Anti-Oxidative and Anti-Proliferative Activity on Human Prostate Cancer Cells Lines of the Phenolic Compounds from Corylopsis coreana Uyeki
College of Pharmacy, Chung-Ang University, Seoul 156-756, Korea
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2013, 18(5), 4876-4886; https://doi.org/10.3390/molecules18054876
Submission received: 4 January 2013
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Revised: 20 April 2013
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Accepted: 23 April 2013
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Published: 24 April 2013
(This article belongs to the Section Natural Products Chemistry)
Abstract
:Fifteen phenolic compounds, including three caffeoyl derivatives, four gallotannins, three ellagitannins and five flavonoids, were isolated from an 80% MeOH extract of the leaves of Corylopsis coreana Uyeki (Korean winter hazel; CL). The anti-oxidative activities [1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity and xanthine oxidase superoxide scavenging activities (NBT)] and the anti-proliferative activity on human prostate cancer cell lines (DU145 and LNCaP) were also evaluated.
1. Introduction
Corylopsis coreana Uyeki (Korean winter hazel; CL) belongs to the Hamamelidaceae or witch hazel family, [1]. CL is cultivated as an ornamental plant in South Korea. Some species of the genus Corylopsis, such as Hamamelis virginiana (witch hazel) have been a folk medicine for the treatment of irritated skin and inflammatory disease [2] and witch hazel bark are widely used in skin care products for sun burn, atopic eczema, etc. [3]. It has been reported that hamamelitannin and simple phenolics were isolated from the bark of witch hazel [4], and their anti-mutagenic activities and anti-cancer activities against various forms of cancer were also reported [5]. This paper describes the isolation of compounds from the leaves of CL and evaluation of its anti-oxidative activities and the anti-proliferation properties of the isolated compounds.
2. Results and Discussion
2.1. Isolation and Identification
Anti-oxidant activity-guided chromatographic fractionation of leaves of CL afforded fifteen phenolic compounds (Scheme 1 and Table 1). The structures of compounds 1–15 were identified as 3-caffeoylquinic acid methyl ester (1) [6], 4-caffeoylquinic acid (2) [6], 3-caffeoylquinic acid (3) [6], 3-O-galloyl-β-d-glucopyranoside (4) [7], bergenin (5) [8], nor-bergenin (6) [8], 11-galloylbergenin (7) [9], tellimagrandin I (8) [10], tellimagrandin II (9) [11], casuarinin (10) [12], quercetin (11) [13], quercitrin (12) [14], quercetin 3-O-β-d-glucuronide (13) [15], datiscetin 3-O-β-d-rhamnpyranoside (14) [16] and myricetin 3-O-β-d-rhamnopyranoside (15) [17], respectively (Figure 1), by comparing the spectral (MS, NMR) data with the values reported in the literature.
Scheme 1.
Extraction and Isolation of Compounds 1–15 from CL.
| Fractions | DPPH radical scavenging activity SC50 (mg/mL) | Superoxide scavenging activity SC50 (mg/mL) |
|---|---|---|
| 1 | >100 e | 59.02 ± 1.07 d |
| 2 | 43.16 ± 0.48 d | 23.64 ± 0.92 c |
| 3 | 20.26 ± 0.43 c | 13.35 ± 1.09 b |
| 4 | 11.22 ±0 24 b | 5.89 ± 0.91 a |
| 5 | 5.89 ± 0.03 a | 2.42 ± 0.73 a |
| Ascorbic acid | 6.68 ± 0.11 a | - |
| Allopurinol | - | 1.70 ± 0.92 a |
Values represent means ± S.D. of three determinations. Values bearing different superscripts in the same column are significantly different (p < 0.05).
Figure 1.
Structures of compounds 1–15 isolated from CL.
2.2. Anti-Oxidative Activity (DPPH Radical, Superoxide Scavenging Activity)
Oxidative damage appears to be related to various diseases and inflammation conditions [18,19]. Polyphenols reduce oxidative stress and provide activity associated with anti-cancer, anti-allergic, and anti-inflammatory effects [20]. In order to evaluate the anti-oxidative activities of the compounds 1–10 from CL, their DPPH radical [21] and superoxide scavenging activities were tested [22]. Among the compounds 1–10 from CL, 8, 9 and 10 showed more potent free radical scavenging activity than ascorbic acid (SC50 = 8.22 ± 0.64 μM), with SC50 values of 3.12 ± 0.05, 2.97 ± 0.04 and 3.29 ± 0.26 μM (p < 0.05) (Table 1), due to presence of a galloyl groups plus an HHDP group in their structures, which plays an important role in anti-oxidation by donating hydrogen atoms to active free radicals [23]. In addition, 8, 9 and 10 also showed more potent superoxide scavenging activity than allopurinol (SC50 = 2.39 ± 0.09 μM), with SC50 values of 0.29 ± 0.69, 0.09 ± 0.02 and 0.16 ± 0.02 μM (p < 0.05) (Table 2).
2.3. Cell Viability and Inhibition of Cancer Cell Proliferation
The cell viability was measured using the MTT assay (Figure 2), which is based on the mitochondria-dependent reduction of MTT to formazan [24]. In order to evaluate the anti-proliferation activities of the compounds 1–15 from CL, cell viability were tested on DU145 and LNCaP prostate cancer cells. The anti-proliferative effects of hydrolysable tannins in sarcoma cells and HeLa cells were reported [25] and the functional groups the hydrolysable tannins are also important factors determining their anti-proliferation activity [26]. Among the ellagitannins 8–10, compound 10 showed higher androgen sensitive anti-proliferation activity, suggesting the importance of the HHDP group. Since 9 was more potent than 10, the presence of both HHDP and galloyl groups might be necessary. Compound 9 was also more potent than 8, suggesting the importance of a galloyl group in the C-l position [27]. The compounds 8, 9 and 10 inhibited the proliferation of both DU145 and LNCaP prostate cancer cells (Table 3).
Table 2.
DPPH radical scavenging and superoxide scavenging activities of each compounds 1–15 from CL.
| Compounds | DPPH radical scavenging activity SC50 (μM/mL) | Superoxide scavenging activity SC50 (μM/mL) |
|---|---|---|
| 1 | 23.05 ± 0.92 d,e | 13.47 ± 0.05 b |
| 2 | 51.49 ± 0.77 g | 11.71 ± 0.36 b |
| 3 | 21.65 ± 0.72 d,e | 22.68 ± 0.35 d |
| 4 | 13.41 ± 0.10 c | 10.81 ± 0.07 c |
| 5 | >100 i | >100 e |
| 6 | 36.34 ± 0.93 f | 13.68 ± 0.74 b, c |
| 7 | 21.63 ± 0.70 e | 3.85 ± 0.03 a |
| 8 | 3.12 ± 0.05 a | 0.29 ± 0.69 a |
| 9 | 2.97 ± 0.04 a | 0.09 ± 0.02 a |
| 10 | 3.29 ± 0.26 a | 0.16 ± 0.02 a |
| 11 | 49.09 ± 0.92 g | 12.18 ± 0.14 b,c |
| 12 | 60.96 ± 0.70 h | 12.43 ± 0.24 b,c |
| 13 | 17.06 ± 0.15 d | 3.17 ± 0.78 a |
| 14 | 36.87 ± 0.44 f | 2.59 ± 0.75 a |
| 15 | 19.45 ± 0.05 d,e | 1.45 ± 0.24 a |
| Ascorbic acid | 8.22 ± 0.64 b | - |
| Allopurinol | - | 2.39±0.09 a |
Values represent means ± S.D. of three determinations. Values bearing different superscripts in the same column are significantly different (p < 0.05).
Figure 2.
Cell viability of compounds 1–15 from CL on RAW 264.7 cell lines.
| Compounds | Anti-proliferative activity of LNCaP cancer cell line IC50 (μM/mL) | Anti-proliferative activity of Du-145 cancer cell line IC50 (μM/mL) |
|---|---|---|
| 1 | >100 c | >100 a |
| 2 | >100 c | >100 a |
| 3 | >100 c | >100 a |
| 4 | >100 c | >100 a |
| 5 | >100 c | >100 a |
| 6 | >100 c | >100 a |
| 7 | >100 c | >100 a |
| 8 | 66.35 ± 1.44 b | >100 a |
| 9 | 43.08 ± 0.63 a | >100 a |
| 10 | 40.56 ± 1.41 a | >100 a |
| 11 | >100 c | >100 a |
| 12 | >100 c | >100 a |
| 13 | >100 c | >100 a |
| 14 | >100 c | >100 a |
| 15 | >100 c | >100 a |
Values represent means ± S.D. of three determinations. Values bearing different superscripts in the same column are significantly different (p < 0.05).
3. Experimental
3.1. General Methods
Sephadex LH-20 column (10–25 µm, GE Healthcare Bio-Science AB, Uppsala, Sweden) and Daisogel ODS-B with MPLC system (5 × 80 cm, Mitsubishi Chemical Co., Tokyo, Japan), 110UV/VIS detector (Gilson, Middleton, WI, USA) and TBP 5002 pump (Tauto Biotech, Shanghai, China) were used for column chromatography. TLC was carried out on pre-coated silica gel 60 F254 plates (Merck, Darmstadt, Germany); spots were detected under UV radiation (254 nm) and by spraying with FeCl3 solution and 10% H2SO4 followed by heating. The 1H- and 13C-NMR spectra were recorded at 300 MHz on a Gemini 2000 instrument (Varian, Palo Alto, CA, USA) and 1H-NMR, 600 MHz; 13C-NMR, 150 MHz on a Varian VNS (Varian, Palo Alto, CA, USA) and the resolution fast atom bombardment mass spectrum (LRFAB-MS) were measured with a JMSAX505WA instrument (JEOL, Tokyo, Japan).
3.2. Plant Material
The leaves of CL (1.8 kg) were collected from the Korea Forest Research Institute, Suwon, Korea in September 2010 and certified by Minwon Lee (Phamacognosy Lab, College of Pharmacy, Chung-Ang University). The voucher specimen (CL2010-9) was deposited at the herbarium of the College of Pharmacy, Chung-Ang University.
3.3. Extraction and Isolation
The dry leaves of CL (1.8 kg) were extracted for 72 h at room temperature with 80% aqueous MeOH (8.0 L). The concentrated extracts were subjected to preparative thin layer chromatography (TLC) using as solvent systems C:M:W (chloroform:MeOH:H2O = 6:4:1) or B:E:F (benzene:ethyl formate:formic acid = 1:7:1). The spots were detected under UV radiation (254 nm) and by spraying with FeCl3 and 10% H2SO4 or anisaldehyde-H2SO4 followed by heating. The CL aqueous layer (270 g) was concentrated and applied to a Sephadex LH-20 column (10–25 µm, 2 kg, 10 × 80 cm), and eluted with H2O containing increasing proportions of MeOH to afford from sub-fraction, 1 (134.6 g), 2 (23.5 g), 3 (10.9 g), 4 (33.3 g) and 5 (49.6 g). Repeated column chromatography of sub-fraction 2 on Daisogel ODS-B with MPLC system (300 μm, 500 g, 5 × 80 cm, Mitsubishi Chemical Co.), using a H2O:MeOH gradient yielded compounds 2 (481 mg), 4 (300 mg), 5 (15.5 g), 6 (87.5 mg). The sub-fraction 3 gave compounds 1 (370 mg), 3 (692 mg), sub-fraction 4 afforded compounds 7 (810 mg), 8 (4.2 g), 11 (1.1 g), 12 (10.3 g), 13 (126.3 mg), 14 (1.8 g) and 15 (475 mg). Finally, sub-fraction 5 contained compound 9 (458 mg) and 10 (11 g), respectively (Figure 1).
3-Caffeoyl quinic acid Methyl ester (1). Dark brown amorphous powder; Negative FAB-MS m/z: 367 [M−H]−, 179 [M−quinic acid methyl ester:caffeic acid]−. 1H-NMR (300 MHz, MeOH-d4): δ 2.17 (2H, m, H-6'), 2.22 (2H, m, H-2'), 3.75 (3H, s, OCH3), 3.77 (1H, m, H-4'), 4.19 (1H, m, H-5'), 5.33 (1H, m, H-3'), 6.29 (1H, d, J = 16.2 Hz, H-8), 6.90 (1H, d, J = 8.4 Hz, H-5), 7.06 (1H, dd, J = 0.6, 8.4 Hz, H-6), 7.18 (1H, d, J = 0.6 Hz, H-2), 7.57 (1H, d, J = 16.2 Hz, H-7).
4-Caffeoyl quinic acid (2). Dark brown amorphous powder; Negative FAB-MS m/z: 353 [M−H]−, 179 [M−quinic acid:Caffeic acid]−, 1H-NMR (300 MHz, MeOH-d4): δ 1.90 (2H, m, H-2'), 2.06 (2H, m, H-6'), 3.73 (1H, m, H-5'), 4.13 (1H, m, H-3'), 5.18 (1H, m, H-4'), 6.26 (1H, d, J = 16.8 Hz, H-8), 6.76 (1H, d, J = 7.8 Hz, H-5), 7.00 (1H, dd, J = 1.8, 7.8 Hz, H-6), 7.04 (1H, s, H-2), 7.48 (1H, d, J = 16.8 Hz, H-7).
3-Caffeoyl quinic acid (3). Dark brown amorphous powder; 1H-NMR (300 MHz, MeOH-d4): δ 2.20 (2H, m, H-6'), 2.24 (2H, m, H-2'), 3.77 (1H, m, H-4'), 4.22 (1H, m, H-5'), 5.37 (1H, m, H-3'), 6.29 (1H, d, J = 15.6 Hz, H-8), 6.87 (1H, d, J = 8.1 Hz, H-5), 7.13 (1H, dd, J = 1.8, 8.1 Hz, H-6), 7.15 (1H, d, J = 1.8 Hz, H-2), 7.57 (1H, d, J = 15.6 Hz, H-7).
3-O-galloyl-β-d-glucopyranoside (4). Yellow amorphous powder; Negative FAB-MS m/z: 331 [M−H]−, 169 [M−glucoside:Gallic aicd]−, 1H-NMR (300 MHz, MeOH-d4): δ 3.20 (1H, m, H-3'), 3.33 (1H, m, H-4'), 3.54 (2H, m, H-6', 5'), 3.76 (1H, m, H-6'), 3.81 (1H, m, H-2'), 5.57 (1H, d, J = 7.8Hz, H-1'), 7.07 (2H, s, H-2, 6), 13C-NMR (150 MHz, MeOH-d4): δ 60.8 (C-6'), 69.8 (C-4'), 73.2 (C-2'), 76.8 (C-3'), 78.5 (C-5'), 94.9 (C-1'), 109.3 (C-2. 6), 119.3 (C-1), 139.0 (C-4), 145.8 (C-3, 5), 165.0 (C-7).
Bergenin (5). White amorphous powder; Negative FAB-MS m/z: 327 [M−H]−, 1H-NMR (600 MHz, MeOH-d4): δ 3.47 (1H, t, 1H J = 9.3 Hz, H-3'), 3.73 (2H, m, H-11), 3.84 (1H, t, 1H, t, J = 8.1 Hz, H-2'), 3.89 (3H, s, OCH3), 4.04 (1H, t, J = 9.6 Hz, H-4'β), 4.09 (1H, t, J = 9.6 Hz, H-4'α), 4.96 (1H, d, J = 10.2 Hz, H-1'), 7.07 (1H, s, H-7), 13C-NMR (150 MHz, MeOH-d4): δ 59.4 (C-12), 61.2 (C-11), 70.4 (C-3'), 72.8 (C-10β), 74.2 (C-4'β), 80.0 (C-4'α), 81.7 (C-2'), 109.7 (C-7), 115.9 (C-10α), 118.0 (C-6α), 140.8 (C-9), 148.0 (C-10), 150.8 (C-8), 164.3 (C-6).
Norbergenin (6). White amorphous powder; 1H-NMR (300 MHz, MeOH-d4): δ 3.47 (1H, t, 1H J = 9.0 Hz, H-3'), 3.73 (2H, m, H-11), 3.84 (1H, t, J = 8.1 Hz, H-2'), 4.04 (1H, t, J = 9.6 Hz, H-4'β), 4.09 (1H, d, J = 9.6 Hz, H-4'α), 5.26 (1H, d, J = 10.2 Hz, anomeric H-1'), 7.08 (1H, s, H-7).
11-Galloylbergenin (7). White amorphous powder; Negative FAB-MS m/z: 479 [M−H]−. 1H-NMR (300 MHz, MeOH-d4): δ 3.70 (1H, t, J = 9.3, H-3'), 3.88 (3H, s, OCH3), 3.95 (2H, m, H-11), 4. 13 (1H, t, J = 10.2 Hz, H-2'), 4.30 (1H, dd, J = 3, 12 Hz, H-4'β), 4.66 (1H, dd, J = 12, 6,6 Hz, H-4'α), 5.05 (1H, d, J = 10.2 Hz, H-1'), 7.11 (1H, s, H-7), 7.18 (1H, s, H-2, 6), 13C-NMR (150 MHz, MeOH-d4): δ 60.3 (C-12), 63.7 (C-11), 70.2 (C-3'), 72.7 (C-10β), 73.8 (C-4'β), 79.1 (C-4'α), 80.0 (C-2'), 109.1 (C-7), 110.7 (C-7'), 116.1 (C-10α, 10'α), 118.6 (C-6α), 119.6 (C-6'α), 139.0 (C-9), 141.0 (C-9'), 145.6 (C-10, 10'), 148.2 (C-8), 151.0 (C-8'), 166.3 (C-6), 166.8 (C-6').
Tellimagrandin I (8). Dark yellow amorphous powder; Positive FAB-MS m/z: 787 [M+H]+, 1H-NMR (600 MHz, Aceton-d4+D2O): δ 3.79 (1H, dd, J = 13.2, 1.8 Hz, H-6"β), 3.87 (1H, dd, J = 13.2, 1.8 Hz, H-6"α), 4.28 (1H, dd, J = 6.6, 9.6 Hz, H-4"α), 4.69 (1H, dd, J = 6.6, 9.6 Hz, H-4"β), 5.11 (1H, m, H-5"α), 5.12 (1H, m, H-5"β), 5.14 (1H, d, J = 7.8 Hz, H-1"β), 5.25 (1H, dddd, J = 1.2, 10.2 Hz, H-2"α), 5.27 (1H, dddd, J = 1.2, 10.2 Hz, H-2"β), 5.29 (1H, t, J = 6.6 Hz, H-6"β), 5.31 (1H, t, J = 6.6 Hz, H-6"α), 5.57 (1H, d, J = 3.6 Hz, H-1"α), 5.62 (1H, t, J = 10.2, 9.6 Hz, H-3"β), 5.89 (1H, t, J = 10.2, 9.6 Hz, H-3"α), 6.49 (2H, s, HHDP-3'), 6.66 (2H, s, HHDP-3'), 6.95 (2H, s, G-2, 6), 6.99 (2H, s, G-2, 6), 7.05 (2H, s, G-2, 6), 7.06 (2H, s, G-2, 6), 13C-NMR (150 MHz, Aceton-d4+D2O): δ 63.0 (C-6"α, 6"β), 66.3 (C-5"α), 70.4 (C-4"α, 4"β), 70.6 (C-3"α, 2"α), 70.6 (C-5"β), 72.0 (C-3"β), 73.9 (C-2"β), 90.1 (C-1"α), 95.5 (C-1"β), 105.9 (HHDP-3), 106.0 (HHDP-3'), 109.1 (HHDP-1, 1'), 109.3 (G-1, 1'), 115.6 (G-2), 118.8 (G-2'), 124.3 (HHDP-5, 5'), 124.9 (HHDP-2, 2'), 135.6 (G-4'), 138.9 (G-4), 144.6 (HHDP-4, 4'), 144.8 (HHDP-6, 6'), 145.4 (G-3), 145.7 (G-3'), 165.5 (-COO ), 165.8 (-COO), 167.3 (-COO), 168.0 (-COO).
Tellimagrandin II (9). Dark yellow amorphous powder; Negative FAB-MS m/z: 953 [M−H]−, 169 [M−tellimagrandin I:Gallic acid]−, 1H-NMR (600 MHz, Aceton-d4+D2O): δ 3.92 (1H, d, J = 6.6 Hz, H-6"β) 4.58 (1H, dd, J = 1.2, 6.6 Hz, H-4"), 5.26 (1H, t, J = 8.4, 9.6 Hz, H-5"), 5.38 (1H, dd, J = 6.6 Hz, H-6"α), 5.64 (1H, dd, J = 1.2, 8.4 Hz, H-2"), 5.87 (1H, t, J = 8.4, 9.6 Hz, H-3"), 6.22 (1H, d, J = 8.4 Hz, H-1"), 6.68 (2H, s, HHDP-3'), 7.00 (2H, s, G-2, 6), 7.03 (2H, s, G-2, 6), 7.13 (2H, s, G-2, 6), 13C-NMR (150 MHz, Aceton-d4+D2O): δ 62.2 (C-6"), 69.8 (C-4"), 71.0 (C-2"), 72.2 (C-5"), 72.4 (C-3"), 92.8 (C-1"), 107.0 (HHDP-3), 107.2 (HHDP-3'), 109.2 (HHDP-1, 1'), 109.3 (G-1', 1",1"'), 114.8 (G-2"'), 118.8 (G-2', 2"), 124.8 (HHDP-2, 2'), 125.0 (HHDP-5, 5'), 135.6 (G-4", 4"'), 138.9 (G-4'), 144.6 (HHDP-4, 4'), 144.9 (HHDP-6, 6'), 145.1 (G-3", 3"'), 145.3 (G-3'), 164.2 (-COO), 165.0 (-COO), 165.6 (-COO), 166.9 (-COO), 167.3 (-COO).
Casuarinin (10). Dark yellow amorphous powder; Positive FAB-MS m/z: 937 [M+H]+, 1H-NMR (600 MHz, Aceton-d4+D2O): δ 3.72 (1H, t, J = 13.2 Hz, H-6"β), 3.79 (1H, t, J = 13.2 Hz, H-6"α), 4.43 (1H, dd, J = 6.6, 9.6 Hz, H-4"α), 4.46 (1H, dd, J = 6.6, 9.6 Hz, H-4"β), 4.83 (1H, m, H-5"α), 4.88 (1H, m, H-5"β), 4.79 (1H, m, H-2"α) 4.82 (1H, m, H-2"β), 4.83 (1H, d, J = 7.8 Hz, H-1"β), 4.96 (1H, m, H-6"β), 4.98 (1H, m, H-6"α), 5.32 (1H, d, J = 3.6 Hz, H-1"α), 5.47 (1H, t, J = 10.2, 9.6 Hz, H-3"β), 5.66 (1H, t, J = 10.2, 9.6 Hz, H-3"α), 5.90 (2H, s, G-2, 6), 6.26 (2H, s, HHDP-3), 6.81 (2H, s, HHDP-3), 6.86 (2H, s, HHDP-3), 6.92 (2H, s, HHDP-3), 13C-NMR (150 MHz, Aceton-d4+D2O): δ 63.0 (C-6"α, 6"β), 66.2 (C-5"α), 70.3 (C-4"α, 4"β), 70.4 (C-3"α, 2"α), 70.8 (C-5"β), 72.0 (C-3"β), 72.5 (C-2"β), 90.2 (C-1"α), 95.4 (C-1"β), 103.2 (HHDP-3), 105.6 (HHDP-3'), 108.6 (HHDP-1), 109.1 (HHDP-1'), 109.3 (G-1, 1'), 115.5 (G-2), 118.8 (G-2'), 124.0 (HHDP-5, 5'), 124.2 (HHDP-2, 2'), 135.5 (G-4'), 139.0 (G-4), 142.8 (HHDP-4, 4'), 144.7 (HHDP-6, 6'), 145.5 (G-3), 145.7 (G-3'), 165.6 (-COO), 165.8 (-COO), 167.3 (-COO), 168.0 (-COO).
Quercetin (11). Yellow amorphous powder; 1H-NMR (300 MHz, DMSO-d6+D2O): δ 6.19 (1H, d, J = 2.1 Hz, H-6), 6.41 (1H, d, J = 1.8 Hz, H-8), 6.89 (1H, d, J = 8.4 Hz, H-5'), 7.55 (1H, dd, J = 2.1, 8.4 Hz, H-6'), 7.68 (1H, d, J = 2.1 Hz, H-2').
Quercitrin (12). Yellow amorphous powder; Negative FAB-MS m/z: 447 [M−H]−, 301 [M−rhamnose:Quercetin]−, 1H-NMR (300 MHz, DMSO-d6+D2O): δ 0.80 (3H, d, J = 6.6 Hz, H-6"), 3.18 (3H, m, H-3", 5", 4"), 3.97 (1H, dd, J = 4.5 Hz, H-2"), 5.24 (1H, s, H-1"), 6.22 (1H ,d, J = 1.8 Hz, H-6), 6.41 (1H, d, J = 1.8 Hz, H-8), 6.88 (1H, d, J = 8.4 Hz, H-5'), 7.26 (1H, dd, J = 2.1, 8.4 Hz, H-6'), 7.29 (1H, d, J = 2.1 Hz, H-2').
Quercetin 3-O-β-d-glucuronide (13). Yellow amorphous powder; Negative FAB-MS m/z: 477 [M−H]−, 301 [M−glucuronide:Quercetin]−, 1H-NMR (300 MHz, DMSO-d6+D2O): δ 3.08 (2H, m, H-6"), 3.21 (1H, m, H-2"), 3.33 (2H, m ,H-4", 3"), 3.58 (1H, m, H-5"), 5.48 (1H, d, J = 7.8 Hz, H-1"), 6.22 (1H, d, J = 2.1 Hz, H-6), 6.42 (1H, d, J = 2.1 Hz, H-8), 6.87 (1H, d, J = 8.7 Hz, H-5'), 7.57 (1H, dd, J = 2.1, 8.7 Hz, H-6'), 7.59 (1H, d, J = 2.1 Hz, H-2').
Datiscetin 3-O-β-d-rhamnpyranoside (14). Yellow amorphous powder; Positive FAB-MS m/z: 447 [M−H]−, 283 [M−rhamnose:Datiscetin]−, 1H-NMR (300 MHz, DMSO-d6+D2O): δ 0.83 (3H, d, J = 6.6 Hz, H-6"), 3.18 (3H, m, H-3", 5", 4"), 3.96 (1H, dd, J = 4.5 Hz, H-2"), 5.24 (1H, s, H-1"), 6.22 (1H, d, J = 1.2 Hz, H-6), 6.42 (1H, d, J = 1.2 Hz, H-8), 6.88 (2H, d, J = 7.6, 8.4 Hz, H-3', 5'), 7.29 (1H, dd, J = 7.6, 8.4 Hz, H-4'), 7.59 (1H, d, J = 7.5 Hz, H-6').
Myricetin 3-O-β-d-rhamnopyranoside (15). Yellow amorphous powder; Negative FAB-MS m/z: 447 [M−H]−, 317 [M−rhamnose:Myricetin]−, 1H-NMR (300 MHz, DMSO-d6+D2O): δ 0.81 (3H, d, J = 6.6 Hz, H-6"), 3.15 (1H, d, J = 9.4, H-5"), 3.16 (1H, t, J = 9.4, 6.1, H-, 4"), 3.32 (1H, dd, J = 9.4, 3.3 Hz, H-3"), 3.97 (1H, bs, J = 1.4 Hz, H-2"), 5.19 (1H, s, H-1"), 6.39 (2H, d, J = 1.2 Hz, H-6, 8), 6.88 (2H, s, H-2', 6').
3.4. Antioxidant Activity
3.4.1. Measurement of DPPH Radical Scavenging Activity
Each sample in absolute EtOH was added to DPPH solution (0.1 mM, in absolute EtOH). After mixing gently for 30 min, optical densities were measured at 518 nm using a microplate reader (TECAN, Salzburg, Austria). L-Ascorbic acid (Sigma, St. Louis, MO, USA) was used as a positive control [21].
3.4.2. Xanthine Oxidase Superoxide Scavenging Activity
After each sample was added to 50 mM phosphate buffer (pH 7.5) containing 0.05 mM EDTA, 0.2 mM hypoxanthine and 0.1 mM NBT, xanthine oxidase (1.2 U/μL) was then added to this mixture. After mixing gently for 10 min, optical densities were measured at 612 nm using a microplate reader (Tecan). Allopurinol was used as a positive control [22].
3.5. Anti-Proliferation and Cytotoxicity Assays
3.5.1. Cell Culture
RAW 264.7 macrophage, DU-145 and LNCaP human prostate cancer cell lines were purchased from the Korean Cell Line Bank. The RAW 264.7 macrophage cell and human prostate cancer cell lines was grown at 37 °C in a humidified atmosphere (5% CO2) in DMEM (Sigma) and RPMI (Sigma) containing 10% fetal bovine serum, 10 IU/mL penicillin G and 100 μg/mL streptomycin (Gibco BRL, Grand Island, NY, USA).
3.5.2. Measurement of Cell Viability
After culturing of RAW 264.7 macrophage (3.5 × 105 cells/200 μL medium) in 96-well plates and incubating for 2 h, in 96-well plates and incubating for 24 h, the cells were treated with the test samples. The cells were incubated for an additional 24 h, and the medium was replaced with fresh medium containing 0.5 mg/mL 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) (Sigma). Incubation was continued for 4 h at 37 °C. The medium was then removed and the MTT-formazan produced was dissolved in dimethyl sulfoxide (DMSO). The extent of the reduction of MTT to dark purple crystals within the cells was quantified by measuring the absorbance at 540 nm using the microplate reader (Tecan) [24].
3.5.3. Anti-Proliferation Assays
After culturing of DU145 and LNCaP human prostate cancer cell lines (1 × 104 cells/ 200 μL medium) in 24-well plates and incubating for 24 h, the cells were treated with the test samples. Plates were incubated for 72 h after which bioassays were performed. LNCaP cells were handled in a similar manner, and the medium was replaced with fresh medium containing 0.5 mg/mL 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) (Sigma). Incubation was continued for 4 h at 37 °C. The medium was then removed and the MTT-formazan produced was dissolved in dimethyl sulfoxide (DMSO). The extent of the reduction of MTT to dark purple crystals within the cells was quantified by measuring the absorbance at 540 nm using the microplate reader (Tecan) [24].
3.6. Statistical Analysis
All data are expressed as mean ± S.D. Values were performed by one-way analysis of variance (ANOVA) followed by Student-Newman-Keuls (S-N-K) test using the SPSS software package; the values were considered significantly different when the p value was less than 0.05.
4. Conclusions
Fifteen phenolic compounds 1–15, inclusing three caffeoyl derivatives 1–3, four gallotannins 4–7, three ellagitannins 8–10 and five flavonoids 11–15 were isolated from CL. DPPH radical scavenging and superoxide scavenging activity, as well as, anti-proliferative activity on prostate cancer call lines (DU145 and LNCaP) of the isolated compounds were evaluated. As a results, the ellagitannin derivatives 8–10 showed potent anti-oxidative and anti-proliferative activities on prostate cancer cell lines. These results suggested that CL extract and its phenolic compounds could potentially be developed as ingredients with anti-oxidative and androgen sensitive anti-proliferation activity.
Acknowledgments
This study was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2010-0022929).
References
- Zhang, Z.; Zhang, H.; Peter, K.E. Hamaelidaceae. In Flora of China; Science Press & Missouri Botanical Garden: Beijing, China and St. Louis, MO, USA, 2003; Volume 9, pp. 18–42. [Google Scholar]
- Huafu, W.; Gordon, J.P.; Keith, H. Determination of hamameli-tannin, catechins and gallic acid in witch hazel bark, twig and leaf by HPLC. J. Pharm. Biomed. Anal. 2003, 33, 539–544. [Google Scholar] [CrossRef]
- Korting, H.C.; Schäfer-Korting, M.; Klövekorn, W.; Klövekorn, G.; Martin, C.; Laux, P. Comparative efficacy of hamamelis distillate and hydrocortisone cream in atopic eczema. Eur. J. Clin. Pharmacol. 1995, 48, 461–465. [Google Scholar]
- Dauer, A.; Metzner, P.; Schimmer, O. Proanthocyanidins from the bark of Hamamelis virginiana exhibit antimutagenic properties against nitroaromatic compounds. Planta Med. 1998, 64, 324–327. [Google Scholar] [CrossRef]
- Dauer, A.; Rimpler, H.; Hensel, A. Polymeric proanthocyanidins from the bark of Hamamelis virginiana L. Planta Med. 2003, 69, 89–91. [Google Scholar] [CrossRef]
- Hideo, I.; Hideko, M.; Ideko, M.; Noriko, O.; Ryo, K. 3-O-feruloyl-4-O-caffeoylquinic acid from coffee beans. Phytochemistry 1985, 24, 630–632. [Google Scholar] [CrossRef]
- Akdemir, Z.S.; Tatli, I.I.; Saracoglu, I.; Ismailoglu, U.B.; Sahin-Erdemli, I.; Caliş, I. Polyphenolic compounds from Geranium prat-ense and their free radical scavenging activities. Phytochemistry 2001, 56, 189–193. [Google Scholar]
- Zamarrud, A.I.; Hussain, H.; Ahmad, V.U.; Qaiser, M.; Amyn, A.; Mohammad, F.V. Two new antioxidant Bergen-in derivatives from the stem of Rivea hypocrateriformis. Fitoterapia 2011, 82, 722–725. [Google Scholar] [CrossRef]
- Dong, W.; Zhu, H.T.; Zhang, Y.J.; Yang, C.R. A carbon-carbon-coupled dimeric bergenin derivative biotransformed by Pleu-rotus ostreatus. Bioorg. Med. Chem. Lett. 2005, 15, 4073–4075. [Google Scholar] [CrossRef]
- Lee, M.W.; Tanaka, T.; Nonaka, G.I.; Nishioka, I. Hirsunin, an ellagitannin with a diarylheptanoid moiety, from Alnus hirsuta var. Microphylla. Phytochemistry 1992, 31, 967–970. [Google Scholar]
- Jin, Z.X.; Ito, H.; Yoshida, T. Dimeric and trimeric ellagitannins from corylus heterophylla. Phytochemistry 1998, 48, 333–338. [Google Scholar]
- Jeng, D.S.; Toshihiko, O.; Shunro, K.; Mitsuo, N. Tannin antioxidants from Osbeckia chinensis. Phytochemistry 1988, 27, 1315–1319. [Google Scholar]
- Lommen, A.; Godejohann, M.; Venema, D.P.; Hollman, P.C.H.; Spraul, M. Application of directly coupled HPLC-NMR-MS to the identification and confirmation of quercetin glycosides and phloretin glycosides in apple peel. Anal. Chem. 2000, 72, 1793–1797. [Google Scholar]
- Philippe, O.D.B.; Dijoux, M.G.; Gilbert, C.; Anne-marie, M.I. Quercitrin T-sulphate fromleaves of leea G uinensis. Phytochemistry 1998, 47, 1171–1173. [Google Scholar]
- Mohamed, B.; Aziz, A.; Christian, R. Regio- and ster-eoselective synthesis of the major metabolite of quercetin, quercetin-3-O-β-d-glucuronide. Tetrahedron Lett. 2002, 43, 6263–6266. [Google Scholar] [CrossRef]
- Lee, S.H.; Park, Y.H.; Moon, B.H.; Lee, E.J.; Hong, S.W.; Lim, Y.H. Substitution effect of hydroxyl groups on the 1H and 13C Chemical Shifts in Hydroxyflavonols. Bull. Korean Chem. Soc. 2008, 29, 1597–1600. [Google Scholar] [CrossRef]
- Lee, J.I.; Kong, C.S.; Jung, M.E.; Hong, J.W.; Noh, I.; Seo, Y.W. Peroxynitrite-scavenging activity of the halophyte limon-ium tetragonum. Ocean Polar Res. 2011, 33, 185–191. [Google Scholar]
- Park, J.H.; Li, C.; Hu, W.; Wang, M.H. Antioxidant and Free Radical Scavenging Activity of Different Fractions from Hawthorn Fruit. J. Food Sci. Nutr. 2010, 5, 44–50. [Google Scholar] [CrossRef]
- Hobbs, A.; Higgs, A.; Moncada, S. Inhibition of nitric oxide synthase as a potential therapeutic target. Ann. Rev. Pharm. Toxicol. 1999, 39, 191–220. [Google Scholar] [CrossRef]
- Alessandra, R.; Venera, C.; Laura, L.; Luca, V.; Angelo, V.; Juan, A.G. Antioxidant activity and antiproliferative action of methanolic extract of Geum quellyon Sweet roots in human tumor cell lines. J. Ethnopharmacol. 2005, 100, 323–332. [Google Scholar] [CrossRef]
- Hatano, T.; Edamatsu, R.; Hiramatsu, M.; Mori, A.; Fujita, Y.; Yasuhara, T. Effects of the interaction of tannins with co-exist substances. IV. Effects of tannins and ralated polyphenols on superoxide anion radical, and on 1,1-diphenyl-2-picrylhydrazyl radical. Chem. Pharm. Bull. 1989, 37, 2016–2021. [Google Scholar]
- Christin, A.; Martine, T.; Jacques, H. Superoxide anion involvement in NBT reduction by NADPH-cytochrome P-450 reductase. FEBS Lett. 1978, 89, 26–28. [Google Scholar] [CrossRef]
- Toshiyuki, F.; Hideyuki, I.; Takashi, Y. Antioxidative polyphen-ols from walnuts (Juglans regia L.). Phytochemistry 2003, 63, 795–801. [Google Scholar]
- Mosmann, T. Rapid colorimetric assay for the cellular growth and survival. J. Immunol. Methods 1983, 65, 55–63. [Google Scholar] [CrossRef]
- Yi, Z.C.; Liu, Y.Z.; Li, H.X.; Yin, Y.; Zhuang, F.Y.; Fan, Y.B.; Wang, Z. Tellimagrandin I enhances gap junctional communication and attenuates the tumor phenotype of human cervical carcinoma HeLa cells in vitro. Cancer Lett. 2006, 242, 77–87. [Google Scholar] [CrossRef]
- Miyamoto, K.; Nomura, M.; Murayama, T.; Furukawa, T.; Hatano, T.; Yoshida, T.; Koshiura, R.; Okuda, T. Antitumor activities of ellagitannins against sarcoma-180 in mice. Biol. Pharm. Bull. 1993, 16, 379–387. [Google Scholar] [CrossRef]
- Ken, S.F. Recent progress in ellagitannin chemistry. Phytochemistry 2005, 66, 1984–2000. [Google Scholar] [CrossRef]
- Sample Availability: Samples of the compounds 1–15 are available from the authors.
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Kim, M.H.; Ha, S.Y.; Oh, M.H.; Kim, H.H.; Kim, S.R.; Lee, M.W. Anti-Oxidative and Anti-Proliferative Activity on Human Prostate Cancer Cells Lines of the Phenolic Compounds from Corylopsis coreana Uyeki. Molecules 2013, 18, 4876-4886. https://doi.org/10.3390/molecules18054876
AMA Style
Kim MH, Ha SY, Oh MH, Kim HH, Kim SR, Lee MW. Anti-Oxidative and Anti-Proliferative Activity on Human Prostate Cancer Cells Lines of the Phenolic Compounds from Corylopsis coreana Uyeki. Molecules. 2013; 18(5):4876-4886. https://doi.org/10.3390/molecules18054876
Chicago/Turabian StyleKim, Manh Heun, Sung Yi Ha, Myeong Hwan Oh, Han Hyuk Kim, So Ra Kim, and Min Won Lee. 2013. "Anti-Oxidative and Anti-Proliferative Activity on Human Prostate Cancer Cells Lines of the Phenolic Compounds from Corylopsis coreana Uyeki" Molecules 18, no. 5: 4876-4886. https://doi.org/10.3390/molecules18054876
