Anti-inflammatory Triterpenes from Euonymus alatus Leaves and Twigs on Lipopolysaccharide-activated RAW264.7 Macrophage Cells
Anti-inflammatory Triterpenes from Euonymus alatus Leaves and Twigs on Lipopolysaccharide-activated RAW264.7 Macrophage Cells
Bulletin of the Korean Chemical Society. 2014. Oct, 35(10): 2945-2949
Copyright © 2014, Korea Chemical Society
  • Received : April 10, 2014
  • Accepted : June 05, 2014
  • Published : October 20, 2014
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About the Authors
Eun Ju Jeong
Ji-Yeong Bae
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 660-751, Korea
Jung-Rae Rho
Department of Oceanography, Kunsan National University, Jeonbuk 573-701, Korea
Young Choong Kim
College of Pharmacy and Research Institute of Pharmaceutical Science, Seoul National University, Seoul 151-742, Korea
Mi-Jeong Ahn
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 660-751, Korea
Sang Hyun Sung
College of Pharmacy and Research Institute of Pharmaceutical Science, Seoul National University, Seoul 151-742, Korea

As a part of ongoing phytochemical research on Euonymus alatus leaves and twigs, we have isolated one new reissantane-type triterpene ( 1 ), together with eight known triterpenes, isoarborinol ( 2 ), friedelin ( 3 ), abruslactone A ( 4 ), 3β,22α-dihydroxyolean-12-en-29-oic acid ( 5 ), 3α,22α-dihydroxyolean-12-en-29-oic acid ( 6 ), 3α,22β-dihydroxyolean-12-en-29-oic acid ( 7 ), 22α-hydroxy-3-oxoolean-12-en-29-oic acid ( 8 ), demethylregelin ( 9 ). The structure of 1 has been elucidated as 24,24-dimethyl-reissant-7(8),25-dien-3α-ol, by extensive 1D and 2D spectroscopic methods including 1 H-NMR, 13 C-NMR, 1 H- 1 H COSY, HSQC, HMBC and NOESY. Anti-inflammatory activities of the isolated compounds were determined as potential regulating excessive inflammatory responses in RAW264.7 macrophage cells. Particularly, abruslactone A ( 4 ) and demethylregelin ( 9 ) showed the most potent activity, which effectively reduced the expression of iNOS protein and subsequent nitric oxide production induced by lipopolysaccharide in RAW264.7 cells.
Euonymus alatus (Thunb.) Sieb. (Celastraceae) is a deciduous tree which is commonly known as winged euonymus. The cork cambium on the twigs which is called ‘gui-jun woo’ has been traditionally used to regulate blood circulation, to relieve pain, to eliminate stagnant blood and to treat dysmenorrheal. Known constituents of E . alatus include sesquiterpenes, sesquiterpene alkaloids, triterpenes, flavonoids and phenolic compounds. 1-3 Based on such background studies, we previously reported anti-inflammatory compounds isolated from the leaves and twigs of E . alatus which showed the significant inhibitory activities on nitric oxide production in LPS-stimulated RAW264.7 macrophage cells and BV2 microglia cells. 4,5 Continuous to the previous phytochemical study on E . alatus , we further tried to isolate anti-inflammatory constituents from CHCl 3 soluble fraction of the methanolic extract of E . alatus leaves and twigs.
Macrophages are widely distributed in the body and play important role such as host defense, inflammatory regulation and tissue remodeling by providing an immediate defense against foreign agents prior to leukocyte migration. 6 An effective immune cells, macrophages play pivotal roles in innate and adaptive immune response to pathogens such as phagocystosis, cytokines, bacteria, bacterial products and particulates including lipopolysaccharide (LPS). 7-9 Upon activation, various growth factors, cytokines and lipid mediators that promote inflammatory process are released. Hence, macrophages are recognized as target cells of a variety of immunosuppressants and anti-inflammatory drugs, leading to acquired immunity. 10 The pharmacological reduction of LPS-inducible inflammatory mediators in macrophage has been recognized as an effective target for the development of anti-inflammatory drugs or immunosuppressants.
In the present study, we report the isolation and structural elucidation of compounds 1-9 from E . alatus leaves and twigs, and the inhibitory activities of the isolated compounds on nitric oxide (NO) production and the expression of iNOS in LPS-stimulated RAW264.7 cells.
Plant Material. The leaves and twigs of E . alatus were collected in Nambu forest of Seoul National University, Beagwoon Mountain, Gwangyang city, Jeollanam-do, Korea, in September 2007 and authenticated by Dr. Jong Hee Park, professor of Pusan National University. A voucher specimen (CS-99) has been deposited in Herbarium of the Medicinal Plant Garden, College of Pharmacy, Seoul National University, Koyang, Korea.
Extraction and Isolation of Compounds 1-9. The air-dried leaves and twigs of E . alatus (15 kg) were extracted three times for 3 h each with 80% MeOH (140 L) in room tempearture using an ultrasonic apparatus. Removal of the solvent in vacuo yielded a methanolic extract (1.2 kg). The methanolic extract was then suspended in distilled water and partitioned successively with CHCl 3 (9 L), EtOAc (9 L), and n -BuOH (10 L). The CHCl 3 fraction (112 g) was subjected to column chromatography on a silica gel column using mixtures of CHCl 3 −MeOH−Water of increasing polarity as eluents (100:4:1→50:4:1→25:4:1→15:4:1→10:5:1→5:4:1→MeOH) to give 11 fractions (fr. 1 to 11). Compound 3 (420 mg) was obtained through recrystallization with MeOH from fr. 2. Fr. 4 was applied on silica gel column eluting with a gradient of CHCl 3 −MeOH to yield 6 fractions (fr. 4-1 to 4-6). Compounds 1 (160 mg) and 2 (330 mg) were obtained from fr. 4-6 and fr. 4-5, respectively, by recrystallization with MeOH. Fr. 8 was subjected to ODS gel column chromatography with a gradient elution of MeOH−H 2 O (20% → 80% MeOH) to give eight fractions (fr. 8-1 to 8-8). Fr. 8-6 was chromatographed on silica gel column eluted with n -hexane−EtOAc (1:1→1:5) to yield 8 fractions (fr. 8-6-1 to 8-6-8). Compound 5 (14 mg) was obtained from 8-6-6 by additional C 18 RP HPLC (AcCN−H 2 O 65:35, 2.0 mL/min, 250 × 10 mm, 210 nm, t R 28.01 min). Fr. 8-7 was subjected to silica gel column chromatography eluted with n -hexane−EtOAc (1:1→1:5) and yielded seven subfractions (fr. 8-7-1 to 8-7-7). Compounds 8 (4.4 mg) and 9 (5.2 mg) were isolated by C 18 RP HPLC (AcCN−H 2 O 70:30, 2.0 mL/min, 250 × 10 mm, 210 nm, t R 25.96 and t R 27.54 min) from fr. 8-7-6. Silica gel column chromatography of fr. 8-8 with a gradient elution of n -hexane-EtOAc afforded six subfractions (fr. 8-8-1 to 8-8-6). Fr. 8-8-1 was further purified by recrystallization with MeOH to yield compound 4 (8.2 mg). Compounds 6 (3.7 mg) and 7 (4.5 mg) were isolated by C 18 RP HPLC (AcCN−H 2 O 70:30, 2.0 mL/min, 250 × 10 mm, 210 nm, t R 39.04 and t R 45.36 min) from fr. 8-8-6.
24,24-Dimethyl-reissant-7(8)-25-dien-3a-ol (1). White amorphous powder, HREIMS m/z 454.4202 [M] + (calcd. for C 32 H 54 O, 454.4175); mp 219-220 ℃,
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+72.0° ( c 1.0, CHCl 3 ); IR (KBr) v max cm −1 : 3477, 2943, 2871, 1457, 1377, 758; NMR data, see Table 1 .
NMR data of compound1in CDCl3a
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aAll assignments were made by extensive analysis of 1D and 2D NMR. bMain observed HMBC and COSY correlations are presented.
Cell Cultures. RAW264.7 macrophage cells were obtained from Korea Cell Line Bank (Seoul, Korea). The cell line was maintained in DMEM containing 20 mM HEPES, 2 mM ʟ-Glutamine, 10% FBS with penicillin (100 IU/mL) and streptomycin (10 mg/mL) at 37 ℃ in a humidified atmosphere of 95% air-5% CO 2 .
Determination of NO Content. RAW264.7 cells were seeded in 48 well plates (1 × 10 5 cells/well) and incubated at 37 ℃ for 24 h. Then, the cell culture was washed and the medium was replaced with Griess medium to remove any trace of phenol red, and treated with test sample for 1 h before exposure to 0.1 mg/mL of LPS. After 24 h incubation, nitrite in culture medium was measured to assess NO production in RAW264.7 cells using Griess reagent. The absorbance at 550 nm was measured on a microplate reader and the concentration was determined using nitrite standard curve.
Estimation of Cell Viability. After 100 mL of sample aliquot was collected for Griess assay, MTT (0.2 mg/mL) was directly added to cultures, followed by incubation at 37 ℃ for 2 h. The supernatant was then aspirated and 100 mL of DMSO was added to dissolve the formazan. After insoluble crystals were completely dissolved, absorbance at 540 nm was measured using a microplate reader. Data were expressed as percent cell viability relative to control cultures.
Western Blotting. RAW264.7 cells were plated overnight in 6-well plates at a density of 1 × 10 6 cells per well. The medium was changed to fresh one and treated with test sample for 1 h before exposure to 0.1 ug/mL of LPS. After 8 h incubation, cells were washed twice with phosphatebuffered saline (PBS). The washed cell pellet was lysed in 200 μL of extraction lysis buffer (50 mM HEPES pH 7.0, 250 mM NaCl, 5 mM EDTA, 5 mM NaF, 0.5 mM sodium orthovanadate, protease inhibitor cocktail, 1% glycerol) and incubated for 30 min at 4 ℃. Cell lysate was centrifuged at 12,000 rpm for 15 min at 4 ℃ and the supernatant was collected, followed by quick freezing. Protein content was determined using Bradford reagent according to the manufacture’s instruction. Equal amounts of protein (40 ug) were loaded per lane onto 8% SDS-PAGE gel. Protein was transferred to PVDF membranes and subsequently blocked in 5% skim milk for 30 min at room temperature. Anti-iNOS (1:1000 dilution; Cell Signaling Technology) antibodies were employed in 1 % skim milk. The membrane was incubated with the primary antibody for 1 h at room temperature. After washing three times with TBST, the immunoreactive bands were visualized by using immunopure peroxidase conjugated goat anti-rabbit IgG (1:10000 dilution; Pierce, Rockford, IL, USA). The Blot was washed three times and then developed by enhanced chemiluminescence (iNtRON Biotechnology, Seongnam, Korea).
Results and Discussion
Isolation of Compounds 1-9 from E. alatus Leaves and Twigs. The methanolic extract of E . alatus leaves and twigs was suspended in water and successively partitioned with CHCl 3 , EtOAc and n -BuOH. Each fraction was evaluated for its inhibitory activity on NO production in LPS-stimulated RAW264.7 cells. Among the fractions, the CHCl 3 soluble fraction showed the greatest inhibitory activity on NO production in RAW264.7 cells ( Table 2 ). The CHCl 3 (112 g) was further subjected to repeated column chromatography to yield one new C 32 reissantane-type triterpene together with eight arborane, freidelane, oleanane, ursanetype triterpenes. Eight known compounds were identified as isoarborinol ( 2 ), friedelin ( 3 ), abruslactone A ( 4 ), 3β,22α-dihydroxyolean-12-en-29-oic acid ( 5 ), 3α,22α-dihydroxyolean-12-en-29-oic acid ( 6 ), 12 3α,22β-dihydroxyolean-12-en-29-oic acid ( 7 ), 13 22α-hydroxy-3-oxoolean-12-en-29-oic acid ( 8 ), demethylregelin ( 9 ) respectively, by comparison of spectroscopic data with those previously reported ( Figure 1 ). Compounds 2 and 4-9 are reported for the first time from this plant.
Inhibitory effects of total extract and each fraction ofE.alatusleaves and twigs on NO production in LPS-stimulated RAW264.7 cells
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aValue of RAW264.7 cells not treated with LPS. bValue of RAW264.7 cells treated with 100 ng/mL LPS for 24 h. Mean value is significantly different (*P < 0.001) from the value of the LPS-treated.
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Structures of compounds 1-9 isolated from CHCl3 fraction of E.alatus leaves and twigs.
Structural Elucidation of Compound 1. Compound 1 was obtained as white amorphous powder with
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+72.0 ( c 0.1, MeOH). Its IR spectrum showed the presence of OH group (3477 cm −1 ) and exomethylene (889 cm −1 ). The molecular formula of 1 was determined as C 32 H 54 O from [M] + ion peak at m/z 454.4202 (calc. 454.4175) in HREIMS. The 1 H-NMR spectrum of 1 displayed signals due to nine methyl groups; seven singlets corresponding to tertiary methyl groups (δ H 0.76, 0.84, 0.94, 0.99, 0.99, 1.00, 1.04), one doublet of a secondary methyl group (δ H 0.85, J = 6.6 Hz) and one vinylic methyl group (δ H 1.66). The 1 H-NMR spectrum also showed signals assignable to one oxymethine proton at δ H 3.41, one olefinic at δ H 5.15 (1H, dd, J = 6.5, 1.6 Hz) and one exomethylene at [δ H 4.66 (1H, br s), 4.72 (1H, br s)]. The 13 C-NMR spectrum exhibited 32 carbon signals sorted by DEPT experiment as nine methyl groups, ten methylenes (including one sp 2 carbon at δ C 109.3), six methines (including one oxygenated at δ C 76.5 and one olefinic carbon at δ C 117.6) and seven quaternary carbons. The location of OH group was evidenced by HMBC correlations between C-3 (δc 76.5) and Me-28 (δ H 0.94), Me-29 (δ H 0.76). The relative configuration of H-3 was determined as equatorial position from the small coupling constant of H-3 (δ H 3.41, br s).
Further structural details were obtained by two dimensional NMR experiments (COSY, HSQC, and HMBC), which coupled with literature data, allowed unambiguous assignment of all carbon signals ( Table 1 ). The elucidated basal structure of 1 was very closed to the series of 19(10→9) abeo -8α,9β,10α-euphane triterpene, which was first time found from Mallotous stenanthusz 17 also called as reissantane-type triterpene. From the 1 H- 1 H COSY correlations between H-10 and H-5, H-5 and H-6, H-6 and H-7, and the HMBC correlations of Me-19 with C-8, C-9, C-10 and C-11, it was suggested that 1 was reissantane-type triterpene with double bond between C-7 and C-8 ( Figure 2 ). The stereochemistry of 1 was determined from the cross peaks observed in NOESY spectrum between Me-19 and H-5, Me-29, between Me-28, Me-29 and H-6, between Me-30 and H-17 ( Figure 2 ). Two extra methyl groups, Me-31 (δ H 0.99) and Me-32 (δ H 0.99) showed the same HMBC correlations with C-23, C-24 and C-25 indicating 24,24-dimethyl position. The presence of 10 carbon side chain was further supported by the characteristic fragment peaks in MS spectrum at m/z 439 (M−Me), 421 (M−H 2 O−Me), 315 (M–side chain), 313 (M–side chain–2H). 18 The remaining exomethylene was determined at C-25 from the HMBC correlations between C-24 (δ C 38.7) and H-26 (δ H 4.66 and 4.72), H-27 (δ H 1.66). The chemical shift (δ H 0.85, d, J = 6.6 Hz) of Me-21 in 1 H-NMR spectrum, and the positive optical rotation of 1 (+72.0°) also indicated that the relative configuration of the side chain belonged to the euphane rather than the tirucallane series. 19 From above data, compound 1 was determined as a C 32 reissantane-type triterpenoid which possesses extra two methyl groups at C-24 in the side chain. On the basis of these data, compound 1 was determined to be 24,24-dimethyl-reissant-7(8), 25-dien-3α-ol.
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The selected HMBC and NOESY correlations in compound 1.
Anti-inflammatory Activities of Compounds 1-9 in LPS-activated RAW264.7 Cells. Inhibitory effects of compounds 1−11 on LPS-induced NO production in RAW264.7 cells were evaluated using the Griess reaction. The treatment of LPS resulted in a significant increment of nitrite concentration in the medium compared to control. Among the compounds isolated, compounds 4, 5, 6, and 9 showed the strong or moderate inhibitory effects on NO production ( Table 2 ) while the others were inactive. Oleanane-type triterpenoids 4-8 characteristically possessed oxygenated C-3, hydroxyl group at C-22 and carboxyl group at C-29. In those triterpenes, compound 4 in which hydroxyl group at C-22 and carboxyl group at C-29 were connected by ester linkage showed the most potent activity compared to those of compounds 5-7 with free forms of carboxyl group and hydroxyl group. In addition, compound 7 with β-hydroxy group at C-22, and compound 8 with ketone group at C-3 were found to be inactive. At the concentration of 100 μM, the NO production was significantly decreased up to 20 ± 1.5% and 15 ± 0.8% of control level by the pretreatment of compounds 4 and 9 , respectively. To verify whether the reduced cell numbers which were caused by the cytotoxicity of these compounds resulted in decrease of NO production, cell viability was measured employing MTT assay. All the compounds tested showed no cytotoxicity at the concentration ranging from 10 μM to 100 μM.
Inhibitory effects of compounds4, 5, 6and9on NO production induced by LPS in RAW264.7 cells
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aRelative NO production (%) calculated as 100 × (NO of LPS + sampletreated − NO of untreated control)/(NO of LPS-treated − NO of untreated control). bValue of RAW264.7 cells not treated with LPS. cValue of RAW264.7 cells treated with 100 ng/mL LPS for 24 h. NO concentration (μM) of control and LPS-treated cultures were 3.2 ± 0.1 and 15.8 ± 0.3, respectively. dNAME (ω-nitro-l-arginine methyl ester) positive control. Mean value is significantly different (*P < 0.01, **P < 0.001) from the value of the LPS-treated.
Since NO has been known to be produced by iNOS in LPS-stimulated RAW264.7 cells, the inhibitory effects of compounds 4 and 9 , which showed the most potent inhibitory activity on NO production, on the expression of iNOS protein were measured. Treatment of RAW264.7 cells with LPS resulted in the increment of iNOS expression and subsequent NO production. Pretreatment of RAW264.7 cells with compounds 4 or 9 significantly inhibited the expression level of iNOS protein compared to cells treated with LPS-only. The inhibition of iNOS expression was more remarkable in the treatment of compound 9 at the concentration of 100 μM ( Figure 3 ).
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Inhibitory effects of compounds 4 and 9 on LPS-induced iNOS expression in RAW264.7 cells. RAW264.7 cells were pretreated with compounds 4 or 9 for 1 h, then exposed to LPS for 24 h. Cell lysate (40 μg protein) was prepared from the cells and subjected to Western blot analysis using an antibody specific for iNOS as described in the Methods. The values shown are mean ± SD of data from three independent experiments. Significant compared with LPS alone, *P < 0.01, **P < 0.001.
Nine triterpenenes including one new reissantane-type was isolated from E . alatus leaves and twigs. Among the compounds isolated, abruslactone A ( 4 ) and demethylregelin ( 9 ) showed the potent inhibitory activities on NO production and iNOS expression in LPS-stimulated RAW264.7 cells. Though further investigations are required to clarify the detailed anti-inflammatory actions of bioactive compounds from E . alatus , the triterpenes isolated herein are thought contribute to anti-inflammatory effects of E . alatus and might possess beneficial therapeutic potential against various inflammation-related diseases.
This work was supported by grants from the Connected Cooperation Projects of Metropolitan Economic Areas (Grant # A004500005 to M-J Ahn), Ministry of Knowledge Economy, and also partially supported by grants from the Next-Generation BioGreen 21 Program (SSAC, grant#: No. PJ0095062013 to M-J Ahn), and Cooperative Research Program for Agriculture Science & Technology Development (Grant # PJ009804 to EJ Jeong), Rural Development Administration, Republic of Korea.
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