Identification of active compounds from Caesalpinia sappan L. extracts suppressing IL-6 production in RAW 264.7 cells by PLS

• Published in: Journal of ethnopharmacology Vol. 148; no. 1; pp. 37 - 44
• Main Authors: Chu, Ming-Juan, Wang, You-Zhi, Itagaki, Kiyoshi, Ma, Hong-Xing, Xin, Ping, Zhou, Xue-Gang, Chen, Guo-You, Li, Sen, Sun, Shi-Qin
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 21.06.2013
• Subjects: Active compounds; Animals; burning; Caesalpinia; Caesalpinia sappan; Caesalpinia sappan L; carbon dioxide; Cell Line; dysentery; enzyme-linked immunosorbent assay; Ethanol - chemistry; IL-6; interleukin-6; Interleukin-6 - antagonists & inhibitors; Interleukin-6 - metabolism; ionization; least squares; Least-Squares Analysis; leprosy; Lipopolysaccharides; mass spectrometry; medicine; Mice; osteoarthritis; Plant Extracts - analysis; Plant Extracts - pharmacology; PLS; prognosis; RAW 264.7; rheumatoid arthritis; Solvents - chemistry; ultra-performance liquid chromatography; Wood - chemistry; South East Asia; Caesalpinia sappan L; RAW 264.7; Active compounds; PLS; IL-6
• ISSN: 0378-8741; 1872-7573
• DOI: 10.1016/j.jep.2013.03.050

Caesalpinia sappan L. is distributed in Southeast Asia and also used as herbal medicine for the treatment of various diseases such as burning sensations, leprosy, dysentery, osteoarthritis and rheumatoid arthritis (RA). The overproduction of IL-6 plays an important role in the prognosis of RA, but the active compounds from the extracts of Caesalpinia sappan L. suppressing IL-6 production remain unknown. Identifying the main active compounds of Caesalpinia sappan L. extracts inhibiting the IL-6 production in LPS-stimulated RAW 264.7 cells by partial least squares (PLS). Sixty-four samples with different proportions of compounds were prepared from Caesalpinia sappan L. by supercritical CO2 fluid extraction (SCFE) and refluxing. Each of 64 samples was applied to RAW 264.7 cells with LPS to evaluate whether IL-6 production by LPS is affected by addition of each sample. The IL-6 production in medium was determined by ELISA and the inhibitory activity of each sample was analyzed. In addition, the fingerprints of these 64 samples were also established by ultra-performance liquid chromatography electrospray ionization tandem mass spectrometry (UPLC–MS). We used the PLS, a simplified method, to evaluate the results from IL-6 production and fingerprints. Each of 64 samples markedly suppressed LPS-induced IL-6 production in RAW cells. The fingerprints by UPLC–MS clearly revealed variations among 64 samples produced in different extract conditions. The PLS analysis with IL-6 production and fingerprints by UPLC–MS suggested that the peaks 71, 93, 150, 157, 168 have more influence on the inhibitory activity of Caesalpinia sappan L. extracts. The peaks 71, 93, 150 are likely representing sappanone A, protosappanin E and neoprotosappanin, respectively. The peaks 157 and 168 are still at large. This is the first report that sappanone A, protosappanin E, neoprotosappanin and two unidentified compounds can be considered as possible active compounds that might inhibit IL-6 production. Further studies are needed to confirm the effectiveness of these five compounds on IL-6 production and possible mechanism. [Display omitted]