中华麻醉学杂志
中華痳醉學雜誌
중화마취학잡지
CHINESE JOURNAL OF ANESTHESIOLOGY
2011年
8期
964-967
,共4页
佘高明%谢红%张力元%胡丽芳%孙锐%王琛
佘高明%謝紅%張力元%鬍麗芳%孫銳%王琛
사고명%사홍%장력원%호려방%손예%왕침
麻醉药,吸入%性别因素%cAMP反应元件结合蛋白质%海马%神经元
痳醉藥,吸入%性彆因素%cAMP反應元件結閤蛋白質%海馬%神經元
마취약,흡입%성별인소%cAMP반응원건결합단백질%해마%신경원
Anesthetics,inhalation%Sex factors%Cyclic AMP response element-binding protein%Hippocampus%Neurons
目的 评价七氟醚对不同性别大鼠海马神经元磷酸化cAMP反应元件结合蛋白1(p-CREB1)表达的影响.方法 健康成年雌性SD大鼠30只,3月龄,体重180~220 g,采用随机数字表法,将大鼠随机分为2组(n=15):对照组(Fc组)和七氟醚组(Fs组);健康成年雄性SD大鼠28只,3月龄,体重380-440 g,采用随机数字表法,将大鼠随机分为2组(n=14):对照组(Mc组)和七氟醚组(Ms组).Fc组和Mc组吸入95%氧气(流量4 L/min)2 h,Fs组和Ms组吸入3%七氟醚2h.于停止吸入七氟醚后2d时行避暗实验;于停止吸入七氟醚后3~7d时行Morris水迷宫实验,第7天认知功能测定结束后处死大鼠,取脑组织,剥离海马,采用Western blot法检测海马组织p-CREB1及Bcl-2、caspase-8的表达水平.结果 与Fc组比较,Fs组停止吸入七氟醚后3d时逃避潜伏期延长,游泳总路程增加,海马组织p-CREB1和Bcl-2表达下调,caspase-8表达上调(P<0.05);与Mc组比较,Ms组停止吸入七氟醚后3~6d时逃避潜伏期延长,游泳总路程增加,海马组织p-CREB1和Bcl-2表达下调,caspase-8表达上调(P<0.05);与Fs组比较,Ms组停止吸入七氟醚后4~6d时逃避潜伏期延长,游泳总路程增加,海马组织p-CREB1和Bcl-2表达下调(P<0.05).结论 七氟醚可通过抑制海马神经元CREB1蛋白磷酸化,上调caspase-8蛋白表达,下调Bcl-2蛋白表达,促进神经元凋亡,导致大鼠认知功能减退,且对雄性大鼠的效应更明显.
目的 評價七氟醚對不同性彆大鼠海馬神經元燐痠化cAMP反應元件結閤蛋白1(p-CREB1)錶達的影響.方法 健康成年雌性SD大鼠30隻,3月齡,體重180~220 g,採用隨機數字錶法,將大鼠隨機分為2組(n=15):對照組(Fc組)和七氟醚組(Fs組);健康成年雄性SD大鼠28隻,3月齡,體重380-440 g,採用隨機數字錶法,將大鼠隨機分為2組(n=14):對照組(Mc組)和七氟醚組(Ms組).Fc組和Mc組吸入95%氧氣(流量4 L/min)2 h,Fs組和Ms組吸入3%七氟醚2h.于停止吸入七氟醚後2d時行避暗實驗;于停止吸入七氟醚後3~7d時行Morris水迷宮實驗,第7天認知功能測定結束後處死大鼠,取腦組織,剝離海馬,採用Western blot法檢測海馬組織p-CREB1及Bcl-2、caspase-8的錶達水平.結果 與Fc組比較,Fs組停止吸入七氟醚後3d時逃避潛伏期延長,遊泳總路程增加,海馬組織p-CREB1和Bcl-2錶達下調,caspase-8錶達上調(P<0.05);與Mc組比較,Ms組停止吸入七氟醚後3~6d時逃避潛伏期延長,遊泳總路程增加,海馬組織p-CREB1和Bcl-2錶達下調,caspase-8錶達上調(P<0.05);與Fs組比較,Ms組停止吸入七氟醚後4~6d時逃避潛伏期延長,遊泳總路程增加,海馬組織p-CREB1和Bcl-2錶達下調(P<0.05).結論 七氟醚可通過抑製海馬神經元CREB1蛋白燐痠化,上調caspase-8蛋白錶達,下調Bcl-2蛋白錶達,促進神經元凋亡,導緻大鼠認知功能減退,且對雄性大鼠的效應更明顯.
목적 평개칠불미대불동성별대서해마신경원린산화cAMP반응원건결합단백1(p-CREB1)표체적영향.방법 건강성년자성SD대서30지,3월령,체중180~220 g,채용수궤수자표법,장대서수궤분위2조(n=15):대조조(Fc조)화칠불미조(Fs조);건강성년웅성SD대서28지,3월령,체중380-440 g,채용수궤수자표법,장대서수궤분위2조(n=14):대조조(Mc조)화칠불미조(Ms조).Fc조화Mc조흡입95%양기(류량4 L/min)2 h,Fs조화Ms조흡입3%칠불미2h.우정지흡입칠불미후2d시행피암실험;우정지흡입칠불미후3~7d시행Morris수미궁실험,제7천인지공능측정결속후처사대서,취뇌조직,박리해마,채용Western blot법검측해마조직p-CREB1급Bcl-2、caspase-8적표체수평.결과 여Fc조비교,Fs조정지흡입칠불미후3d시도피잠복기연장,유영총로정증가,해마조직p-CREB1화Bcl-2표체하조,caspase-8표체상조(P<0.05);여Mc조비교,Ms조정지흡입칠불미후3~6d시도피잠복기연장,유영총로정증가,해마조직p-CREB1화Bcl-2표체하조,caspase-8표체상조(P<0.05);여Fs조비교,Ms조정지흡입칠불미후4~6d시도피잠복기연장,유영총로정증가,해마조직p-CREB1화Bcl-2표체하조(P<0.05).결론 칠불미가통과억제해마신경원CREB1단백린산화,상조caspase-8단백표체,하조Bcl-2단백표체,촉진신경원조망,도치대서인지공능감퇴,차대웅성대서적효응경명현.
Objective To investigate the difference in the effects of sevoflurane inhalation on hippocampal neuronal phosphorylated cAMP response element-binding protein between male and female rats.Methods Fiftyeight healthy SD rats aged 3 months weighing 180-440 g were randomly divided into 4 groups:group female control (Fc group,n = 15) ; group female sevoflurane (Fs group,n = 15) ; group male control (Mc group,n = 14) and group male sevoflurane (Ms group,n = 14).The 2 control groups (Fc group,Mc group) inhaled 95% 02 for 2 h,while the 2 sevoflurane groups (Fs group,Ms group) inhaled 3% sevoflurane for 2 h.The cognitive function was assessed by passive avoidance task performed on the 2nd day after sevoflurane inhalation and Morris water maze test once a day for 5 consecutive days from day 3-7 after sevoflurane.The animals were sacrificed after last cognitive function assessment test on the 7th day after sevoflurane inhalation and their brains were removed for determination of expression of hippocampal neuronal p-CREB1,Bcl-2 and caspase-8 protein expression.Results Sevoflurane inhalation significantly increased the escape latency and swimming distance at day 3 after sevoflurane inhalation in group Fs and at days 3-6 in group Ms as compared with their control groups (Fc group,Mc group) in Morris water maze test.The escape latency and swimming distance were significantly longer at 4-6 d in Ms group than in Fs group.Sevoflurane significantly decreased p-CREB1 and Bcl-2 protein expression and increased caspase-8 expression in groups Fs and Ms as compared with their control groups (Fc group,Mc group).Bcl-2 protein expression was significantly higher in group Fs than in group Ms.Conclusion Two hour 3 % sevoflurane inhalation can induce hippocampal neuronal apoptosis by down-regulating CREB1 phosphorylation and Bcl-2 expression and up-regulating caspase-8 expression.The effects are greater in male rats than in female rats.