Evidence map›Paper›PMID 15876424›Full record

ArticleBiochemical pharmacology2005

Role of P-glycoprotein in transplacental transfer of methadone.

Tatiana Nanovskaya, Ilona Nekhayeva, Nedra Karunaratne, Kenneth Audus, Gary D V Hankins, Mahmoud S Ahmed

Open access · greenAbstract readComparative Study
In one paragraph

Article in Biochemical pharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.9field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Increased risk of severe neonatal opioid withdrawal syndrome in pregnancies with low placental ABCB1 DNA methylation.Journal of perinatology : official journal of the California Perinatal Association · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Cytotoxicity of Endocytosis and Efflux Inhibitors in the BeWo Cell Line.Journal of pharmaceutical research international · 2017
    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

6 authors at 2 institutions in 1 country.

Tatiana NanovskayaDepartment of Obstetrics & Gynecology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555-0587, USA.
Ilona Nekhayeva
Nedra Karunaratne
Kenneth Audus
Gary D V Hankins
Mahmoud S Ahmed
The University of Texas Medical Branch at Galveston · USUniversity of Kansas · US

Funding

TROPHOBLAST MDR EFFLUX SYSTEM AND FETAL PROTECTIONP01HD039878 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SOARES, MICHAEL J · 2002 to 2006
$4.7M
Medications Development for the Pregnant Opiate AddictR01DA013431 · NIDA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI AHMED, MAHMOUD S · 2001 to 2010
$3.1M
NICHD NIH HHS HD39878-03NICHD NIH HHS P01 HD039878NIDA NIH HHS DA-13431-05NIDA NIH HHS R01 DA013431
6 · The paper itself

Abstract

Methadone is the therapeutic agent of choice for treatment of the pregnant opiate addict. However, little is known on the factors affecting its concentration in the fetal circulation during pregnancy and how it might relate to neonatal outcome. Therefore, a better understanding of the function of placental metabolic enzymes and transporters should add to the knowledge of the role of the tissue in the disposition of methadone and its relation to neonatal outcome. We hypothesized that the expression and activity of the placental efflux transporter P-glycoprotein (P-gp) would affect the transfer of methadone to the fetal circulation. Data obtained utilizing dual perfusion of placental lobule and monolayers of Be-Wo cell line indicated that methadone is extruded by P-gp. Transfer of methadone to the fetal circuit was increased by 30% in the presence of the P-gp inhibitor GF120918 while the transfer of paclitaxel, a typical substrate of the glycoprotein, was increased by 50%. In the Be-Wo cell line, methadone and paclitaxel uptake was also increased in the presence of the P-gp inhibitor cyclosporin A. Moreover, the expression of P-gp in placental brush-border membranes varied between term placentas. Taken together, these data strongly suggest that the concentration of methadone in the fetal circulation is affected by the expression and activity of P-gp. It is reasonable to speculate that placental disposition of methadone affects its concentration in the fetal circulation. If true, this may also be directly related to the incidence and intensity of neonatal abstinence syndrome (NAS).

Indexed as

ATP Binding Cassette Transporter, Subfamily B, Member 1Cell LineDose-Response Relationship, DrugFemaleHumansMaternal-Fetal ExchangeMethadonePregnancyProtein BindingATP Binding Cassette Transporter, Subfamily B, Member 1Methadone

Identifiers

PMID15876424
PMCPMC2263002
OpenAlexW1999304753

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.