Evidence map›Paper›PMID 42834149›Full record

ArticleArchives of toxicology2026

Diabetogenic effects of arsenic exposure in C57BL/6 N mice carrying the human AS3MT gene: the role of sex and exposure window.

Navkaran Singh, Christelle Douillet, Yelyzaveta Minaieva, Bingzhen Shang, Fernando Pardo-Manuel de Villena, Rebecca C Fry, Miroslav Styblo

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Navkaran Singh *Department of Nutrition, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7461, USA.
Christelle Douillet *Department of Nutrition, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7461, USA.
Yelyzaveta MinaievaDepartment of Nutrition, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7461, USA.
Bingzhen ShangDepartment of Nutrition, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7461, USA.
Fernando Pardo-Manuel de VillenaDepartment of Genetics, School of Medicine, The University of North Carolina at Chapel Hill, NC, Chapel Hill, 27599-7264, USA.
Rebecca C FryDepartment of Environmental Science and Engineering, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, NC, Chapel Hill, 27599-7431, USA. rfry@email.unc.edu.
Miroslav StybloDepartment of Nutrition, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7461, USA. styblo@med.unc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic exposure to inorganic arsenic (iAs) has been linked to diabetes in both humans and laboratory mice. Prior studies highlight that the mechanism underlying the diabetogenic effects of iAs and the manifestation of iAs-associated diabetes depend, in part, on the exposure window. We have shown that exposure to iAs prior to conception or in utero consistently produced diabetic phenotypes in wild-type (WT) C57BL/6J mice and that this phenotype was characterized primarily by insulin resistance. The effects of postnatal iAs exposures have been less consistent. However, significance of these findings for human exposure remains unclear because WT mice metabolize and detoxify iAs more efficiently than humans. The present study describes the diabetogenic effects of iAs in humanized C57BL/6 N mice that express the human arsenic methyltransferase and exhibit human-like patterns of iAs metabolism. We examined diabetes indicators in male and female offspring of parents exposed to 0 (controls) or 200 ppb iAs (arsenite) prior to conception (PC), and offsprings exposed to iAs in utero (IU), or during the whole life, including the PC and IU windows. We found that only PC exposure produced diabetic phenotype in male offspring. This phenotype was characterized by elevated fasting blood glucose (FBG) and decreased HOMA-B, the indicator of beta cell function. However, fasting plasma insulin and HOMA-IR, the indicator of insulin resistance, were not affected. FBG was also higher in male mice after IU exposure as compared to control male mice, but this difference was not statistically significant. LL exposure had no significant effects in male offspring. No differences in diabetes markers were found between iAs-exposed and control female mice regardless of exposure window. These results suggest that PC exposure produced fasting hyperglycemia in the humanized male mice by impairing the function of insulin secreting beta cells. However, postnatal iAs exposure appeared to attenuate these effects, suggesting that activation of compensatory mechanisms may take place after birth. These findings may inform designs of population studies that examine iAs-associated diabetes, as well as the interpretation of data collected in these studies.

Indexed as

ArsenicAS3MT humanized miceBeta cell functionDiabetesExposure windowFasting glycemiaSex

Identifiers

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.