Evidence map›Paper›PMID 25671547›Full record

ArticlePloS one2015

Human ghrelin mitigates intestinal injury and mortality after whole body irradiation in rats.

Zhimin Wang, Weng Lang Yang, Asha Jacob, Monowar Aziz, Ping Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Ghrelin Induces CluInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Radiomitigators: Breakthroughs in Post-Radiation Recovery.Antioxidants (Basel, Switzerland) · 2026
    Review
  4. Article
  5. Article
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  7. Radioprotective potential of probiotics against gastrointestinal and neuronal toxicity: a preclinical study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
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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

5 authors at 2 institutions in 1 country.

Zhimin WangTheraSource LLC, Manhasset, NY, United States of America.
Weng Lang YangCenter for Translational Research, The Feinstein Institute for Medical Research, Manhasset, NY, United States of America; TheraSource LLC, Manhasset, NY, United States of America.
Asha JacobCenter for Translational Research, The Feinstein Institute for Medical Research, Manhasset, NY, United States of America; TheraSource LLC, Manhasset, NY, United States of America.
Monowar AzizCenter for Translational Research, The Feinstein Institute for Medical Research, Manhasset, NY, United States of America.
Ping WangCenter for Translational Research, The Feinstein Institute for Medical Research, Manhasset, NY, United States of America.
TheraSource (United States) · USFeinstein Institute for Medical Research · US

Funding

PHS HHS R33A1080536PHS HHS R43A10696777
6 · The paper itself

Abstract

Widespread use of ionizing radiation has led to the realization of the danger associated with radiation exposure. Although studies in radiation countermeasures were initiated a half century ago, an effective therapy for a radiomitigator has not been identified. Ghrelin is a gastrointestinal hormone, and administration of ghrelin is protective in animal models of injuries including radiation combined injury. To test whether ghrelin can be protective in whole body irradiaton (WBI) alone, male Sprague Dawley (SD) rats were treated with human ghrelin (20 nmol/rat) daily for 6 days starting at either 24 h or 48 h after 10 Gray (Gy) WBI and survival outcome was examined. The 10 Gy WBI produced a LD70/30 model in SD rats (30% survival in 30 days). The survival rate in rats treated with ghrelin starting at 24 h was significantly improved to 63% and when treatment was initiated at 48 h, the survival remained at 61%. At 7 days post WBI, plasma ghrelin was significantly reduced from the control value. Ghrelin treatment starting at 24 h after WBI daily for 6 days improved histological appearance of the intestine, reduced gut permeability, serum endotoxin levels and bacterial translocation to the liver by 38%, 42% and 61%, respectively at day 7 post WBI. Serum glucose and albumin were restored to near control levels with treatment. Ghrelin treatment also attenuated WBI-induced intestinal apoptosis by 62% as evidenced by TUNEL staining. The expression of anti-apoptotic cell regulator Bcl-xl was decreased by 38% in the vehicle and restored to 75% of the control with ghrelin treatment. Increased expression of intestinal CD73 and pAkt were observed with ghrelin treatment, indicating protection of the intestinal epithelium after WBI. These results indicate that human ghrelin attenuates intestinal injury and mortality after WBI. Thus, human ghrelin can be developed as a novel mitigator for radiation injury.

Indexed as

AnimalsApoptosisBlood GlucoseCell MovementEndotoxinsGhrelinHumansIntestinal MucosaIntestinesLeukocytesMalePermeabilityRadiation Injuries, ExperimentalRadiation-Protective AgentsRatsRats, Sprague-DawleyBlood GlucoseEndotoxinsGhrelinRadiation-Protective AgentsSerum Albumin

Identifiers

PMID25671547
PMCPMC4325005
OpenAlexW2073925044

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.