Evidence map›Paper›PMID 21770760›Full record

ArticleJournal of neurotrauma2011

The effect of progesterone dose on gene expression after traumatic brain injury.

Gail D Anderson, Federico M Farin, Theo K Bammler, Richard P Beyer, Alicia A Swan, Hui-Wen Wilkerson, Eric D Kantor, Michael R Hoane

Abstract read
In one paragraph

Article in Journal of neurotrauma, 2011. 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
2.4field-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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Hypertonic Saline Alleviates Brain Edema After Traumatic Brain Injury via Downregulation of Aquaporin 4 in Rats.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  7. Article
  8. Ischemia/Reperfusion Induces Interferon-Stimulated Gene Expression in Microglia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Progesterone for neuroprotection in pediatric traumatic brain injury.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2015
    Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Gestational age-dependent changes in gene expression of metabolic enzymes and transporters in pregnant mice.Drug metabolism and disposition: the biological fate of chemicals · 2013
    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

8 authors at 1 institution in 1 country.

Gail D AndersonDepartment of Pharmacy, University of Washington, Seattle, Washington 98195, USA. gaila@washington.edu
Federico M Farin
Theo K Bammler
Richard P Beyer
Alicia A Swan
Hui-Wen Wilkerson
Eric D Kantor
Michael R Hoane
Southern Illinois University Carbondale · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
Pharmacological Optimization of Poly-Drug Therapy in Traumatic Brain InjuryR01HD061944 · NICHD · UNIVERSITY OF WASHINGTON · PI ANDERSON, GAIL, HOANE, MICHAEL R. · 2009 to 2013
$3.1M
NICHD NIH HHS R01 HD061944NICHD NIH HHS R01 HD061944-01NIEHS NIH HHS P30ES07033
6 · The paper itself

Abstract

Microarray-based transcriptional profiling was used to determine the effect of progesterone in the cortical contusion (CCI) model. Gene ontology (GO) analysis then evaluated the effect of dose on relevant biological pathways. Treatment (vehicle, progesterone 10 mg/kg or 20 mg/kg given i.p.) was started 4 h post-injury and administered every 12 h post-injury for up to 72 h, with the last injection 12 hr prior to death for the 24 h and 72 h groups. In the CCI-injured vehicle group compared to non-injured animals, expression of 1,114, 4,229, and 291 distinct genes changed >1.5-fold (p<0.05) at 24 h, 72 h, and 7 days, respectively. At 24 h, the effect of low-dose progesterone on differentially expressed genes was <20% the effect of higher dose compared to vehicle. GO analysis identified a significant effect of low- and high-dose progesterone treatment compared to vehicle on DNA damage response. At 72 h, high-dose progesterone treatment compared to vehicle affected expression of almost twice as many genes as did low-dose progesterone. Both low- and high-dose progesterone resulted in expression of genes regulating inflammatory response and apoptosis. At 7 days, there was only a modest difference in high-dose progesterone compared to vehicle, with only 14 differentially expressed genes. In contrast, low-dose progesterone resulted in 551 differentially expressed genes compared to vehicle. GO analysis identified genes for the low-dose treatment involved in positive regulation of cell proliferation, innate immune response, positive regulation of anti-apoptosis, and blood vessel remodeling.

Indexed as

AnimalsApoptosisBrain InjuriesCerebral CortexDose-Response Relationship, DrugGene ExpressionMaleProgesteroneProgestinsRatsRats, Sprague-DawleyProgesteroneProgestins

Identifiers

PMID21770760
PMCPMC3172874
OpenAlexW2035174661

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.