Evidence map›Paper›PMID 22531820›Full record

ArticleToxicology letters2012

Renal efflux transporter expression in pregnant mice with Type I diabetes.

Lindsay L Yacovino, Lauren M Aleksunes

Abstract read
In one paragraph

Article in Toxicology letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Multidrug resistance-associated protein 4 (Mrp4) is a novel genetic factor in the pathogenesis of obesity and diabetes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  3. Article
  4. Review
  5. Endocrine and metabolic regulation of renal drug transporters.Journal of biochemical and molecular toxicology · 2012
    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

2 authors at 1 institution in 1 country.

Lindsay L YacovinoDepartment of Pharmacology and Toxicology, Rutgers University Ernest Mario School of Pharmacy, 170 Frelinghuysen Rd, Piscataway, NJ 08854, USA.
Lauren M Aleksunes
Rutgers, The State University of New Jersey · US

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Emily S Barrett · 1988 to 2026
$47.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
Disposition of Environmental Chemicals During PregnancyR01ES020522 · NIEHS · RUTGERS, THE STATE UNIV OF N.J. · PI ALEKSUNES, LAUREN M · 2011 to 2015
$2.1M
Protective Role of Mrp2 During Chemotherapy-Induced Kidney InjuryR00DK080774 · NIDDK · RUTGERS, THE STATE UNIV OF N.J. · PI ALEKSUNES, LAUREN M · 2009 to 2011
$695k
Protective Role of Mrp2 During Chemotherapy-Induced Kidney InjuryK99DK080774 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ALEKSUNES, LAUREN M · 2008 to 2008
$90k
NIDDK NIH HHS K99 DK080774NIDDK NIH HHS R00 DK080774NIDDK NIH HHS R01DK080774NIEHS NIH HHS P30 ES005022NIEHS NIH HHS P30ES005022NIEHS NIH HHS R01 ES020522NIEHS NIH HHS R01ES020522NIEHS NIH HHS T32 ES007148NIEHS NIH HHS T32ES007148
6 · The paper itself

Abstract

Prior research suggests that sex hormones and metabolic changes, such as obesity and hyperglycemia, can alter renal transporter expression in rodents. The purpose of this study was to characterize the expression of kidney efflux transporters and regulatory transcription factors in response to Type I diabetes and pregnancy. Female C57BL/6 mice were treated with multiple low doses of streptozotocin (STZ) to induce hyperglycemia and then mated with normoglycemic male mice. Transporter mRNA and protein expression were quantified in kidneys from vehicle- and STZ-treated non-pregnant and pregnant mice on gestation day 14. Pregnancy decreased the expression of Mdr1b, Mrp4, and 5 proteins and increased the mRNA and protein expression of Mrp3 by 50-60%. STZ treatment elevated Mrp1, 2, 4, and 5 and reduced Mrp3, 6, and Mdr1b mRNA and/or protein in non-pregnant mice. Pregnancy had little effect on STZ-mediated changes in renal efflux transporter expression. Transcriptional profiles of Hnf1α, PXR, AhR, and Nrf2 were altered in patterns similar to some efflux transporters suggesting potential involvement in their regulation. Taken together, these results suggest that renal drug efflux transporters and regulatory signaling pathways are altered by endocrine and metabolic changes that occur during pregnancy and Type I diabetes.

Indexed as

AnimalsATP Binding Cassette Transporter, Subfamily BBlood GlucoseBlotting, WesternCarrier ProteinsConstitutive Androstane ReceptorDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1FemaleFluorescent Antibody Technique, IndirectGene ExpressionHepatocyte Nuclear Factor 1-alphaKidneyMiceMice, Inbred C57BLNF-E2-Related Factor 2ATP Binding Cassette Transporter, Subfamily BBlood GlucoseCarrier ProteinsConstitutive Androstane ReceptorHepatocyte Nuclear Factor 1-alphaHnf1a protein, mouseNF-E2-Related Factor 2PPAR alphaPregnane X ReceptorReceptors, Aryl HydrocarbonReceptors, Cytoplasmic and NuclearReceptors, SteroidRNA, Messenger

Identifiers

PMID22531820
PMCPMC3370395
OpenAlexW2026936704

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.