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Three quinolizidine dimers from the seeds of Sophora alopecuroides and their hepatoprotective activities
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Xiang Yuan, Jianshuang Jiang, Yanan Yang, Xu Zhang, Ziming Feng, Peicheng Zhang*
Chinese Chemical Letters | 2022, 33(6) : 2923 - 2927
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Chinese Chemical Letters | 2022, 33(6): 2923-2927
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Three quinolizidine dimers from the seeds of Sophora alopecuroides and their hepatoprotective activities
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Xiang Yuan, Jianshuang Jiang, Yanan Yang, Xu Zhang, Ziming Feng, Peicheng Zhang*
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  • State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China
Published: 2022-06-15 doi: 10.1016/j.cclet.2021.10.085
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Sophoralines A-C, three novel [2 + 2] cycloaddition dimers of matrine-based alkaloids with an unprecedented 6/6/6/6/4/6/6/6/6 nonacyclic skeleton containing 11 stereogenic centers, were isolated from Sophora alopecuroides. Their structures were determined by spectroscopic methods, and the absolute configurations were further determined by single-crystal X-ray diffraction analysis for 1 and quantum chemical calculations of electronic circular dichroism (ECD) spectra for 2 and 3. Moreover, 1 exhibited excellent hepatoprotective activities in acetaminophen-induced liver injury in vitro and in vivo.

Alkaloids  /  Sophora alopecuroides  /  X-ray diffraction  /  Hepatoprotective activities
Xiang Yuan, Jianshuang Jiang, Yanan Yang, Xu Zhang, Ziming Feng, Peicheng Zhang. Three quinolizidine dimers from the seeds of Sophora alopecuroides and their hepatoprotective activities[J]. Chinese Chemical Letters, 2022 , 33 (6) : 2923 -2927 . DOI: 10.1016/j.cclet.2021.10.085
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Sophora alopecuroides L. (Leguminosae) is widely distributed in northwestern China, and is commonly used as the traditional Chinese medicine "Kudouzi" for the treatment of eczema, sore throat, acute dysentery, and gastrointestinal hemorrhage [1-5]. Phytochemical investigations of S. alopecuroides have revealed that it contains large amounts of quinolizidine alkaloids. Since 1895, more than 50 alkaloids have been reported from Sophora species [6-9], and these alkaloids have been shown to exhibit anti-human immunodeficiency virus, antitumor, and hepatoprotective activities [10, 11]. Among them, approximately 10 dimeric quinolizidine alkaloids, which are linked by a C-C or C-N single bond, have been identified. Recently, a number of studies on natural product dimers with structural diversity and pharmacological significance have been published, resulting in increased interest among various scientific communities [12-19]. In the present study, three new alkaloid dimers were isolated and identified from S. alopecuroides, namely sophoralines A-C (1-3), which represent the first [2 + 2] cycloaddition dimeric matrine-based alkaloid possessing an unprecedented 6/6/6/6/4/6/6/6/6 nonacyclic skeleton (Fig. 1). The biological studies showed that pretreatment with 1 markedly alleviated acetaminophen (APAP)-induced acute liver injury via inhibiting oxidative stress in vitro and in vivo.
Sophoraline A (1), colorless crystal (MeOH), was assigned its molecular formula C30H42N4O2 by the high resolution electrospray ionization mass spectroscopy (HRESIMS) ion at m/z 491.3382 [M + H]+, suggesting 12 degrees of unsaturation. The characteristic infrared radiation (IR) absorption at 1666 cm−1 and UV absorption at 277 nm suggested the presence of an α, β-unsaturated amide group in 1.
The 1H nuclear magnetic resonance (NMR) spectrum of 1 exhibited the presence of two olefinic protons at δH 6.36 (dd, J = 10.0, 5.5 Hz) and 5.80 (d, J = 10.0 Hz) and two methylenes connected to heteroatoms at δH 4.25 (dd, J = 13.5, 4.5 Hz), 4.06 (dd, J = 13.5, 4.5 Hz), 3.07 (overlapped), and 2.65 (overlapped). The 13C NMR and distortionless enhancement by polarization transfer (DEPT) spectra showed the existence of 30 carbons (Supporting information Table S1), including two carbonyls (δC 170.8 and 165.7), two sp2 methines (δC 138.7 and 125.6), a quaternary carbon (δC 71.0), ten sp3 methines (δC 64.1, 58.9, 53.2, 51.6, 51.3, 44.9, 39.6, 35.7, 32.8 and 27.6) and fifteen sp3 methylene carbons (six of which were connected to heteroatom at δC 58.3, 58.2, 54.8, 45.5, 42.2 and 42.2). The carbonyls and double bond accounted for three degrees of unsaturation, indicating the presence of nine rings in the structure of 1. The aforementioned spectroscopic evidences, particularly the molecular formula, suggested that 1 was likely a dimeric alkaloid.
Analysis of the 1H-1H correlation spectroscopy (COSY) spectrum aided by the heteronuclear single quantum correlation spectroscopy (HSQC) experiment led to the assignment of two isolated spin systems as depicted with bolded blue lines in Fig. 2. The heteronuclear multiple bond correlation spectroscopy (HMBC) cross peaks from H-14 to C-12 and C-15, H2-17 to C-11 and C-15 indicated the presence of a δ-lactam. The planar structure of unit A was further constructed by the key correlations of H2-17 to C-4, C-5 and C-6, and H-6 to C-2, C-5, C-7, C-11, and C-17, together with 1H-1H COSY correlations of H2-2/H2-3/H2-4/H-5/H-6/H-7/H2-8/H2-9/H2-10, suggesting that unit A was similar to (−)-13, 14-dehydrosophoridine [20]. The most notable difference was chemical shifts of C-7, C-11 and C-12 in (−)-13, 14-dehydrosophoridine from δC 39.6, 53.5 and 29.9 to δC 51.6, 71.0 and 39.6, respectively, in unit A, caused by the formation of dimer. The unit B was subsequently established by the HMBC correlations of H-14ʹ to C-12ʹ, C-13ʹ and C-15ʹ, and H-11ʹ to C-6ʹ, C-8ʹ and C-13ʹ, together with H-6ʹ to C-2ʹ, C-5ʹ, C-7ʹ, C-10ʹ, C-11ʹ and C-17ʹ. The HMBC correlations between H-12 and C-12ʹ, C-13ʹ, H-13 and C-13ʹ, and contiguous 1H-1H COSY correlations extending from H-14 to H-11ʹ distinctly confirmed the connection of units A and B via the C-12-C-13ʹ bond. Different from other reported alkaloid dimers, the 12 degrees of unsaturation immanent in the molecular formula of 1 and the aforementioned NMR data, which represent two moieties of the structure occupying 11 degrees of unsaturation suggested that the dimer should possess one additional ring structure. Three methine groups (δC 51.3, 39.6 and 32.8) and a quaternary carbon (δC 71.0) were observed in 1, as well as the key HMBC correlations from H-13 to C-12 and C-13ʹ, H-12 to C-12ʹ, C-13ʹ and C-14ʹ, and H-7 to C-11 and C-14ʹ, indicating that unit A is linked to unit B via a four-membered ring.
The rotating frame overhauser effect spectroscopy (ROESY) experiment was used to assign the relative configurations of the stereocenters in 1. In unit A, ROESY correlations of H-5/H-17b, H-6/H-7 and H-6/H-17a (Fig. 2) indicate that H-6 and H-7 were the same oriented, whereas H-5 was assigned to the opposite side. In unit B, the ROESY correlations of H-13ʹ/H-12, H-13ʹ/H-11ʹ and H-13ʹ/H-14ʹ for unit B demonstrated that H-12, H-11ʹ, H-13ʹ and H-14ʹ were cofacial. Furthermore, the ROESY correlations of H-6ʹ/H-5ʹ and H-6ʹ/H-7ʹ suggest that H-5ʹ, H-6ʹ and H-7ʹ have the same spatial orientation. Ultimately, the single crystal X-ray diffraction research was undertaken to elucidate the absolute configurations. The absolute configurations of 1 were unambiguously confirmed by X-ray diffraction with a Flack parameter of 0.02 (8). Finally, the result was confirmed through a comparison of the calculated and experimental electronic circular dichroism (ECD) spectra (Fig. 3). Therefore, the absolute configurations of 1 were determined as 5R, 6S, 7S, 11S, 12R, 5ʹS, 6ʹS, 7ʹR, 11ʹR, 13ʹS, 14ʹS and named sophoraline A.
Sophoraline B (2) was assigned its molecular formula C30H42N4O3 by the HRESIMS ion at m/z 507.3326 [M + H]+. Detailed analyses of the molecular formula and NMR data in 2 possessed an extra "O" in comparison to that of 1. Regardless of the stereochemistry, this indicated that 2 might be an oxidation congener of 1. This speculation was confirmed by the 1H-1H COSY spectrum that exhibited the same spin systems as 1 (Fig. S3 in Supporting information). The chemical shifts of C-2, C-6 and C-10 from δC 54.8, 58.9 and 45.5 in 1 to 71.5, 73.7 and 57.8 in 2, respectively, suggested that unit A was N-oxide congener. Further interpretation of the HMBC correlation peaks were used to construct the planar architectural structure of 2 (Fig. 1).
The relative conformation of 2 was deduced based on biosynthetic pathway and ROESY experiment referencing to those of 1. The correlations of H-5/H-17b, H-6/H-7 and H-17a, H-6ʹ/H-5ʹ and H-7ʹ, and H-13ʹ/H-11ʹ suggested that 2 shared the same relative conformation of 1. Furthermore, similar Cotton effects in the experimental circular dichroism (CD) spectra of the two compounds indicated that they may share the same absolute configurations. To further confirm its absolute configurations, calculated ECD spectrum of 2a was compared with experimental data (Fig. 3), which eventually determined the absolute configurations of 2 to be 5R, 6S, 7S, 11S, 12R, 5ʹS, 6ʹS, 7ʹR, 11ʹR, 13ʹS, 14ʹS and named sophoraline B.
Sophoraline C (3) was assigned its molecular formula C30H44N4O2 by the HRESIMS ion at m/z 493.3526 [M + H]+, suggesting 11 degrees of unsaturation. Further analyses of the molecular formula and NMR data of 3 also indicated that 3 showed highly similar planar structure as 1. In comparison with the spectra of 1, the upfield movement of C-13 and C-14 from δC 138.7 and 125.6 to δC 31.1 and 22.4 in 3, respectively, suggesting that the double bond is saturated. Based on the 1H-1H COSY spectrum correlations, a complicated spin system was observed in 3 (Fig. 4). The HMBC correlations from H-6ʹ to C-2ʹ, C-5ʹ, C-7ʹ, C-10ʹ, C-11ʹ and C-17ʹ, as well as from H-11ʹ to C-6ʹ, C-7ʹ, C-12ʹ and C-13ʹ suggested that the planar structure of unit B was similar to that of 1. Together with the HMBC correlations from H-6 to C-2, C-5, C-7, C-10, C-11 and C-17, as well as from H-12 to C-7, C-11, C-13 and C-14 determined a planar structure of unit A. Finally, two moieties are linked to form a four-membered ring system, which supported by the key HMBC correlations from H-7 to C-11 and C-14ʹ, H-12 to C-13ʹ and C-14ʹ, H-13ʹ to C-12 and C-13. The planar structure of 3 was unambiguously established as shown in Fig. 1.
The ROESY correlations of H-5/H-17b, H-6/H-7, H-6ʹ/H-5ʹ and H7ʹ, H-12/H-13ʹ, H-13ʹ/H-14ʹ and H-14ʹ/H-11ʹ, suggested that 3 shared the same relative conformation of 1. The absolute configuration of 3 was also established by comparison of the experimental and calculated ECD spectra (Fig. 3), allowing assignment of the absolute configurations as 5R, 6S, 7S, 11S, 12R, 5ʹS, 6ʹS, 7ʹR, 11ʹR, 13ʹS, 14ʹS, and named sophoraline C.
Three novel [2 + 2] cycloaddition dimers of matrine-based alkaloids, with an unprecedented 6/6/6/6/4/6/6/6/6 nonacyclic skeleton containing 11 stereogenic centers, were isolated from the seeds of S. alopecuroides. These compounds represent the first example of an unusual pattern of [2 + 2] dimerization between two matrine-type alkaloids with highly fused polycyclic carbon skeletons. A plausible biosynthetic pathway is proposed in Scheme 1. The [2 + 2] cycloaddition reaction between two moieties is a key step in biosynthesis of 1−3. Quinolizidine alkaloid may originate via the lysine pathway [21]. In vivo, 1 with tension cyclobutane structure could be formed from intermolecular [2 + 2] cycloaddition of two our previous isolated compounds, neosophocarine and sophoramine, by enzymatic processes. Furthermore, 1 could be oxidized to yield 2 and hydrogenated to obtain 3.
Although the discovery of 1-3 has aroused great interest, it also raises the question whether they are natural products or handling artifacts. Thus, neosophocarine and sophoramine were performed for attempting [2 + 2] cycloaddition reactions under different conditions with heat, ultraphonic and UV, etc., while no dimers were detected (see Supporting information).
Furthermore, the hepatoprotective effect of 1 against APAP-induced hepatotoxicity in HepG2 cells and a mice model were evaluated. All animal experiments were approved by the Animal Experimentation Ethics Committee of Chinese Academy of Medical Sciences in complete compliance with the guidelines of Institutional Animal Care and Use Committees of Chinese Academy of Medical Sciences (Beijing, China). In the in vitro experiment, 1 could alleviate damage to the hepatocyte induced by APAP in HepG2 cells. As shown in Fig. 5A, the viability of HepG2 cells was significantly decreased by 46.21% after exposure to 10 mmol/L APAP. However, cells were pretreated with 1 significantly against APAP-induced cell damage, and increased cells viability to 77.50%. The flow cytometry results showed that 1 inhibited cell apoptosis and the intracellular reactive oxygen species (ROS) levels in APAP-induced HepG2 cells in a dose-dependent manner (Figs. 6 and 7). The down-regulation expression of oxidative stress proteins, heme oxygenase-1 (HO-1), NAD(P)H dehydrogenase quinone 1 (NQO-1), and catalytic or modify subunit of glutamate-cysteine ligase (GCLC/GCLM), was markedly reversed by the pretreatment of 1. To assess the protective effects of 1 in vivo, a mice model with acute liver injury (ALI) induced by APAP administration was established. As shown in Fig. 7, the levels of serum alanine transaminase (ALT) and aspartate transaminase (AST) in the APAP group sharply increased to 1429.22 ± 82.84 and 1455.47 ± 97.41 U/L, respectively, compared with 36.17 ± 2.96 and 78.37 ± 4.56 U/L in the control group. Pretreatment with 1 (10, 20 and 30 mg/kg) significantly attenuated APAP-induced elevation of ALT and AST levels in a dose-dependent manner. ALT activities decreased to 298.95 ± 20.26, 120.75 ± 13.42, and 66.35 ± 11.03 U/L when pretreated with 10, 20, and 30 mg/kg of 1, respectively, and AST activities decreased to 608.55 ± 29.90, 224.95 ± 23.42 and 169.70 ± 8.67 U/L, respectively. In addition, the APAP-induced hepatic glutathione (GSH) and superoxide dismutase (SOD) depletion (2.80 ± 0.62 µmol/g protein and 192.39 ± 8.23 U/mg protein, respectively) was significantly prevented by pretreatment with 1 at 30 mg/kg (GSH levels increased to 7.16 ± 0.31 µmol/g protein and SOD levels increased to 291.56 ± 13.01 U/mg protein). An evaluation of liver provided further evidence that pretreatment with 1 reversed APAP-induced hepatocellular necrosis, hemorrhaging, and infiltration of inflammatory cells (Fig. 8).
Declaration of competing interest
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The authors declare no competing financial interest.
Acknowledgments
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This work was supported by grants from the National Natural Science Foundation of China (No. 82104032), CAMS Innovation Fund for Medical Sciences (No. 2016-I2M-1-010), and the Drug Innovation Major Project (No. 2018ZX09711001-008).
Supplementary materials
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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2021.10.085
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Year 2022 volume 33 Issue 6
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doi: 10.1016/j.cclet.2021.10.085
  • Receive Date：2021-08-31
  • Online Date：2025-12-19
  • Published：2022-06-15
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  • Received：2021-08-31
  • Revised：2021-10-11
  • Accepted：2021-10-26
Affiliations
    State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China
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表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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