Hydrogen inhalation ameliorates oxidative stress and glucose metabolism disorder in the brain of hindlimb unloading rats

First, authors explain the experiment materials and methods. In the experiment, specific pathogen-free (SPF) facility Sprague-Dawley male rats are purchased from Experiment Animal Center of Wei Tong Li Hua (Beijing, China) and are maintained at the SPF facility of China Astronaut Research and Training Center in SPF with 12-h light/dark cycle at ambient temperature and humidity and fed a standard chow diet. After 7 d, the rats are randomly divided into 4 groups: 1) control (Ctrl) group, where rats were kept under normal conditions; 2) Ctrl + H2 group, where rats were treated with about 5% hydrogen under normal conditions for 90 min each time, 2 times per day; 3) HU, where rats were treated with hindlimb unloading; and 4) HU + H2 group, rats were treated with about 5% hydrogen under hindlimb unloading conditions for 90 min each time, 2 times per day. The 5% H2 is obtained by mixing the H2–O2 (66% hydrogen and 33% oxygen) generated by the hydrogen/oxygen generator and air. All the animal experiments were approved by the Committees of Animal Ethics and Experimental Safety of the China Astronaut Research and Training Center (reference number: ACC-IACUC-2020-006). After 28 d of hindlimb unloading, behavioral assessments, neurotransmitter level analysis, histological analysis, assays for GSSG, GSH, MDA, SOD, and CAT, targeted metabolite profiling, mRNA sequencing, RNA extraction and real-time PCR, western blotting, and statistical analysis are performed.

Then, authors present their experiment analysis results. The results are summarized in to four points. (1) Hydrogen inhalation improved brain function and alleviated the pathological damage in hippocampus induced by hindlimb unloading. (2) Hydrogen inhalation ameliorated the level of oxidative stress induced by hindlimb unloading in rat brain. (3) Hydrogen inhalation ameliorated the perturbation in glucose metabolism induced by hindlimb unloading in rat brain. (4) The potential mechanism of hydrogen in ameliorating unloading-induced rat brain dysfunction: hindlimb unloading may induce cognitive defects via PGC-1α and BDNF by influencing the expression of RGS13, while H₂ alleviated these effects.

Last, authors draw the conclusion. This study suggests that hydrogen plays a protective role in hindlimb-unloading-induced brain damage, which is closely related with the obvious effect of hydrogen treatment in alleviating antioxidant activities and regulation on glucose metabolism. The changes of PGC-1α and BDNF, the key regulators of metabolism and brain function, are probably involved in this process. The underlying mechanism need to be further explored. The function of hydrogen on brain protection provides a potential protective measure for astronauts during spaceflight.