Hydrogen Gas Inhalation Reduces Lung Damage from Bacterial Toxins in Mice
- Authors
- Xiaochen Qiu, Hengyu Li, Hongtai Tang, Yichao Jin, Wuquan Li, YuSun, PingFeng, Xuejun Sun, Zhaofan Xia
- Journal
- International Immunopharmacology
- Year
- 2011
- DOI
- 10.1016/j.intimp.2011.09.007
- Study Type
- Mouse
- Outcome
- Positive
- Peer Reviewed
- Yes
- Country
- China
- Health Condition
- Acute Lung Injury
- Body System
- Respiratory
TL;DR
Breathing in hydrogen gas can help reduce lung damage and improve survival in mice with a severe lung condition caused by an infection.
Key Finding
Mice with induced acute lung injury that inhaled 2% hydrogen gas had improved survival rates, reduced lung swelling, and less inflammatory damage compared to mice breathing normal air.
Summary
Researchers tested whether breathing hydrogen gas could help mice recover from acute lung injury (a serious condition where the lungs become inflamed and fill with fluid). They gave mice a harmful substance called lipopolysaccharide to trigger lung injury, then had some breathe hydrogen-mixed air while others breathed normal air. Mice that inhaled hydrogen survived better, had less fluid in their lungs, showed less inflammation, and had less damage to lung tissue compared to the control group.
Practical Takeaway
This is an early-stage animal study showing hydrogen gas may help protect against severe lung injury caused by specific inflammatory triggers. However, this was only tested in mice, not humans, so it's unclear whether these results would apply to people or to other types of lung disease. More research, including human studies, would be needed before hydrogen inhalation could be considered a treatment for acute lung injury.
Abstract
Acute lung injury (ALI) is a serious illness, the incidence and mortality of which are very high. Free radicals, such as hydroxyl radicals (OH) and peroxynitrite (ONOO(-)), are considered to be the final causative molecules in the pathogenesis of ALI. Hydrogen, a new antioxidant, can selectively reduce OH and ONOO(-). In the present study, we investigated the hypothesis that hydrogen inhalation could ameliorate ALI induced by intra-tracheal lipopolysaccharide (LPS, 5mg/kg body weight). Mice were randomized into three groups: sham group (physiological saline+2% hydrogen mixed gas), control group (LPS+normal air) and experiment group (LPS+2% hydrogen mixed gas). Bronchoalveolar lavage fluid (BALF) was performed to determine the total protein concentrations and pro-inflammatory cytokines. Lung tissues were assayed for oxidative stress variables, wet/dry (W/D) ratio, histological, immunohistochemistry and Western blotting examinations. Our experiments exhibited that hydrogen improved the survival rate of mice and induced a decrease in lung W/D ratio. In addition, hydrogen decreased malonaldehyde and nitrotyrosine content, inhibited myeloperoxidase and maintained superoxide dismutase activity in lung tissues and associated with a decrease in the expression of TNF-α, IL-1β, IL-6 and total protein concentrations in the BALF. Hydrogen further attenuated histopathological alterations and mitigated lung cell apoptosis. Importantly, hydrogen inhibited the activation of P-JNK, and also reversed changes in Bax, Bcl-xl and caspase-3. In conclusion, our data demonstrated that hydrogen inhalation ameliorated LPS-induced ALI and it may be exerting its protective role by preventing the activation of ROS-JNK-caspase-3 pathway.