Protective effect of hydrogen against hyperoxia-induced type II alveolar epithelial cell injury.
- Author:
Lan YAO
1
;
Feng XU
;
Chong LUO
;
Pan YU
;
Xinxin DONG
;
Xuejun SUN
;
Chengjun LIU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Animals, Newborn; Antioxidants; metabolism; Cell Proliferation; Cells, Cultured; Epithelial Cells; drug effects; Female; Hydrogen; pharmacology; Male; Malondialdehyde; metabolism; Membrane Potential, Mitochondrial; Oxidative Stress; drug effects; Oxygen; adverse effects; Pulmonary Alveoli; cytology; Rats; Rats, Sprague-Dawley; Superoxide Dismutase; metabolism
- From: Journal of Southern Medical University 2013;33(2):193-196
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the protective effect of hydrogen against hyperoxia-induced oxidative stress injury in premature rat type II alveolar epithelial cells (AECs).
METHODSThe type II AECs isolated from premature rats were randomly divided into air (21% oxygen) control group, hyperoxia (95% oxygen) control group, air + hydrogen group, and hyperoxia+ hydrogen group. The cells with hydrogen treatment were cultured in the presence of rich hydrogen. After the corresponding exposure for 24 h, the cell morphology was observed microscopically. MTT assay was used to evaluated the cell proliferation ability, and JC-1 fluorescence probe was used to detect the mitochondrial membrane potential (δφ) changes of the type II AECs. The concentration of maleic dialdehyde (MDA) and superoxide dismutase (SOD) activity in the cell supernatant were detected using colorimetric method.
RESULTSNo significant differences were found in cell growth or measurements between air control and air + hydrogen groups. Compared with air control group, the cells exposed to hyperoxia showed significantly suppressed proliferation, reduced mitochondrial membrane potential, increased MDA content, and decreased SOD activity. Intervention with hydrogen resulted in significantly increased cell proliferation and SOD activity and lowered MDA content, and restored the mitochondrial membrane potential in the cells with hyperoxia exposure (P<0.05).
CONCLUSIONHydrogen can significantly reduce hyperoxia-induced oxidative stress injury in premature rat type II AECs, improve the cellular antioxidant capacity, stabilize the mitochondrial membrane potential, and reduce the inhibitory effect of hyperoxia on cell proliferation.