Background/aim: The aim of this study was to investigate whether a hydrogen administration can produce neuroprotective effects after brain ischemia reperfusion in rats. Materials and methods: A brain ischemia reperfusion injury was induced by a 2-h left middle cerebral artery occlusion (MCAO) using an intraluminal filament, followed by 46 h of reperfusion. A hydrogen-rich saline (1 mL/kg body weight i.p.) was administered at the beginning of reperfusion. Saline (1 mL/kg)-treated animals were used as the control. Sham-operated animals were also used. Subsequently, 48 h after the MCAO, histological alternations, heme oxygenase-1 (HO-1) expression, and levels of malondialdehyde (MDA) and superoxide dismutase (SOD) in the cerebral cortex and the hippocampus were examined. Results: Hydrogen significantly alleviated brain tissue histological damage, promoted HO-1 expression, upregulated levels of SOD, and decreased the levels of MDA in brain tissue after the ischemia reperfusion injury. Conclusion: The results suggest that the neuroprotective effects of hydrogen may be mediated by promoting HO-1 expression and attenuated the oxidative injury.
Hydrogen, heme oxygenase-1, brain, cerebral ischemia reperfusion, rats
WANG, XIFENG; ZHANG, LIANSHUANG; ZHAO, WEI; and LIU, TONGSHEN
"The protective effects of hydrogen on HO-1 expression in the brainafter focal cerebral ischemia reperfusion in rats,"
Turkish Journal of Medical Sciences: Vol. 46:
5, Article 39.
Available at: https://journals.tubitak.gov.tr/medical/vol46/iss5/39