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作 者:卫爱武[1] 宋艳丽[2] 成琼[3] 马存亮[4] 倪婷婷[2]
机构地区:[1]河南中医学院第一附属医院妇产科,郑州450003 [2]河南中医学院研究生,郑州450008 [3]河南中医学院第一附属医院病理科,郑州450003 [4]河南中医学院第一附属医院检验科,郑州450003
出 处:《郑州大学学报(医学版)》2009年第3期526-530,共5页Journal of Zhengzhou University(Medical Sciences)
基 金:河南省自然科学基金资助项目0511043700
摘 要:目的:制备异种抗磷脂抗体皮下注射致妊娠丢失大鼠模型的改良方法。方法:将80只10周龄SD孕鼠随机分为A~H组共8组(每组各10只),分别于孕8d、孕12d背部多部位皮下注射25、50、75、100mg/(kg·d)抗心磷脂抗体(ACA,A、B、C、D组)或狼疮抗凝物(LA,E、F、G、H组)蛋白液,以注射健康人血清[75mg/(kg·d)]的SD孕鼠作为空白对照(10只),至孕15d处死后取材,计算各组孕鼠胚胎吸收率、胚胎质量,酶标仪测各组血清ACA的相对含量,以部分凝血酶原时间(APTT)来判定LA的活性。结果:造模后,孕鼠血清ACA、APTT、胚胎吸收率明显增加(P<0.05);胚胎质量明显降低(P<0.05);胎盘切片镜下见胎盘免疫复合物沉积、组织变性坏死、炎性细胞浸润、血管内纤维素凝结及淤血等病理现象;且均与抗体蛋白液剂量呈正相关,其中以注射75mg/(kg·d)ACA蛋白液或LA蛋白液造模最稳定。结论:LA可作为复制本动物模型所需免疫抗体来源之一;75mg/(kg·d)ACA蛋白液或LA蛋白液为本模型所需免疫抗体的稳定有效量;改良后动物模型符合抗磷脂抗体致妊娠丢失患者的生化、产科特点及病理变化。Aim : To investigate the improved methods for setting up rat model of fetal loss induced by human APA. Methods:80 10-week-old SD pregnant rats were randomly divided into 5 groups: A - H and blank control group. On the 8th and 12th day of pregnancy, multi-site subcutaneous injection of the anticardiolipin antibody( ACA ,Group A - D) or lupus anticoagulant ( LA,Group E -H) of protein solution on the back was used to every rat of Group A - H in the dosage of 25,50,75, and 100 mg/(kg · d). Until the 15th day of pregnancy, they were killed for taking samples. Meanwhile, healthy human protein solution was taken as a blank control group. Absorption rate and weight of fetus were calculated ;75 mg/(kg·d) ACA level was measured by enzyme mark instrument and activities of LA determined by APTT. Results: Studying the rat model, we found that the number of ACA in serum and embryo absorption rate increased significantly ( P 〈 0.05 ) , and APTT prolonged, while embryonic weight decreased significantly ( P 〈 0.05 ). The results of pathological observation showed some phenomena such as deposit of plaeenta immune complex, tissue degeneration and necrosis, inflam- matory cell infiltration, fibrin agglutinations and blood stasis in the vessel, etc, which were all positively correlated with dosages of antibody protein solution. In addition, 75 mg/( kg · d) ACA protein solution or LA protein solution is the stable and effective dosage of immune antibody for the model. Conclusion : LA can be one of the immune antibody sources to replicate the animal model; 75 mg/( kg ·d) ACA protein solution or LA protein solution is the stable and effective immune antibody dosage for a model; the improved animal model conforms to the biological, obstetrical and pathological changes of fetus loss patients induced by APA.
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