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Article

Bioactive Constituents Obtained from the Seeds of Lepidium apetalum Willd

1
Tianjin State Key Laboratory of Modern Chinese Medicine, 312 Anshanxi Road, Nankai District, Tianjin 300193, China
2
Tianjin Key Laboratory of TCM Chemistry and Analysis, Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 312 Anshanxi Road, Nankai District, Tianjin 300193, China
*
Authors to whom correspondence should be addressed.
Molecules 2017, 22(4), 540; https://doi.org/10.3390/molecules22040540
Submission received: 25 January 2017 / Revised: 24 March 2017 / Accepted: 25 March 2017 / Published: 28 March 2017
(This article belongs to the Section Natural Products Chemistry)

Abstract

:
Three new compounds, apetalumosides C1 (1), D (2), and 1-thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3), together with twenty-two known ones (425) were obtained from the seeds of Lepidium apetalum Willd. Among the known isolates, 58, 1013, 1620, and 25 were obtained from the genus for the first time; 4, 14, 15, and 2124 were isolated from the species for the first time. Meanwhile, the NMR data of 16 was first reported here. Their structures were determined by means of chemical and spectroscopic methods. On the other hand, their inhibitory effects on sodium oleate-induced triglyceride (TG) overloading in HepG2 cells were evaluated. As a result, two new compounds (1 and 2), together with known isolates 711, 13, 14, 1618, 20, 21, and 25 possessed significant inhibitory effects in the cells.

1. Introduction

In our on-going program of screening the phytochemical and bioactive constituents from Lepidium apetalum seed extract [1,2], three new compounds, apetalumosides C1 (1), D (2), and 1-thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3), along with twenty-two known isolates, astragalin (4) [3]; kaempferol 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (5) [4]; drabanemoroside (6) [5]; quercetin 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (7) [4]; quercetin 3-O-α-l-rhamnopyranosyl(1→2)-α-l-arabinopyranoside (8) [6]; isorhamnetin 3-O-β-d-glucopyranoside (9) [7]; isorhamnetin 3,4′-O-β-d-diglucoside (10) [8]; isorhamnetin 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (11) [4]; 2-O-(3,4-dihydroxybenzoyl)-2,4,6-trihydroxyphenylacetic acid 4-O-β-d-glucopyranoside (12) [9]; 4,9-di-O-β-d-glucosyl sinapoyl alcohol (13) [10]; 3′,5′-dimethoxy-4-O-β-d-glucopyranosyl cinnamic acid (14) [11]; sinapoylglucose (15) [12]; sinapoyl-9-sucrosecoside (16); 1(E),2(E)-di-O-sinapoyl-β-d-glucopyranoside (17) [13]; 1,2-disinapoylgentiobiose (18) [14]; lariciresinol 4′-O-β-d-glucopyranoside (19) [15,16]; (7S,8R)-aegineoside (20) [17,18]; l-tryptophan (21) [19]; thymidine (22) [20]; adenosine (23) [21]; stachyose (24) [22]; and TgSSTg (25) [23] were obtained. Among the known isolates, 58, 1013, 1620, and 25 were obtained from the genus for the first time. Meanwhile, 4, 14, 15, and 2124 were isolated from the species for the first time, and the NMR data of 16 was first reported here. Moreover, as the active ingredients of the hypolipidemic effect, several phenolic compounds, including five flavonoids (711), five sinapic acid homologues (13, 14, and 1618), and one lignan (20), together with two new compounds (1 and 2), as well as two other isolates (21 and 25) exhibited significant triglyceride (TG)-lowering effects in HepG2 cells.

2. Results and Discussion

The 50% EtOH extract of L. apetalum seeds was treated with the same experimental process as reported in reference [1,2] to obtain 95% EtOH eluate, which was separated by silica gel, octadecylsilica (ODS), Sephadex LH-20 CC, and finally preparative HPLC to yield compounds 125. Their structures are shown in Figure 1 and Figure 2.
Apetalumoside C1 (1) was isolated as yellow powder with negative optical rotation ([α] D 25 −41.1°, MeOH). Its molecular formula was deduced as C44H50O25 from a [M − H] quasi-molecular ion at m/z 977.2555 (calcd. for C44H49O25, 977.2568) in the negative-ion HRESI–TOF–MS spectrum. The 1H-, 13C-NMR (Table 1) and 2D NMR (1H-1H COSY, HSQC, HMBC, HSQC–TOCSY) spectra revealed the occurrence of one kaempferol aglycon (δ 6.51 (1H, br. s, H-6), 6.85 (1H, br. s, H-8), 6.92 (2H, d, J = 9.0 Hz, H-3′,5′), 8.09 (2H, d, J = 9.0 Hz, H-2′,6′), 12.65 (1H, br. s, 5-OH)); three β-d-glucopyranosyl (δ 4.35 (1H, d, J = 8.0 Hz, H-1′′′′), 5.12 (1H, d, J = 7.0 Hz, H-1′′′), 5.50 (1H, d, J = 8.0 Hz, H-1′′)); along with one sinapoyl (δH 3.81 (6H, s, 3′′′′′,5′′′′′-OCH3), 6.53 (1H, d, J = 16.0 Hz, H-8′′′′′), 7.00 (2H, s, H-2′′′′′,6′′′′′), 7.51 (1H, d, J = 16.0 Hz, H-7′′′′′); δC 166.2 (C-9′′′′′)). Meanwhile, in the HMBC experiment, the long-range correlations from H-1′′ to C-3; H-1′′′ to C-7; H-1′′′′ to C-6′′′; H-3′′′′ to C-9′′′′′ were observed, then the connectivities between oligoglycoside moieties and aglycon or sinapoyl groups were characterized. Finally, a HSQC–TOCSY experiment was developed to assign the badly overlapped protons in the sugar chemical shift range. In the HSQC–TOCSY spectrum, correlations between the following proton and carbon pairs were observed: δC 100.6 (C-1′′) and δH 3.08 (H-4′′), 3.21 (H-2′′), 3.26 (H-3′′), 5.50 (H-1′′); δH 3.08 (H-4′′) and δC 60.8 (C-6′′), 69.8 (C-4′′), 74.2 (C-2′′), 76.3 (C-5′′), 76.8 (C-3′′); δH 5.12 (H-1′′′) and δC 69.2 (C-4′′′), 73.0 (C-2′′′), 76.2 (C-3′′′), 99.7 (C-1′′′); δH 3.71, 3.99 (H2-6′′′) and δC 68.9 (C-6′′′), 69.2 (C-4′′′), 73.0 (C-2′′′), 75.3 (C-5′′′), 76.2 (C-3′′′); δC 103.5 (C-1′′′′) and δH 3.22 (H-2′′′′), 3.34 (H-4′′′′), 4.35 (H-1′′′′), 4.90 (H-3′′′′); δH 4.90 (H-3′′′′) and δC 60.7 (C-6′′′′), 68.1 (C-4′′′′), 77.4 (C-5′′′′), 103.5 (C-1′′′′). Acid hydrolysis of 1 yielded d-glucose, which was identified by retention time and optical rotation using chiral detection by HPLC analysis [1,2].
Apetalumoside D (2), white powder, exhibited negative optical rotation ([α] D 25 −35.3°, in MeOH). In the positive-ion HRESI–TOF–MS of 2, the quasi-molecular ion peak was observed at m/z 593.1333 [M + Na]+ (calcd. for C22H34O13S2Na, 593.1333), and its molecular formula was revealed to be C22H34O13S2. The 1H-, 13C-NMR spectra (Table 2) indicated the presences of one symmetrical 1,3,4,5-tetrasubstituted benzene ring (δ 6.58 (2H, s, H-2,6)); two methoxyl (δ 3.75 (6H, s, 3,5-OCH3)); one oxygenated methene (δ 3.18 (1H, br. d, ca. J = 11 Hz), 3.39 (1H, dd, J = 5.0, 11.0 Hz), H2-8); one methine bearing an oxygen function (δ 4.28 (1H, br. d, ca. J = 5 Hz, H-7)); along with two 1-thio-β-d-glucopyranosyl (δ 4.27 (1H, d, J = 10.0 Hz, H-1′′), 4.31 (1H, d, J = 9.5 Hz, H-1′)) [24]. The 1H-1H COSY experiment on 2 indicated the presence of three partial structures shown in bold bonds (Figure 3). Finally, the planar structure of apetalumoside D (2) was determined by the long-range correlations from H-2,6 to C-1, 3–5, 7; 3,5-OCH3 to C-3,5; H-7 to C-1, 2,6, 8, C-1′; H-1′ to C-7; H-1′′ to C-8 observed in its HMBC spectrum. The 1H- and 13C-NMR data of 2 was assigned by the correlations from proton to carbon displayed in the HSQC spectrum.
The molecular formula of 1-thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3) was deduced as C12H22O10S2 from a [M + H]+ quasi-molecular ion at m/z 391.0739 (calcd. for C12H23O10S2, 391.0727). Twelve signals were displayed in its 13C-NMR (Table 3) spectrum, and all of their chemical shifts appeared in the field of 60–100. The correlations from δH 4.68 (1H, d, J = 9.0 Hz, H-1′) to δC 92.4 (C-1′), and δH 5.57 (1H, d, J = 5.5 Hz, H-1) to δC 96.1 (C-1) observed in the HSQC spectrum indicated that there were two sugar units in 3. Combined with its MS and 1H-NMR spectrum (Table 3), the presence of two 1-thio-glucopyranosyl parts were conjectured. Among them, the anomeric proton (δH 4.68 (H-1′)) and a set of 13C-NMR (δC 63.7 (C-6′), 72.1 (C-4′), 74.4 (C-2′), 80.0 (C-3′), 83.1 (C-5′), 92.4 (C-1′)) signals revealed the presence of 1-thio-β-d-glucopyranosyl [23,24]. Meanwhile, the presence of 1-thio-α-d-glucopyranosyl was presumed by the following signals: δH 5.57 (H-1), and δC 63.4 (C-6), 72.3 (C-4), 74.3 (C-2), 76.2 (C-3), 76.4 (C-5), 96.1 (C-1). Moreover, all of the coupling constants between H-2 and H-3, H-3 and H-4, H-4 and H-5 were 9.5 Hz, which indicated that the protons in C-2, 3, 4, 5 were in axial bond. On the other hand, H-1 was suggested to be in equatorial bond by JH-1,2 = 5.5 Hz. Finally, the nuclear overhauser effect (NOE) correlations between H-2 and H-1, H-4; H-3 and H-5 observed in the NOESY experiment, further proved the presence of 1-thio-α-d-glucopyranosyl. The assignment of protons and carbons was reached by the 1H-1H COSY, HSQC, and HMBC spectra. On the basis of the above mentioned evidence, the structure of 3 was elucidated to be 1-thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3).
The L. apetalum isolates were evaluated for their inhibitory activities on TG overloading by the model of sodium oleate (SO)-induced fatty liver in vitro. As shown in Figure 4, compounds 1, 2, 710, 11, 13, 14, 1618, 20, 21 and 25 exhibited significant TG-lowering effects, among which, 10, 13 and 21 showed levels of activities almost equivalent to the positive control—a TG clearance rate of about 22%—and the remainders also reached at least 4.02% ± 1.57%.
According to the results shown in Figure 5, the tested compounds 7, 8, 17, 20 and 25 showed different dose–activity relationships. In response to stimulations of 7, 8 and 17 (at 30, 3 and 0.3 µmol/L), or 20 and 25 (at 100, 30, 3 and 0.3 µmol/L), gradual decrement trends of TG overloading were observed (shown in Table 4 and Table 5).
As for structure–activity relationships, quercetin glycosides (7 and 8) and isorhamnetin glycosides (911) in the current study showed significant TG-lowering effects, while kaempferol glycosides (46) exhibited no obvious activity, which indicated that the 3′-position substitution of hydroxyl or methoxy might play critical roles on the TG-lowering activity of flavone glycosides. For apetalumoside C1 (1), a previous study has reported that the substitution of 7-position by O-glycosides would reduce the inhibitory activities of flavonoid glycosides [2], while in the current study, 1 still exhibited a strong effect with the glycosylation of 7-hydroxyl; this is speculated to be due to the presence of the sinapoyl group in the structure. Meanwhile, five of the six sinapic acid homologues in our study, including 13, 14, and 1618, showed significant TG-lowering activities. By comparing the TG clearance rate of 17 (12.39% ± 0.95%) with that of 18 (5.49% ± 3.17%), at the concentration of 30 µmol/L, as well as the difference of their structures, we speculated that the one additional glycosyl might be the reason for the reduced activity. However, it is noteworthy that sinapoylglucose (15) showed lower activity than that of sinapoyl-9-sucrosecoside (16), which made it complicated to illustrate the influence of the substituted position and amount of glycosyl on the activity of sinapic acid groups.

3. Experimental

3.1. General

Ultraviolet–visible spectroscopy (UV) and Infrared Spectroscopy (IR) spectra were recorded on a Varian Cary 50 UV-Vis (Varian Australia Pty Ltd., Mulgrave, Australia) and Varian 640-IR FT-IR spectrophotometer (Varian, Inc., Hubbardsdon, MA, USA), respectively. Optical rotations were measured on a Rudolph Autopol IV automatic polarimeter (Rudolph Research Analytical, Hackettstown, NJ, USA). NMR spectra were determined on a Bruker 500 MHz NMR spectrometer (Bruker BioSpin AG Industriestrasse, Fällanden, Switzerland) at 500 MHz for 1H- and 125 MHz for 13C-NMR (internal standard: tetramethylsilane). Negative- and positive-ion mode HRESI–TOF–MS were obtained on an Agilent Technologies 6520 Accurate-Mass Q-TOF LC/MS spectrometer (Agilent Corp., Santa Clara, CA, USA).
Column chromatographies (CC) were performed on macroporous resin D101 (Haiguang Chemical Co., Ltd., Tianjin, China), silica gel (48–75 μm, Qingdao Haiyang Chemical Co., Ltd., Qingdao, China), ODS (40–63 μm, YMC Co., Ltd., Tokyo, Japan), and Sephadex LH-20 (Ge Healthcare Bio-Sciences, Uppsala, Sweden). Preparative high performance liquid chromatography (PHPLC) columns, Cosmosil 5C18-MS-II (20 mm i.d. × 250 mm, Nakalai Tesque, Inc., Tokyo, Japan), were used to separate the constituents.

3.2. Plant Material

The seeds of L. apetalum were collected from Anguo city, China, and identified by Dr. Li Tianxiang (The Hall of Traditional Chinese Medicines (TCM) Specimens, Tianjin University of TCM, Tianjin, China). The voucher specimen was deposited at the Academy of Traditional Chinese Medicine of Tianjin University of TCM (No. 20120501).

3.3. Extraction and Isolation

The seeds of L. apetalum (10 kg) were treated with the same experimental process as reported in reference [1,2], as a result, the 95% EtOH (Fraction 1) and H2O (Fraction 2) eluates were obtained.
Fraction 1 (80 g) was subjected to silica gel CC (CHCl3–MeOH (100:0 → 100:5, v/v) → CHCl3–MeOH–H2O (10:3:1 → 6:4:1, lower layer, v/v) → MeOH) to yield sixteen fractions (Fr. 1-1–1-16). Fractions 1-7 (12.5 g) and 1-8 (12.0 g) were isolated by ODS CC (MeOH–H2O (20% → 30% → 40% → 50% → 70% → 100%, v/v)); as a result, fifteen (Fr. 1-7-1–1-7-15) and eleven fractions (Fr. 1-8-1–1-8-11) were obtained, respectively. Fraction 1-7-1 (699.0 mg) was prepared by PHPLC [CH3CN–H2O (5:95, v/v) + 1% HOAc] to give thymidine (22, 11.1 mg). Fraction 1-8-1 (253.1 mg) was purified by PHPLC [CH3CN–H2O (8:92, v/v) + 1% HOAc] to yield 3′,5′-dimethoxy-4-O-β-d-glucopyranosyl cinnamic acid (14, 29.7 mg). Fraction 1-8-3 (579.2 mg) was separated by PHPLC (CH3CN–H2O (1:99, v/v) + 1% HOAc), and adenosine (23, 22.7 mg) was gained. Fraction 1-8-4 (1.3 g) was isolated by PHPLC (CH3CN–H2O (9:91, v/v) + 1% HOAc) to yield seven fractions (Fr. 1-8-4-1–1-8-4-7). Fraction 1-8-4-5 (130.9 mg) was further purified by PHPLC (MeOH–H2O (22:78, v/v) + 1% HOAc) to yield sinapoylglucose (15, 7.3 mg). Fraction 1-8-7 (573.6 mg) was separated by Sephadex LH-20 CC (MeOH–H2O (1:1, v/v)) and PHPLC (CH3CN–H2O (15:85, v/v) + 1% HOAc) to give lariciresinol 4′-O-β-d-glucopyranoside (19, 6.5 mg). Fraction 1-8-8 (1.1 g) was prepared by PHPLC (CH3CN–H2O (16:84, v/v) + 1% HOAc), and (7S,8R)-aegineoside (20, 10.1 mg) was yielded. Fraction 1-8-10 (917.9 mg) was purified by PHPLC (CH3CN–H2O (13:87, v/v) + 1% HOAc) to obtain astragalin (4, 4.6 mg) and isorhamnetin 3-O-β-d-glucopyranoside (9, 21.3 mg). Fraction 1-8-11 (1.3 g) was isolated by PHPLC (CH3CN–H2O (25:75, v/v)) to give 1(E),2(E)-di-O-sinapoyl β-d-glucopyranoside (17, 414.4 mg). Fraction 1-12 (8.0 g) was subjected to ODS CC (MeOH–H2O (10% → 20% → 30% → 40% → 50% → 70% → 100%, v/v)), and nine fractions (Fr. 1-12-1–1-12-9) were given. Fraction 1-12-8 (1.4 g) was further prepared by PHPLC (CH3CN–H2O (14:86, v/v) + 1% HOAc) to yield sinapoyl-9-sucrosecoside (16, 370.6 mg). Fraction 1-12-9 (2.1 g) was purified by PHPLC (MeOH–H2O (40:60, v/v) + 1% HOAc) to obtain 1,2-disinapoylgentiobiose (18, 1.3 g) and drabanemoroside (6, 57.3 mg). Fraction 1-13 (13.7 g) was isolated by PHPLC (MeOH–H2O (15:85 → 30:70 → 38:62 → 48:52, v/v) → MeOH) to give twenty-one fractions (Fr. 1-13-1–1-13-21). Fraction 1-13-3 (606.1 mg) was purified by PHPLC (CH3CN–H2O (5:95, v/v) + 1% HOAc) to gain apetalumoside D (2, 120.0 mg). Fraction 1-13-4 (780.2 mg) was separated by PHPLC (CH3CN–H2O (8:92, v/v) + 1% HOAc) to yield l-tryptophan (21, 102.4 mg). Fraction 1-13-6 (543.7 mg) was further purified by PHPLC (CH3CN–H2O (8:92, v/v)) to obtain 4,9-di-O-β-d-glucosyl sinapoyl alcohol (13, 32.0 mg). Fraction 1-13-16 (217.6 mg) was isolated by PHPLC (CH3CN–H2O (16:84, v/v)), and isorhamnetin 3,4′-O-β-d-diglucoside (10, 35.2 mg) was yielded. Fraction 1-13-17 (369.6 mg) was prepared by PHPLC (CH3CN–H2O (18:82, v/v)) to gain apetalumoside C1 (1, 54.1 mg). Fraction 1-13-20 (779.2 mg) was separated by PHPLC (CH3CN–H2O (16:84, v/v)) to obtain quercetin 3-O-α-l-rhamnopyranosyl(1→2)-α-l-arabinopyranoside (8, 273.6 mg). Fraction 1-14 (8.0 g) was subjected to Sephadex LH-20 CC (MeOH–H2O (1:1, v/v)), and seven fractions (Fr. 1-14-1–1-14-7) were given. Fraction 1-14-7 (477.8 mg) was separated by PHPLC (CH3CN–H2O (14:86, v/v) + 1% HOAc) to yield 2-O-(3,4-dihydroxybenzoyl)-2,4,6-trihydroxyphenylacetic acid 4-O-β-d-glucopyranoside (12, 6.2 mg). Fraction 1-15 (14.1 g) was isolated by PHPLC (CH3CN–H2O (9:91, v/v)), and eleven fractions (Fr. 1-15-1–1-15-11) were obtained. Fraction 1-15-1 (2.5 g) was further prepared by PHPLC (CH3CN–H2O (8:92, v/v)) to give quercetin 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (7, 265.6 mg). Fraction 1-15-5 (2.3 g) was subjected to Sephadex LH-20 CC (MeOH–H2O (1:1, v/v)) and finally separated by PHPLC (CH3CN–H2O (10:90, v/v)) to yield kaempferol 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (5, 197.1 mg). Fraction 1-15-8 (294.4 mg) was purified by PHPLC (CH3CN–H2O (9:91, v/v)) to gain isorhamnetin 3-O-β-d-glucopyranosyl-7-O-β-d-gentiobioside (11, 140.5 mg).
Meanwhile, fraction 2 (4.0 g) was isolated by PHPLC (MeOH–H2O (2:98, v/v)), and seven fractions (Fr. 2-1–2-7) were given. Fractions 2-4 (102.8 mg) and 2-5 (159.6 mg) were further purified by PHPLC (MeOH–H2O (1:99, v/v)) to yield stachyose (24, 40.9 mg) and 1-thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3, 73.3 mg). Fraction 2-6 (102.8 mg) was separated by PHPLC (MeOH–H2O (3:97, v/v) to gain TgSSTg (25, 58.3 mg).
Apetalumoside C1 (1): Yellow powder; [α] D 25 −41.1° (c = 0.95, MeOH); IR υmax (KBr) cm−1: 3362, 2937, 1699, 1653, 1600, 1516, 1457, 1340, 1286, 1179, 1113, 1066, 827; UV λmax (MeOH) nm (log ε): 334 (4.19), 266 (4.09), 245 (4.20). 1H- (DMSO-d6, 500 MHz) and 13C-NMR (DMSO-d6, 125 MHz) spectroscopic data, see Table 1. HRESI–TOF–MS: Negative-ion mode m/z 977.2555 [M − H] (calcd. for C44H49O25, 977.2568).
Apetalumoside D (2): White powder; [α] D 25 −35.3° (c = 0.94, MeOH); IR υmax (KBr) cm−1: 3399, 2922, 1616, 1519, 1463, 1336, 1222, 1113, 1025, 876, 825; UV λmax (MeOH) nm (log ε): 277 (3.28, sh); 242 (3.82). 1H- (DMSO-d6, 500 MHz) and 13C-NMR (DMSO-d6, 125 MHz) spectroscopic data, see Table 2. HRESI–TOF–MS: Positive-ion mode m/z 593.1333 [M + Na]+ (calcd. for C22H34O13S2Na, 593.1333).
1-Thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3): White powder. [α] D 25 +184.5° (c = 0.97, H2O); IR υmax (KBr) cm−1: 3368, 2888, 1636, 1411, 1356, 1273, 1097, 1042, 874; 1H- (D2O, 500 MHz) and 13C-NMR (D2O, 125 MHz) spectroscopic data, see Table 3. HRESI–TOF–MS: Positive-ion mode m/z 391.0739 [M + H]+ (calcd. for C12H23O10S2, 391.0727).
Sinapoyl-9-sucrosecoside (16): Pale yellow powders; The NMR data of 16 in DMSO-d6 is first reported. 1H-NMR (DMSO-d6, 500 MHz) δ: 6.89 (2H, s, H-2,6), 7.60 (1H, d, J = 16.0 Hz, H-7), 6.44 (1H, d, J = 16.0 Hz, H-8), 3.65 ((1H, d, J = 12.5 Hz), 3.69 (1H, d, J = 12.5 Hz), H2-1′), 3.87 (1H, d, J = 10.0, H-3′), 4.12 (1H, dd, J = 8.0, 10.0 Hz, H-4′), 4.18 (1H, m, H-5′), (4.32 (1H, dd, J = 6.0, 12.0 Hz), 4.55 (1H, br. d, ca. J = 12 Hz, H2-6′)), 5.46 (1H, d, J = 3.0 Hz, H-1′′), 3.54 (1H, dd, J = 3.0, 9.5 Hz, H-2′′), 3.82 (1H, dd, J = 9.5, 9.5 Hz, H-3′′), 3.41 (1H, dd, J = 9.5, 9.5 Hz, H-4′′), 4.18 (1H, m, H-5′′), (3.83 (1H, m, overlapped), 3.92 (1H, br. d, ca. J = 11 Hz), H2-6′′), 3.87 (6H, s, 3,5-OCH3); 13C-NMR (DMSO-d6, 125 MHz) δ: 126.5 (C-1), 106.8 (C-2,6), 149.2 (C-3,5), 139.3 (C-4), 147.3 (C-7), 115.5 (C-8), 169.2 (C-9), 64.1 (C-1′), 105.1 (C-2′), 83.6 (C-3′), 76.0 (C-4′), 79.0 (C-5′), 65.1 (C-6′), 93.1 (C-1′′), 73.0 (C-2′′), 74.5 (C-3′′), 71.7 (C-4′′), 71.9 (C-5′′), 64.1 (C-6′′), 56.9 (3,5-OCH3); HRESI–TOF–MS: Negative-ion mode m/z 547.1680 [M − H] (calcd. for C23H31O15, 547.1668).
Acid Hydrolysis of 1: the solution of compound 1 (2.0 mg) in 1 M HCl (1 mL) was treated by using the same method as described in reference [1,2]: 1 was heated under reflux for 3 h. The reaction mixture was then analyzed by CH3CN–H2O (70:30, v/v; flow rate 1.0 mL/min). As a result, d-glucose was detected from the aqueous phase of 1 by comparison of its retention time and optical rotation with that of the authentic sample, d-glucose (tR 8.8 min (positive)).

3.4. Evaluation of Effects on Sodium Oleate-Induced TG Overloading in HepG2 Cells

Materials: HepG2 cells were purchased from Cell Resource Center of Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College (Beijing, China). Dulbecco’s modified Eagle’s medium (DMEM), penicillin and streptomycin were purchased from Thermo Scientific (Waltham, MA, USA). Fetal Bovine Serum (FBS) was obtained from Mediatech (Herndon, VA, USA). TG assay kits were purchased from Biosino Bio-Technology And Science Inc. (Beijing, China). Sodium oleate (SO) and orlistat were obtained from Sigma-Aldrich Corporation (St. Louis, MO, USA).
Cell culture: HepG2 cells were routinely cultured in DMEM-based medium as described before [25]. After cells reached about 80% confluence and were seeded at a density of 80,000 cells/mL in 48-multiwell plates for 24 h, the experiments were then performed.
Induction and evaluation of TG overloading: TG overloading was induced as described before [25]. Briefly, HepG2 cells at 80% confluence were exposed to 200 µmol/L SO for 48 h. Meanwhile, the tested isolates at the indicated concentrations were added in the presence of SO. Orlistat (5 µmol/L) was selected as the positive control and the medium without SO was used as the negative control. At the end of the experiment, the intracellular TG content was determined using a commercial TG assay kit after cells were rinsed by phosphate-buffered saline and lysed. The absorbance was analyzed at 492 nm. Under the selected concentrations in this study, according to pre-tests, no obvious influence was observed on cell viability (data not shown). The measurement was made in triplicate.

3.5. Statistical Analysis

Statistical analyses were undertaken with SPSS v12.0 (SPSS, Chicago, IL, USA). The significance of the differences between the mean values was determined using an analysis of variance (ANOVA). The differences were considered statistically significant at p < 0.05.

4. Conclusions

Summed up, twenty-five compounds (125) including three new ones, apetalumosides C1 (1), D (2), and 1-thio-β-d-glucopyranosyl(1→1)-1-thio-α-d-glucopyranoside (3), were obtained from the seeds of L. apetalum. Among the known isolates, 58, 1013, 1620, and 25 were obtained from the genus for the first time; 4, 14, 15, 2124 were isolated from the species for the first time. Meanwhile, the NMR data of 16 was first reported here. Their structures were determined by means of chemical and spectroscopic methods. Moreover, their inhibitory effects on TG overloading were evaluated in HepG2 cells. The results showed that phenol compounds, including five flavonoids (711), five sinapic acid groups (13, 14, 1618) and one lignin (20), together with two new compounds (1 and 2) as well as two other isolates (21 and 25) have significant TG-lowering effects, among of which, 10, 13 and 21 exhibited a level of activities almost comparable to that of orlistat. It is suggested that the above compounds contained in the L. apetalum might be part of the material basis involved in the lipid metabolism.

Acknowledgments

This work was financially supported by programs for National Natural Science Foundation of China (81673688), Changjiang Scholars and Innovative Research Team in University (PCSIRT, No. IRT_14R41).

Author Contributions

Yi Zhang and Tao Wang designed the research and wrote the manuscript; Sijian Wang, Pingping Shi, and Lu Qu performed the experimental work; Jingya Ruan and Shengcai Yang retrieved literature; Haiyang Yu perfected language. All authors discussed, edited and approved the final version.

Conflicts of Interest

The authors declare no conflict of interest.

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Sample Availability: Samples of all compounds are available from the authors.
Figure 1. The new compounds 13 obtained from the seeds of L. apetalum.
Figure 1. The new compounds 13 obtained from the seeds of L. apetalum.
Molecules 22 00540 g001
Figure 2. The known compounds (425) obtained from the seeds of L. apetalum.
Figure 2. The known compounds (425) obtained from the seeds of L. apetalum.
Molecules 22 00540 g002
Figure 3. The main 1H-1H COSY and HMBC correlations of 13.
Figure 3. The main 1H-1H COSY and HMBC correlations of 13.
Molecules 22 00540 g003
Figure 4. Effects of compounds 125 on TG overloading in HepG2 cells. Cells were treated with 200 µmol/L sodium oleate (SO) for 48 h. Meanwhile, 30 µmol/L-tested compounds or 5 µmol/L-orlistat (Orli.) were co-incubated to evaluate their inhibitory effects, respectively. Each value represents the mean ± S.E.M., n = 4, *** p < 0.001, ** p < 0.01, * p < 0.05 vs. model group (Mod.). Nor. = normal group.
Figure 4. Effects of compounds 125 on TG overloading in HepG2 cells. Cells were treated with 200 µmol/L sodium oleate (SO) for 48 h. Meanwhile, 30 µmol/L-tested compounds or 5 µmol/L-orlistat (Orli.) were co-incubated to evaluate their inhibitory effects, respectively. Each value represents the mean ± S.E.M., n = 4, *** p < 0.001, ** p < 0.01, * p < 0.05 vs. model group (Mod.). Nor. = normal group.
Molecules 22 00540 g004
Figure 5. Concentration-dependent inhibitory effects of compounds 7, 8, 17, 20, and 25 on TG overloading in HepG2 cells. Cells were treated with 200 µmol/L SO for 48 h. Meanwhile, different indicated concentrations of tested compounds were co-incubated to perform the dose dependency study, respectively. Each value represents the mean ± S.E.M., n = 4, *** p < 0.001, ** p < 0.01, * p < 0.05 vs. model group (Mod.). Nor. = normal group.
Figure 5. Concentration-dependent inhibitory effects of compounds 7, 8, 17, 20, and 25 on TG overloading in HepG2 cells. Cells were treated with 200 µmol/L SO for 48 h. Meanwhile, different indicated concentrations of tested compounds were co-incubated to perform the dose dependency study, respectively. Each value represents the mean ± S.E.M., n = 4, *** p < 0.001, ** p < 0.01, * p < 0.05 vs. model group (Mod.). Nor. = normal group.
Molecules 22 00540 g005
Table 1. 1H- and 13C-NMR data for 1 in DMSO-d6.
Table 1. 1H- and 13C-NMR data for 1 in DMSO-d6.
No.δCδH (J in Hz)No.δCδH (J in Hz)
2156.72′′′73.03.28 (dd, 7.0, 9.5)
3133.43′′′76.23.32 (dd, 9.5, 9.5)
4177.64′′′69.23.26 (m, overlapped)
5160.85′′′75.33.75 (m)
699.46.51 (br. s)6′′′68.93.71 (dd, 5.5, 11.5)
7162.7 3.99 (br. d, ca. 12)
894.46.85 (br. s)1′′′′103.54.35 (d, 8.0)
9155.92′′′′71.53.22 (dd, 7.5, 8.0)
10105.63′′′′77.54.90 (dd, 7.5, 9.0)
1′120.74′′′′68.13.34 (dd, 9.0, 9.0)
2′,6′130.98.09 (d, 9.0)5′′′′77.43.08 (m)
3′,5′115.26.92 (d, 9.0)6′′′′60.73.56 (br. d, ca. 12)
4′160.1 3.70 (dd, 5.5, 11.5)
5-OH12.65 (br. s)1′′′′′124.5
1′′100.65.50 (d, 8.0)2′′′′′,6′′′′′105.97.00 (s)
2′′74.23.21 (dd, 7.5, 8.0)3′′′′′,5′′′′′147.9
3′′76.83.26 (m, overlapped)4′′′′′138.0
4′′69.83.08 (m, overlapped)7′′′′′144.97.51 (d, 16.0)
5′′76.33.21 (m)8′′′′′115.56.53 (d, 16.0)
6′′60.83.30 (br. d, ca. 11)9′′′′′166.2
3.50 (dd, 5.5, 10.5)3′′′′′,5′′′′′-OCH356.03.81 (s)
1′′′99.75.12 (d, 7.0)
Table 2. 1H- and 13C-NMR data for 2 in DMSO-d6.
Table 2. 1H- and 13C-NMR data for 2 in DMSO-d6.
No.δCδH (J in Hz)No.δCδH (J in Hz)
1130.24′70.0 a3.07 (m, overlapped)
2,6105.66.58 (s)5′78.13.12 (m, overlapped)
3,5147.56′61.2 b3.46 (dd, 5.0, 12.5)
4134.5 3.70 (br. d, ca. 13)
746.54.28 (br. d, ca. 5)1′′84.74.27 (d, 10.0)
834.83.18 (br. d, ca. 11)2′′80.83.13 (m, overlapped)
3.39 (dd, 5.0, 11.0)3′′78.03.12 (m, overlapped)
3,5-OCH355.93.75 (s)4′′69.9 a3.07 (m, overlapped)
1′83.74.31 (d, 9.5)5′′72.93.01 (dd, 9.5, 10.0)
2′72.93.01 (dd, 8.0, 9.5)6′′61.1 b3.46 (dd, 5.0, 12.5)
3′80.83.13 (m, overlapped) 3.70 (br. d, ca. 13)
a,b Can be exchanged.
Table 3. 1H- and 13C-NMR data for 3 in D2O.
Table 3. 1H- and 13C-NMR data for 3 in D2O.
No.δCδH (J in Hz)No.δCδH (J in Hz)
196.15.57 (d, 5.5)1′92.44.68 (d, 9.0)
274.33.87 (dd, 5.5, 9.5)2′74.43.49 (dd, 9.0, 9.5)
376.23.58 (dd, 9.5, 9.5)3′80.03.52 (dd, 9.5, 9.5)
472.33.44 (dd, 9.5, 9.5)4′72.13.42 (dd, 9.5, 9.5)
576.43.94 (m)5′83.13.50 (m)
663.43.80 (dd, 5.5, 12.5)6′63.73.72 (dd, 5.5, 12.5)
3.88 (dd, 1.5, 12.5) 3.91 (dd, 1.5, 12.5)
Table 4. TG clearance of compounds 7, 8 and 17 at different concentrations.
Table 4. TG clearance of compounds 7, 8 and 17 at different concentrations.
Sample (µmol/L)7817
3030.33030.33030.3
TG clearance (%)9.46 ± 1.897.16 ± 0.873.24 ± 0.3512.00 ± 1.178.27 ± 2.144.15 ± 1.9712.70 ± 2.395.68 ± 1.154.32 ± 1.57
Table 5. TG clearance of compounds 20 and 25 at different concentrations.
Table 5. TG clearance of compounds 20 and 25 at different concentrations.
Sample (µmol/L)2025
1003030.31003030.3
TG clearance (%)4.14 ± 1.403.91 ± 1.792.82 ± 1.061.31 ± 1.0212.66 ± 0.773.91 ± 0.902.96 ± 0.452.00 ± 0.34

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Wang, S.; Shi, P.; Qu, L.; Ruan, J.; Yang, S.; Yu, H.; Zhang, Y.; Wang, T. Bioactive Constituents Obtained from the Seeds of Lepidium apetalum Willd. Molecules 2017, 22, 540. https://doi.org/10.3390/molecules22040540

AMA Style

Wang S, Shi P, Qu L, Ruan J, Yang S, Yu H, Zhang Y, Wang T. Bioactive Constituents Obtained from the Seeds of Lepidium apetalum Willd. Molecules. 2017; 22(4):540. https://doi.org/10.3390/molecules22040540

Chicago/Turabian Style

Wang, Sijian, Pingping Shi, Lu Qu, Jingya Ruan, Shengcai Yang, Haiyang Yu, Yi Zhang, and Tao Wang. 2017. "Bioactive Constituents Obtained from the Seeds of Lepidium apetalum Willd" Molecules 22, no. 4: 540. https://doi.org/10.3390/molecules22040540

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