- Research article
- Open Access
Analysis of the main active ingredients and bioactivities of essential oil from Osmanthus fragrans Var. thunbergii using a complex network approach
https://doi.org/10.1186/s12918-017-0523-0
© The Author(s). 2017
- Received: 30 June 2017
- Accepted: 19 December 2017
- Published: 28 December 2017
Abstract
Background
Osmanthus fragrans has been used as folk medicine for thousands of years. The extracts of Osmanthus fragrans flowers were reported to have various bioactivities including free radical scavenging, anti-inflammation, neuroprotection and antitumor effects. However, there is still lack of knowledge about its essential oil.
Methods
In this work, we analyzed the chemical composition of the essential oil from Osmanthus fragrans var. thunbergii by GC-MS. A complex network approach was applied to investigate the interrelationships between the ingredients, target proteins, and related pathways for the essential oil. Statistical characteristics of the networks were further studied to explore the main active ingredients and potential bioactivities of O. fragrans var. thunbergii essential oil.
Results
A total of 44 ingredients were selected from the chemical composition of O. fragrans var. thunbergii essential oil, and that 191 potential target proteins together with 70 pathways were collected for these compounds. An ingredient-target-pathway network was constructed based on these data and showed scale-free property as well as power-law degree distribution. Eugenol and geraniol were screened as main active ingredients with much higher degree values. Potential neuroprotective and anti-tumor effect of the essential oil were also found. A core subnetwork was extracted from the ingredient-target-pathway network, and indicated that eugenol and geraniol contributed most to the neuroprotection of this essential oil. Furthermore, a pathway-based protein association network was built and exhibited small-world property. MAPK1 and MAPK3 were considered as key proteins with highest scores of centrality indices, which might play an important role in the anti-tumor effect of the essential oil.
Conclusions
This work predicted the main active ingredients and bioactivities of O. fragrans var. thunbergii essential oil, which would benefit the development and utilization of Osmanthus fragrans flowers. The application of complex network theory was proved to be effective in bioactivities studies of essential oil. Moreover, it provides a novel strategy for exploring the molecular mechanisms of traditional medicines.
Keywords
- Osmanthus fragrans Var. thunbergii
- Essential oil
- Complex network
- Active ingredients
- Anti-tumor effect
- Neuroprotective effect
Background
Osmanthus fragrans, also known as sweet olive or fragrant olive, is one of the most famous flowers in China due to attractive color and strong fragrance. Various varieties of Osmanthus fragrans flowers have been developed, and divided into four groups, Semperfloren, Thunbergii, Latifolius and Aurantiacus [1]. The cultivation and production of O. fragrans var. thunbergii group was more abundant than those of other groups [2]. This variation is considered to have higher market value and widely used in food chemistry [3].
Osmanthus fragrans flowers have been used as folk medicine for a long time in the treatment of rheumatism, cough and stomachache [4]. Extracts of Osmanthus fragrans flowers have been reported to exhibit various bioactivities both in vitro and in vivo. Water extract of the flower showed a potential to suppress TGF-β1-induced pulmonary fibrosis in human lung fibroblasts cells [5]. Acetonic extract of the flower exhibited antioxidant activity and melanogenesis inhibitory effect in murine melanoma cells [6]. Ethanol extract of the flower was reported to have neuroprotective and free radical scavenging effects [7]. Moreover, it also showed the ability of reducing allergic airway inflammation and oxidative stress in mice [8].
Essential oil is the volatile oil extracted from plants with strong aromatic components and distinctive odour, which has been widely used as a major raw material of perfume or cosmetic [9]. The essential oil is an excellent source of bioactive compounds, and exhibits various activities such as antioxidant and antimicrobial effects [10]. Therefore, it is considered to be partly responsible for the biomedical functions of plants [11]. Previous reports about O. fragrans var. thunbergii essential oil were mainly focused on its chemical composition. A broad group of low-molecular compounds were found in this essential oil, including linalool oxide, ocimene, 2,6-octadien-1-ol, 3,7-dimethyl-2-butanone, 3,7-dimethyl-β-ionone, and so on [12, 13]. However, the main active ingredients and bioactivities of this essential oil were still not fully elucidated.
One of the main causes for difficulties in the bioactivity study of O. fragrans var. thunbergii essential oil is the complexity of its chemical composition. Recently, complex network approach has emerged in the pharmacological researches, which was also known as “network pharmacology” or “system pharmacology” [14, 15]. This methodology holds a significant potential for extracting biological information from large amounts of chemical data [16], and enables to predict the target profiles and pharmacological actions of herbal compounds [17, 18]. For instance, Chandran et al. performed a network to evaluate the immunomodulatory activity of Withania somnifera, and revealed a series of novel bioactive immune target combinations. Chen et al. constructed a multi-parameter network model on the basis of three important parameters to tentatively explain the anti-fibrosis mechanism of herbal medicine Sophora flavescens [19]. Luo et al. used systems pharmacology strategies for anticancer drug discovery based on natural products [20]. In addition, Gogoi et al. developed a network pharmacology-based virtual screening of natural products from Clerodendrum species for identification of novel anti-cancer therapeutics [21]. These studies demonstrate that complex network approach has real potential for bioactivity study of natural products [22, 23].
In this study, we applied the complex network method to evaluate the main active ingredients and bioactivities of O. fragrans var. thunbergii essential oil. GC-MS was used to analyze ingredients of this essential oil. An ingredient-target-pathway network was constructed, and that statistical characteristics of the network were calculated to determine the key nodes. The nodes associated with the key pathway were extracted and reorganized as a core subnetwork to explore the underlying mechanism. Furthermore, a pathway-based protein association network was also built to investigate interrelationships between target proteins of O. fragrans var. thunbergii essential oil.
Methods
Plant material and sample preparation
Fresh flowers of O. fragrans var. thunbergii were collected from the campus of Baoji University of Art and Science (106°18′ E, 33°35’N, 618 m altitude), Baoji, China, in late September, 2015. The plant species was identified and confirmed by Prof. Xiaomei Wang, Shaanxi Key Laboratory of Phytochemistry, Baoji University of Art and Sciences. The flowers (BJWLXY-CC-SKLP150915) were dried in the shade at 25 °C until the humidity lower than 30%, and conserved in an airtight polyethylene bag at −20 °C. Samples (10 g) were extracted by steam distillation. The distilled liquid was then extracted with n-hexane, and dehydrated with anhydrous magnesium sulfate, followed by evaporation. Residual essential oil was stored at −20 °C until use.
Chemical ingredients database building
GC-MS was used to analyze chemical ingredients of O. fragrans var. thunbergii essential oil. The essential oil was diluted in n-hexane (≥99%, GC grade, Sigma-Aldrich), and filtrated using a 0.22 μm filter. A blank (n-hexane) was prepared equally as the essential oil sample, and used as control sample. A measure of 1 μL sample was injected into a Trace 1300 GC coupled with an ISQ LT MS (Thermo, USA). Chromatographic separation was accomplished on a TG-5 column (30 m × 0.25 mm i.d.; film thickness: 0.25 μm; Thermo, USA). Temperature programming was set to 60 °C held for 2 min, then rose to 120 °C at 3 °C/min, maintained for 4 min, finally increased to 290 °C at 3 °C/min and held for 2 min. The inlet temperature was kept at 280 °C and ion source temperature was 270 °C. Helium was used as carrier gas at a constant flow rate of 1 mL/min. Electron impact ionization source (70 eV) was used at full scan mode (m/z 50-550).
Ingredients of O. fragrans var. thunbergii essential oil were identified by NIST 14 (National Institute of Standards and Technology, Gaithersburg, MD, USA) with a similarity of more than 70%. Retention indexes (RI) was also evaluated, using a saturated n-alkane mixture (C9-C36, Sigma Chemical, St. Louis, MO, USA). RI value for each component was calculated by AMDIS version 2.70 (Automated Mass Spectrometry Deconvolution and Identification System).
Lipinski’s five rules were applied to evaluate drug-like properties of the identified compounds in O. fragrans var. thunbergii essential oil [24]. A few important pharmaceutical properties were investigated using Pubchem (https://pubchem.ncbi.nlm.nih.gov/) and TCMSP (http://ibts.hkbu.edu.hk/LSP/tcmsp.php) [25], including molecular weight (MW < 500), number of donor atoms for H-bonds (HBD < =5), number of acceptor atoms for H-bonds (HBA < =10), and octanol-water partition coefficient (Mlog P < =5).
Collection of target proteins and pathways analysis
Potential target proteins of the ingredients in O. fragrans var. thunbergii essential oil were collected using cyber tools such as SuperPred (http://prediction.charite.de/) and DrugBank (https://www.drugbank.ca/). Targets having interaction data for less than five compounds have been removed in the database. Information of all the selected proteins were converted and uniformed by Uniprot (http://www.uniprot.org/). In addition, ingredients without any target proteins were excluded.
Pathway analysis was performed on the selected target proteins utilizing KEGG pathway database (http://www.kegg.jp/kegg/). The database contains information about signal transduction, biological processes of cells, and homologous conservative path information of more than 700 species. The queried species in this study is Homo sapiens. Pathway analysis was carried out with a P-value threshold of 0.01.
Network construction
The collected data were analyzed using complex network method. First, an ingredient-target-pathway network was constructed based on their interrelationships, designed to screen main active components and bioactivities of O. fragrans var. thunbergii essential oil. In this network, nodes represented ingredients, target proteins or pathways collected in previous steps, respectively. If a protein was the hit target of any ingredients, or involved in any pathways, connections were made between these nodes. Subsequently, targets and ingredients connected to the most important biological pathway were extracted from the ingredient-target-pathway network, and reconstructed as a core subnetwork to explore the underlying mechanism. Moreover, a pathway-based protein association network was built to evaluate the closeness of interaction between target proteins. If two proteins were both involved in common pathways, a connection was made between them. Isolated nodes were excluded from the network. All the networks for O. fragrans var. thunbergii essential oil were constructed and visualized by Pajek ver. 2.00 (Batagelj and Mrvar, 2009).
Statistical analysis of the network
A series of parameters of the networks for O. fragrans var. thunbergii essential oil were investigated for more interpretation. Degree (k) was first calculated and ranked to evaluate the importance of a node. The degree k i indicates the number of edges connecting to the node i. Mean value of k i for all nodes in the network is defined as average degree, denoted as ⟨k⟩. Degree distribution, the proportion of randomly selected nodes with a certain number of connections, was represented as P(k).
Results
Chemical composition of O. fragrans Var. thunbergii essential oil
The yield of O. fragrans var. thunbergii essential oil was 0.19% (w/w, on a dry weight basis). Pharmaceutical potentials of herbal medicines are determined by their chemical compositions [27]. In the present study, a total of 91 compounds were identified from the essential oil, including alcohols, ketones, esters, hydrocarbons, terpenes, aldehydes, acids, and so on. Total ions chromatogram (TIC) of the sample was shown in Additional file 1, and that chemical information of identified compounds was listed in Additional file 2. Alcohols and ketones were major ingredients of the essential oil. This essential oil has highest concentration of dihydro-β-ionol, followed by β-ionone, (2,6,6-trimethyl-2-hydroxycyclohexylidene) acetic acid lactone and γ-decalactone. In order to narrow the scope of potential active ingredients, pharmaceutical properties of these compounds were researched. After the preliminary screening, 79 ingredients were reserved for the next step.
In previous reports, Xin et al. characterize the volatiles in flowers of four cultivar groups of sweet osmanthus (Wuhan, China), and that 71 compounds were found in Thunbergii cultivars. β-ionone, cis-linalool oxide (furan), trans-linalool oxide (furan) and linalool were the most common volatiles [3]. Hu et al. identified 52 components from O. fragrans var. thunbergii essential oil (Xianning, China), and that 1,2-epoxy linalool was the main component. Lei et al. identified 45 compounds in water-soluble essential oil components from O. fragrans var. thunbergii flowers (Hangzhou, China), which was rich in linalool oxide, 4-methoxyphenethyl and 4-hydroxyphenethyl alcohol [28]. Chemical composition of O. fragrans var. thunbergii essential oil revealed in the present study was generally consistent with other reports, but differed in percentages of individual components. This might because that compounds in O. fragrans var. thunbergii flowers varied among different geographical origins and flowering stages [2, 29].
Target proteins and related pathways
Proteins are crucial for herbal medicines to achieve therapeutic effects in vivo. In order to explore potential bioactivities, we collected target proteins for the selected ingredients of O. fragrans var. thunbergii essential oil. A total of 191 target proteins were obtained (Additional file 3), including ornithine decarboxylases, adenosine receptors, hydroxyacid oxidases, and so on. It suggested that this essential oil might have various bioactivities. In addition, we excluded ingredients with no hit targets. Only 44 ingredients were reserved for further study (Additional file 3).
Pathway analysis was applied on target proteins of O. fragrans var. thunbergii essential oil for further interpretation, and the results showed that these proteins were involved in 70 biological pathways (Additional file 3), calcium signaling pathway, nitrogen metabolism, pentose and glucuronate interconversions, cytochrome P450, and so on. These pathways were critical in several important biological processes such as signal transduction, drug metabolism and energy metabolism, which indicated that O. fragrans var. thunbergii essential oil might have various bioactivities.
The ingredient-target-pathway network
Ingredient-target-pathway network of O. fragrans var. thunbergii essential oil. The network consisted of 44 compounds (red nodes), 191 hit targets (yellow nodes), 70 related pathways (green nodes), and 879 connections. Numbers and names of nodes are listed in Additional file 3
Degree distribution of the ingredient-target-pathway network. k represents degree values, and that P(k) indicates degree distribution
Main active ingredients of O. fragrans Var. thunbergii essential oil
As interaction between small molecule and protein plays a critical role in modulating the intrinsic biological processes, the information related to protein targets and small molecule has been highly valued by biomedical and pharmaceutical sciences. Target proteins are often those important ones in the development of specific diseases within the organism. Perturbing their functions by druggable molecules will help to cure the disease or relieve the symptoms [30]. Therefore, more attention was paid to highly connected ingredients of O. fragrans var. thunbergii essential oil in this study.
Degree values (k) of all nodes in the ingredient-target-pathway network, shown in descending order
Potential anti-tumor effect of O. fragrans Var. thunbergii essential oil
In the target proteins of O. fragrans var. thunbergii essential oil, MAPK1 (MK01, k = 33) and MAPK3 (MK03, k = 31) had much higher degree values than others (Fig. 3). This indicated that the two proteins were associated with most ingredients and pathways in the network. They were considered as hub nodes and had significant impact on bioactivities of the essential oil. MAPK1 and MAPK3 were members of MAPKs family, which played an important role in MAPK/ERK cascade. Once universally activated, this pathway could block apoptosis, whereas the inhibition of MAPK/ERK is closely associated with anti-tumor effect [38]. MAPK1 and MAPK3 have been reported to be associated with various types of cancer, such as prostate cancer, colorectal cancer and gastric cancer [39–41].
A few compounds in this essential oil also showed a potential strong tumor-inhibiting activity through some other target proteins. p53 is one of the most intensively studied tumor suppressor proteins, with mutations that lead to loss of wild-type p53 activity frequently detected in many different tumor types [42]. In this study, p53 was the target protein of cis-anethol. It was involved in 15 pathways in the network, which were all closely correlated to tumor progression, such as apoptosis, pancreatic cancer, glioma, and melanoma. This protein, together with the hub proteins MAPK1 and MAPK3, all belong to MAPK signaling pathway (k = 12).
EGFR is another important protein in relation to tumor development [43]. Signaling by EGFR plays a key role in tumorigenesis prompted efforts to target this receptor in anticancer therapy [44]. It was the target protein of the selected main active ingredients, geraniol and eugenol. This protein was involved in 18 pathways in the network, most of which were tumor-related, such as ErbB signaling pathway, bladder cancer, endometrial cancer and colorectal cancer.
In addition, pathway analysis showed that several target proteins of O. fragrans var. thunbergii essential oil were involved in many tumor-related pathways (Additional file 2), including cytochrome P450 (k = 22), non-small cell lung cancer (k = 10), prostate cancer (k = 8), small cell lung cancer (k = 7), VEGF signaling pathway (k = 6), prostate thyroid cancer (k = 6), Wnt signaling pathway (k = 5), tyrosine metabolism (k = 4), and so on. These data suggested a potential anti-tumor effect of O. fragrans var. thunbergii essential oil.
There were also many reports about the anti-tumor effect of Osmanthus fragrans. Compounds isolated from ethyl acetate extract of Osmanthus fragrans var. aurantiacus flower could inhibit the growth of human colon cancer cell line HCT-116 [45]. Pomolic acid, isolated from flowers of O. fragrans var. aurantiacus Makino, could induce apoptosis in SK-OV-3 human ovarian adenocarcinoma cells [46]. These reports were consistent with the assumption that O. fragrans var. thunbergii essential oil had a potential anti-tumor effect.
Potential neuroprotective effect of O. fragrans Var. thunbergii essential oil
The key pathway node of the network was neuroactive ligand-receptor interaction (Fig. 3). This pathway was connected with a total of 50 proteins, which meant that more than a quarter of target proteins of O. fragrans var. thunbergii essential oil were involved in it. Neuroactive ligand-receptor interaction contains a collection of receptors and ligands, and is closely related to neurological function and neurodegeneration diseases [47]. Coincidentally, some target proteins of this essential oil were proved to be enriched in Alzheimer’s disease (k = 8, Additional file 2), one of the best known neurodegeneration diseases. Besides, it has been reported that ethanol extract of dried O. fragrans var. thunbergii flowers had neuroprotective effect in Wistar rat [7]. Extract of this flower was also found to protect D-galactose induced aging in mouse model [48]. These data suggested a possible neuroprotection of O. fragrans var. thunbergii essential oil.
The core subnetwork
Core subnetwork of O. fragrans var. thunbergii essential oil. The network consisted of 59 nodes and 150 connections. Red nodes represent ingredients, yellow nodes indicate target proteins, and that green nodes refers to neuroactive ligand-receptor interaction. Numbers and names of the nodes are listed in Additional file 3
Eugenol has been reported to protect neuronal cells from excitotoxic and oxidative injury [49]. Neuroprotective efficacy of eugenol was also found in acrylamide-induced neuropathy in rats [50]. Geraniol showed a neuroprotective effect in an acrylamide model of neurotoxicity in Drosophila melanogaster [51]. Additionally, geraniol was reported to be beneficial for the treatment of Parkinson’s disease associated with neuromuscular disability. These reports further confirmed that eugenol and geraniol played an important role in the neuroprotective effect of O. fragrans var. thunbergii essential oil.
The pathway-based protein association network
Pathway-based protein association network of Osmanthus fragrans var. thunbergii essential oil. The network consisted of 142 nodes and 2102 connections. Nodes represent target proteins of selected ingredients in Osmanthus fragrans var. thunbergii essential oil. Connections indicate that two proteins are involved in common pathway. Numbers and names of the nodes are listed in Additional file 3
Statistics for the degree distribution of the pathway-based protein association network
k | Frequency a | Frequency% b | k | Frequency | Frequency% | k | Frequency | Frequency% |
---|---|---|---|---|---|---|---|---|
58 | 1 | 0.70 | 24 | 4 | 2.82 | 11 | 9 | 6.34 |
57 | 10 | 7.04 | 23 | 2 | 1.41 | 10 | 12 | 8.45 |
55 | 1 | 0.70 | 21 | 1 | 0.70 | 9 | 2 | 1.41 |
54 | 1 | 0.70 | 20 | 1 | 0.70 | 8 | 4 | 2.82 |
53 | 15 | 10.56 | 19 | 3 | 2.11 | 7 | 5 | 3.52 |
49 | 24 | 16.90 | 17 | 1 | 0.70 | 4 | 1 | 0.70 |
48 | 3 | 2.11 | 16 | 2 | 1.41 | 3 | 1 | 0.70 |
42 | 1 | 0.70 | 15 | 2 | 1.41 | 2 | 5 | 3.52 |
28 | 13 | 9.15 | 14 | 6 | 4.23 | 1 | 1 | 0.70 |
27 | 3 | 2.11 | 13 | 2 | 1.41 | |||
26 | 3 | 2.11 | 12 | 3 | 2.11 |
Distribution of clustering coefficient of the pathway-based protein association network. N represents number of nodes with a specific value of clustering coefficient
Top ten nodes with the highest values of centrality indices in the pathway-based protein association network
No. a | Protein name b | Cd c | No. | Protein name | Cb d | No. | Protein name | Cc e |
---|---|---|---|---|---|---|---|---|
175 | EGFR | 0.411 | 166 | PGH2 | 0.177 | 207 | KPCA | 0.500 |
149 | ADRB1 | 0.404 | 234 | PP2BA | 0.109 | 126 | MK01 | 0.496 |
156 | BKRB2 | 0.404 | 207 | KPCA | 0.093 | 232 | MK03 | 0.496 |
170 | DRD1 | 0.404 | 252 | HCD2 | 0.082 | 234 | PP2BA | 0.496 |
194 | ACM3 | 0.404 | 126 | MK01 | 0.082 | 175 | EGFR | 0.447 |
195 | ACM2 | 0.404 | 232 | MK03 | 0.082 | 149 | ADRB1 | 0.445 |
197 | ACM5 | 0.404 | 175 | EGFR | 0.069 | 156 | BKRB2 | 0.445 |
198 | ACM1 | 0.404 | 282 | TYRO | 0.049 | 170 | DRD1 | 0.445 |
209 | 5HT2C | 0.404 | 192 | AOFA | 0.036 | 194 | ACM3 | 0.445 |
210 | 5HT2A | 0.404 | 261 | ADH1B | 0.027 | 195 | ACM2 | 0.445 |
Three-dimensional diagram illustrating centrality indices of nodes in the pathway-based protein association network
KPCA, also known as protein kinase C alpha type, is involved in several important processes such as cell proliferation, apoptosis, tumorigenesis, cardiac hypertrophy and angiogenesis. The expression levels of KPCA were reported to be closely related to esophageal carcinoma [39]. EGFR is the abbreviation of epidermal growth factor receptor. Mutation in EGFR could induce non-small cell lung cancer [41]. PP2BA (serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform) has a role in the calmodulin activation of calcineurin, and is considered to be associated with human neurodegenerative disease [40]. These reports further supported the assumption that O. fragrans var. thunbergii essential oil had anti-tumor and neuroprotective effects.
Previous network analysis has revealed that MAPK1 (mitogen-activated protein kinase 1) and MAPK3 (mitogen-activated protein kinase 3) were hub nodes of the ingredient-target-pathway network. Furthermore, they were also screened as key proteins of the pathway-based protein association network. Consistency of the results indicated that the two proteins were not only associated with most ingredients and pathways, but also closely related to other target proteins of the essential oil. These data provided further support for the potential anti-tumor effect of O. fragrans var. thunbergii essential oil.
Discussion
Although geraniol and eugenol together accounted for only 1.5% of the O. fragrans var. thunbergii essential oil (Additional file 2), these two compounds showed potential of strong bioactivity and acceptable cytotoxicity at the level of quantity according to previous reports. Geraniol originated from geranium essential oil was reported to show 312.5 μg/mL minimum inhibitory concentrations (MIC) against many species of bacteria such as E. coli, Mycobacterium smegmatis, Pseudomonas aeruginosa, Salmonella typhi, and Yersinia enterocolitica. Moreover, 100 μg/mL strong activity of geraniol was also found against Staphylococcus epidermidis and Streptococcus mutans [55]. Inhibitory concentration 50% values (IC50) for the anti-HSV effects of eugenol were 25.6 mg/mL and 16.2 mg/mL for HSV-1 and HSV-2 respectively, together with a maximum dose of 250 mg/mL for cytotoxicity test in the mouse model [56]. These reports supported the assumption that eugenol and geraniol were the main active ingredients of O. fragrans var. thunbergii essential oil.
Conclusions
This study presents one of the first complex network analysis for evaluating active ingredients and bioactivities of plant essential oil. We analyzed the ingredients of O. fragrans var. thunbergii essential oil, and collected target proteins and related pathways for the selected compounds. Three networks were constructed based on these data to investigate the interrelationships. Topological Statistical analysis of these networks revealed that eugenol and geraniol were the main active ingredients of this essential oil. The essential oil also showed potential anti-tumor and neuroprotective effect, which were strongly supported by previous reports about Osmanthus fragrans [45, 46, 48, 49, 51]. Results of this work suggested a possible application of O. fragrans var. thunbergii essential oil in oncotherapy and neurological disorders, that would benefit the development and utilization of Osmanthus fragrans flowers. Complex network theory was also proved to be effective in bioactivities studies of essential oil. Moreover, it provides a novel strategy for exploring the molecular mechanisms of traditional medicines.
Declarations
Acknowledgments
None.
Funding
This work is supported and sponsored by the Shaanxi Science and Technology Commission (No. 2014JM2058), and Shaanxi Education Commission (No. 13JS005), the Key Project of Baoji University of Arts and Sciences (ZK 16053), the Innovation and Entrepreneurial Programme for Undergraduate (201610721019).
Availability of data and materials
Datasets supporting the results of this article are also included in the additional files.
Authors’ contributions
LW and TN collected data for the study. LW and TN performed data analysis. HW and JH conceived and designed the study. LW and XW wrote the manuscript. DD, LM, JX revised the manuscript. All authors have read and approved the manuscript.
Ethics approval and consent to participate
Not applicable
Consent for publication
Not applicable
Competing interests
The authors declare that they have no competing interests.
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Authors’ Affiliations
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