中华手外科杂志
中華手外科雜誌
중화수외과잡지
CHINESE JOURNAL OF HAND SURGERY
2015年
2期
138-141
,共4页
吴建龙%巨积辉%周广良%刘跃飞%张广亮%侯瑞兴
吳建龍%巨積輝%週廣良%劉躍飛%張廣亮%侯瑞興
오건룡%거적휘%주엄량%류약비%장엄량%후서흥
外科皮瓣%再灌注损伤%雌二醇%p38丝裂原活化蛋白激酶
外科皮瓣%再灌註損傷%雌二醇%p38絲裂原活化蛋白激酶
외과피판%재관주손상%자이순%p38사렬원활화단백격매
Surgical flaps%Reperfusion injury%Estradiol%p38 MAPK
目的 研究雌二醇(Estradiol,E2)对大鼠皮瓣缺血再灌注损伤p38丝裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)信号通路的影响以及对皮瓣的保护作用.方法 取Wistar大鼠40只,随机分为健康对照组(Ⅰ组)、缺血再灌注组(Ⅱ组)、生理盐水组(Ⅲ组)、E2组(Ⅳ组),每组10只大鼠.分别制作大鼠腹部皮瓣缺血再灌注损伤模型,术后观察各组皮瓣一般情况、测定皮瓣成活率、检测蒂部腹壁浅静脉血清中性粒细胞(NEU)和肿瘤坏死因子α(TNF-α)的浓度.切取皮瓣行组织学观察,并应用Western Blot法检测皮瓣p38 MAPK及丝裂原活化蛋白激酶磷酸酶-2(MKP-2)的表达变化.结果 术后7d皮瓣成活率Ⅳ组显著高于Ⅱ、Ⅲ组(P<0.05).Ⅳ组蒂部静脉血NEU及TNF-α浓度明显低于Ⅱ、Ⅲ组(P<0.05).缺血再灌注后,Ⅱ、Ⅲ组p38 MAPK表达明显高于Ⅰ组(P<0.05),而Ⅳ组p38 MAPK表达较Ⅱ、Ⅲ组显著降低(P<0.05).Ⅳ组MKP-2表达较Ⅰ、Ⅱ、Ⅲ组均显著增加(P<0.05).结论 E2可通过抑制p38 MAPK表达,减轻皮瓣内NEU介导的炎性反应级联反应,减少TNF-α释放,从而减轻皮瓣缺血再灌注损伤,提高皮瓣成活率.其作用可能与MKP-2对p38 MAPK活性的抑制有关.
目的 研究雌二醇(Estradiol,E2)對大鼠皮瓣缺血再灌註損傷p38絲裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)信號通路的影響以及對皮瓣的保護作用.方法 取Wistar大鼠40隻,隨機分為健康對照組(Ⅰ組)、缺血再灌註組(Ⅱ組)、生理鹽水組(Ⅲ組)、E2組(Ⅳ組),每組10隻大鼠.分彆製作大鼠腹部皮瓣缺血再灌註損傷模型,術後觀察各組皮瓣一般情況、測定皮瓣成活率、檢測蒂部腹壁淺靜脈血清中性粒細胞(NEU)和腫瘤壞死因子α(TNF-α)的濃度.切取皮瓣行組織學觀察,併應用Western Blot法檢測皮瓣p38 MAPK及絲裂原活化蛋白激酶燐痠酶-2(MKP-2)的錶達變化.結果 術後7d皮瓣成活率Ⅳ組顯著高于Ⅱ、Ⅲ組(P<0.05).Ⅳ組蒂部靜脈血NEU及TNF-α濃度明顯低于Ⅱ、Ⅲ組(P<0.05).缺血再灌註後,Ⅱ、Ⅲ組p38 MAPK錶達明顯高于Ⅰ組(P<0.05),而Ⅳ組p38 MAPK錶達較Ⅱ、Ⅲ組顯著降低(P<0.05).Ⅳ組MKP-2錶達較Ⅰ、Ⅱ、Ⅲ組均顯著增加(P<0.05).結論 E2可通過抑製p38 MAPK錶達,減輕皮瓣內NEU介導的炎性反應級聯反應,減少TNF-α釋放,從而減輕皮瓣缺血再灌註損傷,提高皮瓣成活率.其作用可能與MKP-2對p38 MAPK活性的抑製有關.
목적 연구자이순(Estradiol,E2)대대서피판결혈재관주손상p38사렬원활화단백격매(mitogen-activated protein kinase,MAPK)신호통로적영향이급대피판적보호작용.방법 취Wistar대서40지,수궤분위건강대조조(Ⅰ조)、결혈재관주조(Ⅱ조)、생리염수조(Ⅲ조)、E2조(Ⅳ조),매조10지대서.분별제작대서복부피판결혈재관주손상모형,술후관찰각조피판일반정황、측정피판성활솔、검측체부복벽천정맥혈청중성립세포(NEU)화종류배사인자α(TNF-α)적농도.절취피판행조직학관찰,병응용Western Blot법검측피판p38 MAPK급사렬원활화단백격매린산매-2(MKP-2)적표체변화.결과 술후7d피판성활솔Ⅳ조현저고우Ⅱ、Ⅲ조(P<0.05).Ⅳ조체부정맥혈NEU급TNF-α농도명현저우Ⅱ、Ⅲ조(P<0.05).결혈재관주후,Ⅱ、Ⅲ조p38 MAPK표체명현고우Ⅰ조(P<0.05),이Ⅳ조p38 MAPK표체교Ⅱ、Ⅲ조현저강저(P<0.05).Ⅳ조MKP-2표체교Ⅰ、Ⅱ、Ⅲ조균현저증가(P<0.05).결론 E2가통과억제p38 MAPK표체,감경피판내NEU개도적염성반응급련반응,감소TNF-α석방,종이감경피판결혈재관주손상,제고피판성활솔.기작용가능여MKP-2대p38 MAPK활성적억제유관.
Objective To investigate the p38 MAPK changes in flap ischemia reperfusion injury and the protective effect of estradiol (E2).Methods The superficial epigastric artery flap ischemia reperfusion injury model was created in forty adult Wistar rats which were randomly divided into control group (group Ⅰ),ischemiareperfusion group(group Ⅱ),saline group (group Ⅲ),estradiol group (groupiⅣ).The general condition of the flap was observed at 3,5,and 7 days after operation.At 7 days after operation,the survival rate of the flap was detected,the p38 MAPK and MKP-2 expression and protein level were quantified with Westem Blot,the flaps were harvested to perform histology observation and neutrophils (NEU) scoring.The NEU and the TNF-α levels of the superficial epigastric vein were tested.Results The survival rates of the flap 7 days after operation of groupⅣ was higher than group Ⅱ and Ⅲ significantly (P < 0.05).The general and histological observation showed that the degree of inflammatory exudation and necrotic area in the flap edge in group Ⅱ and Ⅲ was more serious than that of groupⅣ at 7 days postoperatively.The NEU and TNF-α in groupⅣ was lower than that in group Ⅱ and Ⅲ (P < 0.05).After ischemia-reperfusion,the p38 MAPK expression in groupⅡ and Ⅲ was significantly higher than that in group Ⅰ (P < 0.05).The expression of p38 MAPK in groupⅣ is lower than that in groupⅡ and Ⅲ (P<0.05),the MKP-2 expression in groupⅣ is higher than that in group Ⅰ,Ⅱ and Ⅲ (P < 0.05).Conclusion The E2 could inhibit neutrophil infiltration significantly,decrease the TNF-α level in plasma and improve skin flap survival rate by preventing the expression of p38 MAPK.