摘要
目的建立脂多糖(LPS)诱导小鼠持续内毒素血症血小板减少(TCP)模型,观察小鼠模型平均血小板体积(MPV)、血小板生成素(TPO)的变化。方法 C57/BL小鼠随机分为4组,低剂量LPS5mg/kg连续给药组(LL-c组),低剂量LPS5mg/kg单次给药组(LL组),高剂量LPS50mg/kg单次给药组(HL组),对照组(C组);于给药前测定各组小鼠血小板计数(PLT)和MPV作为基线,观察给药后小鼠PLT、TPO、MPV水平及存活情况。结果 LL-c组小鼠注射LPS后PLT下降,并持续处于基线30%左右的水平,与基线相比较差异均有统计学意义(P<0.01),LL组与HL组均先降低后升高;LL-c组注射LPS后MPV持续处于增大水平,与基线相比较差异有统计学意义(P<0.01),HL、LL组MPV均先增大后减小;7d时LL-c组小鼠TPO高于C组(P<0.05);LL-c组、LL组与HL组小鼠造模7d时分别死亡5只、0只、14只。结论连续低剂量腹腔注射LPS可诱导小鼠持续TCP模型。
Objective To establish a model of mouse continuing endotoxemia thrombocytopenia (TCP) induced by li- popolysaccharide (LPS), observe changes of the mean platelet volume (MPV) and thrombopoietin (TPO) in this model. Meth- ods C57/BL mice were randomly divided into four groups, LPS low dose (5 mg/kg) of continue injection (LL-c) group, LPS low dose (5 mg/kg) of single injection (LL) group, LPS high dose (50 mg/kg) of single injection (HL) group and physiological sa- line injection (control) group. The blood platelet count (PLT) and MPV were detected before injection as the base line. The val- ues of PLT, TPO, MPV and mortality were observed after treatment. Results The value of PLT was significantly lower in LL-c group than that of basic line (P 〈 0.01), which was continued in the baseline level of about 30%. The PLT levels were lower and then higher in HL and LL groups. The value of MPV was significantly higher in LL-c group than that of basic line (P 〈 0.01), which was augmentation and then diminution in HL group and LL group. The TPO level of 7-day was significantly higher in LL-c group than that of control group (P 〈 0..05). The mortality were respectively 5 rats, 0 rat and 14 rats in LL-c group, LL group and HL group. Conclusion The model of continuing endotoxemia TCP can be induced by consecutive low dose LPS intraperitoneal injection.
出处
《天津医药》
CAS
北大核心
2013年第5期468-470,共3页
Tianjin Medical Journal
基金
国家临床重点专科建设项目[卫办医政函(2011)873号]
天津市卫生局科技基金资助项目(项目编号:10KG104)