Evidence map›Paper›PMID 19049898›Full record

ArticleProstaglandins & other lipid mediators2009

Regulation of the fetal mouse ductus arteriosus is dependent on interaction of nitric oxide and COX enzymes in the ductal wall.

Jeff Reese, Patrick W O'Mara, Stanley D Poole, Naoko Brown, Chelsea Tolentino, Delrae M Eckman, Judy L Aschner

Open access · greenAbstract read
In one paragraph

Article in Prostaglandins & other lipid mediators, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. KCommunications medicine · 2026
    Article
  2. Article
  3. A novel role for PGEAmerican journal of physiology. Heart and circulatory physiology · 2023
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Renal lymphatic vessel dynamics.American journal of physiology. Renal physiology · 2020
    Article
  9. Article
  10. Review
  11. Review
  12. Selective serotonin reuptake inhibitor exposure constricts the mouse ductus arteriosus in utero.American journal of physiology. Heart and circulatory physiology · 2016
    Article
  13. Article
  14. Aminoglycoside-mediated relaxation of the ductus arteriosus in sepsis-associated PDA.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Omental grafting: a cell-based therapy for blood vessel repair.Journal of tissue engineering and regenerative medicine · 2013
    Article
  20. 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 2 institutions in 1 country.

Jeff ReeseDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232-0656, USA. jeff.reese@vanderbilt.edu
Patrick W O'Mara
Stanley D Poole
Naoko Brown
Chelsea Tolentino
Delrae M Eckman
Judy L Aschner
Vanderbilt University Medical Center · USWake Forest University · US

Funding

Mechanisms of Ductus Arteriosus RegulationR01HL077395 · NHLBI · VANDERBILT UNIVERSITY · PI REESE, JOHN JEFFREY · 2006 to 2010
$2.0M
Hsp90/Client Protein Interactions in the Newborn LungR01HL075511 · NHLBI · VANDERBILT UNIVERSITY · PI ASCHNER, JUDY LYNN · 2005 to 2008
$1.5M
NHLBI NIH HHS HL-075511NHLBI NIH HHS HL-77395NHLBI NIH HHS R01 HL075511NHLBI NIH HHS R01 HL077395
6 · The paper itself

Abstract

Nitric oxide (NO) and cyclooxygenase (COX)-derived prostaglandins are critical regulators of the fetal ductus arteriosus. To examine the interaction of these pathways within the ductus wall, the ductus arteriosus of term and preterm fetal mice was evaluated by pressurized myography. The isolated preterm ductus was more sensitive to NOS inhibition than at term. Sequential NOS and COX inhibition caused 36% constriction of the preterm ductus regardless of drug order. In contrast, constriction of the term ductus was dependent on the sequence of inhibition; NOS inhibition prior to COX inhibition produced greater constriction than when inhibitors were given in reverse order (36+/-6% versus 23+/-5%). Selective COX-1 or COX-2 inhibition prior to N(G)-nitro-l-arginine methyl ester (l-NAME) induced the expected degree of constriction. However, NOS inhibition followed by selective COX-2 inhibition caused unexpected ductal dilation. These findings are consistent with NO-induced activation of COX in the ductus arteriosus wall and the production of a COX-2-derived constrictor prostanoid that contributes to the balance of vasoactive forces that maintain fetal ductus arteriosus tone.

Indexed as

15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAnimalsCyclooxygenase InhibitorsDrug InteractionsDuctus ArteriosusFemaleFetusIndomethacinIn Vitro TechniquesMiceMyographyNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide DonorsPregnancyProstaglandin-Endoperoxide Synthases15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidCyclooxygenase InhibitorsIndomethacinNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide DonorsProstaglandin-Endoperoxide SynthasesVasoconstrictor Agents

Identifiers

PMID19049898
PMCPMC2813040
OpenAlexW2057755427

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.