首页> 外文期刊>American Journal of Perinatology Reports >The Effect of BML-111 in Preeclampsia Rat Model Induced by the Low Dose of Cadmium Chloride
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The Effect of BML-111 in Preeclampsia Rat Model Induced by the Low Dose of Cadmium Chloride

机译:BML-111在小剂量氯化镉诱导的子痫前期大鼠模型中的作用

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Aim?This article determines the optimal time and dose of cadmium chloride (CdClsub2/sub) injected to pregnant rat to establish experimental preeclampsia (PE) model. In addition, the therapeutic potential of BML-111, a lipoxin A4 analogue, in the CdClsub2/sub-induced PE model was also evaluated. Methods?Peritoneal injection of two dose of CdClsub2/sub for successive 6 days was tested in the pregnant rats starting from various gestational days (GDs). During this process, the systolic blood pressure and the body weight of pregnant rats and neonatal rats were monitored. The pathological changes of the placenta and kidney were evaluated by hematoxylin and eosin staining. The phosphorylation of extracellular signal-regulated kinase 1/2 and signal transducer and activator of transcription 3 in the placentas was detected by Western blot, and the messenger ribonucleic acid expression of interleukin (IL)-6, tumor necrosis factor-α, and IL-10 in the placentas were detected by real-time polymerase chain reaction. BML-111 at the dose of 1?mg/kg/day was peritoneally injected into the rat after establishing the PE model to test its therapeutic potential. Results?In the present study, we successfully established the PE model in pregnant rats by intraperitoneally injection of CdClsub2/sub at the dose of 0.125?mg/kg/day from GD 9 to 14. We recapitulated multiple features of clinical PE in CdClsub2/sub-induced rat, including high blood pressure, renal dysfunction, and inflammatory response in placenta. Furthermore, treatment with BML-111 significantly relieved multiple features in our PE rat model. Conclusions?BML-111 has a potential therapeutic effect in pregnant rats with CdClsub2/sub-induced PE, which appears to be mediated through inhibition of inflammatory processes in the placenta.
机译:目的确定注射到怀孕大鼠体内的氯化镉(CdCl 2 )的最佳时间和剂量,以建立先兆子痫(PE)模型。此外,还评估了脂蛋白A4类似物BML-111在CdCl 2 诱导的PE模型中的治疗潜力。方法:从妊娠各个天(​​GDs)开始,对妊娠大鼠进行连续6天腹膜内注射两剂CdCl 2 的试验。在此过程中,监测孕鼠和新生鼠的收缩压和体重。用苏木精和曙红染色评价胎盘和肾脏的病理变化。 Western blot检测胎盘中细胞外信号调节激酶1/2及信号转导和转录激活因子3的磷酸化,信使核糖核酸表达白介素(IL)-6,肿瘤坏死因子-α和白介素实时聚合酶链反应检测胎盘中的-10。建立PE模型后,以1?mg / kg /天的剂量将BML-111腹膜注射到大鼠中以测试其治疗潜力。结果?在本研究中,我们通过腹膜内注射CdCl 2 从GD 9到14剂量为0.125?mg / kg /天成功建立了PE大鼠模型。概括了多种特征CdCl 2 诱导的大鼠临床PE的变化,包括高血压,肾功能不全和胎盘的炎症反应。此外,用BML-111治疗可显着减轻PE大鼠模型的多个功能。结论BML-111对CdCl 2 诱导的PE大鼠具有潜在的治疗作用,其作用可能是通过抑制胎盘中的炎症过程介导的。

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