Department of Pharmacology, College of Korean Medicine, Sang-ji University, Wonju-si, Gangwon-do 26339, Republic of Korea.
Department of Korean Medical Science, School of Korean Medicine and Healthy Aging Korean Medical Research Center, Pusan National University, Yangsan, Gyeongnam 50612, Republic of Korea.
J Nat Prod. 2020 Apr 24;83(4):1183-1189. doi: 10.1021/acs.jnatprod.9b01210. Epub 2020 Mar 19.
Oleanolic acid (OA) is a natural, biologically active pentacyclic triterpenoid found in . Although and OA have antiproliferative actions, the effects and mechanisms of OA in benign prostatic hyperplasia (BPH) are unclear. We examined the effect of OA in an animal model of testosterone-induced BPH. Male rats were injected with testosterone propionate with or without OA. The inhibitory effect of OA on BPH-1 cells was determined . Rats with BPH exhibited outstanding BPH symptoms, including prostatic enlargement, upregulated dihydrotestosterone and 5α-reductase 2 levels, and histological changes. Compared with the BPH group, the OA group showed fewer pathological alterations and regular androgen events. OA inhibited prostate cell proliferation by downregulating the expression of proliferating cell nuclear antigen (PCNA) and cell cycle markers in BPH-induced animals. This indicated that OA has superior therapeutic effect in the BPH animal model than finasteride. studies demonstrated upregulation of PCNA and cell cycle proteins, whereas OA clearly reduced this upregulation. Thus, OA may inhibit the development of BPH by targeting cell cycle progression markers. These suggest that OA is a potential agent for BPH treatment.
齐墩果酸(OA)是一种天然的、具有生物活性的五环三萜,存在于。虽然 和 OA 具有抗增殖作用,但 OA 在良性前列腺增生(BPH)中的作用和机制尚不清楚。我们在雄激素诱导的 BPH 动物模型中研究了 OA 的作用。雄性大鼠用丙酸睾酮加或不加 OA 注射。测定 OA 对 BPH-1 细胞的抑制作用。患有 BPH 的大鼠表现出突出的 BPH 症状,包括前列腺增大、二氢睾酮和 5α-还原酶 2 水平上调以及组织学变化。与 BPH 组相比,OA 组的病理改变较少,雄激素事件较为规律。OA 通过下调 BPH 诱导动物中增殖细胞核抗原(PCNA)和细胞周期标志物的表达抑制前列腺细胞增殖。这表明 OA 在 BPH 动物模型中的治疗效果优于非那雄胺。研究表明 PCNA 和细胞周期蛋白的上调,而 OA 明显降低了这种上调。因此,OA 可能通过靶向细胞周期进程标志物来抑制 BPH 的发展。这些表明 OA 是一种治疗 BPH 的潜在药物。