Hepatoprotective Effects of Different Extracts From Triphala Against CCl4-Induced Acute Liver Injury in Mice

Background: Triphala is a traditional polyherbal formula used in Indian Ayurvedic and Chinese Tibetan medicine. A wide range of biological activities have been attributed to Triphala, but the impact of various extraction methods on efficacy has not been determined. Purpose: The study aimed to evaluate Triphala extracts obtained by various methods for their hepatoprotective effects and molecular mechanisms in a mouse model of carbon tetrachloride (CCl4)-induced liver injury. Methods: HPLC fingerprinting was used to characterize the chemical characteristics of Triphala extracts obtained by (a) 0.5 h ultrasonication, (b) 2 h reflux, and (c) 4 h reflux. Hepatoprotective efficacy was evaluated in a mouse model of CCl4-induced liver damage. Serum levels of alanine transaminase (ALT) and aspartate aminotransferase (AST) were measured, as well as the liver antioxidant and inflammatory markers malondialdehyde superoxide dismutase glutathione peroxidase (GSH-Px), TNF-α, and IL-6. Gene and protein expression of Nrf-2 signaling components Nrf-2, heme oxygenase (HO-1), and NADPH Quinone oxidoreductase (NQO-1) in liver tissue were evaluated by real-time PCR and western blotting. Results: Chemical analysis showed a clear difference in content between extracts produced by ultrasonic and reflux methods. The pharmacological analysis showed that all three Triphala extracts reduced ALT, AST, MDA, TNF-α, and IL-6 levels and increased SOD and GSH-Px. Triphala extracts also induced transcript and protein expression of Nrf-2, HO-1, and NQO-1. Conclusion: Triphala extract prevents CCl4-induced acute liver injury. The ultrasonic extract of Triphala was most effective, suggesting that hepatoprotection may be related to the larger tannins via activation of Nrf-2 signaling.


INTRODUCTION
As one of the largest metabolic organs in the human digestive system, the liver has functions of transformation, excretion, immunity, and detoxification and is susceptible to chemical liver injury caused by various pathogenic and stimulating factors. Aggravated liver cell damage, if left unchecked, can lead to hepatitis, liver fibrosis, or irreversible cirrhosis, which eventually leads to liver cancer (Gu and Manautou, 2012). Studies have shown that the primary pathogenic mechanism of chemical liver injury is the oxidative stress caused by the accumulation of reactive oxygen radicals in the liver and the resulting inflammatory response (Souza et al., 2018).
Triphala is a traditional polyherbal medicine comprised of Terminalia chebula Retz., Terminalia bellirica (Gaertn.) Roxb.., and Phyllanthus emblica Linn., each of which contains a variety of chemical substances with biological activity (Baliga et al., 2012;Zhao et al., 2015;Chen et al., 2019;Nigam et al., 2020). Triphala has a long history in Indian and Chinese traditional medicine as a complementary and alternative therapy for chronic diseases (Jaiswal et al., 2016;Prasad and Srivastava, 2020). Triphala is considered a multipurpose therapeutic drug with antiinflammatory, analgesic, hypoglycemic, antibacterial, and antioxidant properties (Srikumar et al., 2006;Rasool and Sabina, 2007;Peterson et al., 2017;Luo et al., 2019). In traditional usage, Triphala is applied in the treatment of gastritis, hepatitis, colitis and other digestive diseases (Deep et al., 2005;Li et al., 2018a;Nariya et al., 2011;Olennikov et al., 2015;Rayudu and Raju, 2014;Wang et al., 2018). Triphala also has potential uses in the treatment of obesity and diabetes, as well as retinopathy and cardiovascular and cerebrovascular diseases (Saravanan et al., 2007;Gurjar et al., 2012;Kamali et al., 2012;Lu et al., 2012;Ganeshpurkar et al., 2015). Although Triphala is widely used throughout Asia, clinical safety data are lacking. In Thailand, a phase I clinical observational trial was performed in 20 healthy volunteers (10 male, 10 female) to verify the safety of Triphala. In that study, a water extract of Triphala had no obvious side effects (Phetkate et al., 2020). Pharmaceutical analyses have shown that Triphala is rich in saponins, terpenes, tannins, flavonoids, and phenolic acids (Avula et al., 2013). The hydrolyzed tannins in Triphala are considered the primary inducers of biological activity (Pawar et al., 2009;Russell et al., 2011).
Tannins are known to provide hepatoprotection (Olennikov et al., 2015). There are various research models for inducing liver injury in which Triphala and related plant medicinals have been tested for hepatoprotective activity. However, the preparation methods used in these studies vary and may confound the results ( Table 1). In a previous study Huang et al. (2019), we found that the Phyllanthus emblica component of Triphala exhibited hydrolytic tannin conversion in heat-and refluxmediated extraction, suggesting various extraction methods may yield extracts with variable biological activities. Published studies include the use of common hot and cold extraction methods for Triphala and related plants, but extraction temperature influences the chemical composition of Triphala.
In this study, we compared the hepatoprotective efficacy of Triphala extracts obtained by various methods. We established a mouse model of carbon tetrachloride (CCl 4 )induced liver damage, then monitored for the presence of oxidative damage markers alanine transaminase (ALT) and aspartate aminotransferase (AST), as well as the liver antioxidant and inflammatory markers malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), as well as inflammatory factors and Nrf2 signaling-related genes and proteins to explore the protective effect and mechanism of the various Triphala extracts. The results of this study will support future clinical applications of Triphala.

Sample Preparation
Plant materials were prepared in traditional proportions (3 Terminalia chebula: 2 Terminalia bellirica: 2.4 Phyllanthus emblica). Triphala is extracted in water solvent and extracted by ultrasonication for 0.5 h (U-0.5 h) at 20°C, reflux for 2 h (R-2 h) at 100°C, and reflux for 4 h (R-4 h) at 100°C. The solution concentration was 0.24 g/ml, and the extraction values of the three methods were 12.74%, 34.91%, and 41.30%, respectively. The extracts were filtered, and the filtrates were stored in a refrigerator at 4°C.

Experimental Animals
Kunming mice (30 ± 2 g) were supplied by Dashuo Laboratory Animal Co. Ltd. (Chengdu, China). The animals were housed at room temperature under a 12:12 light:dark schedule with food and water ad libitum. All experiments were performed in strict accordance with the recommendations of China's "Guidelines for the Care and Use of Laboratory Animals." The experimental protocol was approved by the Ethics Committee of the Affiliated Hospital of Chengdu University of TCM (Approval ID: 2018BL-002).
The animals were divided into nine groups, with an average of six mice per group. The experimental groups received one of the three Triphala extracts (U-0.5, R-2, and R-4 h), with treatments administered by gavage at 1.2 g/kg for the low-dose group (L) and 2.4 g/kg for the high-dose group (H). Dosages were calculated based on the clinical dosage of Triphala by the body surface area Dried fruits were ground to a powder, then mixed in distilled water (5 g in 100 ml) and mixed for 3 h at 40°C Chakraborty and Verma (2010) Phyllanthus emblica L. bark Ethanol-induced hepatotoxicity Dried bark powder (100 g) was extracted in 250 ml of a 7:3 mixture of absolute ethanol and water. In a rotary evaporator, the extract was evaporated to a dry state by vacuum distillation Chaphalkar et al. (2017) Terminalia chebula t-BHP-induced acute liver injury Samples (100 g) were extracted in 1 L distilled water, boiled for 90 min, centrifuged for 15 min, and the supernatant lyophilized Choi et al. (2015) Phyllanthus emblica L. fruit High fat diet-induced liver injury The dried powder was extracted with water using a rotary shaker at room temperature for 24 h and dried by vacuum evaporation Huang et al. (2017) Terminalia bellirica (Gaertn) Roxb. Fruit CCl 4 -induced hepatotoxicity Dried fruits were minced and extracted with ethanol, then dried under reduced pressure Jadon et al. (2007) Emblica officinalis fruit Iron dextran-induced l hepatotoxicity A mixture of 100 g powder and 500 ml methanol: Water (7:3) was stirred with a magnetic stirrer for 15 h, then the mixture was centrifuged. The supernatant was collected, concentrated in a rotary evaporator, and freeze-dried Sarkar et al. (2015) Terminalia bellirica and Terminalia sericea leaf D-galactosamine-induced liver damage Leaves were air-dried, ground, and extracted with methanol at room temperature for 3 days, then freeze-dried method. Positive controls received DDB (7.5 mg/kg) by gavage. Normal (N) and Model (M) controls were given the same volume of distilled water by gavage. All groups were treated intragastrically once daily for a week. Two hours after treatment on the last day, all mice but those in the N group were given 0.1% CCl 4 vegetable oil solution (10 ml/kg body weight) by intraperitoneal injection, while the mice in the group N were merely given the same amount of vegetable oil. All animals were fasted overnight and sacrificed after 16 h. Blood and liver tissues were collected immediately. The collected blood was centrifuged at 4,000 rpm at 4°C for 10 min and stored at -20°C. The liver tissues were dissected and immediately rinsed  with ice-cold saline. One portion was immediately refrigerated at -80°C, and the other was fixed with 4% paraformaldehyde for histopathological analysis.

UPLC-Q-Orbitrap HRMS Conditions and Analysis
The analysis was performed on ultra-high performance liquid chromatography coupled with quadrupole-orbitrap high resolution mass (UPLC-Q-Orbitrap HRMS) (Thermo Fisher, United States). Chromatographic separation was carried out at 30°C on Thermo Scientific Accucore C 18 (2.1 mm × 100 mm, 2.6 μm). The mobile phase consisted of (A) water with 0.1% formic acid and (B) methanol. The gradient was as follows: 0-25 min, 5% B isocratic; 25-30 min, 5-95% B linear; 30-35 min, 50% B isocratic. The flow rate was 0.3 ml/min. The MS acquisition was performed using both positive and negative ionization mode. The heated electrospray ionization parameters as follows: sheath gas flow 35 arb (arbitrary units), auxiliary gas flow 10 arb, spray voltage 3.0 kV for positive ionization and negative ionization, capillary temperature 320°C, probe heater temperature 350°C, the ion scanning range is m/z 100-1500. Under the above conditions, the chemical constituents of the three extracts of Triphala were qualitatively analyzed. Use Xcalibur 3.0 software to process the total ion chromatogram of the sample in positive and negative ion mode, match the measured spectrum with the mzCloud and mzVault network databases, and then combine the precise relative molecular mass of the target component, reference substances, MassBank, and Human Metabolome database (HMDB), PubMed, ChemSpider and related references, for manual identification and identification.

Calculation of Body Weight and Liver Index
Every two days throughout the experiment, the mice were weighed, and changes were noted. Dissected mouse livers were weighed, and the liver index was calculated as liver index liver mass (g)/mouse body weight (g) × 100%.

Biochemical Examinations of Serum ALT, AST Levels
Serum levels of ALT and AST were determined using standard kits according to the manufacturer's instructions.

Histopathology
The liver tissue stored in 4% paraformaldehyde solution at 4°C was embedded in paraffin, then sliced by microtome, stained by hematoxylin and eosin (H&E), and finally examined under an optical microscope (Nikon eclipse ci, Japan).

Measurement of Hepatic MDA, GSH-Px, SOD, TNF-α and IL-6 Levels
Hepatic levels of MDA, SOD, GSH-Px, TNF-α, and IL-6 were determined according to the manufacturer's instructions of standard assay kits.

RNA Extraction, Reverse Transcription-PCR, and RT-PCR
Total RNA was extracted from mouse liver using Trizol (Invitrogen Life Technologies), followed by reverse transcription to cDNA (Applied Biological Materials Inc.) and PCR amplification (Shanghai Hongshi Medical Technology Co., Ltd.). Amplification conditions were: initial denaturation at 95°C for 10 min, followed by 40 cycles of denaturation at 95°C for 15 s, annealing at 60°C for 15 s, and extension for 60 s. Amplification targets were the Nrf-2, NQO-1, and HO-1 genes, with primers described in Supplementary Table S1. Relative expression was determined by the 2 −ΔΔCT method.

Western Blot Analysis
Liver tissue was weighed, washed 2-3 times with ice-cold PBS, mixed with a 10-fold volume of RIPA, homogenized on ice, centrifuged at 12,000 g for 10 min, and the supernatant collected. Protein concentration was determined by the BCA method. Total protein (15 μL) was separated by 10% SDS-PAGE, then transferred to a PVDF membrane (Millipore Corporation, United States) overnight at 25 V. The membrane was sealed in 5% defatted milk/TBST for 1 h and incubated with primary antibody overnight at 4°C. The membrane was rinsed three times with TBST at room temperature, incubated with secondary antibody at room temperature for 30 min, then washed three times with TBST. Protein bands were detected by ECL, and the images were collected with a chemiluminescence imaging system (Shanghai Clinx Scientific Instrument Co., Ltd.). Grayscale analysis was performed with the on-instrument ChemiScope software.

Statistical Analysis
Data analysis was performed using SPSS 21.0 statistical analysis software with results expressed as mean ± standard deviation. Analysis of variance (ANOVA) and LSD t-tests were used to compare multiple groups. Significance was defined as p < 0.05.

Chemical Analysis
HPLC chromatograms are shown in Figure 1A. Through the comparison of reference substance, we carried out quantitative analysis of 15 components, as shown in Table 2. We compared the differences of 9 components with large changes in peak area during the decoction of Triphala ( Figure 1B). Multivariate statistical methods were used to analyze the fingerprint data, and SIMCA-P 13.0 software was used to perform PCA analysis. The PCA score chart shows Origin 1 is U-0.5 h; Origin 2 is R-2 h; Origin 3 is R-4 h.
Frontiers in Pharmacology | www.frontiersin.org July 2021 | Volume 12 | Article 664607 differences between the products of the three extraction methods, particularly between the ultrasonic and reflux methods ( Figure 1C). Orthogonal projections to latent structures discriminant (OPLS-DA) and S-plot analysis were used to find differences in chemical markers. The S-plot is a loading profile that depicts the influence of variables on biomarker selection. Among all the 186 variables in the S-plot, we identified 10 chemical markers that differed most between the Triphala preparations ( Figure 1D). The retention times for these markers were 15.230, 56.484, 54.018, 8.614, 79.821, 60.271, 32.466, 12.475, 64.938, and 76.437. By comparison with the reference substance's retention time, nine of the components were determined to be gallic acid, 1,3,6tri-O-galloylglucose, corilagin, chebulic acid, ellagic acid, epicatechin gallate, catechin, chebulagic acid, and chebulinic acid. These 9 identified actives have a wide range of biological activities ( Table 3). The component most reduced by extraction is hydrolyzed tannin (chebulinic and chebulagic acid), while tannin hydrolysate was greatly increased (corilagin, gallic acid, chebulic acid, and ellagic acid). Chebulinic acid decreased most dramatically during the decoction of Triphala, likely due to its chemical structure. Chebulinic acid is formed by the condensation of small molecule tannins and glucose through five ester bonds. It is not stable under heat and easily decomposes into one molecule of chebulic acid and one molecule of 1,3,6-Tri-O-galloyl glucose, which is then decomposed into three molecules of gallic acid and one molecule of glucose. Chebulagic acid is also unstable under heated conditions and is hydrolyzed to produce one molecule of chebulic acid and one molecule of corilagin. Corilagin is composed of a galloyl, a hexahydroxybiphenoyl (HHDP) and a glucosyl moiety by three ester bonds. When heated, it will continue to hydrolyze to produce gallic acid, ellagic acid, and glucose. A schematic diagram of the hydrolysis of chebulinic and chebulagic acid is shown in Figure 2. Triphala also contains catechins, condensed tannins that undergo condensation reactions and precipitate, thus reducing the final extract's content.
Through the UPLC-Q-Orbitrap HRMS, a total of 106 compounds were identified in the three extracts of Triphala, among which 76 were common components, as shown in Table 4. The results showed that Triphala mainly contained tannins, phenolic acids, flavonoids, alkaloid sugars and glycosides, vitamins, amino acids, fatty acids, organic acids, and a small amount of coumarins, terpenoids, sterols, lignin.

Effects of Triphala on Physiological Growth
There was no significant difference in animal weights between groups (Supplementary Table S2). Treatments yielded no adverse reactions, including nausea, vomiting, and loss of appetite. The dosages chosen had no significant impact on physiological growth and had no obvious toxic side effects.

Effects of Triphala on Liver Index
The liver index is an important indicator of pathological changes caused by liver injury (Figure 3). Compared with the N group, the model groups' liver index increased significantly (p < 0.01), indicating that hepatotoxicity was successfully modeled. Compared with the M group, the liver index of the treatment group was reduced. Group DDB and U-0.5 h differed significantly (p < 0.01), and the high dose R-2 h also differed significantly (p < 0.01). The results show that all Triphala extracts alleviated liver damage in mice, but the ultrasonic extraction method was most effective.

Effects of Triphala on Serum ALT and AST Levels
Compared with the N group, ALT and AST levels in group M were significantly increased (p < 0.01; Figure 4A,B). In contrast, all mice treated with U-0.5, R-2, and the high dose R-4 h exhibited significantly reduced ALT and AST (p < 0.01). However, mice treated with a low dose of the 4-h reflux extract showed a slight but insignificant decrease in enzyme activity (p > 0.05).

Histopathology
As in Figure 4C, in the normal group, the hepatic lobules were clear in structure, the cords were neatly arranged, and the hepatocytes were rich in cytoplasm and normal in morphology. In the model group, the hepatic lobule structure was destroyed, most hepatocytes were swollen, many hepatocytes were steatotic and necrotic, and many inflammatory cells were infiltrated. In contrast, the liver tissues of the DDB group were nearly normalized; the degree of the hepatocellular lesion was relatively mild. In the U-0.5 h treatment group, the dose dependence was not significant, the hepatic lobule structure was clear, the hepatocyte cytoplasm was abundant, the morphological structure was normal, and a small amount of hepatocyte necrosis, nuclear fragmentation, or dissolution was seen at the edge of the local tissue. In the R-2 h treatment group, the dose dependence was significant. In the high-dose group, the hepatic lobule structure was clear, more hepatocytes showed mild degeneration, and smaller round vacuoles were seen in the cytoplasm. In the low-dose group, a large amount of hepatocyte necrosis, nuclear fragmentation, and dissolution was seen around the central vein and the junction area, and a small amount of hepatocyte balloon-like degeneration was seen at the edge of the necrotic focus. The cells were swollen, the nuclei were centered, and the cytoplasm was vacuolated. In the R-4 h treatment group, the degree of liver cell damage was similar to the model group. The hepatic lobule structure was destroyed, and many inflammatory cells were infiltrated.

Effects of Triphala on Lipid Peroxidation
Compared with the N group, MDA levels in the model group were significantly increased. The levels of SOD and GSH-Px were significantly reduced (p < 0.01; Figure 5), indicating that the liver tissue experienced intense oxidative stress and mounted a lipid peroxidation response. Compared with the M group, MDA levels in the different treatment groups were significantly reduced (p < 0.01), the levels of SOD were significantly increased (p < 0.01), and the levels of GSH-Px were also significantly increased (p < 0.05 or 0.01). Thus, we conclude that Triphala improved the antioxidant response, relieving liver damage caused by CCl 4 .

Effects of Triphala on Anti-inflammatory Markers
Compared with the N group, IL-6 and TNF-α levels in the model group were significantly increased (p < 0.01; Figure 6). Compared with the M group, the levels of TNF-α were significantly reduced in the treatment groups (p < 0.01). IL-6 levels were significantly reduced in the U-0.5 and H-R-2 h groups (p < 0.01) and significantly differed in the L-R-2 and R-4 h groups (p < 0.05). Thus, the ultrasonic extract of Triphala provided a greater antiinflammatory effect.
Effect of Triphala on Nrf-2, HO-1 and NQO-1 Genes and Protein Expression The expression levels of Nrf-2, HO-1, and NQO-1 mRNA in the nuclei of liver tissues in the treatment groups were significantly increased in the treatment groups ( Figure 7). Specifically, Nrf-2, HO-1, and NQO-1 mRNA expression was highest in the group treated with the ultrasonic Triphala extract (p < 0.01). CCl 4 also promotes the expression of these genes. Expression levels of Nrf-2, HO-1, and NQO-1 protein in the nuclei of liver tissues significantly increased in the treatment groups ( Figure 8), with no substantial difference between extraction methods. CCl 4 also promotes the expression of these proteins.

CONCLUSION AND DISCUSSION
Liver disease carries high morbidity and mortality worldwide. Reactive oxygen species (ROS) play a pivotal role in the occurrence and development of chronic liver disease (Kuriakose et al., 2017). Plants are rich in antioxidant ingredients, which are important in reducing the pathogenesis FIGURE 6 | Comparison of liver levels of IL-6 (A), TNF-α (B) (x ± s, n 6). Compared with group N, # p < 0.05, ## p < 0.01; compared with group M, *p < 0.05, **p < 0.01.
Frontiers in Pharmacology | www.frontiersin.org July 2021 | Volume 12 | Article 664607 of oxidative stress due to their free radical scavenging effect (Firuzi et al., 2011). Nevertheless, before plants are used as therapies in modern medical systems, they need to be systematically verified and screened. Triphala has been used as a traditional Ayurvedic medicine for centuries and has been shown to have great potential to promote antioxidant activity (Prasad and Srivastava, 2020). The compound is known to scavenge free radicals, restore antioxidant enzyme and non-enzyme levels, reduces lipid peroxidation, and has good therapeutic prospects for liver diseases. As the main active ingredient of Triphala, tannin is also the main substance of antioxidant activity. CCl4 is widely used in the preparation of liver injury models and is one of the commonly used chemical drugs to verify the hepatoprotective activity of plant-based drugs. The oxidative damage caused by CCl 4 is a good model for screening antiplant drugs for liver protection activity (Nada et al., 2010). Free radicals (·CCl3) are the active metabolites of CCl 4 , mainly related to liver damage caused by CCl 4 (Wu et al., 2007), reacting with oxygen to form trichloromethyl peroxide radical (CCl 3 OO·), which initiates a chain reaction of lipid peroxidation and attacks and destroys polyunsaturated fatty acids, especially those related to phospholipids (Szymonik-Lesiuk et al., 2003;Ranawat et al., 2010).
This study examined three Triphala extracts for protective activity with DDB as a positive control drug. The results show that the three tested extracts have a protective effect on damaged liver cells, but the most protective was the ultrasonic extraction, which significantly reduced serum ALT and AST and MDA in liver tissues increased SOD and GSH-Px activities. These results show that Triphala can better improve free radical scavenging and reduce cell damage caused by free radicals. In addition, CCl 4 -induced oxygen free radicals can produce Kupffer cells, which mediate the liver inflammatory response by inducing TNFα and interleukin (Yu et al., 2014). Current research shows that Triphala can reduce the overexpression of TNF-α and IL-6 in CCl 4 -induced mouse liver tissues, inhibit inflammation, and provide a hepatoprotective effect.
The Nrf-2 signaling pathway is one of the body's most important signaling pathways to cope with oxidative stress injury. It can increase the antioxidant level by up-regulating antioxidant proteins in liver cells (Li et al., 2015). Under normal conditions, Nrf-2 is in a state of inhibition. When free radicals attack the body, Nrf-2 enters the nucleus and activates heme oxygenase-1 (HO-1) and phosphoramidite adenine dinucleotide quinone oxidoreductase-1 (NQO-1), further catalyzing heme degradation and eliminating free radicals from the body (Hseu et al., 2012). This study has shown that Triphala can significantly increase both transcript and protein expression of Nrf-2, HO-1, and NQO-1 in damaged liver tissues, regulates the Nrf-2 signaling pathway, and improves the performance of the body's antioxidant system.
In summary, the three tested Triphala extracts have a hepatoprotective effect, but there were clear differences in efficacy between preparations. The ultrasonic preparation of Triphala was most effective, suggesting that macromolecular substances mediate the protective effect against liver injury, and the loss of macromolecular substances to hydrolysis reduces hepatoprotective potency. During the hydrolysis of FIGURE 7 | Relative expression of Nrf-2 (A), HO-1 (B) and NQO-1 (C) mRNA (x ± s, n 6). Compared with group N, # p < 0.05, ## p < 0.01; compared with group M, *p < 0.05, **p < 0.01.
Triphala, small molecules such as gallic and ellagic acid increase, but studies have found that gallic acid and ellagic acid exhibit poor absorption, low bioavailability, and easy saturation. When the content is saturated, the increase in content has little effect on the efficacy (Seeram et al., 2004;Ahmed et al., 2018). Structure-activity analysis has shown a large number of phenolic hydroxyl groups in the molecular structure of chebulagic and chebulinic acid, suggesting significant antioxidant activity. Therefore, treatment with botanical medicines rich in hydrolyzed tannin must be prepared in a way that optimizes efficacy. There are various preparation processes, but extraction methods should be controlled to meet the consistency requirements for the biological activities of medications. This study's most significant finding is that low-temperature extraction is essential to retaining bioactive hydrolyzed tannins and improving Triphala's hepatoprotective efficacy.

DATA AVAILABILITY STATEMENT
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.

ETHICS STATEMENT
The animal study was reviewed and approved by Ethics Committee of the Affiliated Hospital of Chengdu University of TCM.

AUTHOR CONTRIBUTIONS
Revision of the manuscript was done by XW and DZ. XW, CL, FR, and WL performed the experiments. Acquisition and analysis of experimental data were carried out by XW. YH, HH, gave some advice for improving the paper. Study concept and design were the responsibility of JL and LH.