Evidence map›Paper›PMID 22524730›Full record

ArticleComparative hepatology2012

Severe diabetes and leptin resistance cause differential hepatic and renal transporter expression in mice.

Vijay R More, Xia Wen, Paul E Thomas, Lauren M Aleksunes, Angela L Slitt

Open access · hybridAbstract read
In one paragraph

Article in Comparative hepatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Diabetes Induces Aberrant DNA Methylation in the Proximal Tubules of the Kidney.Journal of the American Society of Nephrology : JASN · 2015
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Alcohol cirrhosis alters nuclear receptor and drug transporter expression in human liver.Drug metabolism and disposition: the biological fate of chemicals · 2013
    Article
  16. Endocrine and metabolic regulation of renal drug transporters.Journal of biochemical and molecular toxicology · 2012
    Review
  17. Article
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

5 authors at 3 institutions in 1 country.

Vijay R MoreDepartment of Biomedical and Pharmaceutical Sciences, University of Rhode Island, Kingston, RI, 02881, USA. aslitt@uri.edu.
Xia Wen
Paul E Thomas
Lauren M Aleksunes
Angela L Slitt
Rutgers, The State University of New Jersey · USUniversity of Rhode Island · USEnvironmental and Occupational Health Sciences Institute · US

Funding

Effect of nutritional status on MRP2 expression and biliary excretion of bisphenoR01ES016042 · NIEHS · UNIVERSITY OF RHODE ISLAND · PI SLITT, ANGELA L · 2008 to 2012
$2.4M
Role of Nrf2 during cholestsis and gallstone formationK22ES013782 · NIEHS · UNIVERSITY OF RHODE ISLAND · PI SLITT, ANGELA L · 2007 to 2009
$323k
NIEHS NIH HHS K22 ES013782NIEHS NIH HHS R01 ES016042
6 · The paper itself

Abstract

backgroundType-2 Diabetes is a major health concern in the United States and other Westernized countries, with prevalence increasing yearly. There is a need to better model and predict adverse drug reactions, drug-induced liver injury, and drug efficacy in this population. Because transporters significantly contribute to drug clearance and disposition, it is highly significant to determine whether a severe diabetes phenotype alters drug transporter expression, and whether diabetic mouse models have altered disposition of acetaminophen (APAP) metabolites.

resultsTransporter mRNA and protein expression were quantified in livers and kidneys of adult C57BKS and db/db mice, which have a severe diabetes phenotype due to a lack of a functional leptin receptor. The urinary excretion of acetaminophen-glucuronide, a substrate for multidrug resistance-associated proteins transporters was also determined. The mRNA expression of major uptake transporters, such as organic anion transporting polypeptide Slco1a1 in liver and kidney, 1a4 in liver, and Slc22a7 in kidney was decreased in db/db mice. In contrast, Abcc3 and 4 mRNA and protein expression was more than 2 fold higher in db/db male mouse livers as compared to C57BKS controls. Urine levels of APAP-glucuronide, -sulfate, and N-acetyl cysteine metabolites were higher in db/db mice.

conclusionA severe diabetes phenotype/presentation significantly altered drug transporter expression in liver and kidney, which corresponded with urinary APAP metabolite levels.

Identifiers

PMID22524730
PMCPMC3416584
OpenAlexW2165282595

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Registered trials

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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.