Department of Physiology and Neurobiology, Xinxiang Medical University, Xinxiang, Henan Province, China.
Neural Regen Res. 2015 Jun;10(6):932-7. doi: 10.4103/1673-5374.158353.
The present study aimed to explore the mechanism underlying the protective effects of hydrogen sulfide against neuronal damage caused by cerebral ischemia/reperfusion. We established the middle cerebral artery occlusion model in rats via the suture method. Ten minutes after middle cerebral artery occlusion, the animals were intraperitoneally injected with hydrogen sulfide donor compound sodium hydrosulfide. Immunofluorescence revealed that the immunoreactivity of P2X7 in the cerebral cortex and hippocampal CA1 region in rats with cerebral ischemia/reperfusion injury decreased with hydrogen sulfide treatment. Furthermore, treatment of these rats with hydrogen sulfide significantly lowered mortality, the Longa neurological deficit scores, and infarct volume. These results indicate that hydrogen sulfide may be protective in rats with local cerebral ischemia/reperfusion injury by down-regulating the expression of P2X7 receptors.
本研究旨在探讨硫化氢对脑缺血/再灌注引起的神经元损伤的保护作用机制。我们通过缝线法建立了大鼠大脑中动脉闭塞模型。大脑中动脉闭塞 10 分钟后,动物通过腹腔注射给予硫化氢供体化合物硫氢化钠。免疫荧光显示,硫化氢处理可降低脑缺血/再灌注损伤大鼠大脑皮质和海马 CA1 区 P2X7 的免疫反应性。此外,硫化氢处理可显著降低这些大鼠的死亡率、Longa 神经功能缺损评分和梗死体积。这些结果表明,硫化氢可能通过下调 P2X7 受体的表达对局部脑缺血/再灌注损伤的大鼠具有保护作用。