Shraibom Nadav, Madaan Alka, Joshi Vidushi, Verma Ritu, Chaudhary Anika, Mishra Gautam, Awasthi Anshumali, Singh Anu Taneja, Jaggi Manu
Sirbal Limited, 11, Agathonos Kapsalos, 3087, Limassol. Cyprus.
Dabur Research Foundation, 22, Site IV, Sahibabad, Ghaziabad, Uttar Pradesh-201010. India.
Antiinflamm Antiallergy Agents Med Chem. 2017;16(2):94-111. doi: 10.2174/1871523016666170720160037.
We have developed a novel aqueous polyherbal formulation (SIRB-001) consisting of 3 herbs; Rheum palmatum L., Lonicera Japonica and Rehmannia glutinosa Libosch in the ratio 1:1:3. SIRB-001 has demonstrated efficacious effects in psoriasis patients.
This study was aimed at scientifically evaluating the in vitro antipsoriatic activity of SIRB-001.
The in vitro anti-psoriatic properties of SIRB-001 were assessed in human keratinocyte cell line; HaCaT. Anti-proliferative effect was studied using MTT assay. Apoptosis was examined by flow cytometry and colorimetric methods. Inflammatory markers and VEGF were determined by ELISA. IL-17/IL-23 secretion was assessed in immune cells. Signaling markers (kinases) by enzymatic assay and Topoisomerase-II activity by Kinetoplast DNA Cleavage assay was tested.
SIRB-001 significantly inhibited (p<0.01) proliferation of HaCaT cells and induced apoptosis. Significant (p<0.01) downregulation of pro-inflammatory markers (TNF- α, IFN-γ, IL-6, NO, sPLA2) and VEGF was observed. IL-17/IL-23 secretion was significantly (p<0.01) alleviated in immune cells (RAW264.7 and THP-1). Inhibition of signaling markers (AKT1, FLT3, MAPK1, PRKCA, MAP2K) was observed. SIRB-001 demonstrated inhibition of Topoisomerase-II activity. High Performance Liquid Chromatography (HPLC) analysis of SIRB-001 was carried out using standard marker compounds chlorogenic acid (tR=13.98min), Acteoside (tR=24.22 min) and Rhein (tR=53.76 min).
The in vitro results substantiate the anti-psoriatic effect of SIRB-001 in patients. SIRB-001 exerted anti-psoriatic effects at cellular level via multiple arms (antiproliferative, pro-apoptotic, anti-inflammatory, anti-angiogenic). This study provides insight into mechanism of action of SIRB-001 and highlights its promising potential for development as a herbal therapeutic agent for psoriasis, emphasizing the need of further pharmacological evaluation and toxicological studies.
我们研发了一种新型水性多草药配方(SIRB - 001),其由三种草药组成,分别是掌叶大黄、忍冬和地黄,比例为1:1:3。SIRB - 001已在银屑病患者中显示出有效作用。
本研究旨在科学评估SIRB - 001的体外抗银屑病活性。
在人角质形成细胞系HaCaT中评估SIRB - 001的体外抗银屑病特性。使用MTT法研究抗增殖作用。通过流式细胞术和比色法检测细胞凋亡。采用酶联免疫吸附测定法(ELISA)测定炎症标志物和血管内皮生长因子(VEGF)。在免疫细胞中评估白细胞介素17(IL - 17)/白细胞介素23(IL - 23)的分泌。通过酶促测定法检测信号标志物(激酶),并采用动质体DNA切割测定法检测拓扑异构酶II的活性。
SIRB - 001显著抑制(p<0.01)HaCaT细胞的增殖并诱导细胞凋亡。观察到促炎标志物(肿瘤坏死因子α、干扰素γ、白细胞介素6、一氧化氮、分泌型磷脂酶A2)和VEGF显著(p<0.01)下调。免疫细胞(RAW264.7和THP - 1)中IL - 17/IL - 23的分泌显著(p<0.01)减轻。观察到信号标志物(蛋白激酶B1、FMS样酪氨酸激酶3、丝裂原活化蛋白激酶1、蛋白激酶Cα、丝裂原活化蛋白激酶激酶)受到抑制。SIRB - 001显示出对拓扑异构酶II活性的抑制作用。使用标准标志物化合物绿原酸(保留时间tR = 13.98分钟)、毛蕊花糖苷(tR = 24.22分钟)和大黄酸(tR = 53.76分钟)对SIRB - 001进行了高效液相色谱(HPLC)分析。
体外实验结果证实了SIRB - 001对患者的抗银屑病作用。SIRB - 001通过多种途径(抗增殖、促凋亡、抗炎、抗血管生成)在细胞水平发挥抗银屑病作用。本研究深入了解了SIRB - 001的作用机制,并突出了其作为银屑病草药治疗剂开发的潜在前景,强调了进一步进行药理学评估和毒理学研究的必要性。