- PMID: 17486089
- DOI: 10.1038/nm1577
Abstract
Acute oxidative stress induced by ischemia-reperfusion or
inflammation causes serious damage to tissues, and persistent oxidative
stress is accepted as one of the causes of many common diseases
including cancer. We show here that hydrogen (H(2)) has potential as an
antioxidant in preventive and therapeutic applications. We induced acute
oxidative stress in cultured cells by three independent methods. H(2)
selectively reduced the hydroxyl radical, the most cytotoxic of reactive
oxygen species (ROS), and effectively protected cells; however, H(2)
did not react with other ROS, which possess physiological roles. We used
an acute rat model in which oxidative stress damage was induced in the
brain by focal ischemia and reperfusion. The inhalation of H(2) gas
markedly suppressed brain injury by buffering the effects of oxidative
stress. Thus H(2) can be used as an effective antioxidant therapy; owing
to its ability to rapidly diffuse across membranes, it can reach and
react with cytotoxic ROS and thus protect against oxidative damage.
Source: https://pubmed.ncbi.nlm.nih.gov/17486089/