Evidence map›Paper›PMID 22807110›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2012

In vivo-formed versus preformed metabolite kinetics of trans-resveratrol-3-sulfate and trans-resveratrol-3-glucuronide.

Satish Sharan, Otito F Iwuchukwu, Daniel J Canney, Cheryl L Zimmerman, Swati Nagar

Erratum issuedOpen access · bronzeAbstract readComparative Study
In one paragraph

Article in Drug metabolism and disposition: the biological fate of chemicals, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Chemopreventive efficacy of oral curcumin: a prodrug hypothesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  4. Article
  5. "Target-Site" Drug Metabolism and Transport.Drug metabolism and disposition: the biological fate of chemicals · 2015
    Article
  6. Article
  7. Herb-drug interactions: challenges and opportunities for improved predictions.Drug metabolism and disposition: the biological fate of chemicals · 2014
    Article
  8. Review
  9. Pulmonary metabolism of resveratrol: in vitro and in vivo evidence.Drug metabolism and disposition: the biological fate of chemicals · 2013
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Satish SharanDepartment of Pharmaceutical Sciences, Temple University School of Pharmacy, Philadelphia, PA, USA. swati.nagar@temple.edu
Otito F Iwuchukwu
Daniel J Canney
Cheryl L Zimmerman
Swati Nagar
Temple University · USUniversity of Minnesota · US

Funding

Conjugation of anticancer drugsR03CA133943 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI NAGAR, SWATI · 2009 to 2010
$150k
Colorectal cancer chemoprevention with phytochemical combinationsR03CA159389 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI NAGAR, SWATI · 2012 to 2013
$148k
NCI NIH HHS R03 CA133943NCI NIH HHS R03-CA133943NCI NIH HHS R03 CA159389NCI NIH HHS R03-CA159389
6 · The paper itself

Abstract

Metabolites in safety testing have gained a lot of attention recently. Regulatory agencies have suggested that the kinetics of preformed and in vivo-formed metabolites are comparable. This subject has been a topic of debate. We have compared the kinetics of in vivo-formed with preformed metabolites. trans-3,5,4'-Trihydroxystilbene [trans-resveratrol (RES)] and its two major metabolites, resveratrol-3-sulfate (R3S) and resveratrol-3-glucuronide (R3G) were used as model substrates. The pharmacokinetics (PK) of R3S and R3G were characterized under two situations. First, the pharmacokinetics of R3S and R3G were characterized (in vivo-formed metabolite) after administration of RES. Then, synthetic R3S and R3G were administered (preformed metabolite) and their pharmacokinetics were characterized. PK models were developed to describe the data. A three-compartment model for RES, a two-compartment model for R3S (preformed), and an enterohepatic cycling model for R3G (preformed) was found to describe the data well. These three models were further combined to build a comprehensive PK model, which was used to perform simulations to predict in vivo-formed metabolite kinetics. Comparisons were made between in vivo-formed and preformed metabolite kinetics. Marked differences were observed in the kinetics of preformed and in vivo-formed metabolites.

Indexed as

AnimalsArea Under CurveBiotransformationGlucuronidesHalf-LifeInjections, Intra-ArterialMaleMetabolic Clearance RateMiceMice, Inbred C57BLModels, BiologicalResveratrolStilbenesSulfatesGlucuronidesResveratrolresveratrol-4'-O-glucuronideStilbenesSulfates

Identifiers

PMID22807110
PMCPMC3463825
OpenAlexW2161782556

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.