皖南医学院学报
皖南醫學院學報
환남의학원학보
ACTA ACADEMIAE MEDICINAE WANNAN
2015年
3期
230-231,239
,共3页
肝内胆汁淤积%缺氧诱导因子%胎盘
肝內膽汁淤積%缺氧誘導因子%胎盤
간내담즙어적%결양유도인자%태반
intrahepatic cholestasis%hypoxia inducible factor%placenta
目的:检测妊娠期肝内胆汁淤积症( ICP)患者胎盘组织缺氧诱导因子HIF-2α蛋白的含量,探讨其在ICP胎儿宫内缺氧中的作用。方法:选取2010年2~8月在弋矶山医院剖宫产分娩的40例孕妇为研究对象,其中正常足月孕妇10例,ICP轻度组15例,重度组15例。采用蛋白免疫印迹法检测各组孕妇胎盘组织中HIF-2α蛋白的表达水平。结果:3组孕妇HIF-2α蛋白表达差异有统计学意义(P<0.05),轻、重度ICP组HIF-2α蛋白表达较正常对照组有统计学意义(P<0.05);轻、重度ICP组间HIF-2α蛋白表达差异无统计学意义(P>0.05)。结论:ICP患者HIF-2α蛋白在胎盘组织中的高表达,可能在胎盘-胎儿系统对缺氧的自稳和代偿反应中起重要的调节作用。
目的:檢測妊娠期肝內膽汁淤積癥( ICP)患者胎盤組織缺氧誘導因子HIF-2α蛋白的含量,探討其在ICP胎兒宮內缺氧中的作用。方法:選取2010年2~8月在弋磯山醫院剖宮產分娩的40例孕婦為研究對象,其中正常足月孕婦10例,ICP輕度組15例,重度組15例。採用蛋白免疫印跡法檢測各組孕婦胎盤組織中HIF-2α蛋白的錶達水平。結果:3組孕婦HIF-2α蛋白錶達差異有統計學意義(P<0.05),輕、重度ICP組HIF-2α蛋白錶達較正常對照組有統計學意義(P<0.05);輕、重度ICP組間HIF-2α蛋白錶達差異無統計學意義(P>0.05)。結論:ICP患者HIF-2α蛋白在胎盤組織中的高錶達,可能在胎盤-胎兒繫統對缺氧的自穩和代償反應中起重要的調節作用。
목적:검측임신기간내담즙어적증( ICP)환자태반조직결양유도인자HIF-2α단백적함량,탐토기재ICP태인궁내결양중적작용。방법:선취2010년2~8월재익기산의원부궁산분면적40례잉부위연구대상,기중정상족월잉부10례,ICP경도조15례,중도조15례。채용단백면역인적법검측각조잉부태반조직중HIF-2α단백적표체수평。결과:3조잉부HIF-2α단백표체차이유통계학의의(P<0.05),경、중도ICP조HIF-2α단백표체교정상대조조유통계학의의(P<0.05);경、중도ICP조간HIF-2α단백표체차이무통계학의의(P>0.05)。결론:ICP환자HIF-2α단백재태반조직중적고표체,가능재태반-태인계통대결양적자은화대상반응중기중요적조절작용。
Objective:To investigate the role of hypoxia-inducible factor-2α(HIF-2α) protein in placenta in intrahepatic cholestasis of pregnancy(ICP). Methods:Forty women undergone cesarean section delivery were included between February and August of 2010 in our hospital.Of them,10 were normal full-term pregnancy women,15 were complicated with mild ICP and another 15,with severe ICP.Western blot was performed determine the protein level of placental HIF-2α.Results:HIF-2αlevel was different among the three groups(P <0.05),and higher in mild and severe ICP group as compared with nor-mal controls (P <0.05),yet difference was not significant between mild and severe ICP group(P <0.05).Conclusion:HIF-2αprotein is highly ex-pressed in placenta in ICP pregnancy,suggesting that it play an important role in regulating the compensatory homeostatic response to hypoxemia of placen-ta-fetus system.