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新生大鼠缺氧缺血性脑损伤后白细胞介素-1β基因转录的动态观察

A Dynamic Observation on Interleukin 1 β Gene Transcription in Neonate Rats with Hypoxic Ischemic Brain Damage
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摘要 目的为探讨HIBD发病机制方法制备左脑缺氧缺血性脑损伤(HIBD)的新生大鼠模型,用IL1β寡核苷酸探针,通过DNARNA斑点杂交技术,检测HIBD后海马、皮质不同时间IL1β及mRNA。结果斑点杂交技术敏感特异,最低可检出1pg总RNA,且IL1β寡核苷酸探针只能特异地与其相应核酸杂交。HIBD后1小时mRNA水平开始增高,3小时为高峰表达,12小时基本消失。其海马表达略高于皮质。结论IL1β转录水平表达在HIBD后早期出现,其作用可能与HIBD发病过程的炎性过程有关。 Objective To study the change of interleukin 1 β gene transcription in the animal model of hypoxic ischemic brain damage(HIBD).Methods A model of HIBD in left brain of neonate rats was established and IL 1 β mRNA in the lesioned ischemic cortex and hippocampus at different times by DNA RNA Dot blot hybridization with IL 1 β oligonucleotide probe was detected.Results Dot blot hybridization was sensitive and specific.The probe can detect 1pg of total RNA,and hybridize only to the homologous nucleic acid.Level of IL 1 β mRNA was elevated as early as 1 hour and peaking expression was 3 hour after HIBD,IL 1 β expression in hippocampus was higher than that in cortex.Conclusions IL 1 β gene expression appears early after HIBD,it may play an important role in the response of inflammatory to HIBD.
出处 《小儿急救医学》 1999年第1期14-15,共2页 Pediatric Emergency Medicine
关键词 新生大鼠 缺氧缺血脑损伤 白细胞介素 斑点杂交 neonatal rats hypoxic ischemic brain damage interleukin 1 β Dot blot hybridization
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