For Manuscript Submission, Check or Review Login please go to Submission Websites List.
For the academic login, please select your country in the dropdown list. You will be redirected to verify your credentials.
Effect of Heavy Metals on, and Handling by, the KidneyBarbier O. · Jacquillet G. · Tauc M. · Cougnon M. · Poujeol P.
Unité Mixte de Recherche-Centre National de la Recherche Scientifique 6548, Université de Nice-Sophia Antipolis, Nice, France Corresponding Author
Dr. Philippe Poujeol
UMR-CNRS 6548, Bâtiment Sciences Naturelles
Université de Nice–Sophia Antipolis, Parc Valrose
FR–06108 Nice Cedex 2 (France)
Tel. +33 4 9207 6852, Fax +33 4 9207 6850, E-Mail email@example.com
Heavy metals such as cadmium (Cd), mercury (Hg), lead (Pb), chromium (Cr) and platinum (Pt) are a major environmental and occupational hazard. Unfortunately, these non-essential elements are toxic at very low doses and non-biodegradable with a very long biological half-life. Thus, exposure to heavy metals is potentially harmful. Because of its ability to reabsorb and accumulate divalent metals, the kidney is the first target organ of heavy metal toxicity. The extent of renal damage by heavy metals depends on the nature, the dose, route and duration of exposure. Both acute and chronic intoxication have been demonstrated to cause nephropathies, with various levels of severity ranging from tubular dysfunctions like acquired Fanconi syndrome to severe renal failure leading occasionally to death. Very varied pathways are involved in uptake of heavy metals by the epithelium, depending on the form (free or bound) of the metal and the segment of the nephron where reabsorption occurs (proximal tubule, loop of Henle, distal tubule and terminal segments). In this review, we address the putative uptake pathways involved along the nephron, the mechanisms of intracellular sequestration and detoxification and the nephropathies caused by heavy metals. We also tackle the question of the possible therapeutic means of decreasing the toxic effect of heavy metals by increasing their urinary excretion without affecting the renal uptake of essential trace elements. We have chosen to focus mainly on Cd, Hg and Pb and on in vivo studies.
© 2005 S. Karger AG, Basel
Divalent cations are essential to cell homeostasis. Among these cations trace elements as Zn2+, Fe2+ and Cu2+ participate in the regulation of numerous physiological functions (e.g. nucleic acid and protein synthesis, enzymatic reactions, membrane stabilization, immune system function, antioxidant defenses, oxidative phosphorylation, etc.). These metals are effective at very low concentrations, and their concentration in body fluids must be tightly regulated: deficiency or excess both cause severe illness and death. Thus, urinary excretion by the kidney, together with the gastrointestinal absorption rate, plays an important role in regulating the plasma level of these elements. Although the renal handling of cations is not fully understood, it is probable that each segment of the nephron is involved in their reabsorption, even so 70% of the transport occurs along the proximal tubule . Over the past decade, our knowledge of divalent cation transport has been considerably advanced by the molecular cloning of the divalent metal transporter 1 (DMT1). DMT1 was identified first in the gastrointestinal tract and is clearly involved in the transport of trace elements. DMT1 is highly expressed in renal tissue  and is therefore a good candidate for trace element transport. Unfortunately, DMT1 is also involved in the transport of some highly toxic divalent cations such as Cd2+, Pb2+, Co2+, Ni2+ and Pt2+. Therefore, when the body is contaminated with these poisons the kidney will be confronted with two problems: (1) the entry of the toxic metal into the renal cells and (2) the concomitant decrease of the essential trace element entry due to competition with the toxin. However, DMT1 is probably not the only renal transporter involved in toxic metal transport. There is evidence that Zn2+ could also be transported in the proximal tubule complexed with cysteine or histidine via a sodium-amino acid cotransporter  and toxic metals might bind these amino acids and compete with Zn2+. This is particularly the case for Hg2+ and Cd2+ which easily form cysteine conjugates. Such examples of interactions between a toxic heavy metal and its non-toxic homologue underline the necessity of elucidating their transport systems.
In this review, we address the transport mechanisms of toxic heavy metals (mainly Cd2+, Pb2+ and Hg2+) along the different segments of the nephron. This has been done on the basis that a decreased toxic effect can be achieved by increased urinary excretion of heavy metals without a modification in the reabsorption of essential trace elements. For this reason, we have focused our review mainly on in vivo studies.
As divalent cations, plasma heavy metals (toxic or not) exist as non-diffusible (protein-bound) and diffusible (complexed and ionized) forms. Tubular reabsorption will depend on the main form present in the glomerular ultrafiltrate. In turn, the ultrafiltrate composition will depend on the dosage and the mode of intoxication. Many accidental intoxications are due to absorption of heavy metal salt leading initially to an increase of the inorganic form in the plasma. Heavy metal ions bind rapidly to albumin, the most abundant protein in plasma. The affinity to albumin is probably not the same for all the heavy metals. They readily bind to the free sulfhydryl group of terminal cysteine residues and to histidine residues . However, a small fraction escapes to this binding and the plasma also contains the free form of the heavy metal. Since a small fraction of albumin is always filtered by the glomerulus, luminal fluid delivered to the early proximal tubule will contain both albumin-bound heavy metal and the ionized form. This situation arises primarily in cases of acute intoxications. It is noteworthy that after systemic injection of a single dose of Cd2+, the heavy metal is rapidly cleared from the blood although urinary excretion of Cd2+ remains undetectable [O.B., unpubl. data]. This indicates that under these conditions the entire bulk of the injected metal is quickly sequestered by different tissues, mainly in the liver (60–80%) and the kidney [, and O.B., unpubl. data]. Finally, renal uptake following acute intoxication is probably due to the membrane transport of both albumin-bound and free forms of heavy metals. During chronic intoxication, the concentration of heavy metal-binding proteins increases in the blood. Heavy metals are known to be potent inducers of metallothioneins and glutathione in renal and liver tissues . Their synthesis is induced by the free form of the heavy metal . Metallothioneins are low weight cysteine-rich proteins and glutathione is a tripeptide containing one cysteine. Both peptides, synthesized in the liver and the kidney, protect against heavy metal toxicity by trapping the metal inside the cells by conjugate formation . The renewal of liver cells during intoxication leads to the release of these conjugates into the systemic circulation where they are subsequently delivered to the kidneys .
As discussed above, heavy metals are present in the tubular fluid under free and bound forms.
Transport of Ionized Forms. The ionized forms of toxic heavy metals are present during acute intoxication. Owing to their properties to form complex or conjugate in the blood, the concentration of the free ionized forms represents less than 10% of the total metal concentration. Clearance measurements in the rat showed that during acute intoxication 99% of filtered Cd2+ was absorbed . Other studies have demonstrated that Hg2+ and Pb2+ are subject to similar renal handling. Finally, in the kidney, heavy metals are primarily absorbed through the apical membrane and do not readily exit from the basolateral membrane. For instance, less than 10% of the Hg2+ taken up from luminal side appears on the basolateral side . This is also the case for Cd2+, which is undetectable in the peritubular capillary after being microinjected into the lumen of the nephron .
Techniques such as micropuncture, microinjection [1, 6, 18] and microperfusion of isolated tubules  have made it possible to map the reabsorption of the heavy metals along the different segments of the nephron.
Proximal Tubule. Using 109Cd microinjections into the rat proximal tubule, Felley-Bosco and Diezi  and Barbier et al.  found that 70 and 95%, respectively, of injected 109Cd was taken up by the proximal tubule. The addition of Fe2+, Co2+ or Zn2+ to the microinjection decreased proximal Cd reabsorption. Conversely, Cd2+ decreased proximal reabsorption of microinjected 65Zn . Taken together, these data suggest common competitive transcellular pathways for divalent metals in the proximal tubule. In recent years, molecular and cellular biology techniques have been used to identify transporters involved in the reabsorption of ionized forms. The first heavy metal transporter was described by Palmiter and Findley  and known as ZnT1 (zinc transporter 1). In addition to Zn2+, ZnT1 could also transport Cd2+ and Cu2+ with a low affinity. However, it is mainly located in the basolateral membrane. Among the transporters, DMT1 could mediate Fe2+, Zn2+, Mn2+, Cd2+, Pb2+, Co2+, Ni2+ and Pt2+ reabsorption, but its expression in the apical membrane of the proximal tubule remains controversial. The ‘zinc transporters’ belonging to the Zrt, IRT-like protein (ZIP) family, involved in the uptake of Zn2+, Fe2+, Co2+ and Cu2+ or the ATP-binding cassette (ABC) type transporter family, involved in the uptake of Ni2+, Mn2+, Fe2+ and Mo2+, could also be candidates. However, their expression in the kidney has not been clearly demonstrated. Stretch-activated cation channels (SAC) could also be involved in the uptake of heavy metal divalent forms since Barbier et al.  have demonstrated the existence of proximal uptake of Cd2+ sensitive to gadolinium (Gd3+). These examples demonstrate that heavy metals could be transported by a large variety of transporters in the proximal tubule; the involvement of each remains to be elucidated.
Loop of Henle and Terminal Segment (Distal Tubule and Connecting Tubule). Although the proximal tubule is the main site of reabsorption, downstream segments of the nephron also exhibit a high permeability for essential and toxic metals. Wareing et al.  demonstrated that the loop of Henle (LH) and the terminal segments could participate in Fe2+ reabsorption. Zn2+ and Cd2+ are also transported in these segments . In the LH, transcellular and paracellular pathways are probably both involved in the transport of heavy metals . The paracellular passive reabsorption of cations is driven by a lumen-positive voltage generated by apical Na+K+2Cl– cotransport and K+ recycling. Microinjections of 55Fe by Wareing et al.  suggest that, in the LH, Fe2+ is taken up by the DMT1 transporter. This transporter has been localized in the apical membrane of the LH, the DCT and the collecting ducts . The role of DMT1 in Cd2+ reabsorption has been demonstrated by Barbier et al.  using 109Cd microinjections. They showed that Fe2+, Co2+ and Zn2+ decreased 109Cd uptake in both LH and distal tubule (DT). Furthermore, Leazer et al.  reported that increase of renal expression of DMT1 and increase of Cd accumulation are closely related in the pregnant rat; using rats which suffer from a mutation in the DMT1 gene, Belgrade rat, Chua et al.  demonstrated that a deficiency in DMT1 impaired the renal reabsorption of Fe2+ and Mn2+. Other transporters have been suggested to drive the distal reabsorption of heavy metals. Thus, Ducoudret et al.  showed that Madin-Darby canine kidney (MDCK) cells, which share some properties of distal nephron cells, expressed a transporter, sensitive to pH, which transports Zn2+, Cd2+ and Cu2+ but not Fe2+, Mn2+ or Co2+. Nagao et al.  described in this cell line a metal transporter involved in the uptake of Co2+, Cu2+, Ni2+, Pb2+ and Zn2+ but not in the uptake of Fe2+ or Mn2+. Unfortunately, in vitroand in vivo data do not yet allow a conclusion as to whether the transporters described in immortalized cell lines are merely modified isoforms of DMT1.
Transport of Bound Forms. During chronic intoxication with heavy metals, liver damage occurs when the capacity of the liver to sequester free forms of metals is exceeded. Then, toxicologically ‘inert’ bound forms, like metal-metallothionein (MT) and metal-glutathione (GSH), are released into the blood and circulate to the kidneys. Hayashi et al.  demonstrated that rat kidney reabsorbs about 50% of the filtered CdMT complexes. Along the proximal tubule this reabsorption occurs via endocytosis: Erfurt et al.  described an internalization of CdMT by endosomes and intracellular storage in immortalized proximal cell lines. Furthermore, parts of the metal-GSH complexes are cleaved by the γ-glutamyltransferase into Cys-metal conjugates that could be transported by the Na+-amino acid cotransporter. This mechanism has been demonstrated for GSH-Hg and GSH-Cd conjugates . The involvement of the Na+/amino acid cotransporter has been suggested by Felley-Bosco and Diezi  who demonstrated, using Cys-109Cd microinjections, that 82% of Cys-109Cd conjugates were reabsorbed by the proximal tubule. Moreover, Gachot et al.  showed that Zn2+ enters renal proximal cells via a saturable carrier-mediated system and also chelated to cysteine or histidine via a Na+/amino acid cotransport mechanism. These putative heavy metal uptake pathways are illustrated in the figure 1.
Toxic Form of Heavy Metals. The ionized form of heavy metals is the toxic form. It appears that conjugates and bound forms of filtered heavy metals are not toxic by themselves but that the divalent form of these metals released from the complexes is responsible for the cellular toxicity.
Renal Pathologies due to Heavy Metals. The severity of renal damage depends, first, on the mode of exposure to the heavy metal. The symptoms observed during acute intoxication will differ from those induced by chronic intoxication. This difference could result from the concentration and the nature of the toxic metal but also from the form of the heavy metal (free or bound). The work of Liu et al.  on MT–/– mice has confirmed that the profile of a Cd2+-induced nephropathy (calciuria, polyuria) is totally different from the profile of a CdMT-induced nephropathy (proximal tubular necrosis and Fanconi syndrome). These data support the idea that during chronic administration the renal toxicity of heavy metals is mainly due to the transport of the filtered conjugate form on the thiol groups of specific or non-specific proteins whereas during acute administration the free ionized form and the conjugates with short peptides and thiol-amino acids could directly participate in this toxicity.
In the rat, an acute perfusion of Cd2+ caused hypercalciuria, hyperphosphaturia and hypokaliuria without modification of glomerular filtration rate (GFR) . By contrast, a single, 20-fold lower dose of Pb2+, Hg2+ induced glomerular and tubular damage characterized by a reduced GFR, glycosuria, proteinuria and a rapid obstruction of the tubular system , illustrating that the pattern of nephrotoxicity differs between heavy metals. Therefore, Pb2+ and Hg2+ are more dangerous than Cd2+ because they induce an irreversible renal insufficiency even during acute intoxication.
Concerning chronic intoxication, most heavy metals (Cd2+, Hg2+, Pb2+) induced a Fanconi syndrome characterized by a decrease of the GFR, an increase in urinary flow rate, proteinuria, glycosuria, aminoaciduria and excessive loss of major ions.
Acute Interactions with Transporters and Ion Channels. It has been demonstrated that heavy metals interact with a number of renal transporters. In the proximal tubule, Cd2+ has been shown to decrease phosphate and glucose transport by inhibiting the NaPi and the Na/glucose cotransporters respectively. In the terminal segments, Cd2+ exerts a blocking effect on ion channels such as the epithelial calcium channel (ECaC) and the renal outer medullary K+ channel (ROMK). Hg2+, Pb2+ and Cr3+ are also potent blockers of the sulfate transporter, Sat-1. Moreover, because they have the ability to compete with the divalent metal carriers of Zn2+ and Fe2+, toxic heavy metals decrease the reabsorption of these essential oligo-metals. Such competition could induce severe deficiency. For example, the decrease of DMT1-mediated Fe2+ transport in the presence of Cd2+ is probably responsible for the anemia in Cd2+ intoxication.
Cellular Effects. The free forms of heavy metals induce an outer membrane rupture and an uncoupling of mitochondrial respiration. This is the case for Cd2+, which inhibits electron transfer and oxidative phosphorylation, resulting in the release of numerous death signals like reactive oxygen species.
It is clear that the danger following exposure to heavy metals comes from the fact that they are accumulated in the renal tissue and poorly excreted in the urine. As discussed above, all the transported forms participate in the toxicity and it is necessary to identify a way to impair their tubular transport, thereby favoring their renal clearance. Concomitantly, decreased heavy metal accumulation could also prevent the induction of binding proteins, inhibit the synthesis of heavy metal-binding protein conjugates and block the delayed deleterious effects observed during chronic intoxication.
Heavy Metal Chelators. For many years, metal chelators have been used to treat heavy metal intoxication. To chelate Cd2+, Hg2+ and Pb2+, the most commonly used chemicals are either non-sulfured conjugates such as ethylenediaminetetraacetate, triethylenetetramine, deferoxamine and deferiprone or sulfured conjugates such as meso-2,3-dimercaptosuccinic acid and 2,3-dimercapto-1-propanesulfonic acid and diethyldithiocarbamate. These molecules have shown real effectiveness in increasing heavy metal elimination through urine. Associated with hemodialysis, the chelators are potent antidotes to cure the acute intoxication with heavy metals such as Pb2+, Hg2+, Cd2+. The efficacy of chelating agents is enhanced by amino acids like methionine that facilitate the cell penetration of chelating agents by reducing their ionic character. However, most chelators also complex essential divalent cations or such as Ca2+, Mg2+, Zn2+, Cu2+, Fe2+ and increase their excretion.
D-Cysteine. The compounds cited above may have secondary effects whereas natural compounds, such as amino acids, can be also used as chelator substances for cadmium. Thus, the administration of cysteine to intoxicated animals reduces the amount of cadmium deposition in the kidney by 40% . In a preliminary study, we investigated whether the D-Cys combated cadmium intoxication by increasing its elimination in the urine. Using in vivo 109Cd microinjection in the rat [O.B., unpubl. data], we found that it was possible to increase by 3-fold the urinary excretion of 109Cd when proximal microinjection was performed in the presence of D-Cys. The D-Cys form is able to bind Cd2+ but the complex is not transported by the Na+-amino acid cotransporter and is not reabsorbed by endocytosis like protein complexes.
Inhibitors and Blockers of Renal Luminal Transport. As stated previously, a few metals, such as Fe2+, Co2+ and Zn2+, compete with heavy metal transport in renal cells and significantly decrease their reabsorption [1, 18]. Based on these properties, an increase in the plasma concentration of these metals could induce an increase of the renal clearance of the toxins. Furthermore, ‘loop diuretics’ like bumetanide could be also used to reduce the paracellular transport of heavy metals in the thick ascending limb . However, the efficiency of these treatments remains to be demonstrated in the intoxicated animal. Moreover, the secondary effects induced by the acute administration of high concentration of essential heavy metals need to be carefully analyzed.
Protection by Zinc. The protective effect of zinc on heavy metal toxicity and especially Cd toxicity has been known for some years. When Zn2+ is administered with Cd2+ during chronic exposure, it prevents the development of renal dysfunction and Fanconi syndrome [O.B., unpubl. data]. The precise mechanisms involved in protection by zinc are still not well known but an action on apoptosis and oxidative stress is highly suspected.
It is evident that exposure to heavy metals is potentially harmful. This is due to the high capacity of renal epithelium to transport and accumulate these toxins. Some positive indications emerge from recent studies: new advances in the discovery of therapeutic tools such as blockers of renal reabsorption of heavy metals, or chelators, or cell protectors such as Zn2+, represent progress in finding preventive and/or curative treatment of populations exposed to toxic heavy metals. Nevertheless, many of the mechanisms involved in heavy metal transport and toxicity are still speculative. This review underlines that more in vivo studies are necessary to elucidate the real physiological handling of heavy metals and to develop effective antidotes against acute and chronic intoxication.
We thank David Shirley for helpful criticism of the manuscript.
Dr. Philippe Poujeol
UMR-CNRS 6548, Bâtiment Sciences Naturelles
Université de Nice–Sophia Antipolis, Parc Valrose
FR–06108 Nice Cedex 2 (France)
Tel. +33 4 9207 6852, Fax +33 4 9207 6850, E-Mail firstname.lastname@example.org
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher or, in the case of photocopying, direct payment of a specified fee to the Copyright Clearance Center.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.