Department of Biology and Pharmaceutical Botany, Medical University of Lodz, Muszynskiego 1, 90-151 Lodz, Poland.
Department of Pharmaceutical Microbiology and Microbiological Diagnostic, Medical University of Lodz, Banacha 12/16, 90-237 Lodz, Poland.
Molecules. 2023 Sep 22;28(19):6759. doi: 10.3390/molecules28196759.
This study evaluates the antioxidant properties and anti-inflammatory potential of polyphenolic acid-rich fractions of 80% methanolic extract from the hairy roots of . The fractionation of the crude extract yielded the following: a diethyl ether fraction rich in caffeic acid (DM1) (25.85 mg/g DWE), an n-butyl fraction rich in rosmarinic acid (DM3) (43.94 mg/g DWE) and a water residue rich in salvianolic acid B (DM4) (51.46 mg/g DWE). The content of these compounds was determined using high-performance liquid chromatography (HPLC). Their antioxidant activity was evaluated based on DPPH (2,2-diphenyl-1-picrylhydrazyl), ABTS (2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt) and FRAP assays. The anti-inflammatory activity of the fractions was determined by their effect on nuclear factor kappa-B (NF-κB) activation and interleukin-1 (IL-1) production in LPS stimulated monocytes. The level of pro-inflammatory IL-1 in cells was measured using ELISA. The activation of NF-κB in THP1-Blue™ cells, resulting in the secretion of SEAP (secreted embryonic alkaline phosphatase), was detected spectrophotometrically using Quanti-Blue reagent. Among the tested fractions, the diethyl ether fraction (DM1) showed the highest antioxidant potential, with an EC value of 15.41 µg/mL in the DPPH assay and 11.47 µg/mL in ABTS and a reduction potential of 10.9 mM Fe(II)/g DWE in FRAP. DM1 at a concentration of 10 mg/mL also efficiently reduced LPS-induced SEAP secretion (53% inhibition) and IL-1 production (47% inhibition) without affecting the normal growth of L929 fibroblast cells.
本研究评估了 80%甲醇提取物的毛状根中多酚酸丰富部分的抗氧化和抗炎潜力。粗提取物的分级分离得到以下产物:富含咖啡酸的二乙醚部分(DM1)(25.85 毫克/克 DWE),富含迷迭香酸的正丁基部分(DM3)(43.94 毫克/克 DWE)和富含丹酚酸 B 的水残基(DM4)(51.46 毫克/克 DWE)。这些化合物的含量使用高效液相色谱法(HPLC)确定。它们的抗氧化活性基于 DPPH(2,2-二苯基-1-苦基肼基),ABTS(2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)二铵盐)和 FRAP 测定法进行评估。通过测定其对 LPS 刺激的单核细胞中核因子 kappa-B(NF-κB)激活和白细胞介素-1(IL-1)产生的影响来确定各部分的抗炎活性。使用 ELISA 测量细胞中促炎细胞因子 IL-1 的水平。THP1-BlueTM 细胞中 NF-κB 的激活导致 SEAP(分泌的胚胎碱性磷酸酶)的分泌,通过使用 Quanti-Blue 试剂分光光度法检测。在所测试的部分中,二乙醚部分(DM1)显示出最高的抗氧化潜力,在 DPPH 测定中 EC 值为 15.41 µg/mL,在 ABTS 中为 11.47 µg/mL,在 FRAP 中为 10.9 mM Fe(II)/g DWE。在 10mg/mL 的浓度下,DM1 还能有效降低 LPS 诱导的 SEAP 分泌(抑制 53%)和 IL-1 产生(抑制 47%),而不影响 L929 成纤维细胞的正常生长。