Hydrogen therapy reduces apoptosis in neonatal hypoxia–ischemia rat model

• DOI: 10.1016/j.neulet.2008.05.077
• Publication Date: 2008-06-04T16:05:03Z
• Authors: Jianmei Cai; Zhimin Kang; Wen Wu Liu; Xu Luo; Sun Qiang; John H. Zhang; Shigeo Ohta; Xuejun Sun; Weigang Xu; Hengyi Tao; Runping Li
• Keywords: Nissl body; Hypoxia; Brain damage

Hypoxia-ischemia (HI) brain injury is a major cause of neuronal cell death especially apoptosis in the perinatal period. This study was designated to examine the effect of hydrogen therapy on apoptosis in an established neonatal HI rat pup model. Seven-day-old rat pups were subjected to left common carotid artery ligation and then 90 min hypoxia (8% oxygen at 37 degrees C). Immediately after HI insult, pups were placed into a chamber filled with 2% H2 for 30 min, 60 min, or 120 min, respectively. 24 h after 2% H2 therapy, the pups were decapitated and brain injury was assessed by 2,3,5-triphenyltetrazoliumchloride (TTC), Nissl, and TUNEL staining, as well as caspase-3, caspase-12 activities in the cortex and hippocampus. H2 treatment in a duration-dependent manner significantly reduced the number of positive TUNEL cells and suppressed caspase-3 and -12 activities. These results indicated H2 administration after HI appeared to provide brain protection via inhibition of neuronal apoptosis.