Glaucumolides A (1) and B (2), novel biscembranes composed of an unprecedented α,β-unsaturated ε-lactone, along with the known metabolites ximaolide A (3) and isosarcophytonolide D (4), were isolated from the cultured soft coral Sarcophyton glaucum. The structures of the new metabolites were determined by extensive spectroscopic analyses. Compounds 1 and 2 were shown to exhibit cytotoxicity against a limited panel of cancer cell lines. In anti-inflammation assay, compounds 1 and 2 displayed strong inhibition of superoxide anion generation and elastase release in human neutrophils stimulated by fMLP/CB. Furthermore, both 1 and 2 were shown to significantly inhibit the accumulation of the pro-inflammatory inducible nitric oxide synthase protein, and compounds 1−3 were found to effectively reduce the expression of cyclooxygenase-2 protein, in lipopolysaccharide-stimulated RAW264.7 macrophage cells.
Many cembrane-type diterpenes have been proven to exhibit cytotoxicity and anti-inflammatory activity1. More than 60 biscembranoids have been isolated from the soft corals of the genera Sarcophyton2, Lobophytum12, Sinularia13. In particular, those belonging to the genus Sarcophyton are the most prolific source of biscembranoids. A common structural feature among these biscembranes is biogenetically derived from Diels-Alder reaction of two different cembranoid units. In our continuing search for structurally unique bioactive metabolites from the genera Sarcophyton14, we carried out the chemical investigation of the cultured soft coral Sarcophyton glaucum (Fig. 1). This study has led to the discovery of two new Diels-Alder cyclized biscembranoids glaucumolides A and B (1 and 2), a known biscembranolide ximaolide A (3)8,11, along with isosarcophytonolide D (4)9, an expected biogenic dienophile precursor of 1 (Fig. 2). The structures of 1 and 2 were deduced by extensive spectroscopic analysis. Based on structural consideration, both 1 and 2 were classified as a new type of biscembranoids as they are biosynthesized using ε-lactonecembrane 6 as a new diene monomer which has not been discovered before the biosynthesis of biscembranoids formed by Diels-Alder reaction. The attracting biological activities of several known biscembranoids13,15 further prompted us to evaluate the cytotoxic and anti-inflammatory activities of isolated metabolites 1–4. The results demonstrated that compounds 1 and 2, possessing a γ- and an ε-lactone rings, exhibited inhibition against the growth of human cancer cell lines, promyelocytic leukemia (HL-60), leukemic lymphoblasts (CCRF-CEM), acute T lymphoblastic leukaemia (MOLT-4), and erythroleukemia (K-562), as well as anti-inflammatory activities by significantly reducing the superoxide anion generation and elastase release in human neutrophils stimulated by N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLP/CB), and the expression of iNOS and COX-2 proteins in LPS-challenged RAW264.7 macrophage cells. In contrast, without the presence of the mentioned lactone rings, 3 only displayed weaker inhibition on COX-2 accumulation in the same macrophage cells.
Glaucumolide A (1), [α]25D −207 (c 0.007, CHCl3), was isolated as an amorphous solid. Its molecular formula, C42H58O8, was established by HRESIMS (713.4022 m/z, [M + Na]+), implying 14 degrees of unsaturation. The presence of the hydroxyl group was suggested by an absorption band at 3499 cm–1 in the IR spectrum. The 13C NMR spectroscopic data of 1 (Table 1) showed the presence of 42 carbon atoms, including eight methyls, 11 methylenes, 11 methines, and 12 quaternary carbons. Its NMR spectrum showed the signals of four vinyl methyls (δH 2.12, s; 1.81, s; 1.65, s; 1.62, s; δc 20.2, 19.6, 17.9, 16.0), one methyl attached to oxygen-bearing quaternary carbon (δH 1.32, s; δc 22.0), one acetoxy group (δH 2.13, s; δc 170.5, C; 21.5, CH3), two methyls of an isopropyl group (δH 2.20, m; 1.10, d, J = 6.8 Hz; 1.08, d, J = 6.8 Hz; δc 25.7, CH; 25.1, CH3; 18.2, CH3); four trisubstituted double bonds (δH 5.93, br s; 5.78, s; 5.14, dd, J = 6.4, 6.4 Hz; 5.11, d, J = 10.0 Hz; δc 161.1, C; 138.7, C; 135.1, CH; 132.8, C; 132.5, C; 127.2, CH; 125.0, CH; 123.0, CH); one tetrasubstituted double bond (δc 132.1, C; 127.4, C); three oxygen-bearing methines (δH 4.82, dd, J = 11.2, 3.2 Hz; 4.16, dd, J = 7.6, 7.6 Hz; 3.95, dd, J = 11.2, 6.0 Hz; δc 84.4, CH; 73.1, CH; 68.3, CH); one oxygenated quaternary carbon (δc 82.9), and four carbonyl carbons (δc 197.4, 177.9, 170.5, 168.9). These evidences indicated the possible presence of a biscembranoid skeleton in compound 1. The COSY spectrum of 1 was used to identify seven different structural units from H2-36 to isopropyl protons H3-16 and H3-17 via H-2, H-3 and H-4; H-5 to H2-6; H-8 to H2-10; H-21 to H-22; H2-24 to H-26; H2-28 to H-30; and H2-32 to H2-33, which were further assembled by HMBC correlations H-5 to C-3 and C-15; H2-14 to C-1, C-2, C-12 and C-13; H3-16 and H3-17 to C-4 and C-15; H3-18 to C-6, C-7 and C-8; H3-19 to C-10, C-11 and C-12; H-21 to C-1, C-2, C-33, C-34 and C-35; H-30 to C-31, C-32 and C-40; H3-37 to C-34, C-35 and C-36; H3-38 to C-22, C-23 and C-24; and H3-39 to C-26, C-27 and C-28 (Fig. 3). Moreover, the HMBC correlations of H-3 and H2-14 to C-20 clearly suggested the presence of an α,β-unsaturated γ-lactone moiety at C-1–C-3 and C-20. Furthermore, the acetoxy group positioned at C-5 was confirmed from the HMBC correlations of H-5 (δ 4.82, dd, J = 11.2, 3.2 Hz) and protons of an acetate methyl (δ 2.13, s) to the ester carbonyl carbon at δ 170.5. In addition, in the 13C NMR spectrum of 1 the signal at δc 68.3, and in the 1H NMR spectrum the signal at δH 4.16 (dd, J = 7.6, 7.6 Hz) could be attributed to a hydroxyl-bearing methine at C-26. On the base of above results and by considering the degrees of unsaturation and molecular formula, C-27 and C-40 should be linked by an oxygen atom to form an ε-lactone ring. The gross structure of 1 was thus established. Metabolite 1 is the first Diels-Alder cyclized biscembranoid possessing not only a saturated γ-lactone but also a seven-membered α,β-unsaturated ε-lactone in the molecule.
The relative configurations of the stereogenic centers in 1 were determined on the basis of NOE relationships and NMR spectroscopic data. It was found that NOESY correlations of H-3 (δ 3.95, dd, J = 11.2, 6.0 Hz) with H-2 (δ 2.33, m) and H-5 (δ 4.82, dd, J = 11.2, 3.2 Hz), H-4 (δ 1.50, d, J = 10.8 Hz) with H-2 and H-5, and H-2 with H-21 (δ 3.05, d, J = 10.0 Hz), and the upfield-shifted δH value of H-21α relative to the H-21β of related biscembranoids in 1H NMR10, indicated the α-orientation for H-2, H-3, H-4, H-5, and H-21. This observation was also strongly supported by the similar 1H NMR spectroscopic data of the above protons including chemical shifts and coupling constants with those of bislatumlide C10. Furthermore, the NOE correlations of H-21 with H-33α (δ 2.16, m) and H3-38, H3-38 with H-26 (δ 4.16, dd, J = 7.6, 7.6 Hz), and H-26 with H-25α (δ 1.82, m), H-29α (δ 2.46, m) and H-30 (δ 5.93, br s), reflected the α-orientations of H-26 and the R*-configuration at C-26. Above results and the NOE correlation between H3-39 (δ 1.32, s) and H-25β (δ 1.36, m) suggested the β-orientation of H3-39 and thus 27S* configuration of 1 as shown in Fig. 4. Further, the 26R* and 27S* configuration, not 26R* and 27R*, could be confirmed by comparing the δ values of C-7 (69.2) and C-8 (82.9) of known compound sartrolide C16 to the corresponding C-26 (68.3) and C-27 (82.9) of 1, while sartrolide A16 with 26R* and 27R* configuration showed C-26 signal at δ 72.7 ppm. The chemical shift values of C-18 (17.9), C-19 (19.6) and C-38 (16.0) reflected the all trans geometry of the trisubstituted double bonds at C-7/C-8, C-11/C-12 and C-22/C-23 in the molecule of 1. From the above observations, NOE correlation between H-30 and one of H2-33 (δ 2.66, m), and further analysis of other NOE interactions (Fig. 4), the relative configuration of 1 with rings A−E could be established.
Glaucumolide B (2), [α]25D −221 (c 0.008, CHCl3), was showed the pseudomolecular ion peak [M + Na]+ at m/z 713.4023 in the HRESIMS, suggesting the molecular formula C42H58O8 and 14 degrees of unsaturation. The IR spectrum also suggested the presence of hydroxyl group in 2 (νmax 3434 cm–1). The 13C NMR spectroscopic data (Table 1) of 2 were found to be resembled to those of 1. Detailed analysis of 1D and 2D NMR spectra of 2 revealed the similar gross structure as that of 1. However, it was found that H-12 (δ 5.98, s) showed significant NOE interaction with H3-19 (δ 1.89, s), and the signal of the C-19 in 2 was remarkably downfield-shifted (δ 19.6 in 1, 24.8 in 2), indicating a Z geometry of Δ11(12) in 2, in contrast to the 11E double bond in 1. These results and other NMR data including NOE correlations, established the structure of compound 2 to be the 11Z isomer of 1.
The absolute configurations of 1 and 2 were further confirmed by comparison of the CD (circular dichroism) spectroscopic data with structurally related compound. As shown in Fig. 5, the CD spectrum of 2 showed a broad negative Cotton effect at 258 nm (Δε = −7.1) due to enone n–π* transition absorption while the intense positive cotton effect at 209 nm (Δε = +27.4) resulted from the π–π* transition of the two isolated Δ22(23) and Δ34(35) double bonds, very similar to that of bislatumlide C10. Thus, the absolute configurations for rings B and C should be the same for both bislatumlide C and 2. One the basis of above results and the fact that both 1 and 2 were isolated from the same organism, the structures and absolute configurations of both 1 and 2 were found to possess the 1S,2R,3S,4S,5S,21S,26R,27S.
A plausible biosynthetic pathway, involving a key Diels–Alder reaction, was postulated for the biosynthesis of compounds 1 and 2 in Figure 6. It is obvious that 4 is one of the two precursors of 1. Another proposed precursor should be the yet to be discovered compound 6. [4+2] Endo cycloaddition of the dienophile 4 and diene 6 occurs between 1,2-Z double bond of 4 and ∆21(34) and ∆35(36) conjugated double bonds diene of 6. Although the possible involvement of a biosynthetic Diels-Alder reaction to afford biscembranoid has been mentioned frequently, no any other bicembranoid was found to be formed by using ε-lactone cembrane 6 or related cembranoidal ε-lactone as the diene precursor. In addition, almost all the previous cembrane dimers exhibited the reactive dienophile double bond at positions C-1 and C-14 (according to the numbering assigned to compound 4), whereas the dienophile double bond in 4 was located at C-1 and C-2. The Diels–Alder addition which arises from supra–supra transition state explains the trans stereochemistry of H-2 and lactone as well as the cis geometry of lactone and H-21. Analogously, the formation of biscembrane 2 by Diels–Alder cyclization of the 11Z isomer of 4, sarcophytonolide A (5)6,9, with compound 6 could be hypothesized.
The cytotoxicity of compounds 1–4 against four human cancer cell lines, HL-60, CCRF-CEM, MOLT-4, and K-562 was investigated. The results (Table 2) demonstrated that compound 2 exhibited significant cytotoxicity against HL-60 and CCRF-CEM cancer cell lines with ED50 values of 3.8 ± 0.9 and 5.3 ± 1.4 μg/mL, respectively. Also, compound 1 exhibited cytotoxicity against the above two cell lines with ED50 values of 6.6 ± 1.2 and 7.4 ± 1.5 μg/mL, respectively. Further, compounds 1 and 2 displayed weaker activity against MOLT-4 and K-562 cell lines (ED50 11.0–19.2 μg/mL). In contrast, compound 3 was inactive toward all the tested cell lines. Perhaps the enhanced cytotoxicity of compounds 1 and 2 relative to 3 is owing to the presence of a α,β-unsaturated ε-lactone ring.
The anti-inflammatory activities of compounds 1–4 on neutrophil pro-inflammatory responses were evaluated by measuring their ability in suppressing fMLP/CB-induced superoxide anion (O2− •) generation and elastase release in human neutrophils, and the results were shown in Table 3. From the results, 1 and 2 showed strong inhibitions (88.42 ± 3.97 and 91.75 ± 3.08%, respectively.) toward superoxide anion generation at 10 μM. Both of them also exhibited potent inhibitory activity against elastase release, with 88.94 ± 6.96 and 103.25 ± 1.89% inhibitions in the same fMLP/CB-stimulated cells at the same concentration. The IC50 values of 1 and 2 in inhibiting the superoxide generation and elastase release were also measured. Although compound 4 did not exhibit strong activity in inhibiting superoxide anion generation, it was shown to display significant inhibitory activity in elastase release.
The in vitro anti-inflammatory activity of compounds 1–3 was also studied. In this assay, the up-regulation of the proinflammatory iNOS and COX-2 proteins of LPS-stimulated RAW264.7 macrophage cells was evaluated using immunoblot analysis. The results (Fig. 7) showed that at concentrations of 5, 10, and 20 μM, compound 1 was found to significantly reduce the levels of iNOS and COX-2 to 59.4 ± 9.0 and 66.5 ± 4.4%; 31.3 ± 6.5 and 78.3 ± 5.0%; and −2.6 ± 2.7 and −0.5 ± 3.2%, respectively. At concentrations of 10 and 20 μM, compound 2 was found to significantly reduce the levels of iNOS and COX-2 to 75.9 ± 3.5 and 64.3 ± 6.9%; and 43.4 ± 5.0 and 6.0 ± 3.6%, respectively. Moreover, at 20 μM, 3 also reduced the level of COX-2 expression to 22.0 ± 6.5% in macrophage cells with LPS treatment. As they did not exhibit cytotoxicity to RAW264.7 cells, they might be promising anti-inflammatory agents. Also, 2 possessing promising cytotoxicity, could become a candidate for future anticancer drug development.
Compounds 1 and 2 are structurally novel as they belong to a new type of biscembranoids using the not yet isolated ε-lactonecembrane 6 as the first time discovered diene precursor for the biosynthesis of biscembranoids by Diels-Alder reaction. Metabolites 1 and 2, with the presence of a α,β-unsaturated ε-lactone ring, were shown to exhibit cytotoxicity against a limited panel of HL-60, CCRF-CEM, MOLT-4 and K-562 cancer cell lines. Compounds 1 and 2 also exhibited potent anti-inflammatory activity in inhibiting the superoxide generation and elastase release in fMLP/CB-induced human neutrophils. Furthermore, both 1 and 2 were shown to significantly inhibit the accumulation of the pro-inflammatory inducible nitric oxide synthase protein, and compounds 1–3 were found to effectively reduce the expression of cyclooxygenase-2 protein, in lipopolysaccharide-stimulated RAW264.7 macrophage cells.
The unusual structural framework with α,β-unsaturated ε-lactone system were reported here for glaucumolides A and B (1 and 2), along with a known biscembranolide ximaolide A (3), and isosarcophytonolide D (4) from the cultured soft coral S. glaucum. From the results of biological activities, it appears that compounds 1 and 2 might be useful for future biomedical applications. The discovery of glaucumolides with a novel carbon scaffold provides additional evidence that cultured soft corals might be a promising source of structurally novel bioactive natural products which could be used for further pharmacological investigation.
General Experimental Procedures
Optical rotations were measured on a Horiba High Sensitivity Polarimeter SEPA-300. Ultraviolet spectra were recorded on a JASCO V-650 spectrophotometer. IR spectra were recorded on a JASCO FT/IR-4100 infrared spectrophotometer. CD spectra were recorded on a JASCO J-815 CD spectrophotometer. NMR spectra were recorded on a Varian 400MR FT-NMR instrument at 400 MHz for 1H and 100 MHz for 13C in CDCl3. LRMS and HRMS were obtained by ESI on a Bruker APEX II mass spectrometer. Silica gel (Merck, 230–400 mesh) was used for column chromatography. Precoated silica gel plates (Merck, Kieselgel 60 F-254, 0.2 mm) were used for analytical TLC. High-performance liquid chromatography was performed on a Hitachi L-2455 HPLC apparatus with a Supelco C18 column (250 × 21.2 mm, 5 μm).
The cultured soft coral Sarcophyton glaucum used in this study was originally collected from the wild and cultured for five years in an 80-ton cultivation tank (height 1.6 m) located in the National Museum of Marine Biology and Aquarium, Taiwan. The tank was a semiclosed recirculating aquaculture system and did not require deliberate feeding. To the best of our knowledge, this is the first farming system for S. glaucum in the world. The specimens were then collected by hand in January 2010 and were stored in a −20 °C freezer. The soft coral was identified by one of the authors (C.-F.D.). A voucher specimen (specimen no. 201001C3) was deposited in the Department of Marine Biotechnology and Resources, National Sun Yat-sen University.
Extraction and Isolation
The frozen bodies of S. glaucum (0.6 kg, wet wt) were minced and extracted exhaustively with CH2Cl2 and MeOH (1:1, 0.5 L × 6). The CH2Cl2 and MeOH extract of the soft coral S. glaucum was partitioned between EtOAc and H2O to afford the EtOAc-soluble fraction. The EtOAc extract (4.5 g) was chromatographed over silica gel by column chromatography and eluted with EtOAc in n-hexane (0–100%, stepwise) and then with MeOH in EtOAc (5–50%, stepwise) to yield 24 fractions. Fraction 15 (23.3 mg), eluting with n-hexane–EtOAc (5:1), was further purified by reversed-phase HPLC using MeOH−H2O (3:1) to afford 4 (2.6 mg). Fraction 20 (69.7 mg), eluting with n-hexane–EtOAc (1:1), was further purified over silica gel using n-hexane–acetone (2:1) to afford six subfractions (A1–A6). Subfraction A3 (13.5 mg) was further purified by reversed-phase HPLC using MeOH−H2O (5:2) to afford 3 (5.2 mg). Subfraction A4 (20.0 mg) was further purified by reversed-phase HPLC using MeOH−H2O (2:1) to afford 1 (4.4 mg) and 2 (2.8 mg).
Glaucumolide A (1)
white amorphous powder; [α]25D −207 (c 0.007, CHCl3); IR (neat) νmax 3499, 2939, 2876, 1734, 1716, 1699, 1375, 1239, 1024, and 755 cm−1; UV (MeOH) λmax (log ε) 205 (3.4) and 236 (3.2) nm; CD (1.9 × 10−4 M, MeOH) λmax (Δε) 244 (−23.7), and 215 (+36.0) nm; 13C and 1H NMR data, see Table 1; ESIMS m/z 713 [M + Na]+; HRESIMS m/z 713.4022 [M + Na]+ (calcd for C42H58O8Na, 713.4024).
Glaucumolide B (2)
white amorphous powder; [α]25D −221 (c 0.008, CHCl3); IR (neat) νmax 3434, 2940, 2878, 1734, 1716, 1698, 1376, 1239, 1024, and 754 cm−1; UV (MeOH) λmax (log ε) 205 (3.3) and 236 (3.2) nm; CD (1.2 × 10−4 M, MeOH) λmax (Δε) 258 (−7.1), and 209 (+27.4) nm; 13C and 1H NMR data, see Table 1; ESIMS m/z 713 [M + Na]+; HRESIMS m/z 713.4022 [M + Na]+ (calcd for C42H58O8Na, 713.4023).
Cell lines were purchased from the American Type Culture Collection (ATCC). Cytotoxicity assays of compounds 1–4 were performed using the Alamar Blue assay18,19. To measure the cytotoxicity activities of tested compounds, three concentrations in DMSO with three replications were performed on each cell line. 5-Fluorouracil and DMSO were used as positive and negative controls, respectively in this assay.
Preparation of Human Neutrophils
Human neutrophils obtained from peripheral blood of healthy adult volunteers (20–30 years old) were enriched using a standard method of dextran sedimentation, Ficoll-Hypaque centrifugation, and hypotonic lysis20,21. Purified neutrophils were resuspended in a Ca2+ -free HBSS buffer (pH 7.4) at 4 °C prior to use.
Measurement of O2− • Generation
The O2− • production was assayed based on the superoxide oxide dismutase inhibitable reduction of ferricytochrome c22. Briefly, neutrophils (6 × 105 cells/mL) incubated with ferricytochrome c (0.5 mg/mL) and Ca2+ (1 mM) were equilibrated at 37 °C for 2 min and then treated with DMSO as control or different concentrations of compounds for 5 min. Neutrophils were activated by 100 nM fMLP for 10 min in the pretreatment of cytochalasin B (CB, 1 μg/mL) for 3 min (fMLP/CB).
Measurement of Elastase Release
The elastase release was assayed using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as the enzyme substrate23,24. Briefly, neutrophils (6 × 105 cells/mL) incubated with MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide (100 μM) were equilibrated at 37 °C for 2 min and treated with compounds for 5 min. Neutrophils were then activated with fMLP (100 nM)/CB (0.5 μg/mL) for 10 min.
Results are expressed as the mean ± SEM, and comparisons were made using Student’s t-test. A probability value of 0.05 or less was considered significant. The software SigmaPlot was used for the statistical analysis.
In Vitro Anti-Inflammatory Assay
Macrophage (RAW264.7) cells were purchased from ATCC. In vitro anti-inflammatory activities of compounds 1–3 were measured by examining the inhibition of lipopolysaccharide (LPS) induced upregulation of iNOS (inducible nitric oxide synthetase) and COX-2 (cyclooxygenase-2) proteins in macrophages cells using Western blotting analysis25. For statistical analysis, all of the data were analyzed by a one-way analysis of variance (ANOVA), followed by the Student-Newman-Keuls post hoc test for multiple comparisons. A significant difference was defined as a p value of <0.05.
How to cite this article: Huang, C.-Y. et al. Glaucumolides A and B, Biscembranoids with New Structural Type from a Cultured Soft Coral Sarcophyton glaucum. Sci. Rep. 5, 15624; doi: 10.1038/srep15624 (2015).
This work was supported by grants from the the National Science Council (NSC-100-2320-B-110-001-M2 and NSC 102-2628-B-110-002-MY2), and Ministry of Education (01C030205) of Taiwan awarded to J.-H.S.