*Corresponding Author:
M. D. Song
Research Institute and College of Biomedical & Health Science (RIBHS), Konkuk University, 268 Chungwon-daero, Chungju-si, Chungbuk, 27478, Korea, Republic of Korea
E-mail: minds@kku.ac.kr
Date of Submission 28 July 2019
Date of Revision 18 September 2019
Date of Acceptance 02 December 2019
Indian J Pharm Sci 2020;82(1):104-113  

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Aster tataricus Linn., (Asteraceae), an oriental and nutrient potential herb used in Asian countries for various health benefits. The present study focused on the protective effects of Aster tataricus against liver fibrosis in cellular and experimental rat model. Cell cytotoxicity, cell cycle and apoptosis functions were analyzed using hepatic stellate cell line following MTT assay, flow cytometry, and Annexin V-FITC/PI staining methods. For in vivo evaluation, thioacetamide-induced hepatofibrosis rat model was established. Sprague-Dawley rats were divided into 5 groups of 10 each (control, thioacetamide, thioacetamide with Aster tataricus extract 100, 500 mg/kg and silymarin 50 mg/kg groups, respectively). Fibrosis was induced by thioacetamide treatment (200 mg/kg, ip) 3 times per week for 13 weeks except for control group. Aster tataricus extract (100 and 500 mg/kg), and silymarin was administrated orally to each group 6 times per week from 7th week to 13th week and various fibrosis related parameters were estimated by real-time polymerase chain reaction using TRIzol Plus RNA purification kit. Results indicated that hepatic stellate cells treated with Aster tataricus extract (0.5 mg/ml) and silymarin (0.05 mg/ml) significantly (p<0.05) induced apoptosis (19.04 and 24.82 %, respectively) compared to the control group (9.78 %). Moreover, rat primary hepatic stellate cells showed morphological changes and degradation of collagen and fibronectin with treatment of Aster tataricus extract at 0.5 mg/kg. In in vivo evaluation Aster tataricus extract at concentrations of 100 and 500 mg/ml attenuated the increased serum levels of alanine transaminase, aspartate transaminase and hydroxyproline and restored the decreased glutathione levels significantly in thioacetamide-induced fibrotic rats (p<0.05). The altered histopathology in thioacetamide-induced liver tissues and changes in fibrosis-related gene expression (TGF-β, α-SMA and Col1α1) were also restored by Aster tataricus extract treatment. In conclusion, A. tataricus can be developed as a potential therapeutic agent to treat liver fibrosis.


Liver fibrosis, thioacetamide, apoptosis, hepatic stellate cells, hydroxyproline

Liver fibrosis, one of the critical disorders in the world population results from chronic hepatic injury, autoimmune hepatitis, hepatitis C infection, alcoholic and non-alcoholic fatty liver and non-alcoholic steatohepatitis with sustained inflammation, formation of scar, altered tissue architecture and organ failure[1]. Deposition of extra cellular matrix (ECM) proteins, a major source of fibrillary and non-fibrillar matrix by hepatic stellate cells (HSCs) activation is considered as one of the important characteristic featuresin the pathogenesis of liver fibrosis[1-3]. HSCs are normally quiescent and possess low proliferation rate, but at conditions of hepatocyte damage or injury they get activated with increased proliferation rate further transforming into myofibroblast-like phenotypic cells.

This condition causes severe damage to the normal architecture of the liver and therefore considered as an important stage during progressive liver disease[4-8]. Inhibiting ECM secretion by activated HSCs and targeting HSCs apoptotic pathways, which are involved in the pathogenesis of liver fibrosis has great significance in ameliorating chronic liver diseases[9]. Several studies on thioacetamide (TAA) in experimental animals revealed similar mechanism of liver fibrogenesis both metabolic and histological when compared with the fibrotic livers of humans including virus-induced cirrhosis[10,11]. Therefore, TAAinduced liver fibrosis in rodents could be a classical model to evaluate therapeutic efficacy of various agents for studying liver damage and liver fibrosis[11]. Use of natural products derived from plants in aiding liver capacity and preventing liver damage such as Ampelopsis brevipedunculata, Orostachys japonicus, Artemisia, Chrysanthemum, Plantago seed, Gardenia jasminoides and Paeonialactiflora have been practiced in Asian countries since centuries[12]. Many factors contribute to herbal medicine’s appeal and supporters of traditional herbal medicine claim that herbs may both treat and prevent liver fibrosis and also act as potential nutrients in strengthening liver functions[13]. Aster tataricus Linn., from the family Asteraceae, is distributed widely in Asian countries and has been used as a common traditional medicine for the relief of coughs and as an expectorant. Scientific studies revealed that A. tataricus possessed diuretic, antitumor, antibacterial, antivirus, antiulcer activities and related hepatic microsomal biotransformation[14,15]. The major constituents of A. tataricus are terpenoids, sterols, flavonoids, polysaccharides and cylclopeptides[16-17]. Recently, the roots and rhizomes of A. tataricus have been reported to inhibit HBV DNA replications and the human gastric carcinoma cell growth indicating that it could act as a natural anticancer agent[16,17]. A. tataricus was also reported to have antioxidant activity and reduce the levels of alanine aminotransferase (ALS), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) in hepatotoxic effect induced by Fr-2[18,19]. More recently, potential inhibitors were isolated from Aster tataricus which exhibited antiinflammatory effects bypreventing the downstream activation of the mitogen-activated protein kinase signaling pathway[20,21]. A. tataricus was found to protect retinal damage in diabetic rats due to the antioxidant and antiinflammatory effects[22] and attenuated neuroinflammation by decreasing the oxidative stress and inhibiting the cytokine production in LPS-stimulated rat astrocytoma cell line (C6) and THP-1 cells[23]. Further, A. tataricus extract was also reported to possess antiinflammatory and anticancer activity in LPS-induced acute lung injury model and by effectively attenuating the growth of SCC-9 cancer cells by virtue of its cytotoxic and anticlonogenic activity[24,25]. Owing to its immense pharmacological properties, in the present study the antihepatofibrotic effects of A. tataricus extract was investigated in HSCs and in a TAA-induced liver fibrosis rat model.

Materials and Methods

Hydroxyproline, TAA, glutathione (GSH), chloramine-T, 5,5-dithiobis-2-nitrobenzoic acid (DTNB), nicotinamide adenine dinucleotide phosphate (β-NADPH), p-dimethylaminobenzaldehyde,1,1,3,3- tetraethoxypropane (TEP) and 3-(4,5-demethylthiazol- 2yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) were purchased from Sigma (St. Louis, Missouri, USA). Annexin V-Fluorescein isothiocyanate (FITC) and propidium iodide (PI) Apoptosis Detection Kit I and GOT-GPT assay kits were obtained from BD Biosciences (San Jose, CA, USA). Perchloric acid was purchased from GFS chemical Co, (Columbus, Ohio, USA). All other chemicals used were of highest quality commercially available.

Plant collection and extraction:

The root of A. tataricus collected during June-July, 2018, was purchased from Ichanbang Medical Herb Co., Jecheon, Chungcheongbuk-do, South Korea. For extraction, Soxhlet extraction technique was used as described previously[21]. Briefly, finely powdered A. tataricus (1 kg) was extracted with 5 l of ethanol (95%) for 3 d and the collected extract was concentrated under reduced pressure, lyophilized and stored in a refrigerator at 4°. The final yield of A. tataricus extract (ATE) was 12.5 % (w/w). ATE stock for use in each experiment was prepared by dissolving ATE in 10% dimethyl sulfoxide (DMSO, Junsei Chemical Co., Ltd., Tokyo, Japan) and then filtered through a 0.22 μM syringe filter. The final concentration of DMSO used for the study was not more than 0.1 %.

Cell lines and culture:

An immortalized rat hepatic stellate cell line (HSC-T6) was obtained from Korean Hospital of Daejeon University, Daejeon, South Korea. Chang liver cell lines was purchased from American Type Culture Collection (Manassas, VA, USA). HSC-T6 cells were cultured in Dulbecco`s modified Eagle media (DMEM, Invitrogen, Carlsbad, CA, USA) supplemented with 5 % fetal bovine serum (FBS, Invitrogen, Carlsbad, CA, USA) and 1 % antibiotic-antimycotic (Invitrogen, Carlsbad, CA, USA) in a humidified atmosphere of 5% CO2 at 37°. The Chang liver cell line was used as a normal human cell line derived from normal liver tissue and cultured as described previously[26]. HSC-T6 cells were activated by serum starvation before treatment with ATE. The protocol for primary HSCs isolation and culture was performed as described previously[27,28].

Cell viability assay:

The effect of ATE on overall cell viability was evaluated using MTT assay and the results were measured on an ELISA reader at 540 nM as described previously[26]. Briefly, the cells were treated with ATE (24 h) at various concentrations (0, 0.1, 0.5, 1.0 mg/ml) and were incubated with 0.5 mg/ml MTT for 3 h, and then the reaction was interrupted by addition of DMSO. The viability of control cells were used as the control values at 100 %.

Cell cycle and apoptosis analysis:

Cell cycle analysis in HSC-T6 cells was evaluated using ATE at 0.1 and 0.5 mg/ml concentrations measured by flow cytometer (FACSCalibur, BD Biosciences, San Jose, CA, USA) using a method reported previously[26]. For apoptosis, Annexin V-FITC and PI apoptosis detection kit I was used according to manufacturer’s instructions. Data analysis was performed with CellQuest software obtained from BD Biosciences. For cell death determination, both early (Annexin V+ and PI-) and late (Annexin V+ and PI-) apoptotic cells were included.

Quantitative Real-time polymerase chain reaction (qRT-PCR):

The protocol for qRT-PCR was followed as described previously[26]. Briefly, total RNA was extracted from tissue samples using TRIzol Plus RNA Purification Kit (Qiagen, Valencia, CA, USA). From total RNA (2 μg), cDNA was synthesized in a 20 μl reaction using a high-capacity cDNA reverse transcription kit (Applied Biosystems, Foster, CA, USA). The internal control was β-actin and the primers used in the study was shown in Table 1.

Table 1: The Primers Used In the Study

qRT-PCR Primer sequences
Cn type 1 α 1 Forward 5'-CCCAGCGGTGGTTATGACTT-3'

Experimental animals:

Specific-pathogen-free Sprague Dawley (SD) rats (6-w old, 190-210 g) of either sex obtained from a commercial animal breeder (Orient Bio, Seongnam, Gyeonggi-do, Korea) were used for experiments approved by the Committee of Laboratory Animals according to the Institutional Guidelines of Konkuk University, Republic of Korea (IACUC No. KU15148). The animals were housed in conventional cages under controlled conditions of temperature (23±3°), relative humidity (50±20 %), and 12/12-h light/dark cycle with standard laboratory chow and purified water ad libitum.

Experimental design:

After one week of adaptation, a total of 50 rats were divided randomly into 5 groups consisting of 10 rats each, the normal control group, TAA group (TAA only), ATE 500 group (TAA with 500 mg/kg ATE), ATE 100 group (TAA with 100 mg/kg), and positive control silymarin group (TAA with 50 mg/kg silymarin). Liver fibrosis was induced by intraperitoneally injecting TAA (200 mg/kg) thrice a week for 13 w to 4 groups of rats except to the normal control group, which received normal saline ip ATE (100 or 500 mg/kg), silymarin (50 mg/kg), or distilled water was given by gastric gavage 6 times per week starting from the w 7 to 13. All animals were fasted for 18 h after the last administration of ATE or silymarin and then blood was collected by cardiac puncture under CO2 anesthesia. For tissue analysis, liver from each rat was excised and separated as two portions. One portion of tissue was fixed in Bouin’s solution for histomorphological findings and another portion of liver tissue was stored at -80° for individual fibrosis-related gene expression.

Analysis of serum biomarkers (AST/ALT), GSH and hydroxyproline:

For analysing serum biochemical parameters serum was separated using a centrifuge (3000 g, 15 min) and the levels of AST and ALT were determined using a GOT-GTP assay kit[26]. Total GSH content was determined according to the method of Ellman[29] and the hydroxyproline estimation was performed using a previously reported method with a slight modification[30]. The optical density of the reaction product of GSH and hydroxyproline was read at 405 and 558 nM, respectively using a spectrophotometer (Tecan, Morrisville, NC, USA).


After sacrificing the animals, the liver was quickly removed and fixed in Bouin’s solution, embedded in paraffin and cut into 5 μM thick sections. The tissue sections were stained with Hematoxylin and Eosin (HE) and Masson’s trichrome. After regular gradient alcohol dehydration and mounting the sections were observed under a light microscope (Olympus BX-50 Microscope, Leica Microsystems, USA) and then photographed. For collagen expression analysis, the blue-stained areas in the Masson’s trichrome stained sections were measured on an image analyzer (Image J, NIH, Bethesda, MD, USA).

Statistical analysis:

Data are expressed as the mean±standard error of the mean (SEM, n=10). Statistically significant differences between groups were analyzed using one-way analysis of variance (ANOVA) followed by student’s t-test. A value of p<0.05 was considered statistically significant.

Results and Discussion

Liver fibrosis and treatment regimen remains a major challenge and health problem because of its complex pathogenesis causing significant morbidity and mortality. Although research to understanding the molecular consequences of liver fibrosis and its pathogenesis has been steadily growing over the last 2 decades, potential treatment for liver fibrosis is still in its infancy[31]. Traditional herbs and nutrient therapy in the management of liver diseases including fibrosis is the central component of medical practice in many parts of Asia[32]. In this study, ATE exhibited potential therapeutic benefits in ameliorating hepatofibrosis in experimental cellular and animal model.

Initially to determine the optimal concentration of ATE for in vitro evaluations, various concentrations of ATE (0.1, 0.25, 0.5, 1.0 mg/ml) were added to Chang cells and HSC-T6 cells and cell viability was assessed using the MTT assay. ATE treatment up to 0.5 mg/ml or DMSO (0.1 %) did not exhibit any signs of cytotoxicity or altered the overall cell viability in both HSC-T6 and Chang cells (figure 1A). Therefore, further in vitro studies were carried out using either 0.1 mg/ml and/or 0.5 mg/ml as these concentrations were considered non-toxic and pharmacologically effective.


Figure 1: Effect of ATE in cell viability assay on Chang liver/HSC-T6 cells and morphological changes in primary HSCs
(A) Chang liver image and HSC-T6 cells image were incubated with ATE at indicated concentrations for 24 h and cell viability was determined by MTT assay. (B) Primary HSCs were cultivated for 1 w and exposed to the ATE (0.5 mg/ml) for 24 h (C). Pictures were taken after 24 h treatment with ATE. Magnification was 100X. Arrows indicate HSCs. The data are expressed as means±SEM (n=10), using one-way analysis of variance (ANOVA) followed by Student’s t-test. *P<0.05 compared to the control group, NS-not significant compared to the control group

It is well documented that deposition and qualitative changes in ECM in the liver by activated HSCs is a crucial event during liver fibrogenesis[33]. HSCs under activated state exhibit enhanced proliferation rate, contractility and collagen scar around cells with increased accumulation of ECM proteins. Thus, suppressing the effects observed in activated HSCs morphology, proliferation and collagen scar indicates attenuation of liver fibrosis[33]. In this study, the altered morphology in activated HSCs (day 7, figure1B) was restored with ATE (0.5 mg/ml) treatment for 24 h (day 8) with cell degradation and decreased collagen fiber morphology (figure 1C).

Earlier reports revealed that inhibition of HSC proliferation by blocking the cell cycle transition from G1 to S phase might aid in HSC inactivation and can prevent the progression of hepatic fibrosis[34,35]. In the activated HSC proliferation process, apoptosis is responsible for mediating HSC loss during recovery from the fibrosis and therefore, induction of HSC apoptosis might has an antifibrotic effect[36,37]. In this study, the cell cycle distribution showed marked effects in silymarin and ATE 0.5 mg/ml treated groups (figure 2A). The percentage of cell cycle distribution revealed that treatment with 0.1 mg/ml of ATE alone did not exhibit any alterations and was similar to untreated control group (1.08 % for control and 1.24 % for ATE 0.1 mg/ml). However, ATE treatment at 0.5 mg/ml showed 2.58 % of cells in the sub-G1 phase compared to the untreated control group. The positive control silymarin showed 3.93 % of cells in the sub-G1 phase compared to the untreated group (figure 2B).


Figure 2: Effect of ATE on the cell cycle in HSC-T6 cells
DNA content in different phases of cell cycle was measured using flow cytometry with propidium iodide. The cell cycle distribution for each treatment group and % cell cycle distribution represented as A. graphs and B. histograms, respectively, image G2, imageS, image G1 image G0

Further, annexin V and PI double staining was performed to confirm the ability of ATE in inducing apoptosis. In Annexin V-FITC/PI assay, ATE (0.5 mg/ ml) and silymarin significantly (p<0.05) increased apoptosis in HSC-T6 cells when compared with the control group (figure 3A-3D). In agreement with the cell cycle distribution data, ATE 0.1 mg/ml did not exhibit marked effects in inducing apoptosis. The percent of cells undergoing apoptotic cell death in control group was 12.09±2.54, which was markedly increased to 42.12±2.74 in the silymarin group, while it was 26.71±3.89 in the 0.5 mg/ml ATE-treated group and 11.72±3.09 in the 0.1 mg/ml ATE-treated group at 24 h. When compared to the Annexin V positive cells in the control group, ATE (0.5 mg/ml) and silymarin (0.05 mg/ml) induced more than two-fold increase in Annexin V positive cells (figure 3E). These results suggested that ATE at 0.5 mg/ml significantly (p<0.05) induced cell death and apoptosis in HSC-T6 cells and also reversed the altered morphology of HSCs.


Figure 3: Effect of ATE on apoptosis in activated HSC-T6 cells
(A) Control cells. Flow cytometry data indicate apoptosis in HSC-T6 cells after incubation with ATE (0.5 mg/ml) and silymarin 0.05 mg/ml (B and D) for 24 h. No effect was observed with ATE treatment at 0.1 mg/ml (C). Data showed the apoptotic (Annexin V+ and PI-) and late apoptotic (Annexin V+ and PI+) cells (E), and represented as mean±SEM (n=10) using one-way analysis of variance (ANOVA) followed by Student’s t-test. *P<0.05 compared with control group

It is well known that TAA induced marked hepatotoxicity and is predominantly used to develop hepatofibrosis in several experimental studies[10,11]. In agreement with the reported data, TAA (200 mg/kg, ip) produced hepatic damage and elevated levels of ALT and AST in serum. AS shown in figures 4A and B, TAA-induced group significantly (p<0.05) increased the serum levels (ALT and AST) and ATE treatment at both concentrations restored these levels significantly (p<0.05). Interestingly, ATE 500 group decreased the tested serum levels to about half compared to TAAtreated group. Silymarin-treated group also showed a significant (p<0.05) positive trend. Further, TAA is known to produce marked hepatotoxicity in exposed animals producing excessive reactive oxygen species (ROS). The antioxidant enzyme GSH, plays an important role in protecting the cell from oxidant damage and is considered as useful marker for detection of liver function when undergoing fibrosis[38,39]. Therefore, the levels of total GSH content were examined in the serum of TAA-treated rats. As shown in figure 4C, a significant (p<0.05) decrease in GSH content was observed in TAA-treated liver tissues compared to those from the control group. However, ATE 500 mg/k-treated group restored the total GSH contents to near normal levels and exhibited superior effect than positive control treated group. These data suggest that the altered antioxidant enzyme status caused by TAA was significantly ameliorated by ATE treatment.


Figure 4: Effect of ATE on serum ALT, AST, total glutathione (GSH) and hydroxyproline levels in TAA-induced rats
Serum levels of (A) ALT and (B) AST, (C) total GSH and (D) hydroxyproline were measured using respective commercial kits as detailed in methods section and spectrophotometry. TAA: Thioacetamide-induced rats (200 mg/kg), Silymarin: positive control (50 mg/kg), ATE 100: ATE 100 mg/kg plus TAA-induced rats, ATE 500: ATE 500 mg/kg plus TAA-induced rats. The data are expressed as mean±SEM (n=10) using one-way analysis of variance (ANOVA) followed by Student’s t-test. #P<0.05 as compared with control group and *p<0.05 compared with TAA group

Hydroxyproline, a major constituent of collagen is well studied as a suitable marker to correlate with ECM accumulation causing HSC proliferation and liver fibrosis[40-43]. Therefore, we evaluated the serum levels of hydroxyproline to confirm whether ATE could positively influence hydroxyproline levels in TAAinduced rats. Results indicated that the hydroxyproline levels in TAA group significantly (p<0.05) increased compared to control group (figure 4D) and ATE treatment (100 and 500 mg/kg) significantly (p<0.05) attenuated this increase when compared to TAA group. Importantly, ATE 500 mg/kg and silymarin treated groupsexhibited similar effects in decreasing the hydroxyproline levels.

It is well documented that TAA treatment causes a significant change in morphological features including tissue deposition with solidified, shrunken, abnormally patterned necrosis and fibrotic scar tissues in liver[39]. HE and Massion’s trichrome are the most important staining techniques used in histopathology and histochemistry for demonstration of general tissues structure as well as several intra-cellular and extra-celluar substances necessary for diagnosis of disease condition in tissues and cells[44,45]. Therefore, whether ATE could recover the TAA-induced histomorphological changes in hepatic tissues were investigated. As shown in figure 5A, normal morphology was observed in control rat liver tissues. However, shrunken and abnormal liver pattern with formation of regenerative nodules were observed in liver tissues from TAA-treated rats (figure 5B). ATE 500 treatment attenuated the altered histological changes with no marked differences observed when treated with lower concentrations (100 mg/kg) of ATE (figures 5C and 5D). To further confirm the effects of ATE on TAAinduced histological changes, Massion’s trichrome staining was also performed. The normal histological pattern observed in control group (figures 6A) was altered in TAA-induced liver tissues (figures 6B) exhibiting excessive collagen accumulation (blue stained areas). In agreement with HE staining data, ATE 500 group alone markedly decreased the collagen accumulation in the liver section with no marked effects observed at ATE 100 mg/kg dose (figures 6C and D). Further, Silymarintreated group showed marked improvement when compared with TAA-induced group (figures 6E). Percent area of fibrosis showed significant (p<0.05) damage in TAA-treated group compared to the control group (figures 6F), which was restored in ATE (100 mg/kg and 500 mg/kg)-treated groups significantly (p<0.05).


Figure 5: Effect of ATE on histomorphology using hematoxylin and eosin (HE) stain of TAA-induced rat liver tissues
Liver tissue samples fixed in Bouin’s solution and sections were stained with HE and observed under light microscopy. (A) control rats, (B) TAA: TAA-induced (200 mg/kg) liver fibrosis rats, (C) ATE 500: ATE 500 mg/kg plus TAA-induced rats, (D) ATE 100: ATE 100 mg/kg plus TAA-induced rats, (E) silymarin (50 mg/kg): positive control rats, scale bar = 200 μM


Figure 6: Effect of ATE on TAA-induced fibrosis by Masson’s trichrome stain of TAA-induced rat liver tissues
This stain was performed similar to H&E stain. (A) control rats, (B) TAA: TAA-induced (200 mg/kg) liver fibrosis rats, (C) ATE 500: ATE 500 mg/kg plus TAA-induced rats, (D) ATE 100: ATE 100 mg/kg plus TAA-induced rats, (E) Silymarin (50 mg/kg): positive control rats, (F) fibrosis area plot. Scale bar = 200 μM. Quantification was done using ImageJ. Values are represented as mean±SEM (n=10) using one-way analysis of variance (ANOVA) followed by Student’s t-test. #P<0.05 as compared with control group, *p<0.05 as compared with TAA group. TAA: Thioacetamide, silymarin: positive control rats, ATE 100: ATE 100 mg/kg plus TAA-treated rats, ATE 500: ATE 500mg/kg + TAA -treated rats

It is well known that transforming growth factor- β (TGF-β)-1 is one of the main cytokines in the generation of ROS and ECM production, which can stimulate the activation and proliferation of HSC by activating its downstream Smad signaling pathway. Α-Smooth muscle actin (α-SMA) is a marker produced in liver fibrosis which regulates essential phenomena for tissue remodeling, such as cytokine synthesis and ECM component production. Therefore, the TGF-β-1/ Smad signaling pathway is considered a potential target for the prevention and treatment of hepatic fibrosis[46]. TGF-β produced by Kupffer cells and HSCs, also promotes the proliferation of HSCs and strongly up regulates the transcription of the collagen-1 and collagen-2 genes to produce a large amount of ECM, contributing to hepatocyte injury and promoting fibrosis[47,48]. In this study, TAA-treated liver showed an up-regulated TGF-β expression while ATE-treated group (500 mg/kg) significantly (p<0.05) downregulated the expression (figure 7A). Further, upregulated α-SMA and collagen-1 alpha 1 (Col1α1) expression in TAA-induced groups were significantly decreased by ATE at both concentrations (p<0.05; figures 7B-7C). The positive control silymarin also exhibited significant (p<0.05) effects in down regulating the expression of selected fibrosis-associated genes. Based on these results, it could be concluded that ATE could attenuate TAA-induced liver fibrosis and this effect might be partially mediated by regulation of the TGF-β1/Smad signaling pathways.


Figure 7: Effect of ATE on TAA-induced fibrosis related gene expression in the liver tissues
Fibrosis related gene expressions of liver tissue were determined by real-time-polymerase chain reaction (RT-PCR). A: TGF-β, B: α-SMA and C: Col1α1. The results are expressed as normalized fold values relative to the control. Values are represented as mean±SEM. (n=10) using one-way analysis of variance (ANOVA) followed by Student’s t-test. *P<0.05 compared to the TAA group. TAA, Thioacetamide; ATE, A. tataricus extract; α-SMA, alpha-smooth muscle actin; Col1α1, collagen type1 alpha 1; TGF-β, transforming growth factor-beta

Traditionally, A. tataricus is used for medicinal and several reports have indicated the presence of numerous bioactive constituents including dietary flavonoids, triterpenes, saponins and specific constituents such as epifriedelinol, caffeoylquinic acids, shionone and aster peptides shionone, epifriedelinol, quercetin, kaempferol, scopoletin, emodin, aurantiamide acetate and 1,7-dihydroxy-6-methyl-anthraquinone[49-52]. Some of these compounds, such as quercetin, saponins, kaempferol, epifriedelinol, caffeoylquinic acids possess strong antioxidant, antiinflammatory and hepatoprotective properties including antifibrotic effects[53-56]. The compounds present in the ATE might act in a synergistic way in promoting potent antihepatofibrosis effect.

In conclusion, the present study provided scientific evidence for the traditional benefits of A. tataricus in the treatment of liver disorders. Further studies on the active constituents and exploring in-depth mechanism is quite necessary to develop A. tataricus as a potential nutrient and medicinal herb against liver fibrosis and related disorders.


This work was supported by Konkuk University in the year 2018.The authors thankProf. Chang-Gue Son from Korean Hospital of Daejeon University, Daejeon, South Korea for generously providing immortalized rat Hepatic Stellate Cell lines.