中华航海医学与高气压医学杂志
中華航海醫學與高氣壓醫學雜誌
중화항해의학여고기압의학잡지
CHINESE JOURNAL OF NAUTICAL MEDICINE AND HYPERBARIC MEDICINE
2013年
6期
384-388
,共5页
刘晓红%高光凯%毛蕊琪%曹永成%秦金燕%毕利泉%时艳辉%耿明
劉曉紅%高光凱%毛蕊琪%曹永成%秦金燕%畢利泉%時豔輝%耿明
류효홍%고광개%모예기%조영성%진금연%필리천%시염휘%경명
高压氧%急性减压病%脊髓损伤%基因表达谱%兔
高壓氧%急性減壓病%脊髓損傷%基因錶達譜%兔
고압양%급성감압병%척수손상%기인표체보%토
Hyperbaric oxygen%Acute decompression sickness%Spinal cord lesion%Gene expression profile%Rabbits
目的 初步探讨急性减压病兔脊髓损伤组织基因表达谱的变化.方法 新西兰大耳白兔10只,5只按文献方法制备急性减压病模型,为急性减压病组;另5只参照空气潜水减压表减至常压,为安全减压组.2组出舱后30 min内各随机选取2只兔,麻醉后解剖,留取胸腰段脊髓,迅速置于液氧中保存.应用基因表达谱芯片对4只兔的脊髓组织进行检测,采用实时定量逆转录聚合酶链反应(reverse transcription polymerase chain reaction,RT-PCR)方法对部分芯片筛选的差异表达基因结果进行验证.结果 芯片杂交结果显示,与安全减压组比较,急性减压病组上调2倍以上的基因9个,下调2倍以上的基因17个,差异表达基因主要涉及炎症、离子通道、细胞周期、物质转运和凋亡等方面.实时定量RT-PCR结果显示,与安全减压组比较,急性减压病组甲状旁腺激素和肿瘤细胞坏死因子分别上调平均6.18倍和6.46倍,酰基辅酶A合成酶和电压门控性离子通道基因分别下调平均2.28倍和3.16倍,与芯片杂交实验结果一致.结论 急性减压病兔脊髓病变差异表达基因主要涉及炎症、细胞周期和凋亡等方面,其意义需要进一步研究.
目的 初步探討急性減壓病兔脊髓損傷組織基因錶達譜的變化.方法 新西蘭大耳白兔10隻,5隻按文獻方法製備急性減壓病模型,為急性減壓病組;另5隻參照空氣潛水減壓錶減至常壓,為安全減壓組.2組齣艙後30 min內各隨機選取2隻兔,痳醉後解剖,留取胸腰段脊髓,迅速置于液氧中保存.應用基因錶達譜芯片對4隻兔的脊髓組織進行檢測,採用實時定量逆轉錄聚閤酶鏈反應(reverse transcription polymerase chain reaction,RT-PCR)方法對部分芯片篩選的差異錶達基因結果進行驗證.結果 芯片雜交結果顯示,與安全減壓組比較,急性減壓病組上調2倍以上的基因9箇,下調2倍以上的基因17箇,差異錶達基因主要涉及炎癥、離子通道、細胞週期、物質轉運和凋亡等方麵.實時定量RT-PCR結果顯示,與安全減壓組比較,急性減壓病組甲狀徬腺激素和腫瘤細胞壞死因子分彆上調平均6.18倍和6.46倍,酰基輔酶A閤成酶和電壓門控性離子通道基因分彆下調平均2.28倍和3.16倍,與芯片雜交實驗結果一緻.結論 急性減壓病兔脊髓病變差異錶達基因主要涉及炎癥、細胞週期和凋亡等方麵,其意義需要進一步研究.
목적 초보탐토급성감압병토척수손상조직기인표체보적변화.방법 신서란대이백토10지,5지안문헌방법제비급성감압병모형,위급성감압병조;령5지삼조공기잠수감압표감지상압,위안전감압조.2조출창후30 min내각수궤선취2지토,마취후해부,류취흉요단척수,신속치우액양중보존.응용기인표체보심편대4지토적척수조직진행검측,채용실시정량역전록취합매련반응(reverse transcription polymerase chain reaction,RT-PCR)방법대부분심편사선적차이표체기인결과진행험증.결과 심편잡교결과현시,여안전감압조비교,급성감압병조상조2배이상적기인9개,하조2배이상적기인17개,차이표체기인주요섭급염증、리자통도、세포주기、물질전운화조망등방면.실시정량RT-PCR결과현시,여안전감압조비교,급성감압병조갑상방선격소화종류세포배사인자분별상조평균6.18배화6.46배,선기보매A합성매화전압문공성리자통도기인분별하조평균2.28배화3.16배,여심편잡교실험결과일치.결론 급성감압병토척수병변차이표체기인주요섭급염증、세포주기화조망등방면,기의의수요진일보연구.
Objective To make a preliminary exploration in the changes of gene expression profile in spinal cord lesion induced by acute decompression sickness in rabbits.Methods Ten New Zealand white rabbits were used for the experiment.Acute decompression sickness model was developed as prescribed in the article in 5 of the animals and were set as the acute decompression sickness group.The other 5 animals were safely decompressed to normal pressure by using the Air Decompression Table,which were set as the safe decompression group.Two rabbits were randomly selected from each group within 30 minutes,when the animals were surfaced out of the chamber.Anatomy was performed after the animals were anesthetized.Sections of thoracic and lumbar spinal cord were taken and preserved in the liquid nitrogen.Gene expression profile chips were used to observe the spinal cord tissues of the 4 rabbits.Selected differential genes contained in some chips were identified with RT-PCR.Results Such were the chip hybridization results:for the acute decompression sickness group,the genes which up-regulated the expressions of genes twice as much were 9,and the genes which down-regulated the expressions of genes twice as much were 17,when comparisons were made with the safe decompression group.Those differential genes were mainly associated with inflammation,ion channels,cell cycle,material transfer and apoptosis,etc.RT-PCR results showed that the expression levels of parathyroid hormone and TNF increased for an average of 6.18 times and 6.46 times respectively for the acute decompression sickness group,when comparisons were made with the safe decompression group.The expression levels of acyl-CoA synthetase and the voltage-gated ion channel gene were down-regulated by an average of 2.28 times and 3.16 times respectively,which was consistent with the experimental Conclusions from chip hybridization,thus confirming the reliability of the research results.Conclusions The differential genes of the involved spinal cord in acute decompression sickness rabbits were mainly associated with inflammation,cell cycle,apoptosis and so on,the significance of which demands further research.