Evidence map›Paper›PMID 21388273›Full record

ArticleRadiation research2011

Pentoxifylline enhances the radioprotective properties of γ-tocotrienol: differential effects on the hematopoietic, gastrointestinal and vascular systems.

Maaike Berbée, Qiang Fu, Sarita Garg, Shilpa Kulkarni, K Sree Kumar, Martin Hauer-Jensen

Abstract read
In one paragraph

Article in Radiation research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Radiomitigators: Breakthroughs in Post-Radiation Recovery.Antioxidants (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Article
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  5. Review
  6. Review
  7. Article
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  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Tocotrienol-Rich Fraction from Rice Bran Demonstrates Potent Radiation Protection Activity.Evidence-based complementary and alternative medicine : eCAM · 2015
    Article
  18. Vitamin E Analogs as Radiation Response Modifiers.Evidence-based complementary and alternative medicine : eCAM · 2015
    Review
  19. Article
  20. Review
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 3 institutions in 1 country.

Maaike BerbéeDivision of Radiation Health, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
Qiang Fu
Sarita Garg
Shilpa Kulkarni
K Sree Kumar
Martin Hauer-Jensen
University of Arkansas for Medical Sciences · USUniformed Services University of the Health Sciences · USCentral Arkansas Veterans Healthcare System · US

Funding

Somatostatin analogues as countermeasures against intestinal radiation toxicityU19AI067798 · NIAID · DUKE UNIVERSITY · PI CHAO, NELSON J. · 2005 to 2024
$82.1M
Endothelial Dysfunction in Intestinal Radiation ToxicityR01CA083719 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI HAUER-JENSEN, MARTIN · 2000 to 2009
$2.8M
NCI NIH HHS CA83719NCI NIH HHS R01 CA083719NIAID NIH HHS AI67798NIAID NIH HHS U19 AI067798
6 · The paper itself

Abstract

The vitamin E analog γ-tocotrienol (GT3) is a potent radioprotector and mitigator. This study was performed to (a) determine whether the efficacy of GT3 can be enhanced by the addition of the phosphodiesterase inhibitor pentoxifylline (PTX) and (b) to obtain information about the mechanism of action. Mice were injected subcutaneously with vehicle, GT3 [400 mg/kg 24 h before total-body irradiation (TBI)], PTX (200 mg/kg 30 min before TBI), or GT3+PTX before being exposed to 8.5-13 Gy TBI. Overall lethality, survival time and intestinal, hematopoietic and vascular injury were assessed. Cytokine levels in the bone marrow microenvironment were measured, and the requirement for endothelial nitric oxide synthase (eNOS) was studied in eNOS-deficient mice. GT3+PTX significantly improved survival compared to GT3 alone and provided full protection against lethality even after exposure to 12.5 Gy. GT3+PTX improved bone marrow CFUs, spleen colony counts and platelet recovery compared to GT3 alone. GT3 and GT3+PTX increased bone marrow plasma G-CSF levels as well as the availability of IL-1α, IL-6 and IL-9 in the early postirradiation phase. GT3 and GT3+PTX were equally effective in ameliorating intestinal injury and vascular peroxynitrite production. Survival studies in eNOS-deficient mice and appropriate controls revealed that eNOS was not required for protection against lethality after TBI. Combined treatment with GT3 and PTX increased postirradiation survival over that with GT3 alone by a mechanism that may depend on induction of hematopoietic stimuli. GT3+PTX did not reduce GI toxicity or vascular oxidative stress compared to GT3 alone. The radioprotective effect of either drug alone or both drugs in combination does not require the presence of eNOS.

Indexed as

AnimalsBlood VesselsChromansDrug SynergismEnzyme InhibitorsHematopoiesisIntestinesMaleMiceOxidative StressPentoxifyllinePeroxynitrous AcidRadiation InjuriesRadiation-Protective AgentsSurvival AnalysisVascular System InjuriesChromansEnzyme InhibitorsPentoxifyllinePeroxynitrous Acidplastochromanol 8Radiation-Protective AgentsVitamin E

Identifiers

PMID21388273
PMCPMC3115470
OpenAlexW2095270172

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.