Efficacy of Buzhong Yiqi decoction on benign prostatic hyperplasia and its possible mechanism.

Jia Lihua, Kuang Haodan, X U Yuan
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引用次数: 1

Abstract

Objective: To explored the mechanism of Buzhong Yigi decoction ( BZYQD) in inhibiting prostatic cell proliferation effect.

Methods: The compounds of BZYQD consisted with eight herbs were searched in TCMSP databases and the putative targets of BZYQD were collected in Drugbank database. Then, "Benign prostatic hyperplasia" (BPH) was used to find the targets based on the GeneCards, Online Mendelian Inheritance in Man (OMIM) and Therapeutic Target Database (TTD) databases, and they were further used to collect further collect the intersection targets between BZYQD and BPH by counter-selection. Next, Herb-Compound-Target-Disease network was constructed by Cytoscape software and protein interaction network was built by Search tool for recurring instances of neighbouring genes (STRING) database. Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment were analyzed by Database for Annotation, Visualization and Integrated Discovery (DAVID) database to predict the mechanism of the intersection targets. Mitogen activated protein kinase 8 (MAPK8), interleukin 6 (IL-6) and quercetin were chosen to perform molecular docking. Then 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay was to detect the bility of BPH-1 (BPH epithelial cell line) by treated with quercetin at the concentrations of 15, 30, 60, 120 μM for 12, 24, 48, 72 h. The production of IL-6, tumor necrosis factor-α (TNF-α), IL-1β and were mRNA expression detected by enzyme-linked immunosorbent assay kit and quantitative real-time polymerase chain reaction. Western blot was used to detect the expression of phospho-p38 mitogen-activated protein kinase (p-P38) and matrix metalloprotein-9 (MMP-9).

Results: A total 151 chemical ingredients of 8 herbs and 1756 targets in BZYQD, 105 common targets of BZYQD and BPH which mainly involving with MAPK8, IL-6, and so on. GO enrichment analysis got 352 GO entries (0.05) which included 208 entries of biological process, 64 entries of cell component and 80 entries of molecular function. KEGG pathway Enrichment analyses got 20 significant pathways which mainly involved with MAPK signaling way. MTT assay indicated quercetin inhibited the viability of BPH-1 cells by time-and dose-dependent manner. Quercetin decreased the IL-6, TNF-α and IL-1β production and mRNA expression, and the expression of p-P38 and MMP-9 were also obviously reduced after treated with quercetin.

Conclusions: BZYQD inhibited BPH through suppressing inflammatory response which might involving with regulating the MAPK signaling way.

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补中益气汤治疗前列腺增生的疗效及其可能机制。
目的:探讨补中益渴汤抑制前列腺细胞增殖的作用机制。方法:在中药中药数据库中检索含有8种中药的化合物,在Drugbank数据库中收集推定靶点。然后,基于GeneCards、Online Mendelian Inheritance in Man (OMIM)和Therapeutic Target Database (TTD)数据库,利用“Benign prostate hyperplasia”(BPH)寻找靶点,并通过反选择进一步收集BZYQD与BPH的交叉靶点。其次,利用Cytoscape软件构建草药-化合物-靶点-疾病网络,利用Search tool for recurring instances of neighbour genes (STRING)数据库构建蛋白质相互作用网络。利用DAVID数据库对基因本体(GO)富集和京都基因基因组百科全书(KEGG)通路富集进行分析,预测交叉靶点的作用机制。选择丝裂原活化蛋白激酶8 (MAPK8)、白细胞介素6 (IL-6)和槲皮素进行分子对接。采用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2- h -溴化四唑(MTT)法检测槲皮素在15、30、60、120 μM浓度下作用12、24、48、72 h后BPH上皮细胞株的增殖能力,采用酶联免疫吸附试剂盒和实时定量聚合酶链反应检测IL-6、肿瘤坏死因子-α (TNF-α)、IL-1β和mRNA表达量。Western blot检测磷酸化-p38丝裂原活化蛋白激酶(p-P38)和基质金属蛋白-9 (MMP-9)的表达。结果:8种中药共151种化学成分,BZYQD的靶点1756个,BZYQD和BPH的共同靶点105个,主要涉及MAPK8、IL-6等。GO富集分析得到352条GO条目(0.05),其中生物过程条目208条,细胞成分条目64条,分子功能条目80条。KEGG通路富集分析得到了20条主要参与MAPK信号通路的重要通路。MTT实验显示槲皮素对BPH-1细胞的活性具有时间和剂量依赖性。槲皮素降低了IL-6、TNF-α、IL-1β的产生和mRNA的表达,p-P38和MMP-9的表达也明显降低。结论:BZYQD通过抑制炎症反应抑制BPH,可能与调节MAPK信号通路有关。
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