中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
THE CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2015年
7期
548-550
,共3页
卢国林%陈小琳%张素晶%毛晓丹%廖鹨
盧國林%陳小琳%張素晶%毛曉丹%廖鷚
로국림%진소림%장소정%모효단%료류
麻醉药%吸入%N-甲基-D-天冬氨酸受体%原位杂交%海马
痳醉藥%吸入%N-甲基-D-天鼕氨痠受體%原位雜交%海馬
마취약%흡입%N-갑기-D-천동안산수체%원위잡교%해마
anesthetics%inhalation%N-methyl-D-aspartate receptor%in situ hybridization%hippocampus
目的:探讨七氟醚对新生大鼠海马 N -甲基-D -天冬氨酸受体( NMDA)亚基mRNA表达的影响。方法新生SD大鼠随机分为2组(均12只),七氟醚组吸入3%七氟醚6 h,而对照组吸入30%氧气6 h。 2组大鼠吸入气体后24 h处死,取海马组织,用原位杂交法检测海马NMDA受体亚基mRNA表达及 NMDA 受体2B 亚基( NR2B)与 NMDA 受体2A 亚基(NR2A)比率的变化。结果与对照组比较,七氟醚组NR2AmRNA表达显著下调(P<0.05),NR2BmRNA表达显著上调(P<0.05),NR2B/NR2A的比率显著上升( P<0.05)。结论七氟醚诱发新生鼠海马神经毒性可能与调控NMDA受体亚基mRNA表达有关。
目的:探討七氟醚對新生大鼠海馬 N -甲基-D -天鼕氨痠受體( NMDA)亞基mRNA錶達的影響。方法新生SD大鼠隨機分為2組(均12隻),七氟醚組吸入3%七氟醚6 h,而對照組吸入30%氧氣6 h。 2組大鼠吸入氣體後24 h處死,取海馬組織,用原位雜交法檢測海馬NMDA受體亞基mRNA錶達及 NMDA 受體2B 亞基( NR2B)與 NMDA 受體2A 亞基(NR2A)比率的變化。結果與對照組比較,七氟醚組NR2AmRNA錶達顯著下調(P<0.05),NR2BmRNA錶達顯著上調(P<0.05),NR2B/NR2A的比率顯著上升( P<0.05)。結論七氟醚誘髮新生鼠海馬神經毒性可能與調控NMDA受體亞基mRNA錶達有關。
목적:탐토칠불미대신생대서해마 N -갑기-D -천동안산수체( NMDA)아기mRNA표체적영향。방법신생SD대서수궤분위2조(균12지),칠불미조흡입3%칠불미6 h,이대조조흡입30%양기6 h。 2조대서흡입기체후24 h처사,취해마조직,용원위잡교법검측해마NMDA수체아기mRNA표체급 NMDA 수체2B 아기( NR2B)여 NMDA 수체2A 아기(NR2A)비솔적변화。결과여대조조비교,칠불미조NR2AmRNA표체현저하조(P<0.05),NR2BmRNA표체현저상조(P<0.05),NR2B/NR2A적비솔현저상승( P<0.05)。결론칠불미유발신생서해마신경독성가능여조공NMDA수체아기mRNA표체유관。
Objective To investigate the effect of sevoflurane on mRNA expression of N -methyl -D -aspartate ( NMDA ) receptor subunit in neonatal rat hippocampi.Methods Twenty-four SD rats were devided into 2 groups( n=12 each) via a random number table:sevoflurane group and control group.The 3.0% sevoflurane and oxy-gen inhalated for 6 h respectively.Rats were sacrificed at 24 h after inhalation of sevoflurane or oxygen.Hippocampi were removed to idendtify the mRNA expression of NMDA subunit and the ratio of NR2 B/NR2 A through in situ hybridization.Results Compared with control group, NR2BmRNA and the ratio of NR2B/NR2A increased, and NR2 AmRNA decreased significantly in sevoflurane group ( P<0.05 ).Conclusion Neurotoxicity of sevoflurane in immature hippocampi might be attributed to regulation of mRNA expression of NMDA subunit in neonatal rat.