Hydrogen Gas Protects Against Muscle Damage from Blood Flow Loss in Mice

Authors
Journal
European Journal of Vascular and Endovascular Surgery
Year
DOI
10.1016/j.ejvs.2024.01.081
Study Type
Mouse
Outcome
Positive
Peer Reviewed
Yes
Country
Japan
Health Condition
Ischemia-Reperfusion Injury
Body System
Musculoskeletal

TL;DR

Breathing in hydrogen gas helped protect mice's leg muscles from damage caused by temporarily cutting off and then restoring blood flow.

Key Finding

Hydrogen gas inhalation reduced inflammatory cell infiltration and muscle tissue damage in mice experiencing ischemia-reperfusion injury (temporary loss and restoration of blood flow to the hindlimb).

Summary

Researchers tested whether breathing hydrogen gas could protect mouse leg muscles from damage caused by temporarily cutting off blood flow and then restoring it—a common problem after surgery. Mice that breathed a mixture containing 1.3% hydrogen gas showed less inflammation, less muscle damage, and better preservation of normal muscle cells compared to mice that breathed regular air.

Practical Takeaway

This early-stage mouse study suggests hydrogen gas may help protect muscle tissue from surgical complications involving blood flow disruption, but human studies are needed to determine if these benefits apply to people. The findings are promising but limited to laboratory animals and cannot yet support health claims for hydrogen water or other hydrogen products in humans.

Abstract

Objective: Ischaemia-reperfusion (I/R) injury is a severe post-operative complication that triggers an inflammatory response and causes severe damage. Hydrogen gas has anti-oxidant and anti-apoptotic properties and has been shown to be safe in humans. The study aimed to investigate whether hydrogen gas protects against skeletal muscle I/R injury. Methods: Experimental basic research using mice. A total of 160 eight to 10 week old albino laboratory bred strain of house mice (25.8 ± 0.68 g) were used in this study. The mice were cable tied to the hindlimb under anaesthesia and then placed in an anaesthesia box filled with air and 2% isoflurane (control group); 80 mice were additionally subjected to 1.3% hydrogen gas in this mix (hydrogen group). After 2 hours, cable ties on the mice were removed to initiate reperfusion, and hydrogen inhalation lasted for 6 hours in the hydrogen group. After 6 hours, the mice were taken out of the box and kept in cages under standard conditions until time for observation at 16 different time points after reperfusion: 0, 2, 4, 6, 8, and 10 hours and one, two, three, four, five, six, seven, 14, 21, and 28 days. Five mice were sacrificed using excess anaesthesia at each time point, and the bilateral hindlimb tissues were harvested each time. The inflammatory effects of I/R injury were assessed by evaluating serum interleukin-6 concentrations using enzyme linked immunosorbent assay, as well as histological and immunohistochemical analyses. Untreated mice with I/R injury were used as controls. Results: Hydrogen gas showed protective effects associated with a reduction in inflammatory cell infiltration (neutrophils, macrophages, and lymphocytes), a reduced area of damaged muscle, maintenance of normal muscle cells, and replacement of damaged muscle cells with neoplastic myocytes. Conclusion: Inhalation of hydrogen gas had a protective effect against hindlimb I/R injury in mice, in part by reducing inflammatory cell infiltration and preserving normal muscle cells.