
Amygdalin ameliorates the progression of atherosclerosis in LDL receptor‑deficient mice
- Authors:
- Published online on: September 25, 2017 https://doi.org/10.3892/mmr.2017.7609
- Pages: 8171-8179
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Copyright: © Lv et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
It is widely acknowledged that atherosclerosis is the principal cause of cardiovascular disease, which ultimately contributes to mortality rates (1,2). Although hypercholesterolemia, smoking, male gender, hypertension, diabetes and age are traditionally considered to be risk factors, accumulating evidence indicates that hyperlipidemia is the major risk factor underlying the formation and development of atherosclerosis (3,4). During the initiation of atherosclerosis, plasma low-density lipoprotein (LDL) accumulates in the arterial wall, oxidized, and recruits circulating monocytes (5). When monocytes transform into macrophages, they uptake oxidized (ox) LDL, resulting in substantial cholesterol accumulation and the formation of foam cells, which ultimately lead to formation of the atherosclerotic lesion. In this multifactorial process, endothelial cells, smooth muscle cells, macrophages and lymphocytes are involved and interact. Increasing experimental evidence suggests that during this process, an array of cytokines and adhesion molecules are involved and promote atherogenesis (6,7). The innate and adaptive immune responses are also pivotal in the pathogenesis of atherosclerosis (8). Therefore, as a result of the multiple interactions, atherosclerotic plaques are formed, which ultimately results in cerebrovascular events and acute coronary syndromes.
Amygdalin (vitamin B17, also known as Laetrile), is extracted from Semen Persicae, the seed of Prunus Persica (L.) Batsch. Amygdalin is also found in abundance in the seeds of apricots, almonds, peaches and other rosaceous plants. To date, amygdalin has been widely used for the treatment of asthma, bronchitis, emphysema, leprosy, diabetes and cancer. The authors' previous study on amygdalin suggested that it may stimulate the immune system and exhibits immune modulation functions by the regulation of regulatory T cells (Tregs) in apolipoprotein E-deficient (ApoE)−/− mice. As ApoE−/− mice are spontaneous atherosclerotic mice, in order to determine whether amygdalin can alleviate high-fat/high-cholesterol induced atherosclerosis, LDLR−/− mice were used in the present study. It has been demonstrated that the cytokines produced by T cells, including interleukin (IL)-6 and tumor necrosis factor (TNF)-α, and macrophages, including IL-1β, affect the extent and nature of the atherosclerotic plaque (9,10). The authors' previous study on the anti-atherosclerotic effect of amygdalin demonstrated that the expression levels of IL-10 and transforming growth factor (TGF)-β were markedly increased in the serum of the amygdalin-treated mice. Therefore, it was hypothesized that amygdalin possesses a broader immune-regulative function on atherogenesis and is critical in the regulation of Tregs in high-fat/high-cholesterol diet-induced atherosclerotic LDLR−/− mice. To confirm this hypothesis, the present study aimed to determine whether the expression levels of TNF-α, IL-1β and IL-6 can be regulated by amygdalin. It is well known that Tregs have a protective role in the progression of atherosclerosis (11) and they are considered to be a therapeutic target for the treatment of atherosclerosis. The authors' previous studies suggested that Tregs can be induced and expanded by amgydalin (12). Therefore, to further substantiate the hypothesis, the expression of forkhead box P3 (Foxp3) was silenced through Foxp3-specific short hairpin (sh)RNAs and the expression levels of the cytokines were observed. Previous clinical investigations of matrix metalloproteinase (MMP)-2 and MMP-9 demonstrated that MMP-9 activity was found in macrophage-rich lesions, whereas the expression of MMP-2 was higher in lesions rich in smooth muscle cells, indicating that MMP-2 and MMP-9 are tightly associated with stable and vulnerable lesions (13). In order to elucidate the mechanism underlying the anti-atherosclerotic function of amygdalin, the present study also examined the expression levels of MMP-2 and MMP-9. Therefore, in order to determine whether amygdalin treatment attenuates plaque progression and alleviates the symptom of atherosclerosis, the present study focused on the immune regulatory function of amygdalin.
Materials and methods
Animals
The LDLR−/− mice were purchased from Jackson Laboratories (Bar Harbor, ME, USA) and maintained in a 12-h light/dark cycle in an atmosphere of 0.03% CO2 with free access to water and food. In accordance with the individual ventilated cage requirements of Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital (Sichuan, China), all mice were raised under specific pathogen-free conditions with controlled temperature (23±2°C). The use and handling of animals were in accordance with the Ethics Committee of Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital.
Study design
Amygdalin was purchased from Changsha Staherb Natural Ingredients Co., Ltd. (Changsha, Hunan, China). The 8-week-old male mice were divided into five groups (n=30 in each group, and body weight range of ~22–24 g): i) LDLR−/− control group (control): 8-week-old male LDLR−/−mice were fed a standard laboratory diet (10% fat, 15% protein and 75% carbohydrate); ii) LDLR−/− high-fat diet (HFD) control group (LDLR−/−): 8-week-old male LDLR−/− mice were fed an HFD containing 40% fat, 14% protein and 46% carbohydrate for 12 weeks; iii) Amygdalin (Low) group: 8-week-old male LDLR−/− mice were fed the HFD for 12 weeks and amygdalin (1 mg/kg/day for 4 weeks consecutively) was injected intraperitoneally; iv) Amygdalin (medium) group: 8-week-old male LDLR−/− mice were fed the HFD for 12 weeks and amygdalin (3 mg/kg/day for 4 weeks consecutively) was injected intraperitoneally; v) Amygdalin (high) group: 8-week-old male LDLR−/− mice were fed the HFD for 12 weeks and amygdalin (10 mg/kg/day for 4 weeks consecutively) was injected intraperitoneally. All groups of mice were sacrificed following 4 weeks of drug delivery.
Lipid profile and cytokine measurements
For measuring total cholesterol content, blood samples were collected from each mouse at the beginning and end of amygdalin treatment. Total plasma cholesterol (TC) and triglyceride (TG) levels were determined using commercial kits (Applygen Technologies, Inc., Beijing, China). The levels of murine IL-1β, TGF-α and IL-6 were assayed using ELISA kits with paired antibodies according to the manufacturer's protocol (R&D Systems, Inc. Minneapolis, MN, USA).
Assessment of aortic sinus atherosclerosis
The hearts and upper sections of the aorta were removed from the mice, fixed, embedded in paraffin and sectioned (5-µm). The sections were then stained with hematoxylin and eosin (cat. no. C0105; Beyotime Institute of Biotechnology, Suzhou, China) and oil red O (cat. no. O0625; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany). Atherosclerotic lesions were quantified by calculating the lesion size in the aortic sinus, as previous described (14,15). The vessel areas were measured using ImageJ software (version 1.47; National Institutes of Health; Bethesda, MD, USA) from images obtained with a Nikon 80i microscope (Nikon Corporation, Tokyo, Japan). For comparisons of plaque areas between the amygdalin groups and control groups, 100 and 200 µm distant sites were used.
Western blot analysis
The proteins were lysed by radioimmunoprecipitation lysis buffer (Beyotime Institute of Biotechnology) and quantified with bicinchoninic method (Beyotime Institute of Biotechnology) as previously described (12). A total of 20 µg protein was loaded onto a NuPageNovex 10% Bis-Tris gel (Thermo Fisher Scientific, Inc.) for electrophoresis. Following electrophoresis, the proteins were transferred onto polyvinylidene fluoride membranes (Pall Life Sciences, Port Washington, NY, USA). The membranes were blocked bovine serum albumin (Sigma-Aldrich; Merck KGaA), and then incubated with primary antibodies overnight at 4°C followed by incubation with horseradish peroxidase (HRP)-conjugated secondary antibody at room temperature for 2 h. Chemiluminescence detection was performed using Immobilon Western Chemiluminescent HRP substrate (EMD Millipore, Billerica, MA, USA), and measured directly using a BioSpectrum imaging system (UVP, Inc., Upland, CA, USA). The mouse monoclonal CD68 (cat. no. sc-20060; 1:1,000), mouse monoclonal MMP-2 (cat. no. sc-13594; 1:500), mouse monoclonal MMP-9 (cat. no. sc-393859; 1:500) and mouse monoclonal β-actin (cat. no. sc-47778; 1:5,000) were purchased from Santa Cruz Biotechnology (Dallas, TX, USA). Rabbit polyclonal monocyte chemoattractant protein-1 (MCP-1; cat. no. ab9899; 1:500) was purchased from Abcam (Cambridge, MA, USA). T cells from the spleen were isolated from the mice in each group. Western blot analysis was performed with mouse monoclonal anti-Foxp3 antibody (cat. no. ab20034; 1:500; Abcam). For the secondary antibody, HRP-conjugated goat anti-mouse IgG polyclonal antibody (cat. no. 115-035-003) and HRP-conjugated goat anti-rabbit polyclonal IgG (cat. no. 111-035-003) were used, which were purchased from Jackson ImmunoResearch Laboratories, Inc. (West Grove, PA, USA). The levels of β-actin were determined as the loading control.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) analysis
Total RNA from the splenocytes and lymphocyte cells was isolated using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.). The primer sequences: FOXP3 forward, 5′-CCCAGGAAAGACAGCAACCTT-3′ and reverse, 5′-TTCTCACAACCAGGCCACTTG-3′; MCP-1 forward, 5′-TTAAAAACCTGGATCGGAACCAA-3′ and reverse, 5′-GCATTAGCTTCAGATTTACGGG-3′; MMP-2 forward, 5′-ACCCAGATGTGGCCAACTAC-3′ and reverse, 5′-TACTTTTAAGGCCCGAGCAA-3′; and MMP-9 forward, 5′-ATGATGGAGGAGAAGCAGTC-3′ and reverse, 5′-AGGTGAAGGGAAAGTGACAT-3′ were used as previously described (12,16,17). The RT-qPCR analysis was performed on an ABI 7900 system using Applied Biosystems Power SYBR® Green PCR Master mix (Thermo Fisher Scientific, Inc.) in triplicate (18). In brief, 0.5 µM forward and reverse primes, 2 µl buffer and 100 ng cDNA templates were added to each tube and the total volume was adjusted to 20 µl by RNase free water (Thermo Fisher Scientific Inc.). Following 3 min denaturation at 95°C; amplification was performed for 35 cycles, including 95°C for 10 sec for denaturation and 55°C for 30 sec for annealing and extension. The copy number was calculated using the 2−ΔΔCq method. The Cq value for GAPDH was used to normalize the samples (19).
Lentivirus preparation and injection
The Foxp3 target sequences were as follows: forward, 5′-GGACACUCAAUGAAAUCUATT-3′; reverse, 5′-UAGAUUUCAUUGAGUGUCCTC-3′ (20). The shRNAs were synthesized and cloned into pTY linkers. Third-generation vectors were used in this experiment. The shRNA lentiviral vector was transiently transfected into 293T cells (Type Culture Collection of the Chinese Academy of Sciences, Shanghai, China). Briefly, the 293T cells were co-transfected with appropriate quantities of vector plasmids, including the helper construct, envelope plasmid, tat plasmid and pTYlinker containing shRNAs. The viral supernatant was harvested at 48 h, filtered through a 0.45-µm filter, subjected to ultracentrifugation (113,000 × g at 4°C for 2 h) for 100-fold concentration and stored at −80°C. Then lentiviral supernatant was thawed at 37°C and diluted in 0.9% saline (Sichuan Kelun Pharmaceuticals, Co., Ltd., Chengdu, Sichuan, China) and polybrene (8 µg/ml final concentration; Sigma-Aldrich; Merck KGaA) to give a dose of 1.6×107 or 1.6×108 transducing units in a 50 µl injection volume. The virus was injected intravenously into the mice with a 30-gauge needle on a 1-cc syringe. After the LDLR−/− mice were confirmed as atherosclerotic, 3 consecutive injections were administered at 3-day intervals (n=6).
Statistical analysis
The effects of treatment on the lesions, plaque compositions, levels of IL-1β, IL-6 and TNF-α, and mRNA levels were calculated using one-way analysis of variance and Bonferroni/Dunn's test or Student's t-test by GraphPad Prism™ software (version 5.0; GraphPad Software Inc., La Jolla, CA, USA). P<0.05 was considered to indicate a statistically significant difference.
Results
Amygdalin regulates lipid composition and the development of atherosclerosis
The authors' previous data indicated that amygdalin attenuated atherosclerosis in ApoE−/− mice. To further examine the therapeutic effect of amygdalin in atherosclerosis, an atherosclerotic mouse model was established in the present study by feeding LDLR−/− mice with an HFD. It was evident from analyzing the lipid profile (Table I), that the TG levels and TC levels were increased in the LDLR−/− mice. However, these changes were alleviated when the mice were treated with amygdalin. A high dose of amygdalin resulted in the 2-fold decrease in TG levels, compared with those in the LDLR−/− mice (P<0.05). By comparing the TC and LDL levels between the drug delivery groups and corresponding control groups, it was found that the mice treated with amygdalin had decreased levels of TC and LDL (P<0.05). In addition, increased levels of HDL were observed in the amygdalin-treated mice (P>0.05). Therefore, amygdalin regulated lipid contents in the HFD-treated LDLR−/− mice.
As the atherosclerotic lesions in the LDLR−/− mice fed with the HFD demonstrated the same morphological characteristics as those of humans, and the mouse model imitated the progression of atherosclerosis, the aortic sinus was stained with H&E and oil red O in the present study (Fig. 1A). The atherosclerotic plaques were well developed in the LDLR−/− mice. By contrast, no atherosclerotic plaques were found in the amygdalin-treated mice. The, vessel areas, lumen areas and plaque areas were also analyzed. As exhibited in Fig. 1B, with the progression of atherosclerosis, the diameters of the aortic sinus increased. In addition, the areas of the lumen were decreased (Fig. 1C) and those of the plaques were increased (Fig. 1D) in the LDLR−/− mice. By contrast, the mice treated with amygdalin exhibited a significantly reduced extent of atherosclerosis, evident by the smaller aortic sinus plaques, smaller aortic sinus and expanded lumen are as. This finding was confirmed by the analysis of atherosclerosis surface coverage areas (Fig. 1E), showing decreased lesions in the amygdalin-treated LDLR−/− mice. Therefore, these data indicated that amygdalin inhibited the HFD-induced increase in atherosclerotic lesions in the LDLR−/− mice.
Amygdalin inhibits the inflammatory response
To investigate whether amygdalin inhibits inflammation in the aorta of LDLR−/− mice, the present study compared the mRNA and protein levels of MCP-1, CD68, MMP-2 and MMP-9 in the atherosclerotic arteries. As shown in Fig. 2A and B, the LDLR−/− mice exhibited a marked increase in the expression levels of CD68, MCP-1, MMP-2 and MMP-9. As expected, decreased activities of CD68, MCP-1, MMP-2 and MMP-9 were observed following amygdalin treatment. In addition, to further confirm the inhibitory function of amygdalin in inflammation, plasma inflammatory markers were assessed. As predicted, the analysis of serum inflammatory cytokines revealed that amygdalin markedly reduced the secretion of IL-1β (Fig. 3A), IL-6 (Fig. 3B), and TNF-α (Fig. 3C).
Amygdalin inhibits the progression of atherosclerosis via the induction of Tregs
To determine whether the presence of Tregs is associated with lipid profile changes and inhibited inflammatory responses following amygdalin delivery, the present study investigated the mRNA and protein levels of Foxp3 in splenocytes and peripheral blood cells. Following quantification of them RNA levels of Foxp3, the mRNA levels in peripheral blood cells were increased by 6.3-fold (Fig. 4A), and the mRNA levels in splenocytes were increased by 3.5-fold (Fig. 4B) in the groups treated with a high-dose of amygdalin, compared with the untreated groups (P<0.05). Even in the groups treated with a low dose of amygdalin, the mRNA levels of Foxp3 in the peripheral blood cells and splenocytes were markedly elevated. There was also a marked increase in the protein levels of Foxp3in the amygdalin-treated groups (Fig. 4C).
A previous report indicated that the deletion of Foxp3 results in the absence of functional Tregs in the periphery and a conditionally active form of Foxp3 induces the reprogramming of human T cells into Tregs (21). To further establish that Tregs are induced by amygdalin, the knockdown of Foxp3mRNA was achieved using a lentiviral vector carrying shRNA (Fig. 5A), following which serum proinflammatory cytokines were assessed. As expected, the levels of IL-1β (Fig. 5B), IL-6 (Fig. 5C) and TNF-α (Fig. 5D) were significantly increased in the amygdalin-treated mice bearing Foxp3 shRNA. These data indicated that amygdalin attenuated the development of atherosclerosis via the regulation of Tregs and proinflammatory cytokines in LDLR−/− mice.
Discussion
The authors' previous studies on amygdalin in ApoE−/− mice demonstrated that amygdalin ameliorated the progression of atherosclerosis by the regulation of Tregs (12). However, to assess the regulatory role of amygdalin on atherosclerosis induced by a western diet, the LDLR−/− mouse model was used in the present study. Unlike ApoE−/− mice, a spontaneous atherosclerotic model, LDLR−/− mice do not develop atherosclerosis if they are not fed with an HFD. A previous study demonstrated that the oral administration of oxLDL induced attenuated atherosclerosis in LDL−/− mice (22), indicating that the abnormal lipid composition is involved in the progression of atherosclerosis. The present study demonstrated that amygdalin significantly inhibited the development of atherosclerosis in LDLR−/− male mice fed an HFD as a western-style diet. These mice, in addition to exhibiting hypercholesterolemia, exhibited hypertriglyceridemia, therefore, they exhibited the clinical features of human hypercholesterolemia and hypertriglyceridemia. On comparing the blood cholesterol levels, blood lipids were significantly decreased following amygdalin treatment. This observation was consistent with our previous study in ApoE−/− mice, indicating that amygdalin is critical in the regulation of lipid profiles. Of note, in the present study, the HFD produced more advanced atherosclerotic lesions in the LDLR−/− mice.
There is increasing evidence that cytokines produced by CD4+ T cells and macrophages, including TNF-α, IL-1β and IL-6, affect the extent and nature of the atherosclerotic plaque. A substantial number of clinical studies have shown that the plasma concentration of TNF-α is associated with the degree of atherosclerosis (23,24). To date, epidemiological studies have found that several inflammatory mediators, including IL-6 and TNF-α, appear to be elevated in association with increased vascular risk, indicating cytokine-mediated inflammation is present in the early stages of atherogenesis (25,26). Huber et al demonstrated that the injection of recombinant IL-6 exacerbated development of the early lesion of atherosclerosis in mice (27). Studies on IL-1β have also indicated that the overexpression of IL-1β occurs in various inflammatory diseases, including atherosclerosis, and a reduction of IL-1β decreases the severity of atherosclerosis in ApoE−/− mice (28,29). Studies by Kirii et al demonstrated a significant decrease in atherosclerotic lesions at the aortic sinus in ApoE−/−/IL-1β−/− mice, and the mRNA levels of MCP-1 in the aorta were improved in these mice (28). Their results indicated that the reduction of IL-1β decreases the severity of atherosclerosis through increasing the expression of MCP-1. It has also been reported that macrophage foam cells and smooth muscle cells express IL-6, indicating that IL-6, in addition to IL-1β and TNF-α, are critical in the progression of atherosclerosis (9). In the present study, it was demonstrated that even a low dose of amygdalin markedly reduces the expression levels of circulating cytokines, including IL-6, IL-1β and TNF-α. However, compared with the low dose group, no significant difference in the reduction of proinflammatory cytokines was observed in when the mice were treated with a high dose of amygdalin.
It is widely acknowledged that Tregs are important in the development of atherosclerosis, confirmed by studies investigating the adoptive transfer of lymphocytes (15,30) and Th2 cytokines produced by Tregs. In the authors' previous study, the anti-atherosclerotic function of amygdalin was demonstrated by its successful induction of Tregs in ApoE−/− mice. However, in the high-fat/high-cholesterol diet-induced atherosclerosis of LDLR−/− mice, whether the anti-atherosclerotic effect of amygdalin is via the regulation of Tregs remains to be elucidated. Foxp3 has been demonstrated to govern the development and function of Tregs (31). Mutations in Foxp3 eliminate CD25+ Tregs and cause autoimmune disorders (32,33). Therefore, the present study also focused on Tregs, and further substantiation of our hypothesis was achieved by the silencing of Foxp3. As expected, elevated mRNA and protein expression levels of Foxp3 were observed in the amygdalin-treated mice. Following silencing of Foxp3, a marked increase in cytokines was observed in the circulation, indicating that the inhibition of Tregs exacerbated the atherosclerotic situation. These results provide evidence that the inhibition of Foxp3 acceleratedthe development of atherosclerosis, even with amygdalin treatment, suggesting that the anti-atherosclerotic effect of amygdalin occurred through the regulation of Tregs.
Although it is widely acknowledged that lipids are central in the pathogenesis of plaques, macrophages, and their secreted cytokines contribute substantially to atherogenesis. It has been reported that M1 macrophages in atheroma may have pro-inflammatory functions, which produce high levels of effectors, including cytokines IL-1β and TNF-α (13). According to the results of the present study, demonstrated in Fig. 3, amygdalin significantly reduced the cytokine secretion of M1 macrophages, suggesting the anti-atherosclerotic effect of amygdalin may be partly due to the inhibition of proinflammatory cytokines. Specifically, the mice treated with a high dose of amygdalin showed significantly decreased expression of CD68, indicating that the high dose of amygdalin exerted a more marked inhibitory effect on proinflammatory cytokines. As atheroma formation also involves the recruitment of T cells and chemokines, the present study examined other factors contributing to atherosclerosis. It has been documented that MCP-1 has a unique and crucial role in the initiation and evolution of atherosclerosis by regulating the migration of monocytes and T-cells into the vessel wall (34,35). In the present study, an increased expression level of MCP-1 was observed in the atherosclerotic mice, however, treatment with amygdalin markedly reduced the chemokine secretion in the region of the lesion. The migration of SMCs also contributes to vascular remodeling during the development and complication of human atherosclerotic lesions. Clinical data show that MMP-2 facilitates the migration and proliferation of SMCs and may be important in atherogenesis (34). Cumulative evidence has demonstrated that MMP-2-deficiency reduces atherosclerotic plaque lesion formation in ApoE−/− mice (7). In clinical studies, that increased MMP-2 and MMP-9 staining was observed in the plaques of expansively remodeled segments, indicating that MMP-2 and MMP-9 may be involved in plaque vulnerability and in expansive arterial remodeling (36). By contrast, deficiency of MMP-9 has also been associated with reduced plaque size, macrophage content and collagen deposition in aortic lesions of ApoE−/− mice (37) and LDLR−/−/Apob100/100 mice (19). In the present study, it was demonstrated that a high dose of amygdalin markedly reduced MMP-9 at the transcription and translation levels, indicating the anti-atherosclerotic effect of amygdalin via the inhibition of MMP-9.
In conclusion, the present study demonstrated that, in the development of atherosclerosis in LDLR−/− mice fed with an HFD (western-style diet), amygdalin inhibited the progression of atherosclerosis. Amygdalin also markedly alleviated hypercholesterolemia and hypertriglyceridemia in the LDLR−/− mice and affected the extent of atherosclerotic lesions. Subsequent investigations on the mechanism of amygdalin-induced anti-atherosclerotic effects revealed that amygdalin inhibited the inflammatory response and induced Tregs. These results demonstrated the potential of amygdalin in the control and treatment of atherosclerosis, and support the potential of the clinical application of amygdalin as a novel anti-inflammatory drug in the prevention of coronary heart disease.
Acknowledgements
The present study was supported in part by the Guangxi Natural Science Foundation for Youth (grant no. 2013GXNSFBA019139), Guangxi Colleges and Universities Science and Technology Research Funding (grant no. ZD2014067), the Guangxi Health and Family Planning Commission Funding (grant no. GZPT13-05), the Guangxi Key Laboratory of Chinese Medicine Foundation Research Funding, Guangxi University of Chinese Medicine (grant no. 13-051-35) and Guangxi Key Laboratory of Common Technology of Traditional Chinese Medicine Preparation Funding, Guangxi University of Chinese Medicine to Dr Jianzhen Lv. The present study was also supported by the Sichuan Health and Family Planning Commission Funding (grant no. 16ZD0253), the Sichuan National Science Research Funding (grant no. 2015JY0183) and the Sichuan Scientific Research Foundation of the Returned Overseas Chinese Scholars to Dr Yi Wang.
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