC, Teubner JK, Ryall RL (1984) Factors affecting measurement of urinary oxalate. Clin Chem 30(8):1339–1343PubMed
43.
Zurück zum Zitat Chalmers AH, Cowley DM, McWhinney BC (1985) Stability of ascorbate in urine—relevance to analyses for ascorbate and oxalate. Clin Chem 31(10):1703–1705PubMed Chalmers AH, Cowley DM, McWhinney BC (1985) Stability of ascorbate in urine—relevance to analyses for ascorbate and oxalate. Clin Chem 31(10):1703–1705PubMed
45.
Zurück zum Zitat Miki K, Sudo A (1998) Effect of urine pH, storage time, and temperature on stability of catecholamines, cortisol, and creatinine. Clin Chem 44(8):1759–1762PubMed Miki K, Sudo A (1998) Effect of urine pH, storage time, and temperature on stability of catecholamines, cortisol, and creatinine. Clin Chem 44(8):1759–1762PubMed
46.
Zurück zum Zitat Wyss M, Kaddurah-Daouk R (2000) Creatine and creatinine metabolism. Physiol Rev 80(3):1107–1213CrossRef Wyss M, Kaddurah-Daouk R (2000) Creatine and creatinine metabolism. Physiol Rev 80(3):1107–1213CrossRef
47.
Zurück zum Zitat Perrone RD, Madias NE, Levey AS (1992) Serum creatinine as an index of renal-function - new insights into old concepts. Clin Chem 38(10):1933–1953PubMed Perrone RD, Madias NE, Levey AS (1992) Serum creatinine as an index of renal-function - new insights into old concepts. Clin Chem 38(10):1933–1953PubMed
48.
Zurück zum Zitat Hamm LL, Simon EE (1987) Roles and mechanisms of urinary buffer excretion. Am J Physiol Renal Physiol 253(4):F595–F605CrossRef Hamm LL, Simon EE (1987) Roles and mechanisms of urinary buffer excretion. Am J Physiol Renal Physiol 253(4):F595–F605CrossRef
49.
Zurück zum Zitat Wamberg S, Hansen AC, Engel K, Kildeberg P (1978) Balance of net base in rat. 3. Effects of oral sodium-bicarbonate and sodium citrate loading. Biol Neonate 34(1–2):24–31CrossRefPubMed Wamberg S, Hansen AC, Engel K, Kildeberg P (1978) Balance of net base in rat. 3. Effects of oral sodium-bicarbonate and sodium citrate loading. Biol Neonate 34(1–2):24–31CrossRefPubMed
50.
Zurück zum Zitat Oster JR, Stemmer CL, Perez GO, Vaamonde CA (1988) Comparison of the effects of sodium-bicarbonate versus sodium-citrate on renal acid excretion. Miner Electrol Metab 14(2–3):97–102 Oster JR, Stemmer CL, Perez GO, Vaamonde CA (1988) Comparison of the effects of sodium-bicarbonate versus sodium-citrate on renal acid excretion. Miner Electrol Metab 14(2–3):97–102
51.
Zurück zum Zitat Brown JC, Packer RK, Knepper MA (1989) Role of organic-anions in renal response to dietary acid and base loads. Am J Physiol Renal Physiol 257(2):F170–F176CrossRef Brown JC, Packer RK, Knepper MA (1989) Role of organic-anions in renal response to dietary acid and base loads. Am J Physiol Renal Physiol 257(2):F170–F176CrossRef
54.
Zurück zum Zitat Hood VL (1985) pH regulation of endogenous acid production in subjects with chronic ketoacidosis. Am J Physiol Renal Physiol 249(2):F220–F226CrossRef Hood VL (1985) pH regulation of endogenous acid production in subjects with chronic ketoacidosis. Am J Physiol Renal Physiol 249(2):F220–F226CrossRef
55.
Zurück zum Zitat Lindinger MI, Franklin TW, Lands LC, Pedersen PK, Welsh DG, Heigenhauser GJF (2000) NaHCO3 and KHCO3 ingestion rapidly increases renal electrolyte excretion in humans. J Appl Physiol 88(2):540–550CrossRefPubMed Lindinger MI, Franklin TW, Lands LC, Pedersen PK, Welsh DG, Heigenhauser GJF (2000) NaHCO3 and KHCO3 ingestion rapidly increases renal electrolyte excretion in humans. J Appl Physiol 88(2):540–550CrossRefPubMed
56.
Zurück zum Zitat Khanna A, Kurtzman NA (2006) Metabolic alkalosis. J Nephrol 19:S86–S96PubMed Khanna A, Kurtzman NA (2006) Metabolic alkalosis. J Nephrol 19:S86–S96PubMed
57.
Zurück zum Zitat Maren TH (1967) Carbonic anhydrase—chemistry physiology and inhibition. Physiol Rev 47(4):595–781CrossRefPubMed Maren TH (1967) Carbonic anhydrase—chemistry physiology and inhibition. Physiol Rev 47(4):595–781CrossRefPubMed
62.
Zurück zum Zitat Ohana E, Shcheynikov N, Moe OW, Muallem S (2013) SLC26A6 and NaDC-1 transporters interact to regulate oxalate and citrate homeostasis. J Am Soc Nephrol 24(10):1617–1626CrossRefPubMedPubMedCentral Ohana E, Shcheynikov N, Moe OW, Muallem S (2013) SLC26A6 and NaDC-1 transporters interact to regulate oxalate and citrate homeostasis. J Am Soc Nephrol 24(10):1617–1626CrossRefPubMedPubMedCentral
63.
Zurück zum Zitat Maren TH (1977) Use of inhibitors in physiological studies of carbonic-anhydrase. Am J Physiol Renal Physiol 232(4):F291–F297CrossRef Maren TH (1977) Use of inhibitors in physiological studies of carbonic-anhydrase. Am J Physiol Renal Physiol 232(4):F291–F297CrossRef
67.
Zurück zum Zitat Higashihara E, Nutahara K, Takeuchi T, Shoji N, Araie M, Aso Y (1991) Calcium-metabolism in acidotic patients induced by carbonic-anhydrase inhibitors—responses to citrate. J Urol 145(5):942–948CrossRefPubMed Higashihara E, Nutahara K, Takeuchi T, Shoji N, Araie M, Aso Y (1991) Calcium-metabolism in acidotic patients induced by carbonic-anhydrase inhibitors—responses to citrate. J Urol 145(5):942–948CrossRefPubMed
Metadaten
Titel
Oxalate transport by the mouse intestine in vitro is not affected by chronic challenges to systemic acid–base homeostasis
verfasst von
Jonathan M. Whittamore
Marguerite Hatch
Publikationsdatum
14.06.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Urolithiasis / Ausgabe 3/2019
Print ISSN: 2194-7228
Elektronische ISSN: 2194-7236
DOI
https://doi.org/10.1007/s00240-018-1067-5

Weitere Artikel der Ausgabe 3/2019

Urolithiasis 3/2019 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

Stufenschema weist Prostatakarzinom zuverlässig nach

22.04.2024 Prostatakarzinom Nachrichten

Erst PSA-Test, dann Kallikrein-Score, schließlich MRT und Biopsie – ein vierstufiges Screening-Schema kann die Zahl der unnötigen Prostatabiopsien erheblich reduzieren: Die Hälfte der Männer, die in einer finnischen Studie eine Biopsie benötigten, hatte einen hochgradigen Tumor.

Harnwegsinfektprophylaxe: Es geht auch ohne Antibiotika

20.04.2024 EAU 2024 Kongressbericht

Beim chronischen Harnwegsinfekt bei Frauen wird bisher meist eine Antibiotikaprophylaxe eingesetzt. Angesichts der zunehmenden Antibiotikaresistenz erweist sich das Antiseptikum Methenamin-Hippurat als vielversprechende Alternative, so die Auswertung einer randomisierten kontrollierten Studie.

Update Urologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.