中华麻醉学杂志
中華痳醉學雜誌
중화마취학잡지
CHINESE JOURNAL OF ANESTHESIOLOGY
2009年
12期
1106-1108
,共3页
岳立辉%陈静%王茂爱%赵砚丽%卢大儒
嶽立輝%陳靜%王茂愛%趙硯麗%盧大儒
악립휘%진정%왕무애%조연려%로대유
血红素氧化酶(脱环)%病毒融合蛋白质类%肝移植%低温保存%炎症
血紅素氧化酶(脫環)%病毒融閤蛋白質類%肝移植%低溫保存%炎癥
혈홍소양화매(탈배)%병독융합단백질류%간이식%저온보존%염증
Heme oxygenase (decyclizing)%Viral fusion proteins%Liver transplantation%Cryopreservation%Inflammation
目的 探讨HIV-1反式激活蛋白-血红素氧合酶-1(TAT-HO-1)融合蛋白对大鼠供肝冷保存期炎性反应及肝功能的影响.方法 成年健康雄性SD大鼠48只,体重250~300 g,开腹游离腹主动脉并结扎,于左右髂总动脉分叉处向心端穿刺腹主动脉,切断肝上下腔静脉,随机灌注4℃HTK液(C组,U=24)或4℃含TAT-HO-1融合蛋白50 μg/ml的HTK液(P组,n=24),至流出灌洗液清亮后停止灌注,取肝脏,置于相应保存液中冷保存.分别于冷保存即刻、6、12和18 h时取保存液并切取肝组织.采用全自动生化分析仪测定保存液谷草转氨酶(AST)、谷丙转氨酶(ALT)及乳酸脱氢酶(LDH)活性,免疫组化法检测肿瘤坏死因子α(TNF-α)的表达,光镜下观察肝组织形态学.结果 随冷保存时间延长,两组保存液AST、ALT及LDH活性升高,TNF-α表达上调(P<0.05);与C组比较,冷保存6、12、18 h时P组保存液AST、ALT及LDH活性降低,TNF-α表达下调(P<0.05).结论 TAT-HO-1融合蛋白可抑制大鼠供肝冷保存期的炎性反应,对肝功能具有一定保护作用.
目的 探討HIV-1反式激活蛋白-血紅素氧閤酶-1(TAT-HO-1)融閤蛋白對大鼠供肝冷保存期炎性反應及肝功能的影響.方法 成年健康雄性SD大鼠48隻,體重250~300 g,開腹遊離腹主動脈併結扎,于左右髂總動脈分扠處嚮心耑穿刺腹主動脈,切斷肝上下腔靜脈,隨機灌註4℃HTK液(C組,U=24)或4℃含TAT-HO-1融閤蛋白50 μg/ml的HTK液(P組,n=24),至流齣灌洗液清亮後停止灌註,取肝髒,置于相應保存液中冷保存.分彆于冷保存即刻、6、12和18 h時取保存液併切取肝組織.採用全自動生化分析儀測定保存液穀草轉氨酶(AST)、穀丙轉氨酶(ALT)及乳痠脫氫酶(LDH)活性,免疫組化法檢測腫瘤壞死因子α(TNF-α)的錶達,光鏡下觀察肝組織形態學.結果 隨冷保存時間延長,兩組保存液AST、ALT及LDH活性升高,TNF-α錶達上調(P<0.05);與C組比較,冷保存6、12、18 h時P組保存液AST、ALT及LDH活性降低,TNF-α錶達下調(P<0.05).結論 TAT-HO-1融閤蛋白可抑製大鼠供肝冷保存期的炎性反應,對肝功能具有一定保護作用.
목적 탐토HIV-1반식격활단백-혈홍소양합매-1(TAT-HO-1)융합단백대대서공간랭보존기염성반응급간공능적영향.방법 성년건강웅성SD대서48지,체중250~300 g,개복유리복주동맥병결찰,우좌우가총동맥분차처향심단천자복주동맥,절단간상하강정맥,수궤관주4℃HTK액(C조,U=24)혹4℃함TAT-HO-1융합단백50 μg/ml적HTK액(P조,n=24),지류출관세액청량후정지관주,취간장,치우상응보존액중랭보존.분별우랭보존즉각、6、12화18 h시취보존액병절취간조직.채용전자동생화분석의측정보존액곡초전안매(AST)、곡병전안매(ALT)급유산탈경매(LDH)활성,면역조화법검측종류배사인자α(TNF-α)적표체,광경하관찰간조직형태학.결과 수랭보존시간연장,량조보존액AST、ALT급LDH활성승고,TNF-α표체상조(P<0.05);여C조비교,랭보존6、12、18 h시P조보존액AST、ALT급LDH활성강저,TNF-α표체하조(P<0.05).결론 TAT-HO-1융합단백가억제대서공간랭보존기적염성반응,대간공능구유일정보호작용.
Objective To investigate the effect of TAT-heine oxygenase-1 (TAT-HO-1) fusion protein on the inflammatory response and liver function during cold preservation of liver in rots. Methods Forty-eight male SD rats weighing 250-300 g were randomly divided into 2 groups according to the type of preservation solution (n=24 each): control group (group C) and TAT-HO-1 fusion protein group (group P). The livers were harvested according to the method described by Kamada. In control group the livers were flushed and preserved with 4℃ HTK solution while in group P the livers were flushed and preserved with 4℃ HTK solution containing TAT-HO-1 fusion protein 50 μg/ml. Liver specimens and preservation solution samples were collected at 0, 6, 12, and 18 h of cold storage. The activities of aspartato amino-transferase (AST), alanine aminu-transferase (ALT) and lactate dehydrogenase (LDH) in the preservation solution were analyzed. TNF-α expression in the liver was determined. The liver histomorphology was observed by light microscopy. Results The AST, ALT and LDH activities in the preservation solution and TNF-α expression in the liver were significantly increased time-dependendy during cold storage in both groups. The AST, ALT and LDH activities and TNF-α expression were significantly lower at 6, 12 and 18 h of cold storage in group P than in group C.Conclusion TAT-HO-1 fusion protein can reduce the inflammatory response of the liver during cold storage in rats, and has protective effect on liver function to some extent.