Evidence map›Paper›PMID 25868844›Full record

ArticleToxicology and applied pharmacology2015

Toxicological significance of renal Bcrp: Another potential transporter in the elimination of mercuric ions from proximal tubular cells.

Christy C Bridges, Rudolfs K Zalups, Lucy Joshee

Abstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. The Protective Activity ofInternational journal of nephrology · 2024
    Article
  2. Article
  3. Article
  4. Article
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  6. Article
  7. Article
  8. Article
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  10. Article
  11. Renal Drug Transporters and Drug Interactions.Clinical pharmacokinetics · 2017
    Review
  12. Xenobiotic transporters and kidney injury.Advanced drug delivery reviews · 2017
    Review
  13. Chronic Kidney Disease and Exposure to Nephrotoxic Metals.International journal of molecular sciences · 2017
    Review
  14. The aging kidney and the nephrotoxic effects of mercury.Journal of toxicology and environmental health. Part B, Critical reviews · 2017
    Review
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Christy C BridgesDivision of Basic Medical Sciences, Mercer University School of Medicine, Macon, GA, USA. Electronic address: bridges_cc@mercer.edu.
Rudolfs K ZalupsDivision of Basic Medical Sciences, Mercer University School of Medicine, Macon, GA, USA.
Lucy JosheeDivision of Basic Medical Sciences, Mercer University School of Medicine, Macon, GA, USA.
Mercer University · US

Funding

Proximal Tubular Transport of Mercury and Effects of Reduced Renal MassR15ES019991 · NIEHS · MERCER UNIVERSITY MACON · PI BRIDGES, CHRISTY C · 2011 to 2011
$471k
NIEHS NIH HHS ES019991NIEHS NIH HHS R15 ES019991
6 · The paper itself

Abstract

Secretion of inorganic mercury (Hg(2+)) from proximal tubular cells into the tubular lumen has been shown to involve the multidrug resistance-associated protein 2 (Mrp2). Considering similarities in localization and substrate specificity between Mrp2 and the breast cancer resistance protein (Bcrp), we hypothesize that Bcrp may also play a role in the proximal tubular secretion of mercuric species. In order to test this hypothesis, the uptake of Hg(2+) was examined initially using inside-out membrane vesicles containing Bcrp. The results of these studies suggest that Bcrp may be capable of transporting certain conjugates of Hg(2+). To further characterize the role of Bcrp in the handling of mercuric ions and in the induction of Hg(2+)-induced nephropathy, Sprague-Dawley and Bcrp knockout (bcrp(-/-)) rats were exposed intravenously to a non-nephrotoxic (0.5 μmol · kg(-1)), a moderately nephrotoxic (1.5 μmol · kg(-1)) or a significantly nephrotoxic (2.0 μmol · kg(-1)) dose of HgCl2. In general, the accumulation of Hg(2+) was greater in organs of bcrp(-/-) rats than in Sprague-Dawley rats, suggesting that Bcrp may play a role in the export of Hg(2+) from target cells. Within the kidney, cellular injury and necrosis was more severe in bcrp(-/-) rats than in controls. The pattern of necrosis, which was localized in the inner cortex and the outer stripe of the outer medulla, was significantly different from that observed in Mrp2-deficient animals. These findings suggest that Bcrp may be involved in the cellular export of select mercuric species and that its role in this export may differ from that of Mrp2.

Indexed as

AnimalsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2Blood Urea NitrogenCreatinineFecesGene Knockout TechniquesKidneyKidney Tubules, ProximalLiverMaleMembranesMercuric ChlorideMercury CompoundsRatsRats, Sprague-DawleyAbcc2 protein, ratAbcg2 protein, ratATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2CreatinineMercuric ChlorideMercury CompoundsVesicular Transport ProteinsBreast cancer resistance proteinKidneyMercuryMultidrug resistance-associated protein 2Proximal tubule

Identifiers

PMID25868844
PMCPMC4430411
OpenAlexW2007166455

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.