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硫化氢联合浅低温对大鼠脑缺血再灌注损伤的影响
引用本文:苗晓蕾,嵇晴,李丹,徐苗苗,周玉弟,孙晓迪,段满林,徐建国.硫化氢联合浅低温对大鼠脑缺血再灌注损伤的影响[J].中华麻醉学杂志,2010,30(9).
作者姓名:苗晓蕾  嵇晴  李丹  徐苗苗  周玉弟  孙晓迪  段满林  徐建国
摘    要:目的 评价硫化氢(H2S)联合浅低温对大鼠脑缺血再灌注损伤的影响.方法 雄性SD大鼠80只,体重250~300 g,月龄3月,随机分为5组(n=16):假手术组(S组)、脑缺血再灌注组(IR组)、浅低温组(M组)、硫氢化钠组(NaHS组)和硫氢化钠+浅低温组(NM组).IR组、M组、NaHS组、和NM组采用四血管阻塞法建立大鼠脑缺血再灌注模型,缺血15 min后恢复灌注.NaHS组和NM组于再灌注即刻腹腔注射NaHS 14μmol/kg,其余组注射等容量生理盐水.同时M组和NM组于15 min内将直肠温降至32~33 ℃,并维持6 h;其余组采用白炽灯维持直肠温36~37 ℃.再灌注6 h时,各组处死12只大鼠,取海马组织,测定H2S的含量,采用Western b1ot法测定磷酸化cAMP反应原件结合蛋白(p-CREB)的表达,采用RT-PCR法测定脑源性神经营养因子(BDNF)mRNA的表达.于再灌注72 h时,各组处死4只大鼠,取海马组织,观察CA1区病理学结果.结果 M组、NaHS组和NM组病理学损伤较IR组减轻,其中NM组减轻最明显.与S组比较,IR组、M组、NaHS组和NM组海马H2S含量升高(P<0.05);与IR组和M组比较,NaHS组和NM组海马H2S含量升高(P<0.05).与S组比较,IR组、M组、NaHS组和NM组海马p-CREB和BDNF mRNA的表达上调(P<0.05);与IR组比较,M组、NaHS组和NM组海马p-CREB和BDNF mRNA的表达上调(P<0.05);与NaHS组和M组比较,NM组海马p-CREB表达差异无统计学意义(P>0.05),BDNF mRNA表达上调(P<0.05).NahS组和M组各指标比较差异无统计学意义(P>0.05).结论 H2S联合浅低温可减轻大鼠脑缺血再灌注损伤,其机制与上调海马p-CREB和BDNF mRNA的表达有关.

关 键 词:硫化氢  低温  人工  再灌注损伤  

Effect of hydrogen sulfide combined with mild hypothermia on cerebral ischemia-reperfusion in rats
MIAO Xiao-lei,JI Qing,LI Dan,XU Miao-miao,ZHOU Yu-di,SUN Xiao-di,DUAN Man-lin,XU Jian-guo.Effect of hydrogen sulfide combined with mild hypothermia on cerebral ischemia-reperfusion in rats[J].Chinese Journal of Anesthesilolgy,2010,30(9).
Authors:MIAO Xiao-lei  JI Qing  LI Dan  XU Miao-miao  ZHOU Yu-di  SUN Xiao-di  DUAN Man-lin  XU Jian-guo
Abstract:Objective To evaluate the effect of hydrogen sulfide combined with mild hypothermia on cerebral ischemia-reperfusion (I/R) injury in rats. Methods Eighty male SD rats, aged 3 months, weighing 250-300 g, were randomly divided into 5 groups ( n = 16 each): sham operation group (group S), cerebral I/R group,mild hypothermia group (group M), sodium hydrosulfide group (group NaHS) and NaHS + mild hypothermia group (group NM). In group I/R, M, NaHS and NM, cerebral I/R was induced by occlusion of 4 vessels (cauterization of bilateral vertebral arteries and 15 min occlusion of bilateral common carotid arteries) followed by reperfusion. In group NaHS and NM, intraperitoneal NaHS 14 μmol/kg was injected immediately after reperfusion, while the equal volume of normal saline was injected in the other three groups. At the same time, the rectal temperature was reduced to 32-33 ℃ within 15 min, lasting for 6 h, in group M and NM, while it was maintained at 36-37 ℃by physical method in other groups. Twelve rats of each group were sacrificed after 6 h of reperfusion, and then the hippocampus was removed for determination of the content of H2 S by using spectrophotometer and the expression of p-CREB and BDNF mRNA by using Western blot and RT-PCR respectively. Four rats in each group were sacririced after 72 h of reperfusion and then the hippocampus was removed for microscopic examination. Results The cerebral I/R injury was attenuated in group M, NaHS and NM compared with group I/R, with the slightest injury in group NM. The H2S content was significantly higher in group I/R, M, NaHS and NM than in group S, and in group NaHS and NM than in group I/R and M. The expression of p-CREB and BNDF mRNA was significantly higher in group I/R, M, NaHS and NM than in group S, and in group M, NaHS and NM than in group I/R. The BDNF mRNA expression was significantly higher in group NM than in group M and NaHS. There was no significant difference in the H2S content and the expression of p-CREB and BNDF mRNA between group NaHS and M.Conclusion Hydrogen sulfide combined with mild hypothermia can attenuate cerebral I/R injury by up-regulating the expression of p-CREB and BDNF mRNA in hippocampus in rats.
Keywords:Hydrogen sulfide  Hypothermia  induced  Reperfusion injury  Brain
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