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The effect of Jiedu Huoxue decoction on rat model of experimental nonbacterial prostatitis via regulation of miRNAs

机译:Jiedu Huoxue汤对MiRNA调控的实验性非分泌前列腺炎大鼠模型的影响

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Context The underlying mechanisms of Jiedu Huoxue decoction (JDHXD) in treating chronic prostatitis have not been fully explored. Objective This study investigates the miRNAs as potential biomarkers and the effect of JDHXD on the rat model of experimental nonbacterial prostatitis. Materials and methods Fifty-four Sprague-Dawley male rats were randomly divided into normal control, model, JDHXD low dose (0.5?g/kg/day), medium dose (1?g/kg/day), high dose (2?g/kg/day) and western medicine (cernilton 0.094?g/kg/day) groups, and intragastrically administered once daily for 30?days. The control and model (upon successful establishment) groups received distilled water. Differential expression of miRNAs was analysed with high-throughput miRNA sequencing and validated with qRT-PCR and Northern blot. Prediction of specific target genes and functional enrichment analysis were performed with bioinformatics. Results LDsub50/sub test showed no sign of toxicity with maximum feasible dose 4?g/kg JDHXD. Compared with control, 495 miRNAs showed expression changes in CAP/CPPS rats, of which 211 were significantly different and 37 were prostatic-related. There were 181 differentially expressed miRNAs between the model and high dose JDHXD groups, of which 23 were identical with the control and model groups. Compared with control, miR-146a, miR-423 and miR-205 expression increased significantly in the model group, decreased dose-dependently in the JDHXD groups (p??0.05), and vice-versa for miR-96 (p??0.05). The effect of low dose JDHXD was comparable to cernilton (p??0.05). Discussion and conclusions Future studies may explore the contributions of the active components in JDHXD. The study design is generalisable. The effect can be repeatedly verified in clinical trials.
机译:背景信息尚未完全探索Jiedu Huoxue汤(JDHXD)治疗慢性前列腺炎的潜在机制。目的本研究研究了MIRNA作为潜在的生物标志物和JDHXD对实验性非分泌前列腺炎大鼠模型的影响。材料和方法五十四个Sprague-Dawley雄性大鼠随机分为正常对照,模型,JDHXD低剂量(0.5?G / kg /天),中剂量(1?g / kg /天),高剂量(2? G / kg /天)和西医(Cernilton 0.094?g / kg /天)组,每天一次胃内给药30?天。控制和型号(成功建立时)基团接受蒸馏水。用高通量miRNA测序分析miRNA的差异表达,并用QRT-PCR和Northern印迹验证。用生物信息学进行特异性靶基因的预测和功能性富集分析。结果LD 50 测试显示没有毒性的迹象,最大可行剂量4?g / kg jdhxd。与对照相比,495名MiRNA显示帽/ CPP大鼠的表达变化,其中211分显着不同,37例与前列腺有关。在模型和高剂量JDHXD组之间存在181个差异表达的miRNA,其中23与对照组相同。与对照组相比,模型组中MiR-146a,miR-423和miR-205表达显着增加,在JDHXD组中依赖于剂量依赖性(p?<〜0.05),对miR-96反之亦然(p? <?0.05)。低剂量JDHXD的效果与Cernilton相当(P?> 0.05)。讨论和结论未来的研究可能探讨了JDHXD中的活动组分的贡献。研究设计是不断的。可以在临床试验中重复验证效果。

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