Search tips
Search criteria 


Logo of ijmsMDPIhomeThis articleThis journalInstructions for authorsSubscribeIJMS
Int J Mol Sci. 2017 March; 18(3): 620.
Published online 2017 March 13. doi:  10.3390/ijms18030620
PMCID: PMC5372635

A Biomedical Investigation of the Hepatoprotective Effect of Radix salviae miltiorrhizae and Network Pharmacology-Based Prediction of the Active Compounds and Molecular Targets

Maurizio Battino, Academic Editor


Radix salviae miltiorrhizae (Danshen in Chinese), a classic traditional Chinese medicine (TCM) herb, has been used for centuries to treat liver diseases. In this study, the preventive and curative potential of Danshen aqueous extract on acute/chronic alcoholic liver disease (ALD) and non-alcoholic fatty liver disease (NAFLD) was studied. The in vivo results indicated that Danshen could alleviate hepatic inflammation, fatty degeneration, and haptic fibrogenesis in ALD and NAFLD models. In the aspect of mechanism of action, the significant reduction in MDA levels in both ALD and NAFLD models implies the decreased levels of oxidative stress by Danshen. However, Danshen treatment could not activate the internal enzymatic antioxidant system in ALD and NAFLD models. To further explore the hepatoprotective mechanism of Danshen, an in silico-based network pharmacology approach was employed in the present study. The pharmacological network analysis result revealed that six potential active ingredients such as tanshinone iia, salvianolic acid b, and Danshensu may contribute to the hepatoprotective effects of Danshen on ALD and NAFLD. The action mechanism may relate with regulating the intracellular molecular targets such as PPARα, CYP1A2, and MMP2 for regulation of lipid metabolism, antioxidant and anti-fibrogenesis by these potential active ingredients. Our studies suggest that the combination of network pharmacology strategy with in vivo experimental study may provide a forceful tool for exploring the mechanism of action of traditional Chinese medicine (TCM) herb and developing novel bioactive ingredients.

Keywords: Radix salviae miltiorrhizae, hepatoprotective, antioxidant, network pharmacology

1. Introduction

Liver disease is one of the most serious health problems worldwide, affecting more than 10% of the world population [1,2]. Alcoholic liver disease (ALD) and nonalcoholic fatty liver disease (NAFLD) are two common types of liver diseases that represent a major health burden in industrialized countries. ALD is caused by excessive alcohol consumption whereas NAFLD is related with obesity and metabolic disorders, although nonalcoholic steatohepatitis (NASH) has been reported in lean individuals [3]. Both ALD and NAFLD may progress into fibrosis, cirrhosis, and eventually hepatocellular carcinoma as a result of severe and prolonged liver damage [4]. The effect of current synthetic agents in treating ALD and NAFLD is not satisfactory and most of them have undesirable side effects [5]. Thereby, the development of novel agents that can improve the efficacy of ALD and NAFLD prevention and treatment is urgently needed. In recent years, numerous medicinal herbs and phytochemicals have been investigated as complementary and alternative treatments for liver diseases including ALD and NAFLD [2]. However, scientific validation of these herbal medicines’ efficacy is needed.

Danshen is the root part of Salvia miltiorrhiza Bunge. According to the TCM theory, Danshen can unblock meridians, dispel stasis and promote regeneration without damaging healthy “Qi”. It is widely indicated for liver disorders caused by blood stasis accumulation and obstruction [6]. The hepatoprotective effects of Danshen have been proved by several clinical trials in NAFLD and hepatocarcinoma patients in recent years [7,8]. Furthermore, modern pharmacological studies also revealed the hepatoprotective effect of Danshen and its active ingredients for liver diseases in vitro and in vivo. For example, the total extracts of Danshen and its components such as tanshinol A, tanshinone I, tanshinone II A, dihydrotanshinono I, neotanshinone A, cryptanshinono, salvianolic acid A and salvianolic acid B were found to exhibit hepatoprotective effects in various hepatic cell lines and animal models against viral hepatitis, paracetamol-induced hepatitis, hepatic fibrosis and hepatocarcinoma [9,10,11,12,13]. Although Danshen has shown potential hepatoprotective effects in several hepatic dysfunctions models, systematical research on its therapeutic effect and the underlying mechanisms on ALD and NAFLD are still limited. Plenty of studies have shown that oxidative stress plays an important role in mediating the pathogenesis of various liver diseases including ALD and NAFLD. Oxidative stress in the liver could induce lipid peroxidation and subsequently results in death of hepatocyte [14,15]. Nature has evolved multiple layers of antioxidant defense in the liver. Small molecular antioxidants such as vitamins E and C offer the first line of defense to scavenge reactive oxygen/nitrogen species (ROS/RNS) directly and thus prevent or delay the initiation of various oxidative stresses. Besides this defense layer, antioxidant enzymes also serve as a major defense to detoxify ROS/RNS into less reactive species. Substantial evidence have shown that Danshen extracts could suppress oxidative stress by increasing the activity of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT) as well as reducing reactive oxygen species (ROS) and malondialdehyde (MDA) levels in mice diabetic renal tissue and rat paracetamol-induced liver injury [16,17,18]. Thus, the aim of the present study was to investigate the potential antioxidant effects of Danshen extract on ALD and NAFLD and explore the underlying mechanisms.

Over the past few decades, there has been a significant decline in the rate of novel phytochemicals translated into effective drugs. Currently, the most important problem for novel drugs development is a lack of therapeutic efficacy in clinical trials, which account for 33% of failures [19]. Thus, to maximize drug efficacy in pharmaceutical development, network pharmacology has been recently introduced to analyze the biological network of drug candidates in order to design a poly-target drug molecule. Network pharmacology is a developing field based in systems pharmacology that looks at the effect of drugs on both interactome and diseasome [20]. The drug-target network plays an important role in understanding the mechanisms of action of approved and experimental drugs. In recent years, network pharmacology has attracted much attention in the field of revealing the molecular mechanisms of TCM herbs for complicated diseases. Zhang et al. explored an integrative platform of TCM network pharmacology and its application on a herbal formula [21]. Li et al. also determined active compounds and action mechanisms of Ge-Gen-Qin-Lian decoction for treatment of type 2 diabetes by using network pharmacology method [22]. Many active chemical compositions of TCM target multiple proteins in the biological network of human diseases. Molecular docking and text mining assays are available for modeling interactions between small molecules and proteins [23,24]. Thus, research into TCM based on network pharmacology, which is a holistic understanding of the molecular mechanisms responsible for the pharmacological effects of herbal medicines, is well worth undertaking.

In the present research, we hypothesized that Danshen may exhibit both preventive and curative effects against alcoholic and non-alcoholic hepatic injuries via relieving oxidative stress. We investigated the biological effects of Danshen on acute/chronic ALD and NAFLD mice models. Then, we utilized computational tools and resources to develop the pharmacological network of Danshen for predicting the potential active ingredients and intracellular molecular targets. The in silico method combined with in vivo studies in this research may decipher the mystery of Danshen and promote TCM-based drug discovery.

2. Results

2.1. The Hepatoprotective Effect of Danshen on Acute ALD

Treatment with Danshen can decrease the liver weight to body weight ratio. Compared with the control group, alcohol administration slightly reduced body weight in mice, while Danshen treatment had no significant effect on body weight (Figure 1A,B). Alcohol administration exacerbated the development of liver injury in mice, as indicated by augmented liver weight to body weight ratio and increased serum AST and ALT levels. Significantly decreased ALT and AST levels were detected in acute ALD mice after Danshen treatment (Figure 1C,D). Mice liver morphology also appeared normal, accompanied with lower liver damage scoring in the Danshen treatment group. This further postulated that the liver histology results were consistent with the liver function test (Figure 2). The biochemical results showed that Danshen could increase hepatic SOD level, but had no significant influence on hepatic level of CAT or GSH-Px (Figure 1E–H). Our results also showed that administration of alcohol to mice markedly increased MDA levels compared with the normal control group. This result indicates that peroxidation progress of hepatic lipid occurred rapidly after formation of fatty liver by acute alcohol consumption. When mice were orally administered with 0.28 g/kg Danshen, the levels of MDA in hepatic tissues were significantly (p < 0.05) reduced by up to 31.6% of ethanol control group. These results indicate that Danshen can protect against the alcohol-induced hepatic lipid peroxidation process.

Figure 1Figure 1
Liver weight to body weight ratio, body weight measurement, and biochemical assays results after Danshen treatment in acute ALD. (A,B) The liver weight-to-body weight radio and body weight changes; (C) serum ALT level; (D) serum AST level; (E ...
Figure 2
H&E staining results after Danshen treatment in acute ALD (original magnification 100×). (A) The normal group had a clear structure of the hepatic lobule, and there were no visible lesions; (B) In the model group, typical pathological ...

2.2. The Hepatoprotective Effect of Danshen on Chronic ALD

Chronic alcohol consumption did not produce any significant (p < 0.05) changes in body weights of the mice under our experimental conditions as well as the liver weight to body weight ratio. Reduced serum AST and ALT levels after Danshen treatment indicated that Danshen dose-dependently reduced liver injury induced by chronic alcohol consumption (Figure 3). Histological analysis was conducted. As shown in Figure 4A, the hepatocytes and plate from hepatic tissue sample of the normal control group have intact structure, and the boundary between hepatocytes is clear. Insides of cellular structures are clean without impurities and droplets. However, the hepatocytes of chronic ALD model showed the infiltration of lymphocytes and vacuolar degenerations (Figure 4B). Co-administration of Danshen attenuated the above histopathological changes. Scoring on liver damage gave conclusions consistent with the serum AST and ALT test. Hepatic MDA level was significantly reduced in mice treated with Danshen. Hepatic level of SOD was increased after Danshen treatment, but no significant change in the hepatic level of CAT or GSH-Px was detected (Figure 3).

Figure 3
Biochemical assays results of Danshen treatment on chronic ALD (original magnification 100×). (A) Serum ALT level; (B) serum AST level; (CH) the production of MDA and the activity of SOD, CAT, and GSH-Px in liver tissues. DS-L for low ...
Figure 4
H&E staining results after Danshen treatment in chronic ALD (original magnification 100×). Treatment with Danshen for six weeks attenuated the inflammation and macrovacuolar degeneration in chronic ALD mice mode. (A) The normal group had ...

2.3. The Hepatoprotective Effect of Danshen on NAFLD

Treatment of Danshen could significantly reduce the AST level in a dose-dependent manner, and also slightly reduce the ALT level (Figure 5). Although AST is a more specific and sensitive indicator for liver damage in NAFLD [25,26], the results still indicate the effect of Danshen in alleviating NAFLD-induced liver damage. The H&E staining exhibited visible intracellular vacuolization that marked lipid accumulation and obvious inflammatory infiltration in the model group. However, the Danshen-treated group showed decreased levels of accumulated lipid droplets and inflammatory infiltrates. Histological scoring results showed consistent with the conclusion of serum ALT and AST levels (Figure 6). Hepatic MDA level was dose-dependently reduced while GSH-Px level was increased in mice treated with Danshen. However, a minimal effect on hepatic SOD and CAT activity could be detected after Danshen treatment (Figure 5). In addition, the PSR staining revealed a more pronounced development of fibrosis in livers of the model group mice, compared to mice that received Danshen (Figure 7).

Figure 5
Biochemical results of Danshen treatment on mice model of NAFLD. (A) Serum ALT level; (B) serum AST level; (CH) the production of MDA and the activity of SOD, CAT, and GSH-Px in liver tissues. DS-L for low dose of Danshen treatment group (0.093 ...
Figure 6
H&E staining results after Danshen treatment in NAFLD (original magnification 100×). Treatment with Danshen for six weeks attenuated the inflammation and macrovacuolar degeneration in NAFLD. (A) The normal group had a clear structure of ...
Figure 7
Picrosirius red staining results after Danshen treatment in NAFLD (original magnification 100×). Treatment with Danshen attenuated the collagen deposition in NAFLD. (A) The normal group showed little collagen deposition within hepatocytes; (B ...

2.4. In Silico-Based Network Construction and Analysis

The active ingredients of Danshen were predicted through in silico-based pharmacology method. To further illuminate the relationship between bioactive compounds and potential target genes, a drug-target network was built through network analysis (Figure 8). The results showed that six active compounds of Danshen were found to affect different potential targets, which may exhibit hepatoprotective effects (Table S1). Among the six active compounds, Danshensu exhibits the largest number of hepatoprotective target connections (10), followed by salvianolic acid a (8), and salvianolic acid b (6). For the 29 potential targets, the network showed peroxisome proliferator-activated receptor alpha (PPARα) had the largest number of compound interactions (tanshinone iia, salvianolic acid b and Danshensu), followed by CYP1A2 (isoimperatorin and Oleanolic acid) and MMP-2 (tanshinone iia and salvianolic acid a). The remaining 26 targets showed interactions with only one compound. Those high-degree nodes in the network, which had more target–compound interactions, are likely to play a more important role in treating ALD and NAFLD [27]. Information on 29 potential hepatoprotective targets in Danshen can be found in the Supplementary Materials (Table S1); all the data were manually collected from the TTD, PharmGKB, and CTD databases.

Figure 8
Compound–target networks and corresponding compound structures. The Compound-target network related to hepatoprotective effects in ALD and NALFD was shown in (A). The red octagons are active compounds from Danshen and the blue squares represent ...

3. Discussion

In the long history of TCM practice, Danshen has been shown to have multiple pharmacological activities, including hepatoprotective effect. Although the chemistry composition of Danshen has been extensively studied, the active ingredients and related mechanisms that contribute to its hepatoprotective activity in ALD and NAFLD are far from clear. In the present study, we demonstrated that Danshen might exhibit a preventive effect on acute and chronic ALD as well as NAFLD in a mouse model. Danshen could significantly decrease the MDA level in both ALD and NAFLD models. MDA is formed as a result of peroxidation of unsaturated fatty acids, which is the end product of lipid peroxidation. Since the MDA level is considered an indicator of polyunsaturated fatty acid damage, the decreased MDA level indicated attenuated oxidative damage in liver disease [28,29]. Previous studies showed that the detoxification pathway by the internal anti-oxidative system should be the result of an interacting network of multiple enzymes, with SOD catalyzing the first step and then CAT and GSH-Px removing hydrogen peroxide [30,31]. Although our data indicated that Danshen could increase the expression of SOD in ALD model and improve the activity of GSH-Px in NAFLD model, the overexpression of a single antioxidant enzyme in the liver is not sufficient to activate the internal anti-oxidative enzyme system and reduce the toxicity of superoxide [32]. Thus, Danshen seemed to play its anti-oxidation role through some other mechanisms in ALD and NAFLD. This postulation is partly consistent with our network pharmacological analysis results.

Peroxisome proliferator-activated receptor alpha (PPARα), which had the largest number of compound interactions in our network study, was indicated as the key regulator of lipid peroxidation in ALD and NAFLD. Tanshinone iia, salvianolic acid b, and Danshensu might be the potential active compounds of Danshen to target PPARα and related signaling pathways. In previous studies, PPARα may mediate NAFLD through a periostin-dependent pathway. It can regulate fatty acid oxidation by activating the periostin-dependent JNK signaling pathway and further activate hepatosteatosis in vivo and in vitro [33,34,35]. Activation of PPARα is also associated with increased mitochondrial glutathione (GSH) in the liver and decreased levels of circulating fatty acyl-carnitines [36]. Furthermore, PPARα plays a protective role to enhance mitochondrial function in response to chronic alcohol consumption by adaptive transcriptional activation and we suggest that activation of this nuclear receptor may be of therapeutic value in the treatment for ALD [37]. These studies indicated that PPARα may emerge as an intracellular target of Danshen for preventing the development of ALD and NAFLD. Cytochrome P450, family 1, subfamily A, polypeptide 2 (CYP1A2), a member of the cytochrome P450 mixed-function oxidase system, may also be involved in the metabolism of xenobiotics such as ethanol in the liver. Previous research has revealed that CYP1A2 plays an important role in alcohol-induced liver steatosis by catalyzing many reactions involved in ethanol metabolism and synthesis of cholesterol, steroids, and other lipids [38,39]. CYP1A2 could produce ROS to further promote oxidative stress and inflammation. In the early stage of ALD, this enzyme can generate ROS in the liver as a consequence of alcohol exposure. ROS will further produce excessive oxygen free radicals and lead to lipid peroxidation, as well as oxidative stress damage [40,41,42]. Our in silico study results indicated that the active ingredients in Danshen, such as isoimperatorin and oleanolic acid, may regulate the expression of CYP1A2, CYP2B6, and CYP1B1, thus further attenuating oxidative damage in the liver. Furthermore, like PPARα, CYP1A2 activity is also associated with intracellular GSH concentration [43]. GSH, which is one of the most important cellular non-enzymatic antioxidants may be involved in the hepatoprotective and antioxidant activity of Danshen in ALD and NAFLD. Our findings also suggest that Danshen and its potential active compounds (tanshinone iia and salvianolic acid a) may be useful in attenuating hepatic injury in CCl4-induced liver fibrosis in NAFLD model. Matrix metalloproteinase-2 (MMP2) may play a pivotal role in the anti-fibrosis effects of Danshen according to our network study. MMP2 is important in the formation of hepatic fibrosis, degrading certain kinds of extra cellular matrix (ECM) such as collagens and proteoglycans. Downregulation of MMP2 expression and the TGF-β1/Smad signaling pathways can relieve liver fibrosis in rats [44]. MMP2 activity is also critical for TGFβ2-induced matrix contraction, which may promote fibrosis in vitro [45]. Thus, MMP2 may be an important target for tissue repairing and preventing interstitial fibrosis in NAFLD. Generally, in the current study, we found that Danshen may relieve hepatic inflammation, fatty liver, and fibrogenesis in ALD and NAFLD mice without obvious side effects. Although our studies have shown that Danshen extract and its potential active ingredients may alleviate liver diseases in mice models, these animal models cannot predict the actual effect of Danshen on liver diseases in human patients. A randomized, double-blinded, placebo-controlled clinical trial should be performed in a future study to critically examine whether Danshen has a preventive and/or therapeutic effect on ALD and NAFLD patients.

An innovation of this study is combining in vivo studies with network pharmacology research. For the multiple components/multiple targets interaction model of TCM herbal medicines, conventional experimental research faces a situation of long-term investment to investigate the complex interaction mechanisms. Thus, our network pharmacology study, which integrates the systems biology and in silico technologies, may offer a direction for the mechanistic study of hepatoprotective effects of TCM herbal medicines. The pharmacological network analysis results illustrated the potential active ingredients and mechanism of action of Danshen in the management of ALD and NALFD. Therefore, network pharmacology may be a forceful tool for exploring the potential mechanism of action of TCM herbal medicines and developing novel active ingredients. A network pharmacology-based approach combined with in vivo studies might be available for elucidating the relationship between complex diseases such as liver diseases and TCM herbal medicine interventions. Notwithstanding the advances in recent network pharmacology research, there are some crucial technical issues to be addressed and improved for data collection on herbal medicines. First of all, the inventory of herbal products remains incomplete and novel chemical structures are being discovered. Secondly, previous researchers explored and provided only a small number of hepatoprotective target genes. Last but not least, stringently assessing the relationships between compounds and corresponding targets and obtaining accurate action modes such as activated drug–target interactions or inhibited drug–target interactions are still a challenge for the present network pharmacology study [46,47]. To resolve these problems, herbal compound libraries should be established and further enriched to better correlate compound functions with structures. Furthermore, experimental verification of the potential hepatoprotective compounds after in silico screening is needed to validate the accurate interactions between drugs and proteins based on theoretical predictions.

4. Materials and Methods

4.1. Reagents

Ethanol (99.9%, Thermo Scientific, Waltham, MA USA); carbon tetrachloride (CCl4) (99.9%, Thermo Scientific); Liquid ethanol diet (Bio-Serv, Flemington, NJ, USA); Control liquid dextrose diet (Bio-Serv); Choline-deficiency, amino acid-defined diet (CDAA) (Research Diets); Detection Kits for alanine transaminase (ALT), aspartate transaminase (AST), malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT) (Jiancheng, Nanjing, China); Direct Red 80 (Sigma-Aldrich, St. Louis, MO, USA); Picric acid (Sigma-Aldrich); Oil Red O (Sigma-Aldrich); Danshen aqueous extracts was prepared by Vitagreen® (Hong Kong, China), the root of Salvia miltiorrhiza Bunge was cut into small pieces and soaked for 2 h, then boiled for 1 h under a medium-heat fire after first being boiled under a high-heat fire. After being filtered, the residue was boiled again using the same method. All filtrate was collected, combined and then concentrated at 60 °C to a final concentration of 0.5 g/mL.

4.2. Animal Models and Treatments

For the alcohol-induced acute liver injury model, male C57BL/6J mice (four weeks of age) in treatment group were given three doses of Danshen extracts (0.093, 0.28, 0.84 g/kg/day) via gavage for nine days. Normal and Model groups of mice received equal volume (0.2 mL) of saline water. 6 h after the last treatment, the model group and treatment group of mice received ethanol (6 g/kg via gavage). The normal group of mice received the same volume of isocaloric/isovolumetric maltodextrin solution. This model was slightly modified from Enomoto et al. [48]. After 12 h of ethanol treatment, mice were euthanized by cervical sacrificed, and serum and liver samples were collected. For the induction of chronic ALD model, mice were initially fed the control liquid dextrose diet for three days to acclimate them to the liquid diet. Afterward, the mice were fed either the liquid ethanol diet or the control liquid dextrose diet for two weeks, as described by previous studies [49,50]. For the treatment group, mice were given Danshen extracts at different dose (0.093, 0.28, 0.84 g/kg) via gavage daily throughout the experiment. Normal and model groups of mice received equal volume (0.2 mL) of saline water. Twelve hours after the last treatment, mice were euthanized by cervical sacrificed, and serum and liver were collected. To induce chronic NAFLD model, we introduced the CDAA diet as described by Fujita et al. [51]. A low dose of CCl4 (0.4 μL/g body weight, twice/week) was used as promoter of fibrosis. Mice were fed with control chow or CDAA chow for six weeks in this study. Then, three doses of Danshen (0.093, 0.28, 0.84 g/kg) were given to the treatment group through oral administration every day. Normal and model groups of mice received an equal volume (0.2 mL) of saline. At the end point, mice were euthanized by cervical dislocation; serum and liver were collected for further analysis. All experimental protocols involving mice were approved by the Committee on the Use of Live Animals in Teaching and Research (CULATR) of the University of Hong Kong. CULATR number: 3637-15. Project Start Date: 27 March 2015. Animal license was approved by Department of Health, Hong Kong Special Administrative Region Government. Animal license number: (13-671) in DH/HA&P/8/2/3 Pt.54. Approved date: 13 December 2013.

4.3. Biochemical Assays

Serum samples were separated by centrifugation at 3000 rpm for 10 min and were kept at −20 °C until analysis. The serum levels of ALT, AST were determined with commercial kits. All of the procedures were carried out according to the manufacturers’ instructions. Liver tissue was homogenized in lysis buffer, centrifuged at 10,000× g for 5 min at 4 °C, and the supernatants were collected. The activity of GSH-Px, SOD, CAT and the production of MDA were measured according to the manufacturers’ instructions.

4.4. Liver Histology

Formalin-fixed tissues were stained with hematoxylin and eosin (H&E) and analyzed by microscopy. The liver damage score was measured by three individual examiners with the following criteria, 0: no damage; 1–3: mild damage; 4–6: intermediate damage; 7–9: severe damage; 10: destruction of liver structure [52]. In addition, for assessing liver fibrosis, we also conducted Sirius-Red staining in hepatic tissue biopsy. Scoring on the stained sections was made by three individual examiners with the following criteria, 0: no signs of observed fibrosis. 1–3: no extension of portal area fibrosis. 4–6: fibrosis occurring in the portal area with an intact lobule structure. 7–9: fibrosis associated with a broken lobule structure, but no signs of cirrhosis. 10: fibrosis and the formation of cirrhosis [53]. All the stained sections were observed and photographed under a microscope (with 100× magnification).

4.5. Network Pharmacology Analysis

4.5.1. Molecular Database Construction

Chemical ingredients of Danshen were manually collected from related literature and two phytochemical databases: Traditional Chinese Medicine Systems Pharmacology Database (TCMSP) (Available online: and TCM Database@Taiwan (Available online: [31,32,33,34,35,36].

4.5.2. Pharmacokinetic ADME Evaluation

In this step, an in silico integrative model—ADME was used to select the ingredients with favorable pharmacokinetics properties. The ADME system used in this study including PreOB (predict oral bioavailability) and PreCaco-2 (predict Caco-2 permeability). Oral bioavailability (OB) is one of the most vital pharmacokinetic properties of orally administered drugs as it plays an important role for the efficiency of the drug delivery to the systemic circulation [54,55]. Here, a reliable in silico screening model OBioavail 1.1 was employed in OB value calculation of the constituents in Danshen. This model was constructed based on 805 structurally diverse drugs and drug-like molecules. Multiple linear regression, partial least square and support vector machine methods were applied during this model building, ending up with determination coefficient (R2) = 0.80 and standard error of estimate (SEE) = 0.31 for test sets. [56,57]. In addition, for orally administered drugs, another pivotal problem is their movement across the intestinal epithelial barrier, which determines the rate and extent of human absorption and ultimately affects its bioavailability [58]. Thus, a preCaco-2 model was used to predict the efficiency of drug absorption. The phytochemical information of the compounds with their Caco-2 permeability properties were explored using the TCMSP database; detailed parameters information, screening criteria, and calculations can be obtained from TCMSP website (Available online: Finally, compounds with OB ≥ 33% and Caco2 ≥ 0.4 cm/s were regarded as candidate ingredients for further study. It is worth noting that the OB value of salvianolic acid A and salvianolic acid B are lower than 33%, but both of them are widely expected to exhibit hepatoprotective effects in vitro and in vivo [11,59,60,61]. Thus, these two compounds were also regarded as candidate compounds for further analysis.

4.5.3. Identification of Associated Proteins and Genes

The integrative efficacy of the ingredients in Danshen was determined by analyzing the compounds and targets interactions obtained from the Search Tool for Interactions of Chemicals and Proteins (STITCH) database(Available online: [44], HIT (Herbal Ingredients’ Targets) Database (Available online: [45] and omics-based Ligand-Target Chemogenomic model (LTC) [46], respectively. Then, for better defining the role of Danshen in hepatoprotective potentials, these targets were mapped to the Therapeutic Target Database (TTD, Available online: [47], PharmGKB (Available online: [48], and the Comparative Toxicogenomics Database (CTD, Available online: [49] to eliminate the unrelated target protein and provide a more complete and accuracy view on compound-hepatoprotective target associations. The targets with hepatoprotective potentials were retrieved from TTD, PharmGKB and CTD database by using the following search terms: liver disease, hepatic damage, alcoholic liver, non-alcoholic liver, fatty liver, liver fibrosis, oxidative damage, steatosis, oxidative damage, and lipid metabolism.

4.5.4. Network Construction

To further probe the relationships between the compounds and targets associated with hepatoprotective effects, the Compound–Target network plotting was generated by Cytoscape 3.4.0 (Available online: [50]. In the graphical network plot, nodes represent the compounds or proteins, and edges encode the compound–target interactions. In order to specify the importance of a node and how this node influences the communication between two nodes, all the properties of the network were analyzed using Network Analysis plugin. A flowchart to schematically describe the network pharmacology process in this study is shown in Figure 9.

Figure 9
A flowchart to schematically describe the network pharmacology process.

4.6. Statistical Analysis

All the data are presented as the mean ± SD and analyzed by one-way analysis of variance using SPSS17 software (SPSS Inc., Chicago, IL, USA). p < 0.05 was considered statistically significant.

5. Conclusions

Our studies suggested that Danshen could alleviate hepatic inflammation, fatty degeneration, and haptic fibrogenesis in ALD and NAFLD models. The combination of network pharmacology strategy with in vivo experimental study may provide a forceful tool for exploring the mechanism of action of traditional Chinese medicine herb and developing novel bioactive ingredients.


The study was financially supported by grants from the research council of the University of Hong Kong (Project Codes: 104003422, 104004092), the Research Grants Committee (RGC) of Hong Kong, HKSAR (Project Codes: 766211, 17152116), Wong’s Donation on Modern Oncology of Chinese Medicine (Project code: 200006276), Gala Family Trust (Project Code: 200007008), Government-Matching Grant Scheme (Project Code: 207060411), and a donation from Vita Green Health Products Co., Ltd. (Project cord: 200007477). The authors would like to express thanks to Keith Wong, Cindy Lee, and Alex Shek for their technical support.

Supplementary Materials

Supplementary materials can be found at

Author Contributions

Author Contributions

Yibin Feng designed the experiments. Ming Hong performed the experiments and primarily wrote the paper. Sha Li, Ning Wang, Hor-Yue Tan, Fan Cheung revised the paper. All authors analyzed the data and assisted in writing.

Conflicts of Interest

Conflicts of Interest

The authors declare no conflict of interest.


1. Uhl P., Fricker G., Haberkorn U., Mier W. Current status in the therapy of liver diseases. Int. J. Mol. Sci. 2014;15:7500–7512. doi: 10.3390/ijms15057500. [PMC free article] [PubMed] [Cross Ref]
2. Hong M., Li S., Tan H.Y., Wang N., Tsao S.W., Feng Y. Current status of herbal medicines in chronic liver disease therapy: The biological effects, molecular targets and future prospects. Int. J. Mol. Sci. 2015;16:28705–28745. doi: 10.3390/ijms161226126. [PMC free article] [PubMed] [Cross Ref]
3. Loomba R., Sanyal A.J. The global NAFLD epidemic. Nat. Rev. Gastroenterol. Hepatol. 2013;10:686–690. doi: 10.1038/nrgastro.2013.171. [PubMed] [Cross Ref]
4. Wang J., Li P., Jiang Z., Yang Q., Mi Y., Liu Y., Shi R., Zhou Y., Wang J., Lu W., et al. Diagnostic value of alcoholic liver disease (ALD)/nonalcoholic fatty liver disease (NAFLD) index combined with gamma-glutamyl transferase in differentiating ALD and NAFLD. Korean J. Intern. Med. 2016;31:479–487. doi: 10.3904/kjim.2015.253. [PMC free article] [PubMed] [Cross Ref]
5. Gupta N.K., Lewis J.H. Review article: The use of potentially hepatotoxic drugs in patients with liver disease. Aliment. Pharmacol. Ther. 2008;28:1021–1041. doi: 10.1111/j.1365-2036.2008.03822.x. [PubMed] [Cross Ref]
6. Zhu C., Cao H., Zhou X., Dong C., Luo J., Zhang C., Liu J., Ling Y. Meta-analysis of the clinical value of danshen injection and huangqi injection in liver cirrhosis. Evid. Based Complement. Altern. Med. 2013;2013:842824. doi: 10.1155/2013/842824. [PMC free article] [PubMed] [Cross Ref]
7. Wen T., Zheng G., Meng X., Chen L. Evaluation of oral glucose tolerance test in the assessment of reserved function of liver for patients with hepatocellular carcinoma. Hua Xi Yi Ke Da Xue Xue Bao. 1997;28:197–200. [PubMed]
8. Peng H., He Y., Zheng G., Zhang W., Yao Z., Xie W. Meta-analysis of traditional herbal medicine in the treatment of nonalcoholic fatty liver disease. Cell. Mol. Biol. 2016;62:88–95. [PubMed]
9. Yue S., Hu B., Wang Z., Yue Z., Wang F., Zhao Y., Yang Z., Shen M. Salvia miltiorrhiza compounds protect the liver from acute injury by regulation of p38 and NFκB signaling in Kupffer cells. Pharm. Biol. 2014;52:1278–1285. doi: 10.3109/13880209.2014.889720. [PubMed] [Cross Ref]
10. Parajuli D.R., Zhao Y.Z., Jin H., Chi J.H., Li S.Y., Kim Y.C., Sohn D.H., Lee S.H. Anti-fibrotic effect of PF2401-SF, a standardized fraction of Salvia miltiorrhiza, in thioacetamide-induced experimental rats liver fibrosis. Arch. Pharm. Res. 2015;38:549–555. doi: 10.1007/s12272-014-0425-2. [PubMed] [Cross Ref]
11. Li M., Lu Y., Hu Y., Zhai X., Xu W., Jing H., Tian X., Lin Y., Gao D., Yao J. Salvianolic acid B protects against acute ethanol-induced liver injury through SIRT1-mediated deacetylation of p53 in rats. Toxicol. Lett. 2014;228:67–74. doi: 10.1016/j.toxlet.2014.04.011. [PubMed] [Cross Ref]
12. Pan T.L., Wang P.W., Huang C.H., Leu Y.L., Wu T.H., Wu Y.R., You J.S. Herbal formula, Scutellariae radix and Rhei rhizoma attenuate dimethylnitrosamine-induced liver fibrosis in a rat model. Sci. Rep. 2015;5:11734. doi: 10.1038/srep11734. [PMC free article] [PubMed] [Cross Ref]
13. Lee W.Y., Cheung C.C., Liu K.W., Fung K.P., Wong J., Lai P.B., Yeung J.H. Cytotoxic effects of tanshinones from Salvia miltiorrhiza on doxorubicin-resistant human liver cancer cells. J. Nat. Prod. 2010;73:854–859. doi: 10.1021/np900792p. [PubMed] [Cross Ref]
14. Hassan H.M., Guo H., Yousef B.A., Guerram M., Hamdi A.M., Zhang L., Jiang Z. Role of Inflammatory and Oxidative Stress, Cytochrome P450 2E1, and Bile Acid Disturbance in Rat Liver Injury Induced by Isoniazid and Lipopolysaccharide Cotreatment. Antimicrob. Agents Chemother. 2016;60:5285–5293. doi: 10.1128/AAC.00854-16. [PMC free article] [PubMed] [Cross Ref]
15. Koroglu E., Canbakan B., Atay K., Hatemi I., Tuncer M., Dobrucali A. Role of oxidative stress and insulin resistance in disease severity of non-alcoholic fatty liver disease. Turk. J. Gastroenterol. 2016;27:361–366. doi: 10.5152/tjg.2016.16106. [PubMed] [Cross Ref]
16. Xu L., Shen P., Bi Y., Chen J., Xiao Z., Zhang X., Wang Z. Danshen injection ameliorates STZ-induced diabetic nephropathy in association with suppression of oxidative stress, pro-inflammatory factors and fibrosis. Int. Immunopharmacol. 2016;38:385–394. doi: 10.1016/j.intimp.2016.06.024. [PubMed] [Cross Ref]
17. Yue K.K., Lee K.W., Chan K.K., Leung K.S., Leung A.W., Cheng C.H. Danshen prevents the occurrence of oxidative stress in the eye and aorta of diabetic rats without affecting the hyperglycemic state. J. Ethnopharmacol. 2006;106:136–141. doi: 10.1016/j.jep.2005.12.026. [PubMed] [Cross Ref]
18. Zhou X., Cheung C.M., Yang J.M., Or P.M., Lee W.Y., Yeung J.H. Danshen (Salvia miltiorrhiza) water extract inhibits paracetamol-induced toxicity in primary rat hepatocytes via reducing CYP2E1 activity and oxidative stress. J. Pharm. Pharmacol. 2015;67:980–989. doi: 10.1111/jphp.12381. [PubMed] [Cross Ref]
19. Kola I., Landis J. Can the pharmaceutical industry reduce attrition rates? Nat. Rev. Drug Discov. 2004;3:711–715. doi: 10.1038/nrd1470. [PubMed] [Cross Ref]
20. Chen Y., Kern T.S., Kiser P.D., Palczewski K. Eyes on systems pharmacology. Pharmacol. Res. 2016;114:39–41. doi: 10.1016/j.phrs.2016.09.026. [PMC free article] [PubMed] [Cross Ref]
21. Liang X., Li H., Li S. A novel network pharmacology approach to analyse traditional herbal formulae: The Liu-Wei-Di-Huang pill as a case study. Mol. Biosyst. 2014;10:1014–1022. doi: 10.1039/c3mb70507b. [PubMed] [Cross Ref]
22. Li H., Zhao L., Zhang B., Jiang Y., Wang X., Guo Y., Liu H., Li S., Tong X. A network pharmacology approach to determine active compounds and action mechanisms of ge-gen-qin-lian decoction for treatment of type 2 diabetes. Evid. Based Complement. Altern. Med. 2014;2014:495840. doi: 10.1155/2014/495840. [PMC free article] [PubMed] [Cross Ref]
23. Ke Z., Zhang X., Cao Z., Ding Y., Li N., Cao L., Wang T., Zhang C., Ding G., Wang Z., et al. Drug discovery of neurodegenerative disease through network pharmacology approach in herbs. Biomed. Pharmacother. 2016;78:272–279. doi: 10.1016/j.biopha.2016.01.021. [PubMed] [Cross Ref]
24. Wu L., Gao X., Cheng Y., Wang Y., Zhang B., Fan X. Symptom-based traditional Chinese medicine slices relationship network and its network pharmacology study. Zhongguo Zhong Yao Za Zhi. 2011;36:2916–2919. [PubMed]
25. Borsoi Viana M.S., Takei K., Collarile Yamaguti D.C., Guz B., Strauss E. Use of AST platelet ratio index (APRI Score) as an alternative to liver biopsy for treatment indication in chronic hepatitis C. Ann. Hepatol. 2009;8:26–31. [PubMed]
26. Hallsworth K., Thoma C., Hollingsworth K.G., Cassidy S., Anstee Q.M., Day C.P., Trenell M.I. Modified high-intensity interval training reduces liver fat and improves cardiac function in non-alcoholic fatty liver disease: A randomized controlled trial. Clin. Sci. 2015;129:1097–1105. doi: 10.1042/CS20150308. [PubMed] [Cross Ref]
27. Danhof M. Systems pharmacology—Towards the modeling of network interactions. Eur. J. Pharm. Sci. 2016;94:4–14. doi: 10.1016/j.ejps.2016.04.027. [PubMed] [Cross Ref]
28. Guesmi F., Tyagi A.K., Bellamine H., Landoulsi A. Antioxidant Machinery Related to Decreased MDA Generation by Thymus Algeriensis Essential Oil-induced Liver and Kidney Regeneration. Biomed. Environ. Sci. 2016;29:639–649. [PubMed]
29. Tullberg C., Larsson K., Carlsson N.G., Comi I., Scheers N., Vegarud G., Undeland I. Formation of reactive aldehydes (MDA, HHE, HNE) during the digestion of cod liver oil: Comparison of human and porcine in vitro digestion models. Food Funct. 2016;7:1401–1412. doi: 10.1039/C5FO01332A. [PubMed] [Cross Ref]
30. Li S., Hong M., Tan H.Y., Wang N., Feng Y. Insights into the Role and Interdependence of Oxidative Stress and Inflammation in Liver Diseases. Oxid. Med. Cell Longev. 2016;2016:4234061. doi: 10.1155/2016/4234061. [PMC free article] [PubMed] [Cross Ref]
31. Ho Y.S., Magnenat J.L., Gargano M., Cao J. The nature of antioxidant defense mechanisms: A lesson from transgenic studies. Environ. Health Perspect. 1998;106(Suppl. S5):1219–1228. doi: 10.1289/ehp.98106s51219. [PMC free article] [PubMed] [Cross Ref]
32. Tepperman J.M., Dunsmuir P. Transformed plants with elevated levels of chloroplastic SOD are not more resistant to superoxide toxicity. Plant Mol. Biol. 1990;14:501–511. doi: 10.1007/BF00027496. [PubMed] [Cross Ref]
33. Batatinha H.A., Lima E.A., Teixeira A.A., Souza C.O., Biondo L.A., Silveira L.S., Lira F.S., Neto J.C. Association between aerobic exercise and rosiglitazone avoided the NAFLD and liver inflammation exacerbated in PPAR-α knockout mice. J. Cell Physiol. 2016;232:1008–1019. doi: 10.1002/jcp.25440. [PubMed] [Cross Ref]
34. Kostadinova R., Montagner A., Gouranton E., Fleury S., Guillou H., Dombrowicz D., Desreumaux P., Wahli W. GW501516-activated PPARβ/δ promotes liver fibrosis via p38-JNK MAPK-induced hepatic stellate cell proliferation. Cell Biosci. 2012;2:34. doi: 10.1186/2045-3701-2-34. [PMC free article] [PubMed] [Cross Ref]
35. Lu Y., Liu X., Jiao Y., Xiong X., Wang E., Wang X., Zhang Z., Zhang H., Pan L., Guan Y., et al. Periostin promotes liver steatosis and hypertriglyceridemia through downregulation of PPARα J. Clin. Investig. 2014;124:3501–3513. doi: 10.1172/JCI74438. [PMC free article] [PubMed] [Cross Ref]
36. Patterson A.D., Shah Y.M., Matsubara T., Krausz K.W., Gonzalez F.J. Peroxisome proliferator-activated receptor α induction of uncoupling protein 2 protects against acetaminophen-induced liver toxicity. Hepatology. 2012;56:281–290. doi: 10.1002/hep.25645. [PMC free article] [PubMed] [Cross Ref]
37. Li H.H., Tyburski J.B., Wang Y.W., Strawn S., Moon B.H., Kallakury B.V., Gonzalez F.J., Fornace A.J., Jr. Modulation of fatty acid and bile acid metabolism by peroxisome proliferator-activated receptor α protects against alcoholic liver disease. Alcohol. Clin. Exp. Res. 2014;38:1520–1531. doi: 10.1111/acer.12424. [PMC free article] [PubMed] [Cross Ref]
38. Ellefson W.M., Lakner A.M., Hamilton A., McKillop I.H., Bonkovsky H.L., Steuerwald N.M., Huet Y.M., Schrum L.W. Neonatal androgenization exacerbates alcohol-induced liver injury in adult rats, an effect abrogated by estrogen. PLoS ONE. 2011;6:e29463 doi: 10.1371/journal.pone.0029463. [PMC free article] [PubMed] [Cross Ref]
39. Lucas D., Berthou F., Dreano Y., Lozac'h P., Volant A., Menez J.F. Comparison of levels of cytochromes P-450, CYP1A2, CYP2E1, and their related monooxygenase activities in human surgical liver samples. Alcohol. Clin. Exp. Res. 1993;17:900–905. doi: 10.1111/j.1530-0277.1993.tb00861.x. [PubMed] [Cross Ref]
40. Hussain T., Al-Attas O.S., Al-Daghri N.M., Mohammed A.A., De Rosas E., Ibrahim S., Vinodson B., Ansari M.G., El-Din K.I. Induction of CYP1A1, CYP1A2, CYP1B1, increased oxidative stress and inflammation in the lung and liver tissues of rats exposed to incense smoke. Mol. Cell. Biochem. 2014;391:127–136. doi: 10.1007/s11010-014-1995-5. [PubMed] [Cross Ref]
41. Brauze D., Rawluszko A.A. The effect of aryl hydrocarbon receptor ligands on the expression of polymerase (DNA directed) κ (Polκ), polymerase RNA II (DNA directed) polypeptide A (PolR2a), CYP1B1 and CYP1A1 genes in rat liver. Environ. Toxicol. Pharmacol. 2012;34:819–825. doi: 10.1016/j.etap.2012.09.004. [PubMed] [Cross Ref]
42. Kurzawski M., Dziedziejko V., Post M., Wojcicki M., Urasinska E., Mietkiewski J., Drozdzik M. Expression of genes involved in xenobiotic metabolism and transport in end-stage liver disease: Up-regulation of ABCC4 and CYP1B1. Pharmacol. Rep. 2012;64:927–939. doi: 10.1016/S1734-1140(12)70888-5. [PubMed] [Cross Ref]
43. Vibhuti A., Arif E., Mishra A., Deepak D., Singh B., Rahman I., Mohammad G., Pasha M.A. CYP1A1, CYP1A2 and CYBA gene polymorphisms associated with oxidative stress in COPD. Clin. Chim. Acta. 2010;411:474–480. doi: 10.1016/j.cca.2009.12.018. [PubMed] [Cross Ref]
44. Li X.M., Peng J.H., Sun Z.L., Tian H.J., Duan X.H., Liu L., Ma X., Feng Q., Liu P., Hu Y.Y. Chinese medicine CGA formula ameliorates DMN-induced liver fibrosis in rats via inhibiting MMP2/9, TIMP1/2 and the TGF-β/Smad signaling pathways. Acta Pharmacol. Sin. 2016;37:783–793. doi: 10.1038/aps.2016.35. [PMC free article] [PubMed] [Cross Ref]
45. Eldred J.A., Hodgkinson L.M., Dawes L.J., Reddan J.R., Edwards D.R., Wormstone I.M. MMP2 activity is critical for TGFβ2-induced matrix contraction—Implications for fibrosis. Investig. Ophthalmol. Vis. Sci. 2012;53:4085–4098. doi: 10.1167/iovs.12-9457. [PubMed] [Cross Ref]
46. Calvert S., Tacutu R., Sharifi S., Teixeira R., Ghosh P., de Magalhaes J.P. A network pharmacology approach reveals new candidate caloric restriction mimetics in C. elegans. Aging Cell. 2016;15:256–266. doi: 10.1111/acel.12432. [PMC free article] [PubMed] [Cross Ref]
47. Li X., Wu L., Liu W., Jin Y., Chen Q., Wang L., Fan X., Li Z., Cheng Y. A network pharmacology study of Chinese medicine QiShenYiQi to reveal its underlying multi-compound, multi-target, multi-pathway mode of action. PLoS ONE. 2014;9:e95004 doi: 10.1371/journal.pone.0095004. [PMC free article] [PubMed] [Cross Ref]
48. Enomoto N., Ikejima K., Yamashina S., Enomoto A., Nishiura T., Nishimura T., Brenner D.A., Schemmer P., Bradford B.U., Rivera C.A., et al. Kupffer cell-derived prostaglandin E(2) is involved in alcohol-induced fat accumulation in rat liver. Am. J. Physiol. Gastrointest. Liver Physiol. 2000;279:G100–G106. [PubMed]
49. Lieber C.S., de Carli L.M. An experimental model of alcohol feeding and liver injury in the baboon. J. Med. Primatol. 1974;46:263–264. doi: 10.1111/j.1753-4887.1988.tb05447.x. [PubMed] [Cross Ref]
50. Ambade A., Catalano D., Lim A., Kopoyan A., Shaffer S.A., Mandrekar P. Inhibition of heat shock protein 90 alleviates steatosis and macrophage activation in murine alcoholic liver injury. J. Hepatol. 2014;61:903–911. doi: 10.1016/j.jhep.2014.05.024. [PMC free article] [PubMed] [Cross Ref]
51. Fujita K., Nozaki Y., Yoneda M., Wada K., Takahashi H., Kirikoshi H., Inamori M., Saito S., Iwasaki T., Terauchi Y., et al. Nitric oxide plays a crucial role in the development/progression of nonalcoholic steatohepatitis in the choline-deficient, l-amino acid-defined diet-fed rat model. Alcohol. Clin. Exp. Res. 2010;34(Suppl. S1):S18–S24. doi: 10.1111/j.1530-0277.2008.00756.x. [PubMed] [Cross Ref]
52. Krastev Z. Liver damage score—A new index for evaluation of the severity of chronic liver diseases. Hepatogastroenterology. 1998;45:160–169. [PubMed]
53. James J., Bosch K.S., Aronson D.C., Houtkooper J.M. Sirius red histophotometry and spectrophotometry of sections in the assessment of the collagen content of liver tissue and its application in growing rat liver. Liver. 1990;10:1–5. doi: 10.1111/j.1600-0676.1990.tb00428.x. [PubMed] [Cross Ref]
54. Tian S., Li Y., Wang J., Zhang J., Hou T. ADME evaluation in drug discovery. 9. Prediction of oral bioavailability in humans based on molecular properties and structural fingerprints. Mol. Pharm. 2011;8:841–851. doi: 10.1021/mp100444g. [PubMed] [Cross Ref]
55. Saghir S.A. Determination of ADME and bioavailability following intravenous, oral, and dermal routes of exposure. Curr. Protoc. Toxicol. 2009 doi: 10.1002/0471140856.tx0508s41. [PubMed] [Cross Ref]
56. Ru J., Li P., Wang J., Zhou W., Li B., Huang C., Li P., Guo Z., Tao W., Yang Y., et al. TCMSP: A database of systems pharmacology for drug discovery from herbal medicines. J. Cheminform. 2014;6:13. doi: 10.1186/1758-2946-6-13. [PMC free article] [PubMed] [Cross Ref]
57. Wang X., Xu X., Li Y., Li X., Tao W., Li B., Wang Y., Yang L. Systems pharmacology uncovers Janus functions of botanical drugs: Activation of host defense system and inhibition of influenza virus replication. Integr. Biol. 2013;5:351–371. doi: 10.1039/C2IB20204B. [PubMed] [Cross Ref]
58. Pereira C., Araujo F., Barrias C.C., Granja P.L., Sarmento B. Dissecting stromal-epithelial interactions in a 3D in vitro cellularized intestinal model for permeability studies. Biomaterials. 2015;56:36–45. doi: 10.1016/j.biomaterials.2015.03.054. [PubMed] [Cross Ref]
59. Zeng W., Shan W., Gao L., Gao D., Hu Y., Wang G., Zhang N., Li Z., Tian X., Xu W., et al. Inhibition of HMGB1 release via salvianolic acid B-mediated SIRT1 up-regulation protects rats against non-alcoholic fatty liver disease. Sci. Rep. 2015;5:16013. doi: 10.1038/srep16013. [PMC free article] [PubMed] [Cross Ref]
60. Hou J., Tian J., Jiang W., Gao Y., Fu F. Therapeutic effects of SMND-309, a new metabolite of salvianolic acid B, on experimental liver fibrosis. Eur. J. Pharmacol. 2011;650:390–395. doi: 10.1016/j.ejphar.2010.10.019. [PubMed] [Cross Ref]
61. Hu Y.Y., Liu P., Liu C., Xu L.M., Liu C.H., Zhu D.Y., Huang M.F. Actions of salvianolic acid A on CCl4-poisoned liver injury and fibrosis in rats. Zhongguo Yao Li Xue Bao. 1997;18:478–480. [PubMed]

Articles from International Journal of Molecular Sciences are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)