南方医科大学学报 ›› 2019, Vol. 39 ›› Issue (07): 850-.doi: 10.12122/j.issn.1673-4254.2019.07.16

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乌司他丁对异氟烷介导的大鼠海马神经元凋亡的影响

郭远波,王研,张登文,崔灿,李涛,王晟   

  • 出版日期:2019-07-20 发布日期:2019-07-20

Effect of ulinastatin on isoflurane-induced neuronal apoptosis in the hippocampus of rats

  • Online:2019-07-20 Published:2019-07-20

摘要: 目的探讨乌司他丁预处理对异氟烷介导的大鼠海马神经元线粒体途径凋亡的影响及可能的机制。方法36只SD雄性 大鼠随机分为对照组、异氟烷组和乌司他丁组,每组12只。对照组不给与任何处理,异氟烷组和乌司他丁组采用0.75%异氟烷 急性暴露6 h,而乌司他丁组在采用0.75%异氟烷急性暴露前,先给与50000 U/kg乌司他丁预处理。以TUNEL染色检测细胞凋 亡,JC-1探针检测线粒体膜电位(△ψm),Western blot检测细胞色素C释放及caspase-3活性,H2DCFDA探针检测细胞内活性氧 (ROS)。结果与对照组比较,异氟烷组海马神经元凋亡显著增加(P<0.05),而乌司他丁组显著下降(P<0.05);异氟烷组神经元 线粒体△ψm显著降低(P<0.05),乌司他丁组显著提高(P<0.05);异氟烷组海马神经元ROS、细胞色素C释放及caspase-3活性均 显著增加(P<0.05),而乌司他丁组显著降低(P<0.05)。结论乌司他丁可以抑制异氟烷介导的大鼠海马神经元凋亡,其机制可 能与抑制线粒体途径凋亡有关。

Abstract: Objective To investigate the effect of ulinastatin pretreatment on isoflurane-induced mitochondria-dependent neuronal apoptosis in the hippocampus of rats. Methods Thirty-six male SD rats were randomly assigned into control group, isoflurane group and ulinastatin group. In the latter two groups, the rats were subjected to acute exposure to 0.75% isoflurane for 6 h and pretreated with 50 000 U/kg of ulinastatin before isoflurane exposure, respectively. After the treatments, apoptosis of the hippocampal neurons was detected using TUNEL assay, and the mitochondrial membrane potential ( △ ψm) was measured using JC-1 mitochondrial membrane potential kit; cytochrome C release and caspase-3 activity were examined with Western blotting, and intracellular reactive oxygen species (ROS) was detected using the fluorescent probe H2DCFDA. Results Compared with those in the control group, the rats with acute exposure to isoflurane showed markedly increased TUNELpositive cells in the hippocampus (P<0.05), which were obviously reduced by ulinastatin pretreatment (P<0.05). The △ψm of the hippocampal neurons was significantly reduced after isoflurane exposure (P<0.05), and was partly recovered by ulinastatin pretreatment (P<0.05). Acute exposure to isoflurane resulted in obviously increased cellular ROS, cytochrome C release and caspase-3 activity in the hippocampal neurons (P<0.05), and these changes were significantly inhibited by ulinastatin pretreatment (P<0.05). Conclusion Ulinastatin pretreatment provides neuroprotection against isoflurane-induced apoptosis of the hippocampal neurons in rats possibly by inhibiting mitochondria-dependent apoptosis pathway.