中国循证儿科杂志
中國循證兒科雜誌
중국순증인과잡지
CHINESE JOURNAL OF EVIDENCE-BASED PEDIATRICS
2009年
4期
380-384
,共5页
马海燕%李红%王云英%李向红%张采欣
馬海燕%李紅%王雲英%李嚮紅%張採訢
마해연%리홍%왕운영%리향홍%장채흔
铅%大鼠%胎盘组织超微结构%一氧化氮%基质金属蛋白酶-9
鉛%大鼠%胎盤組織超微結構%一氧化氮%基質金屬蛋白酶-9
연%대서%태반조직초미결구%일양화담%기질금속단백매-9
Lead%Rat%Placenta cytoarchitecture%Nitric oxide%Matrix metalloproteinase-9
目的 观察NO和基质金属蛋白酶-9(MMP-9)在孕期铅暴露大鼠胎盘组织中的变化特征,及其与胎盘组织超微结构的相关性.方法 108只大鼠分为4组(A、B、C组和对照组),对照组孕期饮服蒸馏水,A、B和c组分别于孕期不同阶段饮服0.025%醋酸铅溶液.原子吸收光谱法测定血铅水平.硝酸还原酶法测定胎盘组织NO含量.免疫组化法测定胎盘滋养层细胞MMP-9表达阳性率.电镜观察胎盘组织超微结构.结果 ①A和B组孕鼠胎盘组织NO含量均高于对照组,差异有显著统计学意义(P<0.01);②MMP-9评分4组间总体差异有显著统计学意义(H=39.226,P<0.01),以B组的MMP-9阳性表达率最高,C组最低;③各组孕鼠胎盘组织超微结构示:对照组合体滋养层细胞微绒毛致密,胞质内细胞器丰富,内质网致密,有较多的线粒体,细胞间连接和基底膜清晰完整;A组胎盘微血管内皮细胞肿胀,基底膜增厚,微绒毛突起;B组滋养层巨细胞增生,空泡化细胞岛增多;C组滋养层细胞坏死,微绒毛稀疏,线粒体数目减少和粗面内质网池扩张.结论 铅暴露孕鼠胎盘组织中NO含量和MMP-9表达阳性率与胎盘组织超微结构的病理改变密切相关.
目的 觀察NO和基質金屬蛋白酶-9(MMP-9)在孕期鉛暴露大鼠胎盤組織中的變化特徵,及其與胎盤組織超微結構的相關性.方法 108隻大鼠分為4組(A、B、C組和對照組),對照組孕期飲服蒸餾水,A、B和c組分彆于孕期不同階段飲服0.025%醋痠鉛溶液.原子吸收光譜法測定血鉛水平.硝痠還原酶法測定胎盤組織NO含量.免疫組化法測定胎盤滋養層細胞MMP-9錶達暘性率.電鏡觀察胎盤組織超微結構.結果 ①A和B組孕鼠胎盤組織NO含量均高于對照組,差異有顯著統計學意義(P<0.01);②MMP-9評分4組間總體差異有顯著統計學意義(H=39.226,P<0.01),以B組的MMP-9暘性錶達率最高,C組最低;③各組孕鼠胎盤組織超微結構示:對照組閤體滋養層細胞微絨毛緻密,胞質內細胞器豐富,內質網緻密,有較多的線粒體,細胞間連接和基底膜清晰完整;A組胎盤微血管內皮細胞腫脹,基底膜增厚,微絨毛突起;B組滋養層巨細胞增生,空泡化細胞島增多;C組滋養層細胞壞死,微絨毛稀疏,線粒體數目減少和粗麵內質網池擴張.結論 鉛暴露孕鼠胎盤組織中NO含量和MMP-9錶達暘性率與胎盤組織超微結構的病理改變密切相關.
목적 관찰NO화기질금속단백매-9(MMP-9)재잉기연폭로대서태반조직중적변화특정,급기여태반조직초미결구적상관성.방법 108지대서분위4조(A、B、C조화대조조),대조조잉기음복증류수,A、B화c조분별우잉기불동계단음복0.025%작산연용액.원자흡수광보법측정혈연수평.초산환원매법측정태반조직NO함량.면역조화법측정태반자양층세포MMP-9표체양성솔.전경관찰태반조직초미결구.결과 ①A화B조잉서태반조직NO함량균고우대조조,차이유현저통계학의의(P<0.01);②MMP-9평분4조간총체차이유현저통계학의의(H=39.226,P<0.01),이B조적MMP-9양성표체솔최고,C조최저;③각조잉서태반조직초미결구시:대조조합체자양층세포미융모치밀,포질내세포기봉부,내질망치밀,유교다적선립체,세포간련접화기저막청석완정;A조태반미혈관내피세포종창,기저막증후,미융모돌기;B조자양층거세포증생,공포화세포도증다;C조자양층세포배사,미융모희소,선립체수목감소화조면내질망지확장.결론 연폭로잉서태반조직중NO함량화MMP-9표체양성솔여태반조직초미결구적병리개변밀절상관.
Objective To investigate the effect of lead exposure during various gestational periods on the expression of rat placental nitric oxide(NO) and matrix metalloproteinase-9 (MMP-9), and their relationship with the placenta cytoarchitecture. Methods 108 Wistar rats were randomly divided into four groups and fed with respective drinking solutions with or without 0.025% lead acetate during various gestational periods. Controls were given distilled water without lead; Group A was given distilled water containing 0. 025% lead acetate throughout days 1 to 10 of gestation. Both group B and group C were fed with the same lead acetate water during days 11 to 20 or 1 to 20 of gestation, respectively. Blood lead levels were determined by atomic absorption spectrophotometry. The levels of NO were determined by nitrate reductase test. The expression of MMP-9 in placenta was determined by immunohistochemistry. Five microscopic fields (×400) in each placenta were randomly selected. The total cells positive for MMP-9 were counted by same observer for the entire study and verified by a second observer blinded to the study. Five random fields per placenta were scored. The immunoreactive intensity was determined according to immunoreactive cell scores and the immtmoreactive chromatosis scores. The immunoreactive cells were scored according to the number of positive cells in each field :0 (≤5 % ), 1 ( - 25 % ), 2 ( - 50% ), 3 ( - 75% ) and 4 ( > 75% ). The immunoreactive chromatosis scores were classified into three grades: hadro-ehromatosis was scored 3, superficial- chromatosis was scored 1 and that between 1 and 3 was scored 2. The immunoreactive intensity was classified into four grades: 0 ( - , negative), - 2 ( +, weakly positive ), - 4 ( + +, moderately positive ) and > 5 ( + + + , strongly positive). Placenta cytoarchitecture was examined by an unmasked observer with a transmission electron microscope ( TEM, Model JEM-1200EX, Jeel Jem, Tokyo). Pieces of placenta were fixed with 2.5% glutaraldehyde and 1% osmium tetroxide, dehydrated in ethanol of gradient concentrations, and permeated using EPON812 embedding solution.brown pigment localizing in the langhans cells and zoarium trophoblastic cells of placental villus, mesenchymal fibroblasts, vascular endothelial cells and contractile fiber cells of vessel wall. The expression of MMP-9 in lead-exposed mrs was significantly higher than that in controls( H = 39.226, P <0.01 ). The expressions of NF-B between any two groups showed significantly differences. placental microangium endotheliocytes, basal membrane thickening and microvilli evagination were observed under electronic microscopy. In group B, trophoblast giant corpuscles and vacuolization cells were increased in number. In group C, rat placental trophoblast showed cell necrosis, rongh endoplasmic reticula appeared distended, mitochondria decreased in number and microvilli quantity decreased. Conclusions The expressions of rat placental NO and MMP-9 were associated with placenta cytoarchitectural changes.