Evidence map›Paper›PMID 20599802›Full record

ArticleBiochemical pharmacology2010

Role of transporter-mediated efflux in the placental biodisposition of bupropion and its metabolite, OH-bupropion.

Sarah J Hemauer, Svetlana L Patrikeeva, Xiaoming Wang, Doaa R Abdelrahman, Gary D V Hankins, Mahmoud S Ahmed, Tatiana N Nanovskaya

Open access · greenAbstract read
In one paragraph

Article in Biochemical pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Racial association and pharmacotherapy in neonatal opioid withdrawal syndrome.Journal of perinatology : official journal of the California Perinatal Association · 2019
    Observational
  5. Article
  6. Placental control of drug delivery.Advanced drug delivery reviews · 2017
    Review
  7. Review
  8. Review
  9. Article
  10. ATP-binding cassette proteins BCRP, MRP1 and P-gp expression and localization in the human umbilical cord.Xenobiotica; the fate of foreign compounds in biological systems · 2016
    Article
  11. Article
  12. Metabolism and disposition of bupropion in pregnant baboons (Papio cynocephalus).Drug metabolism and disposition: the biological fate of chemicals · 2014
    Article
  13. Review
  14. 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

7 authors at 1 institution in 1 country.

Sarah J HemauerDepartment of Obstetrics & Gynecology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0587, USA. sjhemaue@utmb.edu
Svetlana L Patrikeeva
Xiaoming Wang
Doaa R Abdelrahman
Gary D V Hankins
Mahmoud S Ahmed
Tatiana N Nanovskaya
The University of Texas Medical Branch at Galveston · US

Funding

Development of Bupropion for Smoking Cessation During PregnancyR01DA024094 · NIDA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI NANOVSKAYA, TATIANA · 2007 to 2011
$1.5M
NIDA NIH HHS R01 DA024094NIDA NIH HHS R01DA024094
6 · The paper itself

Abstract

Cigarette smoking during pregnancy is a preventable risk factor associated with maternal and fetal complications. Bupropion is an antidepressant used successfully for smoking cessation in non-pregnant patients. Our goal is to determine whether it could benefit the pregnant patient seeking smoking cessation. The aim of this investigation was to determine the role of human placenta in the disposition of bupropion and its major hepatic metabolite, OH-bupropion. The expression of efflux transporters P-gp and BCRP was determined in placental brush border membrane (n=200) and revealed a positive correlation (p<0.05). Bupropion was transported by BCRP (K(t) 3 microM, V(max) 30 pmol/mg protein/min) and P-gp (K(t) 0.5 microM, V(max) 6 pmol/mg protein min) in placental inside-out vesicles (IOVs). OH-bupropion crossed the dually-perfused human placental lobule without undergoing further metabolism, nor was it an efflux substrate of P-gp or BCRP. In conclusion, our data indicate that human placenta actively regulates the disposition of bupropion (via metabolism, active transport), but not its major hepatic metabolite, OH-bupropion.

Indexed as

Antidepressive AgentsATP Binding Cassette Transporter, Subfamily B, Member 1Biological TransportBupropionFemaleHumansMembrane Transport ProteinsPlacentaPregnancyAntidepressive AgentsATP Binding Cassette Transporter, Subfamily B, Member 1BupropionMembrane Transport Proteins

Identifiers

PMID20599802
PMCPMC2940852
OpenAlexW1966937601

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.