Literature DB >> 35552

pH and bicarbonate effects on mitochondrial anion accumulation. Proposed mechanism for changes in renal metabolite levels in acute acid-base disturbances.

D P Simpson, S R Hager.   

Abstract

Mitochondria from rabbit and dog renal cortex were incubated with 1 mM (14)C-weak acid anions in media containing low (10 mM) or high (40 mM) concentrations of bicarbonate and the steady-state accumulation of labeled anion in the matrix was measured. In the absence of an energy source, no concentration of (14)C-anion in the mitochondrial matrix space was present, but the anion concentration was significantly higher at low- than at high-bicarbonate concentration. Addition of an energy source, usually ascorbate plus tetramethyl-p-phenylenediamine, led to increases in matrix space anion levels and to accentuation of the difference in anion uptake between low- and high-bicarbonate media, so that two to four times as much anion was present at low- than at high-bicarbonate concentrations. The anions affected included substrates for which inner membrane carriers are present in mitochondria, such as citrate, alpha-ketoglutarate, malate, and glutamate, as well as substances which diffuse passively across the inner membrane such as acetate and formate. When a nonbicarbonate medium buffered with Hepes was used, pH change did not alter anion uptake although anion concentrations exceeding those in the medium still developed when an energy source was present. The difference in mitochondrial anion accumulation between low- and high-bicarbonate levels diminished with decreasing temperature or with increasing anion concentration in the medium. Estimation of intramitochondrial pH with [(14)C]5,5-dimethyl-oxazolidine-2,4-dione showed that the pH gradient across the inner mitochondrial membrane was significantly greater with 10 than with 40 mM bicarbonate in the medium.A hypothesis is described that relates this effect of pH and bicarbonate on mitochondrial anion accumulation to the very rapid changes in substrate levels in renal cortex, which develop when acute metabolic acidosis or alkalosis is produced in the intact animal. It is suggested that an abrupt fall in systemic pH and bicarbonate is associated with a shift in substrate in renal cortex out of the cytoplasm and into mitochondria, where some of the added substrate is metabolized. Reduction in the size of the cytoplasmic pool of substrate occurs with relatively little accompanying change in the size of the mitochondrial pool, thus causing a net reduction in the total tissue pool. This mechanism accounts for the reduction in tissue levels of many mitochondrial substrates observed acutely in metabolic acidosis. In metabolic alkalosis, reversal of these effects leads to expansion of the cytoplasmic pool, thereby resulting in the rise in tissue levels of substrates which occurs in this condition.

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Year:  1979        PMID: 35552      PMCID: PMC372005          DOI: 10.1172/JCI109353

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  20 in total

1.  TISSUE CITRATE LEVELS AND CITRATE UTILIZATION AFTER SODIUM BICARBONATE ADMINISTRATION.

Authors:  D P SIMPSON
Journal:  Proc Soc Exp Biol Med       Date:  1963-11

2.  The effects of changes in acid-base balance on urinary citrate in the rat.

Authors:  M A CRAWFORD; M D MILNE; B H SCRIBNER
Journal:  J Physiol       Date:  1959-12       Impact factor: 5.182

Review 3.  Recent advances in renal tubular biochemistry.

Authors:  J S Stoff; F H Epstein; R Narins; A S Relman
Journal:  Annu Rev Physiol       Date:  1976       Impact factor: 19.318

4.  The measurement of transmembrane electrochemical proton gradients.

Authors:  H Rottenberg
Journal:  J Bioenerg       Date:  1975-05

5.  Acute effects of acidosis on ammoniagenic pathways in the kidneys of the intact rat.

Authors:  R G Narins; A S Relman
Journal:  Am J Physiol       Date:  1974-10

6.  Parathyroid hormone and renal cell metabolism.

Authors:  N Nagata; H Rasmussen
Journal:  Biochemistry       Date:  1968-10       Impact factor: 3.162

7.  Acid-base behavior of separated canine renal tubule cells.

Authors:  A Struyvenberg; R B Morrison; A S Relman
Journal:  Am J Physiol       Date:  1968-05

8.  The effect of steroids and ammonium chloride acidosis on phosphoenolpyruvate carboxykinase in rat kidney cortex. II. The kinetics of enzyme induction.

Authors:  I D Longshaw; G A Alleyne; C I Pogson
Journal:  J Clin Invest       Date:  1972-09       Impact factor: 14.808

9.  Glutamine transport and metabolism by mitochondria from dog renal cortex. General properties and response to acidosis and alkalosis.

Authors:  D P Simpson; W Adam
Journal:  J Biol Chem       Date:  1975-10-25       Impact factor: 5.157

10.  Renal metabolic response to acid base changes. I. Enzymatic control of ammoniagenesis in the rat.

Authors:  G A Alleyne; G H Scullard
Journal:  J Clin Invest       Date:  1969-02       Impact factor: 14.808

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  8 in total

1.  Acid Stimulation of the Citrate Transporter NaDC-1 Requires Pyk2 and ERK1/2 Signaling Pathways.

Authors:  Miriam Zacchia; Xuefei Tian; Enrica Zona; Robert J Alpern; Patricia A Preisig
Journal:  J Am Soc Nephrol       Date:  2018-04-20       Impact factor: 10.121

2.  Effects of chloride and extracellular fluid volume on bicarbonate reabsorption along the nephron in metabolic alkalosis in the rat. Reassessment of the classical hypothesis of the pathogenesis of metabolic alkalosis.

Authors:  J H Galla; D N Bonduris; R G Luke
Journal:  J Clin Invest       Date:  1987-07       Impact factor: 14.808

3.  Adenosine triphosphate citrate lyase mediates hypocitraturia in rats.

Authors:  J Z Melnick; P A Srere; N A Elshourbagy; O W Moe; P A Preisig; R J Alpern
Journal:  J Clin Invest       Date:  1996-11-15       Impact factor: 14.808

4.  Higher net acid excretion is associated with a lower risk of kidney disease progression in patients with diabetes.

Authors:  Julia J Scialla; John Asplin; Mirela Dobre; Alex R Chang; James Lash; Chi-Yuan Hsu; Radhakrishna R Kallem; L Lee Hamm; Harold I Feldman; Jing Chen; Lawrence J Appel; Cheryl A M Anderson; Myles Wolf
Journal:  Kidney Int       Date:  2016-12-01       Impact factor: 10.612

5.  Segmental chloride and fluid handling during correction of chloride-depletion alkalosis without volume expansion in the rat.

Authors:  J H Galla; D N Bonduris; S L Dumbauld; R G Luke
Journal:  J Clin Invest       Date:  1984-01       Impact factor: 14.808

6.  Citrate inhibition of rat-kidney cortex phosphofructokinase.

Authors:  M M Sola; F J Oliver; R Salto; M Gutiérrez; A Vargas
Journal:  Mol Cell Biochem       Date:  1994-06-29       Impact factor: 3.396

7.  The purine nucleotide cycle in the regulation of ammoniagenesis during induction and cessation of chronic acidosis in the rat kidney.

Authors:  R T Bogusky; K A Steele; L M Lowenstein
Journal:  Biochem J       Date:  1981-04-15       Impact factor: 3.857

8.  Cyclic AMP produced inside mitochondria regulates oxidative phosphorylation.

Authors:  Rebeca Acin-Perez; Eric Salazar; Margarita Kamenetsky; Jochen Buck; Lonny R Levin; Giovanni Manfredi
Journal:  Cell Metab       Date:  2009-03       Impact factor: 27.287

  8 in total

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