Evidence map›Paper›PMID 30487262›Full record

ArticleDiabetes2019

Dynamic Contrast-Enhanced MRI of OATP Dysfunction in Diabetes.

Dorela D Shuboni-Mulligan, Maciej Parys, Barbara Blanco-Fernandez, Christiane L Mallett, Regina Schnegelberger, Marilia Takada, Shatadru Chakravarty, Bruno Hagenbuch, Erik M Shapiro

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Species-Specific Hepatic Uptake of [Molecular imaging and biology · 2025
    Article
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  12. Article
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  16. Review
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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

9 authors at 2 institutions in 1 country.

Dorela D Shuboni-MulliganDepartment of Radiology, Michigan State University, East Lansing, MI.
Maciej ParysDepartment of Comparative Medicine and Integrative Biology Program, Michigan State University, East Lansing, MI.ORCID 0000-0003-4456-3369
Barbara Blanco-FernandezDepartment of Radiology, Michigan State University, East Lansing, MI.
Christiane L MallettDepartment of Radiology, Michigan State University, East Lansing, MI.
Regina SchnegelbergerDepartment of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, MO.
Marilia TakadaDepartment of Comparative Medicine and Integrative Biology Program, Michigan State University, East Lansing, MI.
Shatadru ChakravartyDepartment of Radiology, Michigan State University, East Lansing, MI.ORCID 0000-0003-0855-318X
Bruno HagenbuchDepartment of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, MO.ORCID 0000-0002-2938-8630
Erik M ShapiroDepartment of Radiology, Michigan State University, East Lansing, MI shapir86@msu.edu.ORCID 0000-0002-0901-5781
Michigan State University · USUniversity of Kansas Medical Center · US

Funding

Molecular Characterization of Hepatic Organic Anion Transporting PolypeptidesR01GM077336 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HAGENBUCH, BRUNO · 2007 to 2019
$3.7M
Quantitative molecular and cellular MRI of hepatocyte transplantationR01DK107697 · NIDDK · MICHIGAN STATE UNIVERSITY · PI SHAPIRO, ERIK · 2015 to 2018
$2.1M
NIDDK NIH HHS R01 DK107697NIGMS NIH HHS R01 GM077336
6 · The paper itself

Abstract

Diabetes is associated with hepatic metabolic dysfunction predisposing patients to drug-induced liver injury. Mouse models of type 2 diabetes (T2D) have dramatically reduced expression of organic anion transporting polypeptide (OATP)1A1, a transporter expressed in hepatocytes and in the kidneys. The effects of diabetes on OATP1B2 expression are less studied and less consistent. OATP1A1 and OATP1B2 both transport endogenous substrates such as bile acids and hormone conjugates as well as numerous drugs including gadoxetate disodium (Gd-EOB-DTPA). As master pharmacokinetic regulators, the altered expression of OATPs in diabetes could have a profound and clinically significant influence on drug therapies. Here, we report a method to noninvasively measure OATP activity in T2D mice by quantifying the transport of hepatobiliary-specific gadolinium-based contrast agents (GBCAs) within the liver and kidneys using dynamic contrast-enhanced MRI (DCE-MRI). By comparing GBCA uptake in control and OATP knockout mice, we confirmed liver clearance of the hepatobiliary-specific GBCAs, Gd-EOB-DTPA, and gadobenate dimeglumine, primarily though OATP transporters. Then, we measured a reduction in the hepatic uptake of these hepatobiliary GBCAs in T2D

Indexed as

AnimalsContrast MediaDiabetes Mellitus, Type 2Gadolinium DTPALiver-Specific Organic Anion Transporter 1Magnetic Resonance ImagingMiceMice, KnockoutOrganic Anion TransportersOrganic Cation Transport ProteinsContrast MediaGadolinium DTPAgadolinium ethoxybenzyl DTPALiver-Specific Organic Anion Transporter 1Organic Anion TransportersOrganic Cation Transport ProteinsSLCO1A1 protein, mouseSlco1b2 protein, mouse

Identifiers

PMID30487262
PMCPMC6341305
OpenAlexW2902000270

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.