Abstract

BackgroundCompared to radiation injury alone (RI), radiation injury combined wound (CI) further enhances acute radiation syndrome and subsequently mortality. We previously reported that therapy with Ghrelin, the 28-amino-acid-peptide secreted from the stomach, significantly increased 30-day survival and mitigated hematopoietic death by enhancing and sustaining granulocyte-colony stimulating factor (G-CSF) and keratinocyte chemoattractant (KC) in the blood and bone marrow; increasing circulating white blood cell depletion; inhibiting splenocytopenia; and accelerating skin-wound healing on day 30 after CI. Herein, we aimed to study the efficacy of Ghrelin on intestinal injury at early time points after CI.MethodsB6D2F1/J female mice were exposed to 60Co-γ-photon radiation (9.5 Gy, 0.4 Gy/min, bilateral), followed by 15% total-body-surface-area skin wounds. Several endpoints were measured: at 4–5 h and on days 1, 3, 7, and 15.ResultsGhrelin therapy mitigated CI-induced increases in IL-1β, IL-6, IL-17A, IL-18, KC, and TNF-α in serum but sustained G-CSF, KC and MIP-1α increases in ileum. Histological analysis of ileum on day 15 showed that Ghrelin treatment mitigated ileum injury by increasing villus height, crypt depth and counts, as well as decreasing villus width and mucosal injury score. Ghrelin therapy increased AKT activation and ERK activation; suppressed JNK activation and caspase-3 activation in ileum; and reduced NF-κB, iNOS, BAX and Bcl-2 in ileum. This therapy recovered the tight junction protein and mitigated bacterial translocation and lipopolysaccharides levels. The results suggest that the capacity of Ghrelin therapy to reduce CI-induced ileum injury is mediated by a balanced NF-κB-AKT-MAPK network that leads to homeostasis of pro-inflammatory and anti-inflammatory cytokines.ConclusionsOur novel results are the first to suggest that Ghrelin therapy effectively decreases intestinal injury after CI.

Highlights

  • Compared to radiation injury alone (RI), radiation injury combined wound (CI) further enhances acute radiation syndrome and subsequently mortality

  • We reported that Ghrelin mitigated CIinduced bone marrow damage by sustaining granulocyte-colony stimulating factor (G-CSF) and keratinocyte chemoattractant (KC) increases in bone marrow and circulation [40]

  • Ghrelin therapy inhibits circulating cytokines and chemokines after RI and CI It is evident that RI alone induced increases in circulatory cytokines/chemokines and CI further induced the increases [6]

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Summary

Introduction

Compared to radiation injury alone (RI), radiation injury combined wound (CI) further enhances acute radiation syndrome and subsequently mortality. CI has been observed to accelerate body-weight loss; amplify cytokine/chemokine imbalance and systemic bacterial infection [6, 16]; enhance leukocytopenia, thrombocytopenia, erythrocytopenia [7, 9, 10, 15], acute myelosuppression, immune system inhibition, fluid imbalance, macro- and microcirculation failure, massive cellular damage and disruption of vital organ functions. These subsequently led to multiple organ dysfunction (MOD) and multiple organ failure (MOF). Death occurs as a result of CI [1, 20, 25, 26]

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