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2000
Volume 27, Issue 5
  • ISSN: 1381-6128
  • E-ISSN: 1873-4286

Abstract

Radiation-induced lung injury is characterized by an acute pneumonia phase followed by a fibrotic phase. At the time of irradiation, a rapid, short-lived burst of reactive oxygen species (ROS) such as hydroxyl radicals (•OH) occurs, but chronic radiation-induced lung injury may occur due to excess ROS such as HO, O2•−, ONOO−, and •OH. Molecular hydrogen (H) is an efficient antioxidant that quickly diffuses cell membranes, reduces ROS such as •OH and ONOO−, and suppresses damage caused by oxidative stress in various organs. In 2011, through the evaluation of electron-spin resonance and fluorescent indicator signals, we had reported that H can eliminate •OH and can protect against oxidative stress-related apoptotic damage induced by irradiation of cultured lung epithelial cells. We had explored for the first time the radioprotective effects of H treatment on acute and chronic radiation-induced lung damage in mice by inhaled H gas (for acute) and imbibed H-enriched water (for chronic). Thus, we had proposed that H be considered a potential radioprotective agent. Recent publications have shown that H directly neutralizes highly reactive oxidants and indirectly reduces oxidative stress by regulating the expression of various genes. By regulating gene expression, H functions as an anti-inflammatory and anti-apoptotic molecule and promotes energy metabolism. The increased evidence obtained from cultured cells or animal experiments reveal a putative place for H treatment and its radioprotective effect clinically. This review focuses on major scientific advances in the treatment of H as a new class of radioprotective agents.

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/content/journals/cpd/10.2174/1381612827666210119103545
2021-02-01
2025-06-30
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