Abstract

Background and objectives: Pneumonitis and fibrosis are the most common consequences of lung exposure to a high dose of ionizing radiation during an accidental radiological or nuclear event, and may lead to death, after some months to years. So far, some anti-inflammatory and antioxidant agents have been used for mitigation of lung injury. In the present study, we aimed to detect possible mitigatory effects of melatonin and metformin on radiation-induced pneumonitis and lung fibrosis. Materials and methods: 40 male mice were divided into 4 groups (10 mice in each). For control group, mice did not receive radiation or drugs. In group 2, mice were irradiated to chest area with 18 Gy gamma rays. In groups 3 and 4, mice were first irradiated similar to group 2. After 24 h, treatment with melatonin as well as metformin began. Mice were sacrificed after 100 days for determination of mitigation of lung pneumonitis and fibrosis by melatonin or metformin. Results: Results showed that both melatonin and metformin are able to mitigate pneumonitis and fibrosis markers such as infiltration of inflammatory cells, edema, vascular and alveolar thickening, as well as collagen deposition. Conclusion: Melatonin and metformin may have some interesting properties for mitigation of radiation pneumonitis and fibrosis after an accidental radiation event.

Highlights

  • Pneumonitis and fibrosis are the most common consequences of lung exposure to high dose of ionizing radiation

  • Histopathological results showed that irradiation of mice with 18 Gy gamma rays led to remarkable changes in the lung tissues

  • Results showed that irradiation with 18 Gy gamma rays caused severe congestion, inflammation, infiltration of macrophages, lymphocytes and neutrophils, as well as edema

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Summary

Introduction

Pneumonitis and fibrosis are the most common consequences of lung exposure to high dose of ionizing radiation. Irradiation of lung tissue leads to DNA damage and cell death which trigger release of chemokines and cytokines, resulting to accumulation of macrophages and lymphocytes in alveolar. Chronic infiltration of inflammatory cells and continuous production of free radicals and some cytokines such as IL-4, IL-13, TGF-β, and IFN-γ, lead to upregulation of pro-oxidant and pro-fibrotic genes, resulting in accumulation of collagen and incidence of lung fibrosis. Pneumonitis and fibrosis are the most common consequences of lung exposure to a high dose of ionizing radiation during an accidental radiological or nuclear event, and may lead to death, after some months to years.

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