School of Biological Sciences, Seoul National University, Seoul 151-742, Korea.
ViroMed Co. Ltd., Building 203, Seoul National University, Seoul 151-742, Korea.
Nutrients. 2018 Dec 7;10(12):1946. doi: 10.3390/nu10121946.
Benign prostatic hyperplasia (BPH) is a common disease in the elderly male population throughout the world. Among other factors, androgen dysregulation has been known to play major roles in its pathogenesis. HX109 is a botanical formulation prepared from a mixture of , , and , which have traditionally been used-usually along with other plants-to treat urinary diseases. An ethanol extract was prepared from a mixture of these three plants, and its quality was controlled through cell-based bioassays and by quantification of several marker compounds by high-performance liquid chromatography (HPLC). In the testosterone propionate (TP)-induced prostate hyperplasia rat model, oral administration of HX109 ameliorated prostate enlargement and histological changes induced by TP. In LNCaP cells, a human prostate epithelial cell line, HX109 repressed AR-mediated cell proliferation and the induction of androgen receptor (AR) target genes at the transcriptional level without affecting the translocation or expression of AR. Such effects of HX109 on AR signaling were mediated through the control of activating transcriptional factor 3 (ATF3) expression, phosphorylation of calcium/calmodulin-dependent protein kinase kinase β (CaMKKβ), and increases in intracellular calcium, as evidenced by data from experiments involving ATF3-specific siRNA, CaMKKβ inhibitor, and calcium chelator, respectively. Taken together, our data suggest that HX109 might be used as a starting point for developing therapeutic agents for the treatment of BPH.
良性前列腺增生症(BPH)是全世界老年男性人群中的一种常见疾病。除其他因素外,雄激素失调已被证明在其发病机制中起主要作用。HX109 是一种植物配方,由 、 、 三种植物的混合物制成,这些植物传统上一直被用于治疗泌尿系统疾病,通常与其他植物一起使用。从这三种植物的混合物中提取了乙醇提取物,并通过基于细胞的生物测定和通过高效液相色谱(HPLC)定量几种标记化合物来控制其质量。在丙酸睾丸酮(TP)诱导的前列腺增生大鼠模型中,HX109 的口服给药改善了 TP 诱导的前列腺增大和组织学变化。在 LNCaP 细胞(一种人前列腺上皮细胞系)中,HX109 在转录水平上抑制了 AR 介导的细胞增殖和雄激素受体(AR)靶基因的诱导,而不影响 AR 的易位或表达。HX109 对 AR 信号的这种影响是通过控制激活转录因子 3(ATF3)表达、钙/钙调蛋白依赖性蛋白激酶激酶β(CaMKKβ)磷酸化和细胞内钙增加来介导的,这一点可以从涉及 ATF3 特异性 siRNA、CaMKKβ 抑制剂和钙螯合剂的实验数据得到证明。总之,我们的数据表明,HX109 可能被用作开发治疗 BPH 的治疗剂的起点。