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Effect of chronic accumulation of aluminum on renal function, cortical renal oxidative stress and cortical renal organic anion transport in rats

  • Inorganic Compounds
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Abstract

The aim of the present work was to study the nephrotoxicity of aluminum lactate administered for 3 months (0.57 mg/100 g bodyweight aluminum, i.p., three times per week) to male Wistar rats. Renal function was studied after 6 weeks of treatment (urine was obtained from rats in metabolic cages) and at the end of the treatment using clearance techniques. Another group of rats was used as kidneys donors at the end of treatment. The renal cortex was separated and homogenized to determine glutathione (GSH) level, glutathione S-transferase (GST) activity and lipid peroxidation (LPO) level. Renal cortex slices were also used to study the p-aminohippuric acid (PAH) accumulation during steady-state conditions and the kinetics of uptake process. Clearance results, at the end of the treatment, indicated that renal functions in treated-rats were not different from those measured in control rats, although the renal concentration parameters differ when they were measured in treated rats after 24 h of food and water deprivation. Balances of water and sodium were also modified at both 1.5 and 3 months of treatment. The activity of alkaline phosphatase (AP) relative to inulin excreted in urine was significantly impaired: controls 2.2±0.6 IUI/mg, Al-treated 5.1±0.5 IU/mg, P<0.05. These data indicated that proximal tubular cells were loosing apical brush border membranes. Data obtained in cortex homogenates indicated that both GSH and GST activity were significantly decreased, and a significant increase of LPO was noted simultaneously in Al-treated rats. Renal accumulation of PAH, estimated as slice-to-medium ratio, decreased significantly in the Al-treated rats: control rats 3.06±0.02 (n=12), Al-treated rats 2.26±0.04 (n=12), P<0.0001. The maximal rate of uptake was also diminished in treated rats, while the apparent affinity remained unchanged. All these results indicate that aluminum accumulation in renal tissue affects cellular metabolism, promotes oxidative stress and induces alterations in renal tubular PAH transport, together with an impairment in sodium and water balance only detected under conditions of water deprivation, without other evident changes in glomerular filtration rate or other global functions measured by clearance techniques at least at this time of chronic toxicity.

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References

  • Alfrey AC (1980) Metabolism and toxicity of aluminum in renal failure. Am J Clin Nutr 33:1509–1516

    Google Scholar 

  • Berthold R, Herman M, Savory J, Carpenter R, Sturgill CB, Katsetos CD, Vandenberg SR, Wills M (1989) A long-term intravenous model of aluminum maltol toxicity in rabbits: tissue distribution, hepatic, renal and neuronal cytoskeletal changes associated with systemic exposure. Toxicol Appl Pharmacol 98:58–74

    PubMed  Google Scholar 

  • Burnatowska-Hledin MA, Mayor GH, Lau K (1985) Renal handling of aluminum in the rat: clearance and micropuncture studies. Am J Physiol 249:F192–F197

    CAS  PubMed  Google Scholar 

  • Cacini W, Yokel RA (1988) Accumulation of aluminum by rabbit renal cortex. Res Commun Chem Pathol Pharmacol 59:93–105

    CAS  PubMed  Google Scholar 

  • Commandeur JN, Stijntjes GJ, Vermeulen NP (1995) Enzymes and transport systems involved in the formation and disposition of glutathione S-conjugates. Role in bioactivation and detoxication mechanisms of xenobiotics. Pharmacol Rev 47:271–330

    CAS  PubMed  Google Scholar 

  • Cross RT, Taggart, JV (1950) Renal tubular transport: accumulation of p-aminohippurate by rabbit kidney slices. Am J Physiol 161:181–190

    CAS  Google Scholar 

  • Cucarella C, Montoliu C, Hermenegildo C, Saez R, Manzo L, Minana MD, Felipo V (1998) Chronic exposure to aluminum impairs neuronal glutamate–nitric oxide–cyclic GMP pathway. J Neurochem 70:1609–1614

    CAS  PubMed  Google Scholar 

  • Ebina Y, Okada S, Hamazaki S, Midorikawa O (1984) Liver, kidney and central nervous system toxicity of aluminum given intraperitoneally to rats: a multiple dose subchronic study using aluminum nitriloacetate. Toxicol Appl Pharmacol 75:211–218

    CAS  PubMed  Google Scholar 

  • Ecelbarger CA, MacNeil GG, Greger JL (1994a) Importance of kidney function and duration of exposure on aluminum accumulation in mature rats. Nutr Res 14:577–586

    CAS  Google Scholar 

  • Ecelbarger CA, MacNeil GG, Greger JL (1994b) Tissue aluminum accumulation and toxic consequences in rats chronically fed aluminum with and without citrate. J Agric Food Chem 42:2220–2224

    CAS  Google Scholar 

  • Elías MM, Comin EJ, Grosman ME, Galeazzi SA, Rodriguez Garay EA (1982) Inhibitory effect of unconjugated bilirubin on p-aminohippurate transport in rat kidney cortex slices. Biochim Biophys Acta 693:265–272

    PubMed  Google Scholar 

  • Ellman GL (1959) Tissue sulphydryls groups. Arch Biochem Biophys 82:70–73

    CAS  Google Scholar 

  • El-Maraghy SA, Gad MZ, Fahim AT, Hamdy MA, (2001) Effect of cadmium and aluminum intake on the antioxidant status and lipid peroxidation in rats tissues. J Biochem Mol Toxicol 15:207–214

    Article  CAS  PubMed  Google Scholar 

  • Foulkes EC (1971) Effects of heavy metals on renal aspartate transport and the nature of solute movement in kidney cortex slices. Biochim Biophys Acta 241:815–822

    Article  CAS  PubMed  Google Scholar 

  • Girardi G, Elías MM (1991) Effectiveness of N-acetylcysteine in protecting mercuric chloride-induced nephrotoxicity. Toxicology 67:155–164

    Article  CAS  PubMed  Google Scholar 

  • Girardi G, Torres AM, Elías MM (1989) The implication of renal glutathione levels in mercuric chloride nephrotoxicity. Toxicology 58:187–195

    Article  PubMed  Google Scholar 

  • Gómez Alonso C, Fernández Martín JL, Menéndez Rodríguez P, Fernández Soto Y, Virgos MJ, Cannata JB (1990) Aluminum body burden with normal renal function: risk of oral intoxication. Nefrología 10:386–392

  • Habig WH, Pabst MJ, Jakoby WB (1974) Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Biol Chem 249:7130–7139

    CAS  PubMed  Google Scholar 

  • Jeffery EH, Abreo K, Burgess E, Cannata JB, Greger JL (1996) Systemic aluminum toxicity: effects on bone, hematopoietic tissue and kidney. J Toxicol Environ Health 48:649–665

    Article  CAS  PubMed  Google Scholar 

  • Lin JL, Kou MT, Leu ML (1996) Effect of low-term low-dose aluminum-containing agents on hemoglobin synthesis in patients with chronic renal insufficiency. Nephron 74:33–38

    Google Scholar 

  • Lohr JW, Willisky GR, Acara MA (1998) Renal drug metabolism. Pharmacol Rev 50:107–141

    CAS  PubMed  Google Scholar 

  • Mahieu S, Calvo ML (1998) Effect of the chronic poisoning with aluminum on the renal handling of phosphate in the rat. Toxicol Lett 94:47–56

    Article  CAS  PubMed  Google Scholar 

  • Monteagudo FSE, Isaacson LC, Wilson G, Hickman R, Folb PI (1988) Aluminum excretion by the distal tubule of the pig kidney. Nephron 49:245–250

    Google Scholar 

  • Ohkawa H, Ohishi N, Yagi K (1979) Assay of lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95:351–357

    CAS  PubMed  Google Scholar 

  • Quarles LD (1991) Paradoxical toxic and trophic osseous actions of aluminum: potential explanations. Miner Electrolyte Metab 17:233–239

    CAS  PubMed  Google Scholar 

  • Reed DJ (1990) Glutathione. Toxicological implications. Annu Rev Pharmacol Toxicol 30:603–631

    Article  CAS  PubMed  Google Scholar 

  • Roe HH, Epstein JH, Goldstein NP (1949) A photometric method for determination of inulin in plasma and urine. J Biol Chem 178:839–845

    CAS  Google Scholar 

  • Roy AK, Talukder G, Sharma A (1991) Similar effects in vivo of two aluminum salts on the liver, kidney, bone and brain of Rattus novergicus. Bull Environ Contam Toxicol 47:228–295

    Google Scholar 

  • Sahin G, Varol I, Temizer A (1994) Determination of aluminum levels in the kidney, liver and brain of mice treated with aluminum hydroxide. Biol Trace Elem Res 41:129–135

    CAS  PubMed  Google Scholar 

  • Schetinger MR, Bonan CD, Morsch VM, Bohrer D, Valentim LM, Rodrigues SR (1999) Effects of aluminum sulfate on δ-aminolevulinate dehydratase from kidney, brain and liver of adult mice. Braz J Med Biol Res 32:761–766

    CAS  PubMed  Google Scholar 

  • Somova LI, Missankov A, Khan MS (1997) Chronic aluminum intoxication in rats: dose-dependent morphological changes. Methods Find Exp Clin Pharmacol 19:599–604

    CAS  PubMed  Google Scholar 

  • Stein G, Laske V, Muller A, Braunlich H, Lin BW, Fleck G (1987) Aluminum induced damage of the lysosomes in the liver, spleen, and kidney of rats. J Appl Toxicol 7:253–258

    CAS  PubMed  Google Scholar 

  • Sutherland JE, Greger JL (1998) Kinetics of aluminum disposition after ingestion of low moderate pharmacological doses of aluminum. Toxicology 126:115–125

    Article  CAS  PubMed  Google Scholar 

  • Sweet D, Bush K, Nigam S (2001) The organic anion transporter family; from physiology to ontogeny and the clinic. Am J Physiol 281:F197–F205

    CAS  Google Scholar 

  • Torres AM, Rodriguez JV, Ochoa JE, Elías MM (1986) Rat kidney function related to tissue glutathione levels. Biochem Pharmacol 35:3355–3358

    Article  CAS  PubMed  Google Scholar 

  • Tune BM, Burg MB (1971) Glucose transport by proximal renal tubules. Am J Physiol 221:580–585

    CAS  PubMed  Google Scholar 

  • Waugh WH, Beall PT (1974) Simplified measurement of para-aminohippuric acid and other arylamines in plasma and urine. Kidney Int 5:429–436

    CAS  PubMed  Google Scholar 

  • Wedden RP, Vyas BT (1978) Phlorizin stimulation of p-aminohippurate uptake in rat kidney cortex slices. Kidney Int 14:158–168

    PubMed  Google Scholar 

  • Wills MR, Hewitt CD, Sturgill BC, Savory J, Herman MM (1993) Long term oral and intravenous aluminum administration in rabbits. 1. Renal and hepatic changes. Ann Clin Lab Sci 23:1–16

    CAS  PubMed  Google Scholar 

  • Yokel RA, McNamara PJ (1988)Aluminum bioavailability and disposition in adult and immature rabbits. Toxicol Appl Pharmacol 77:344–352

    Google Scholar 

Download references

Acknowledgements

The authors express their appreciation for the technical assistance in statistical analyses to Lic Elena Carrera. This work was supported by grants from Universidad Nacional del Litoral, Argentina (Program C.A.I. + D).

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Correspondence to María Mónica Elías.

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Mahieu, S.T., Gionotti, M., Millen, N. et al. Effect of chronic accumulation of aluminum on renal function, cortical renal oxidative stress and cortical renal organic anion transport in rats. Arch Toxicol 77, 605–612 (2003). https://doi.org/10.1007/s00204-003-0496-1

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  • DOI: https://doi.org/10.1007/s00204-003-0496-1

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