Section of Molecular Pharmacology, Research Innovation and Invention, Dexa Laboratories of Biomolecular Sciences, PT Dexa Medica, Cikarang, West Java, Indonesia.
Int J Womens Health. 2015 Feb 3;7:161-9. doi: 10.2147/IJWH.S74552. eCollection 2015.
DLBS1442 is a bioactive fraction extracted from the fruit of the native Indonesian plant, Phaleria macrocarpa (Scheff.) Boerl (Thymelaceae). This bioactive fraction is a potential treatment for dysmenorrhea and endometriosis. The present study investigated the pharmacological action of DLBS1442 in endometrial cells. The effect of various doses of DLBS1442 (0-200 μg/mL) over 24 hours was studied using the human endometrial RL95-2 cell line to observe its effect on angiogenesis, cell migration, estrogen and progesterone receptor levels, the eicosanoid pathway, cell viability, and apoptosis. The impact of DLBS1442 on nuclear factor kappa B (NFκB) and the eicosanoid pathway was also studied through its marker gene expression using a quantitative real-time polymerase chain reaction method. DLBS1442 showed an ability to inhibit angiogenesis and cell migration in a dose-dependent manner. At a dose of 100 μg/mL, DLBS1442 increased the cell population in sub-G1 phase from 7% to 34%. DLBS1442 also significantly downregulated the estrogen receptor level and upregulated the progesterone receptor level. Further, it inhibited the eicosanoid signaling pathway by reducing the NFκB transcription level and subsequent reduction of inducible nitric oxide synthase. A dose-dependent decrease in viability and increased apoptosis in RL95-2 cells were also evident after exposure to DLBS1442, where the IC50 was obtained at around 100 μg/mL. In conclusion, DLBS1442 is a potential agent for alleviating symptoms of endometriosis via its antiangiogenic, anti-inflammatory, and proapoptotic activity.
DLBS1442 是从印度尼西亚本土植物 Phaleria macrocarpa(Scheff.)Boerl(野牡丹科)的果实中提取的生物活性部分。该生物活性部分是治疗痛经和子宫内膜异位症的潜在方法。本研究探讨了 DLBS1442 在子宫内膜细胞中的药理作用。使用人子宫内膜 RL95-2 细胞系研究了不同剂量的 DLBS1442(0-200μg/mL)在 24 小时内的作用,以观察其对血管生成、细胞迁移、雌激素和孕激素受体水平、类二十烷酸途径、细胞活力和细胞凋亡的影响。还通过定量实时聚合酶链反应方法研究了 DLBS1442 对核因子 kappa B(NFκB)和类二十烷酸途径的影响及其标记基因表达。DLBS1442 表现出抑制血管生成和细胞迁移的能力,呈剂量依赖性。在 100μg/mL 的剂量下,DLBS1442 将细胞群从亚 G1 期的 7%增加到 34%。DLBS1442 还显著下调了雌激素受体水平,上调了孕激素受体水平。此外,它通过降低 NFκB 转录水平和随后减少诱导型一氧化氮合酶来抑制类二十烷酸信号通路。暴露于 DLBS1442 后,RL95-2 细胞的活力呈剂量依赖性下降,凋亡增加,IC50 约为 100μg/mL。总之,DLBS1442 是一种通过抗血管生成、抗炎和促凋亡活性来缓解子宫内膜异位症症状的潜在药物。