Abstract

Hydrogen is the most abundant chemical element in the Universe, but is seldom regarded as a therapeutic agent. Recent evidence has shown that hydrogen is a potent antioxidative, antiapoptotic and anti-inflammatory agent and so may have potential medical applications in cells, tissues and organs. There are several methods to administer hydrogen, such as inhalation of hydrogen gas, aerosol inhalation of a hydrogen-rich solution, drinking hydrogen dissolved in water, injecting hydrogen-rich saline (HRS) and taking a hydrogen bath. Drinking hydrogen solution (saline/pure water/other solutions saturated with hydrogen) may be more practical in daily life and more suitable for daily consumption. This review summarizes the findings of recent studies on the use of hydrogen in emergency and critical care medicine using different disease models.

Highlights

  • Hydrogen is the lightest element in the Periodic Table and the most abundant chemical substance in the Universe

  • In July 2007 researchers from the Japan Medical University Institute of Geriatrics reported that inhaled hydrogen gas has antioxidant and antiapoptotic properties that protect the brain against ischemia–reperfusion (I/R) injury and stroke by selectively reducing hydroxyl radicals (·OH) and ONOO− in cell-free systems [1]

  • This review focuses on the findings of recent studies of the effects of hydrogen in different disease models in

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Summary

Introduction

HRS treatment significantly attenuates the severity of L-arginine-induced acute pancreatitis in rats by inhibiting oxidative stress, apoptosis and NF-κB activation and promoting acinar cell proliferation [35]. HRS treatment significantly attenuated the severity of intestinal I/R injury by inhibiting apoptosis and Hydrogen therapy and trauma It has been reported that administration of HRS reduced acute spinal cord contusion injury by decreasing the number of apoptotic cells, suppressing oxidative stress, increasing the release of brain derived neurotrophic factor and improving locomotor function [44]. Treatment of mice with 2% hydrogen had beneficial effects on sepsis and sepsis associated organ damage, as demonstrated by decreased levels of oxidative products, increased antioxidant enzyme activity and reduced levels of (HMGB1) in serum and tissue. Because of its extensive and diverse effects, hydrogen seems to differ from conventional drugs that act on their pharmacologic targets, the pharmacokinetics, biology and toxicity of hydrogen remains incompletely understood

Conclusions
Findings
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