Evidence map›Paper›PMID 15845419›Full record

ReviewToxicology and applied pharmacology2005

Molecular and ionic mimicry and the transport of toxic metals.

Christy C Bridges, Rudolfs K Zalups

Abstract readReview
In one paragraph

Review in Toxicology and applied pharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 198 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
198citing papers in PubMed, 3 pooled it
10.0field-weighted citation impact, top 1% 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

198 citing papers in PubMed, 3 syntheses or guidelines pooled it, 761 citations in OpenAlex.

  1. Pooled it
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  3. Evaluation of Fetal Exposures to Metals and Metalloids through Meconium Analyses: A Review.International journal of environmental research and public health · 2021
    Pooled it
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138 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Christy C BridgesDivision of Basic Medical Sciences, Mercer University School of Medicine, Macon, GA 31207, USA. bridges_cc@mercer.edu
Rudolfs K Zalups
Mercer University · US

Funding

TRANSPORT-TOXICITY OF INORGANIC MERCURY IN THE NEPHRONR01ES005980 · NIEHS · MERCER UNIVERSITY MACON · PI ZALUPS, RUDOLFS KARLIS · 1993 to 2006
$1.7M
METALLOTHIONEIN, MERCURY AND MONOCYTE ACTIVATIONR01ES011288 · NIEHS · MERCER UNIVERSITY MACON · PI ZALUPS, RUDOLFS KARLIS · 2002 to 2006
$1.5M
MERCURY NEPHROTOXICITY AFTER A REDUCTION OF RENAL MASSR01ES005157 · NIEHS · MERCER UNIVERSITY MACON · PI ZALUPS, RUDOLFS KARLIS · 1995 to 2002
$752k
MECHANISMS FOR RENAL UPTAKE OF MERCURYF32ES012556 · NIEHS · MERCER UNIVERSITY MACON · PI BRIDGES, CHRISTY C · 2003 to 2005
$147k
MERCURY NEPHROTOXICITY AFTER A REDUCTION OF RENAL MASSR29ES005157 · NIEHS · MERCER UNIVERSITY MACON · PI ZALUPS, RUDOLFS KARLIS · 1988 to 1992
–
TRANSPORT AND TOXICITY OF MERCURY IN THE NEPHRONR55ES005980 · NIEHS · GEORGIA STATE UNIVERSITY · PI BARFUSS, DELON W · 1992 to 1992
–
NIEHS NIH HHS ES012556NIEHS NIH HHS ES05157NIEHS NIH HHS ES05980NIEHS NIH HHS ES11288NIEHS NIH HHS F32 ES012556NIEHS NIH HHS R01 ES005980NIEHS NIH HHS R01 ES011288
6 · The paper itself

Abstract

Despite many scientific advances, human exposure to, and intoxication by, toxic metal species continues to occur. Surprisingly, little is understood about the mechanisms by which certain metals and metal-containing species gain entry into target cells. Since there do not appear to be transporters designed specifically for the entry of most toxic metal species into mammalian cells, it has been postulated that some of these metals gain entry into target cells, through the mechanisms of ionic and/or molecular mimicry, at the site of transporters of essential elements and/or molecules. The primary purpose of this review is to discuss the transport of selective toxic metals in target organs and provide evidence supporting a role of ionic and/or molecular mimicry. In the context of this review, molecular mimicry refers to the ability of a metal ion to bond to an endogenous organic molecule to form an organic metal species that acts as a functional or structural mimic of essential molecules at the sites of transporters of those molecules. Ionic mimicry refers to the ability of a cationic form of a toxic metal to mimic an essential element or cationic species of an element at the site of a transporter of that element. Molecular and ionic mimics can also be sub-classified as structural or functional mimics. This review will present the established and putative roles of molecular and ionic mimicry in the transport of mercury, cadmium, lead, arsenic, selenium, and selected oxyanions in target organs and tissues.

Indexed as

AnimalsCadmiumHumansMercuryMetalsMolecular MimicryToxins, BiologicalCadmiumMercuryMetalsToxins, Biological

Identifiers

PMID15845419
PMCPMC2409291
OpenAlexW2127895812

What OpenQuestion holds

Textmetadata
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.