Department of Anesthesiology, Jinling Hospital, School of Medicine, Nanjing University, No. 305 East Zhongshan Road, Nanjing, 210002, Jiangsu, China.
Department of Anaesthesiology, The 117th Hospital of PLA, No.14 Lingyin Road, Hangzhou, 310013, China.
Mol Neurobiol. 2016 Sep;53(7):4865-73. doi: 10.1007/s12035-015-9391-z. Epub 2015 Sep 9.
We investigated whether mild hypothermia combined with sodium hydrosulfide treatment during resuscitation improves neuron survival following cerebral ischemia-reperfusion injury beyond that observed for the individual treatments. Male Sprague-Dawley rats were divided into seven groups (n = 20 for each group). All rats underwent Pulsinelli 4-vessel occlusion. Ischemia was induced for 15 min using ligatures around the common carotid arteries, except for the sham group. Immediately after initiating reperfusion, the mild hypothermia (MH), sodium hydrosulfide (NaHS), hydroxylamine (HA), MH + NaHS, MH + HA, and ischemia-reperfusion (I/R) control groups received an intraperitoneal injection of saline, sodium hydrosulfide, hydroxylamine, sodium hydrosulfide, hydroxylamine, and saline, respectively, and mild hypothermia (32 to 33 °C) was induced in the MH, MH + NaHS, and MH + HA groups for 6 h. The levels of NR2A, NR2B, p-Akt, and p-Gsk-3β in the hippocampus of the MH, NaHS, and MH + NaHS groups were higher than those in the I/R control group, with the highest levels observed in the MH + NaHS group (P < 0.05). Treatment with hydroxylamine reduced the levels of these proteins in the HA and MH + HA groups, compared with the I/R control and MH groups, respectively. The apoptotic index of the CA1 region of the hippocampus was 45.2, 66.5, 63.5, and 84.8 % in the MH + NaHS, MH, NaHS, and I/R control groups, respectively (P < 0.05), indicating that the combination treatment shifted the NR2A/NR2B balance in favor of synaptic neuron stimulation and phosphatidylinositol 3'-kinase (PI3K)/Akt signaling. The combination of mild hypothermia and sodium hydrosulfide treatment for resuscitation following ischemia-reperfusion injury was more beneficial for reducing hippocampal apoptosis and pathology than that of mild hypothermia or hydrogen sulfide treatment alone.
我们研究了在再灌注期间复温与硫氢化钠联合治疗是否能改善脑缺血再灌注损伤后的神经元存活,超过单独治疗的效果。雄性 Sprague-Dawley 大鼠分为七组(每组 20 只)。所有大鼠均进行 Pulsinelli 四血管闭塞。除假手术组外,通过结扎颈总动脉来诱导缺血 15 分钟。再灌注开始后,轻度复温(MH)、硫氢化钠(NaHS)、羟胺(HA)、MH+NaHS、MH+HA 和缺血再灌注(I/R)对照组分别腹腔注射生理盐水、硫氢化钠、羟胺、硫氢化钠、羟胺和生理盐水,MH、MH+NaHS 和 MH+HA 组诱导轻度复温(32 至 33°C)6 小时。MH、NaHS 和 MH+NaHS 组海马 NR2A、NR2B、p-Akt 和 p-Gsk-3β 水平高于 I/R 对照组,其中 MH+NaHS 组水平最高(P<0.05)。与 I/R 对照组和 MH 组相比,羟胺处理降低了 HA 和 MH+HA 组这些蛋白的水平。海马 CA1 区的细胞凋亡指数分别为 MH+NaHS、MH、NaHS 和 I/R 对照组的 45.2%、66.5%、63.5%和 84.8%(P<0.05),表明联合治疗使 NR2A/NR2B 平衡向有利于突触神经元刺激和磷脂酰肌醇 3'-激酶(PI3K)/Akt 信号的方向移动。与单独复温和氢硫化钠治疗相比,在缺血再灌注损伤后复苏中联合使用轻度复温和硫氢化钠治疗更有利于减少海马细胞凋亡和病理变化。