中华麻醉学杂志
中華痳醉學雜誌
중화마취학잡지
CHINESE JOURNAL OF ANESTHESIOLOGY
2010年
4期
494-496
,共3页
李长生%邢孟韬%吕帅国%李廷坤%徐刚%冯艳平
李長生%邢孟韜%呂帥國%李廷坤%徐剛%馮豔平
리장생%형맹도%려수국%리정곤%서강%풍염평
果糖二磷酸盐类%心肌缺血%连接蛋白类
果糖二燐痠鹽類%心肌缺血%連接蛋白類
과당이린산염류%심기결혈%련접단백류
Fructosediphosphates%Myocardial ischemia%Connexins
目的 探讨1,6-二磷酸果糖(FDP)预先给药对大鼠急性心肌缺血时缝隙连接蛋白43(Cx43)的影响.方法 健康成年雄性SD大鼠36只,体重220~280 g,周龄8~12周,随机分为3组(n=12):假手术组(S组)开胸前即刻经股静脉注射生理盐水5 ml,仅游离血管穿线不结扎;缺血组(I组)在心肌缺血前10 min经股静脉注射生理盐水5 ml;FDP组(F组)在心肌缺血前10 min经股静脉注射10%FDP 100 mg/kg (5 m1).I组和F组采用结扎冠状动脉左前降支30 min的方法制备大鼠急性心肌缺血模型,记录结扎后30 min内心律失常的发生情况,评价心律失常严重程度.结扎30 min后快速摘取心脏.测定左心室面积(LVA),缺血区面积(AAR)和梗死区面积(IA),计算AAR/LVA和IA/AAR.测定心肌Cx43表达.结果 与S组比较,I组和F组心肌Cx43表达下调,心律失常严重程度升高(P<0.05).与I组比较,F组心肌Cx43表达上调,IA/AAR降低,心律失常严重程度降低(P<0.05).结论 FDP预先给药可减轻大鼠急性心肌缺血损伤,其机制与上调心肌Cx43表达有关.
目的 探討1,6-二燐痠果糖(FDP)預先給藥對大鼠急性心肌缺血時縫隙連接蛋白43(Cx43)的影響.方法 健康成年雄性SD大鼠36隻,體重220~280 g,週齡8~12週,隨機分為3組(n=12):假手術組(S組)開胸前即刻經股靜脈註射生理鹽水5 ml,僅遊離血管穿線不結扎;缺血組(I組)在心肌缺血前10 min經股靜脈註射生理鹽水5 ml;FDP組(F組)在心肌缺血前10 min經股靜脈註射10%FDP 100 mg/kg (5 m1).I組和F組採用結扎冠狀動脈左前降支30 min的方法製備大鼠急性心肌缺血模型,記錄結扎後30 min內心律失常的髮生情況,評價心律失常嚴重程度.結扎30 min後快速摘取心髒.測定左心室麵積(LVA),缺血區麵積(AAR)和梗死區麵積(IA),計算AAR/LVA和IA/AAR.測定心肌Cx43錶達.結果 與S組比較,I組和F組心肌Cx43錶達下調,心律失常嚴重程度升高(P<0.05).與I組比較,F組心肌Cx43錶達上調,IA/AAR降低,心律失常嚴重程度降低(P<0.05).結論 FDP預先給藥可減輕大鼠急性心肌缺血損傷,其機製與上調心肌Cx43錶達有關.
목적 탐토1,6-이린산과당(FDP)예선급약대대서급성심기결혈시봉극련접단백43(Cx43)적영향.방법 건강성년웅성SD대서36지,체중220~280 g,주령8~12주,수궤분위3조(n=12):가수술조(S조)개흉전즉각경고정맥주사생리염수5 ml,부유리혈관천선불결찰;결혈조(I조)재심기결혈전10 min경고정맥주사생리염수5 ml;FDP조(F조)재심기결혈전10 min경고정맥주사10%FDP 100 mg/kg (5 m1).I조화F조채용결찰관상동맥좌전강지30 min적방법제비대서급성심기결혈모형,기록결찰후30 min내심률실상적발생정황,평개심률실상엄중정도.결찰30 min후쾌속적취심장.측정좌심실면적(LVA),결혈구면적(AAR)화경사구면적(IA),계산AAR/LVA화IA/AAR.측정심기Cx43표체.결과 여S조비교,I조화F조심기Cx43표체하조,심률실상엄중정도승고(P<0.05).여I조비교,F조심기Cx43표체상조,IA/AAR강저,심률실상엄중정도강저(P<0.05).결론 FDP예선급약가감경대서급성심기결혈손상,기궤제여상조심기Cx43표체유관.
Objective To investigate the effect of fructose-1,6-diphosphate (FDP) pretreatment on myocardial connexin43 (Cx43) in a rat model of acute myocardial ischemia.Methods Thirty-six male 8-12 week old SD rata weighing 220-280 g were randomly divided into 3 groups (n=12 each):group Ⅰ sham operation (group S);group Ⅱ ischemia(group Ⅰ)and group Ⅲ FDP+ischemia(group F).The animals were anesthetized with intraperitoneal 10%chloral hydrate 40 mg/100 g,tracheostomized and mechanically ventilated.Acute myocardial ischemia was induced by occlusion of left anterior descending coronary artery for 30 min.Myocardial ischemia was;verified by elevation of S-T segment on ECG.In group F FDP 100 mg/kg was injected iv at 10 min before ischemia.Arrhythmia was recorded within 30 min after occlusion and the severity of arrbythmia was aggesged.The hearts were removed after 30 min myocardial ischemia.The Left ventricle area (LVA),myocardial infarct area (IA) and area at risk (AAR) were measured and AAR/LVA and IA/AAR ratios were calculated.The expression of myocardial Cx43 protein was determined by immuno-histochemestry and analysis of mean optical density.Results The severity of arrhythmia was significantly higher in group F and I than in gropu S.while lower in group F than in group I(P<0.05).The IA,IA/AAR ratio was significantly lower in group F than in group I.The myocardial Cx43 protein expression was down-regulated in group I and F as compared with group S.and was significantly lower in group I than in group F.Conclusion FDP pretreatment can protect myocardium against acute ischemia by up-regulation of myocardial Cx43 expression.