郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2015年
1期
44-47,48
,共5页
王伟%蔡丽霞%崔志瑞%罗向阳
王偉%蔡麗霞%崔誌瑞%囉嚮暘
왕위%채려하%최지서%라향양
宫内感染%脂肪酸结合蛋白%支气管肺发育不良%大鼠
宮內感染%脂肪痠結閤蛋白%支氣管肺髮育不良%大鼠
궁내감염%지방산결합단백%지기관폐발육불량%대서
intra-amniotic infection%fatty acid binding protein 4%bronchopulmonary dysplasia%rat
目的:观察宫内感染肺损伤时脂肪型脂肪酸结合蛋白(FABP4)在早产大鼠支气管肺泡灌洗液(BALF)及肺组织中的表达,探讨其与新型支气管肺发育不良( BPD)发病的关系。方法:定期受孕的SD大鼠分为LPS组和对照组,于孕15 d羊膜腔内注射LPS或生理盐水。2组动物均于出生后第1天(P1)、第4天(P4)和第7天(P7)各取8只,应用ELISA方法检测BALF中FABP4的含量,采用免疫组化法和RT-PCR技术检测肺组织中FABP4蛋白及mRNA的表达水平。结果:FABP4主要在肺泡巨噬细胞、血管内皮细胞及少量支气管上皮细胞表达。 LPS组早产大鼠BALF中FABP4含量、肺组织中FABP4蛋白及mRNA的相对表达量较对照组均升高,且与时间存在交互作用(P均<0.05)。结论:宫内感染肺损伤时FABP4表达升高,可能是引起肺微血管病理性重塑及肺泡化进程受阻,进而导致新型BPD发生发展的重要因素。
目的:觀察宮內感染肺損傷時脂肪型脂肪痠結閤蛋白(FABP4)在早產大鼠支氣管肺泡灌洗液(BALF)及肺組織中的錶達,探討其與新型支氣管肺髮育不良( BPD)髮病的關繫。方法:定期受孕的SD大鼠分為LPS組和對照組,于孕15 d羊膜腔內註射LPS或生理鹽水。2組動物均于齣生後第1天(P1)、第4天(P4)和第7天(P7)各取8隻,應用ELISA方法檢測BALF中FABP4的含量,採用免疫組化法和RT-PCR技術檢測肺組織中FABP4蛋白及mRNA的錶達水平。結果:FABP4主要在肺泡巨噬細胞、血管內皮細胞及少量支氣管上皮細胞錶達。 LPS組早產大鼠BALF中FABP4含量、肺組織中FABP4蛋白及mRNA的相對錶達量較對照組均升高,且與時間存在交互作用(P均<0.05)。結論:宮內感染肺損傷時FABP4錶達升高,可能是引起肺微血管病理性重塑及肺泡化進程受阻,進而導緻新型BPD髮生髮展的重要因素。
목적:관찰궁내감염폐손상시지방형지방산결합단백(FABP4)재조산대서지기관폐포관세액(BALF)급폐조직중적표체,탐토기여신형지기관폐발육불량( BPD)발병적관계。방법:정기수잉적SD대서분위LPS조화대조조,우잉15 d양막강내주사LPS혹생리염수。2조동물균우출생후제1천(P1)、제4천(P4)화제7천(P7)각취8지,응용ELISA방법검측BALF중FABP4적함량,채용면역조화법화RT-PCR기술검측폐조직중FABP4단백급mRNA적표체수평。결과:FABP4주요재폐포거서세포、혈관내피세포급소량지기관상피세포표체。 LPS조조산대서BALF중FABP4함량、폐조직중FABP4단백급mRNA적상대표체량교대조조균승고,차여시간존재교호작용(P균<0.05)。결론:궁내감염폐손상시FABP4표체승고,가능시인기폐미혈관병이성중소급폐포화진정수조,진이도치신형BPD발생발전적중요인소。
Aim:To investigate the expression of fatty acid binding protein 4 ( FABP4) in bronchoalveolar lavage fluid ( BALF) and lung tissue of preterm rats exposed to intra-amniotic endotoxin and to elucidate the relationship between intra-uterine inflammatory exposure and the pathogenesis of bronchopulmonary dysplasia (BPD).Methods:Timed pregnant SD rats were randomly divided into two groups:control group and LPS group .LPS or normal saline were injected into the amni-otic cavity, respectively.The lungs from eight rats of each group aged postnatal day 1(P1), day 4(P4) and day 7(P7) were removed and the level of FABP 4 in BALF was measured by ELISA .The expressions of FABP 4 protein and mRNA in lung tissue were assessed by immunohistochemistry and RT-PCR.Results:FABP4 immunoreactivity was detected in alveo-lar macrophages , endothelial cells and epithelial cells in both groups .Compared with control group , the FABP4 level in BALF, FABP4 protein and mRNA levels in lung tissue of LPS group increased (P<0.05).Conclusion: Intra-amniotic endotoxin could change the expression of FABP 4, which may contribute to BPD .