Metabolomics of Fuzi-Gancao in CCl4 induced acute liver injury and its regulatory effect on bile acid profile in rats

Abstract

BACKGROUND

Fuzi (Radix aconiti lateralis)-Gancao (Radix glycyrrhizae) is one of the most classical drug pairs of traditional Chinese medicine. In clinical practice, decoctions containing Fuzi-Gancao (F-G) are often used in the treatment of liver diseases such as hepatitis and liver failure.

AIM

To investigate the metabolomics of F-G in CCl₄ induced acute liver injury in rats and its regulatory effect on the bile acid profile.

METHODS

The pharmacodynamic effect of F-G on CCl₄ induced acute liver injury in rats was evaluated, and an ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous determination of 92 metabolites from multiple pathways was established to explore the protective metabolic mechanism of F-G in serum on the liver.

RESULTS

Twenty-four differential metabolites were identified in serum samples. The primary bile acid biosynthetic metabolic pathway was the major common pathway in the model group and F-G group. Subsequently, a UPLC-MS/MS method for simultaneous determination of 11 bile acids, including cholic acid, ursodeoxycholic acid, glycochenodeoxycholic acid, glycochenodeoxycholic acid, taurocholic acid, glycocholic acid, chenodeoxycholic acid, deoxycholic acid, taurochenodeoxycholic acid, taurocholic acid, and glycinic acid, was established to analyze the regulatory mechanism of F-G in serum. F-G decreased the contents of these 11 bile acids in serum in a dose-dependent manner compared with those in the model control group.

CONCLUSION

F-G could protect hepatocytes by promoting the binding of free bile acids to glycine and taurine, and reducing the accumulation of free bile acids in the liver. F-G could also regulate the compensatory degree of taurine, decreasing the content of taurine-conjugated bile acids to protect hepatocytes.

Key Words: Radix aconiti lateralis; Radix glycyrrhizae; Liver injury; Metabolites; Bile acid; Fuzi-Gancao

Core Tip: Fuzi-Gancao (F-G) could protect hepatocytes by promoting the binding of free bile acids to glycine and taurine, and reducing the accumulation of free bile acids in the liver. F-G could also regulate the compensatory degree of taurine, decreasing the content of taurine-conjugated bile acids to protect hepatocytes.

INTRODUCTION

The liver is an important metabolic organ of the human body that has the physiological functions of detoxification, phagocytosis, and defense[1]. With the development of modern industry, liver injury caused by environmental pollution is gradually increasing. Liver injury is an important pathophysiological process in the development of hepatitis, liver fibrosis, liver cirrhosis, and liver cancer. Therefore, the treatment of liver injury is important for the prevention, treatment, and recovery of a variety of liver diseases[2,3].

Bile acids are one of the most sensitive indicators for the clinical diagnosis of liver diseases[4,5]. When the liver system is diseased, it can cause a disturbance in the metabolism of bile acids in the body, thus causing a significant change in the amount of bile acids in the blood. Therefore, biomarkers of the bile acid metabolism pathway are very important diagnostic and therapeutic indicators for liver disease[4-6]. Liver diseases such as liver injury, hepatitis, cirrhosis, and hepatocellular carcinoma have significantly increased serum total bile acid levels, and changes in total bile acid levels are usually analyzed in clinical tests but are not highly specific[6,7]. Therefore, the changes in the bile acid profile based on the metabolic pathway of bile acids have important significance for the prevention and treatment of liver diseases. Bile acids can be divided into primary and secondary bile acids[8,9]. Primary bile acids are bile acids synthesized directly from cholesterol by hepatocytes and mainly include cholic acid (CA) and chenodeoxycholic acid (CDCA). Secondary bile acids are free bile acids produced by the primary bile acids deoxycholic acid (DCA) and lithocholic acid (LCA) after 7α-hydroxy deoxygenation of the intestinal flora. These free bile acids bind with glycine and taurine to form conjugated secondary bile acids such as glycocholic acid (GCA), glycochenodeoxycholic acid (GCDCA), glycochenodeoxycholic acid (GDCA), taurocholic acid (TCA), taurochenodeoxycholic acid (TCDCA), ursodeoxycholic acid (UDCA), glycinic acid (GLCA), and taurocholic acid (TUDCA).

Chinese herbal compounds have been used clinically for thousands of years in the treatment of liver system diseases, among which Fuzi (Radix aconiti Lateralis)-Gancao (Radix glycyrrhizae) is one of the most common drug pairs in Chinese herbal compounds, and Chinese herbal compounds containing Fuzi-Gancao (F-G), such as Yinchen Sifu decoction, Sini decoction, and Fuzi Lizhong decoction, are often used in the treatment of liver diseases such as hepatitis and liver failure[10-13]. Modern pharmacological studies have shown that herbal compounds containing Fuzi and Gancao can reduce the biochemical indexes of liver injury model animals by inhibiting inflammatory stress, lipid peroxidation, and apoptosis and have significant pharmacological activity to prevent liver injury[14-16].

Fuzi and Gancao are important medicinal materials in classic prescriptions, such as Sini decoction and Fuzi Lizhong decoction. Aconite alkaloids in Fuzi and flavonoids in Gancao are the main active ingredients in F-G drug pairs. Alkaloids are the main active ingredients in aconite, and thus far, nearly 200 alkaloids have been isolated and identified. These alkaloids are mainly classified into nonester alkaloids, monoester diterpene alkaloids (MDAs), diester diterpene alkaloids (DDAs), and lipoalkaloids according to their structural properties[17]. MDAs and DDAs have very well-defined pharmacological activities, such as cardiotonic[18-20], anti-inflammatory and analgesic[21], antitumor[22], antioxidation[23], and hepatoprotective[24,25] activities. Flavonoids are the main active ingredients of Gancao and have well-defined pharmacological anti-inflammatory[26-28], antibacterial[29], antioxidant[30], hepatoprotective, and antitumor[31] activities. The Chinese Pharmacopoeia (2015 edition) prescribes the compatibility ratio of Fuzi and Gancao as 1:1, which could decrease the toxins caused by aconite alkaloids and enhance the treatment effect compared with other ratios[32-34].

In a previous study, a rapid, convenient, and stable method for the simultaneous quantitative determination of six alkaloids and three flavonoids in Radix aconiti lateralis and Radix glycyrrhizae by ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established[17]. In this study, the effects of the F-G water extract on the prevention of liver injury induced by tetrachloride (CCl₄) were evaluated. Then, the metabolic mechanism was studied by UPLC-MS/MS. Finally, a method of simultaneous quantitative detection of 11 bile acids was established, and the mechanism of F-G in the regulation of the serum bile acid profile was analyzed by UPLC-MS/MS.

MATERIALS AND METHODS

Plant materials

Radix aconiti lateralis (Fuzi) pieces were purchased from Huang Gang Jingui Traditional Chinese Medicine Industry Development Co., Ltd. (Sichuan, China), and Radix glycyrrhizae (Gancao) was purchased from Bozhou Jinshaotang Herbal Decoction Co., Ltd. (Anhui, China). The medicinal materials were identified by Professor Fu Xiao at the First Affiliated Hospital of Jinzhou Medical University.

Chemicals and Reagents

The aspartate aminotransferase (AST) and alanine aminotransferase (ALT) assay kits were purchased from Nanjing Jiancheng Bioengineering Co., Ltd.; silybin was purchased from Solarbio Biotech Co., Ltd.; L-leucine, L-tryptophan, L-kynurenine, 5-Hydroxytryptamine (5-HT), 5-hydroxytryptophan (5-HTP), cholic acid, N-phenylacetylglycine, glutathione (GSH), glutathione oxidized (GSSG), N-ethylmaleimide, and formic acid were purchased from Sigma-Aldrich (United States); L-phenylalanine (Ring-D5) was purchased from Cambridge isotope laboratories; UDCA, GDCA, GCDCA-Na, TCA-Na, and GCA were purchased from Meryer Co., Ltd.; CDCA, DCA, TCDCA, TUDCA, and GLCA were obtained from Shanghai Macklin Biochemical Co., Ltd; d4-GCDCA was purchased from Shanghai Zhenzun Biochemical Co., Ltd; MS-grade methanol and acetonitrile were purchased from Merck; water for MS analysis was prepared using a Milli-Q water purification system; phosphate buffered solution (PBS) was purchased from HyClone Co., Ltd; CCl4 was purchased from Yongsheng Chemical Co., Ltd; alcohol was purchased from Kermel Chemical Co.; pentobarbital sodium was purchased from Shanghai Experimental Chemical Reagent Co., Ltd.; and normal saline was purchased from Qingdao Huaren Pharmaceutical Co., Ltd.

Animals

Male Sprague-Dawley rats (200 g ± 20 g) were purchased from the Laboratory Animal Center of Chinese Medical University (animal license No.: SCXK (Liao) 2008-0005). The rats were housed under SPF laboratory conditions at a temperature of 25 ± 2 °C, a relative humidity of 40 ± 5%, and a 12-h circadian cycle for 1 wk. All procedures were performed according to the National Institute of Health guidelines regarding the principles of animal care.

Preparation of the F-G extract

Fuzi (1.3 kg) and Gancao (1.3 kg) were mixed and soaked in water (26 L) for 0.5 h, and then the mixture was refluxed for 2 h. The supernatant was then concentrated under vacuum to obtain the F-G extract. The extract was diluted with water to a final concentration of 1.5 g/mL (crude drug), and all the extracts were stored at 4 °C before use.

Protective effect of F-G on acute liver injury induced by CCl₄

Forty male rats were randomly divided into five groups (n = 8): Normal control group, model control group, positive control group, F-G group with 15 g/kg crude drug, and F-G group with 30 g/kg crude drug. The positive control group was orally administered with silybin at 50 mg/kg daily, and the normal control group and model control group were given the same volume of normal saline daily by gavage once a day for 8 d.

On the 7^th day, 40% CCl₄ (v/v, olive oil) was intraperitoneally injected in the positive control group, model control group, and F-G groups at a dose of 2 mL/kg. The rats were anesthetized using sodium pentobarbital 2 h after administration on the 8^th day. Blood samples were collected from the abdominal aorta and centrifuged at 3500 rpm for 10 min (4 °C) to obtain serum samples for transaminase (ALT and AST) and metabolic analysis. Liver tissue samples were taken for pathological analysis.

Metabolic analysis

To elucidate the mechanism of F-G in the treatment of liver injury, three groups of serum samples, including that from the normal control group, model control group, and F-G group (30 g/kg), were used for metabolic analysis by UPLC-MS according to a method published by the authors with minor modifications[35].

Preparation of “stripped” serum: One hundred milliliters of rat serum including activated charcoal powder (6 g) was incubated at room temperature for 2 h. After centrifugation at 13000 rpm for 20 min (4 °C), the supernatant was filtered successively through microporous membranes with pore sizes of 5 μm, 1.2 μm, and 0.45 μm to obtain “stripped” serum.

Samples for metabolic analysis: Two hundred microliters of the serum sample was pipetted into a 1.5 mL centrifuge tube, followed by adding 200 μL of PBS solution containing NEM (10 mmol/L) and 1000 μL of methanol solution with L-phenylalanine (Ring-D5; 10 ng/mL, internal standard) in sequence, vortexing for 30 s, and incubating the sample at -20 °C for 15 min after mixing. After incubation, 1000 μL of supernatant was transferred into a 2 mL centrifuge tube by centrifugation at 12000 rpm for 10 min at 4 °C, and the samples were dried with nitrogen and stored at -80 °C. The dried residue was reconstituted with 100 μL of 5% ACN-H₂O solution prior to analysis, vortexed for 1 min, and centrifuged at 12000 rpm for 10 min at 4 °C. Sixty microliters of the supernatant was aspirated accurately into an injection vial, and 10 μL of each sample was injected into UPLC-MS/MS for the analysis of metabolic biomarkers.

Preparation of standard solution: L-Leucine, 5-HT, N-phenylacetylglycine, L-tryptophan, L-kynurenine, 5-HTP, cholic acid, and GSSG were accurately weighed and dissolved in methanol to make stock solutions at a concentration of 1 mg/mL. GSH was accurately weighed and dissolved in methanol containing NEM (10 mmol/L) to make a solution at a concentration of 0.5 mg/mL. Each standard solution was mixed proportionally and serially diluted with 50% methanol-water to obtain a series of mixed standard solutions.

Method validation: Calibrators of the nine metabolites (L-Leu, 5-HT, N-Phe, L-Try, L-Kyn, 5-HTP, CA, GSH, and GSSG) were generated from the mixed standard working solutions in “stripped” serum. The linear regression standard curve was calculated with 1/x weighting and plotted with the concentrations and the peak area ratio of each analyte to the internal standard.

Pooled standard solutions were added to “stripped” serum to prepare QC samples of three different concentrations, which were then processed as described in “Samples for metabolic analysis”. Intraday precision was calculated according to the content of nine metabolites from the QC sample in six consecutive analyses. The interday precision was obtained after continuous analysis of the QC sample for 3 d. Precision is expressed as the relative standard deviation (RSD, %).

Three concentrations of the mixed standard solutions were added to the samples of a definite content and processed for analysis six times to obtain recovery. Recovery was calculated according to the formula:

Recovery (%) = (C-A)/B × 100% (A is the measured content of the test sample, B is the amount of standard content, and C is the measured content).

UPLC-MS/MS analysis: Samples were separated using a Waters ACQUITY ultra-performance liquid chromatographer with a Waters BEH column (1.7 μm, 2.1 × 50 mm, C-18) and a mobile phase consisting of 0.1% formic acid in water (A) and acetonitrile (B) using a gradient system with the following elution procedures: 0-2.0 min, 5% B; 2.0-5.0 min, 5-50% B; 5.0-6.0 min, 50% B; 6.0-17.0 min, 50-95% B; 18.0-22.0 min, 95-5% B; and 22.0-25.0 min, 5% B. The flow rate was 0.3 mL/min, and the column temperature was set at 25 °C. Mass spectral analysis was achieved using an AB 4000 Q-TRAP system with ESI in positive and negative ionization modes and multiple reaction monitoring (MRM) mode. The MS parameters were as follows: Ion spray voltage, ± 4500 V; curtain gas, 20 psi; temperature, 450 °C; and ion source gas, 40 psi. All the metabolites were analyzed using precursor ions (Q1), product ions (Q3), declustering energy, entrance pressure, collision energy, and collision cell exit potential as detection parameters.

Bile acid analysis

Thirty-six male SD rats were randomly divided into six groups (n = 6): Normal control group, model control group, positive control group, and F-G groups including FGL (10 g/kg), FGM (20 g/kg), and FGH (30 g/kg). The positive control group was given 50 mg/kg silybin, the normal group and model group were given the same volume of normal saline, and all the groups were administered for 8 d.

On the 7^th day, 40% CCl₄ (v/v, olive oil) solution was injected intraperitoneally (2 mL/kg), and the same dose of olive oil was injected intraperitoneally in the control group. The rats were anesthetized 2 h after administration on the 8^th day. Blood samples were collected from the abdominal aorta and centrifuged at 4000 rpm for 10 min (4 °C) to obtain serum samples for the analysis of bile acids.

Preparation of standard solutions: CDCA, DCA, UDCA, GLCA, GCDCA, GDCA, GCA, TCDCA, TCDCA, TUDCA, and TCA were accurately weighed and dissolved in methanol to prepare stock solutions at a concentration of 1 mg/mL and stored at -80 °C. Solutions were serially diluted with 50% methanol-water prior to testing. d₄-GCDCA was accurately weighed and dissolved in methanol to make an internal standard solution. All the solutions were stored at -80 °C prior to use.

Sample preparation: Two hundred microliters of serum was added to 1000 μL of methanol containing internal standard (d4-GCDCA, 20 ng/mL). The samples were centrifuged at 12000 rpm for 15 min (4 °C) after mixing, and then 1000 μL of the supernatant was dried with nitrogen and stored at -80 °C. The dried residue was reconstituted with 50 μL of 80% methanol-water solution prior to analysis, vortexed for 1 min, and centrifuged at 12000 rpm for 15 min (4 °C). Then, 30 μL of supernatant was aspirated accurately into an injection vial, and 10 μL of each sample was injected into the UPLC-MS/MS system for bile acid quantification.

UPLC-MS analysis: Samples were separated using a Waters Acquity Uplc instrument and an Agilent ZORBAX SB-C18 column (3.5 μm, 2.1 mm × 100 mm) and a mobile phase consisting of 0.1% formic acid in water (A) and methanol (B) using a gradient system with the following elution procedure: 0-2.0 min, 10% B; 2.0-9.0 min, 10%-80% B; 9.0-11.0 min, 80% B; 11.0-20.0 min, 80%-90% B; and 20.0-25.0 min, 90%-10% B. Ten microliters of the sample was injected at a flow rate of 0.4 mL/min and column temperature of 25 °C. Mass spectral analysis was achieved using a Thermo Scientific TSQ Quantum with ESI in negative ionization mode and MRM mode. The ion spray voltage was -3200 v and the temperature was 380 °C.

Method validation: Eleven bile acids (CDCA, DCA, UDCA, CA, GLCA, GCDCA, GDCA, GCA, TCDCA, TCDCA, TUDCA, and TCA) were diluted with 50% methanol solution to prepare a series of solutions and mixed with “stripped” serum to generate calibrators for validation of the UPLC-MS/MS method. The linear regression standard curve was calculated with 1/x weighting and plotted with the concentrations and the peak area ratio of each analyte to the internal standard.

Pooled standard solutions were added to “stripped” serum to prepare QC samples of three different concentrations for analysis. Intraday precision was calculated according to the contents of 11 bile acids from QC samples for six consecutive analyses. The interday precision was obtained after continuous analysis of QC samples for 3 d. Interday precision and intraday precision are expressed as the relative standard deviation (RSD, %). Three concentrations of mixed standard solutions were added to the samples of a definite content and processed as described above for bile acid analysis six times to obtain recovery.

Three concentrations of 11 mixed bile acid standard solutions were used to investigate the stability of QC samples under different storage conditions and processing procedures. Short-term stability was assessed by analyzing the QC samples that were kept at room temperature for 12 h. Long-term stability was assessed by storing the QC samples at -20 °C for 20 d. Freeze-thaw stability was assessed after the QC samples were frozen at -80 °C and thawed at 4 °C in 1 d for 3 consecutive days. Postpreparation stability was assessed by analyzing the QC samples that were kept at 4 °C for 12 h.

Data analysis

Metabolic analysis was calibrated and integrated using AB Analyst (version 1.6.2, AB Applied Biosystems). Quantitative analyses of bile acids were performed using Thermo Scientific TSQ Quantum Workstation analysis software. Pathway analyses were achieved using SIMCA-P, Metaboanalyst, and KEGG software. The experimental data are expressed as the mean ± SD. The data were analyzed with SPSS 19.0 statistical software (P < 0.05 and P < 0.01).

RESULTS

Effects of F-G on acute liver injury

Histological analysis: The liver tissue of rats in each group was macroscopically observed. The livers of the normal control group rats had a normal morphology, a red color, no adhesion between the lobules, a smooth surface, and no bleeding spots. In the model group, the surface of the liver was milky white, and there was obvious adhesion between the lobules of the liver and the mucous membranes. In the F-G group, the adhesion degree between the lobules and mucous membrane was significantly decreased, and the color was rosier than that of the model rats. The morphological results showed that F-G extract could significantly relieve liver injury induced by CCl₄ (Figure 1).

Figure 1 Histological changes in various groups of rats. HE staining, magnification: 400 ×. A: Normal control group; B: Model control group; C: Fuzi-Gancao (F-G) group (15 g/kg); D: F-G group (30 g/kg); E: Positive control group (silybin).

Histological analysis indicated that the structure of liver tissue in the normal control group was normal, the liver cells were neatly arranged, and there were no pathological changes, such as hepatocyte swelling, inflammatory cell infiltration, blood stasis, or steatosis of hepatocytes. Compared with the normal control group, the model control group showed a significant increase in the number of hepatocytes with extensive hydrodegeneration, steatosis, hepatocyte necrosis, and inflammatory cell infiltration. Compared with the model control group, F-G groups (15 g/kg and 30 g/kg) indicated a decrease in the amount of water-like degeneration in the liver, steatotic cells, and swelling hepatocytes with a significant dose-effect relationship.

Assay of ALT and AST: ALT and AST in the serum of rats were detected by ELISA. The results indicated that the contents of ALT and AST in the model control group were significantly higher than those in the normal control group (P < 0.01). Both transaminase levels were significantly reduced in the F-G groups compared to those in the model control group, but the magnitude of the reduction was still different from that of the positive control group (Table 1).

Table 1 Alanine aminotransferase and aspartate aminotransferase in serum of rats (n = 8).

Group	ALT (U/L)	AST (U/L)
Normal control	43.6 ± 8.7	131.6 ± 25.1
Model control	187.3 ± 29.6a	285.1 ± 31.5a
Positive control	86.7 ± 13.7c	184.2 ± 37.8c
F-G (15 g/kg)	151.2 ± 24.3	246.2 ± 39.8
F-G (30 g/kg)	119.4 ± 19.5c	224.0 ± 34.1b

^aP < 0.01 for the model control group and normal control group.

^bP < 0.05.

^cP < 0.01 for each treatment group and model control group, respectively. F-G: Fuzi-Gancao; ALT: Alanine aminotransferase; AST: Aspartate aminotransferase.

Metabolic analysis

Linearity: The calibration curve of each standard was plotted with the concentrations of nine biomarkers and the ratio of the peak area of each component to that of the internal standard with weighted (1/x) least-square linear regression. The calibration curves of the nine analytes exhibited a good linearity with coefficient of correlation (R²) values better than 0.9926. The lowest concentration of the linear regression for each sample was determined to be the limit of quantification (Table 2).

Table 2 Calibration curve, R², and concentration range of nine metabolites.

Compound	Standard curve	R2	Range (ng/mL)
L-Leu	Y = 0.0627X - 4.9797	0.9952	100-10000
5-HT	Y = 0.0385X - 0.0269	0.9939	0.8-80
N-phe	Y = 0.0229X - 4.9120	0.9958	250-25000
L-Try	Y = 0.0048X - 2.4673	0.9926	600-60000
L-Kyn	Y = 0.0331X + 0.0123	0.9960	5-500
5-HTP	Y = 0.0492X - 0.0001	0.9983	0.2-20
CA	Y = 0.00004X - 0.0010	0.9959	40-4000
GSH	Y = 0.0032X - 0.2362	0.9975	150-20000
GSSG	Y = 0.0001X + 0.0010	0.9949	50-10000

L-Leu: L-leucine; 5-HT: 5-Hydroxytryptamine; N-phe: N-phenylacetylglycine; L-Try: L-tryptophan; L-Kyn: L-kynurenine; 5-HTP: 5-hydroxytryptophan; CA: Cholic acid; GSH: Glutathione; GSSG: Glutathione oxidized.

Accuracy, precision, and recovery: The accuracy and precision of analytes in the QC samples were less than 9.24% and 8.10%, respectively (Table 3), and the recovery of analytes is shown in Table 4. All the analytical values of the nine analytes had satisfactory results within the acceptable criteria according to the bioanalytical method validation guidance of the United States FDA.

Table 3 Accuracy and precision of the developed ultra performance liquid chromatography-tandem mass spectrometry method (n = 6).

Ingredient	Concentration (ng/mL)	Accuracy %	Precision %	Repeatability %	Stability %
L-Leu	750	100.35 ± 3.20	3.19	3.69	0.41
	1000	105.20 ± 6.45	6.13	6.91	1.69
	5000	95.53 ± 4.55	4.76	4.98	1.85
5-HT	6	99.78 ± 8.61	8.63	8.10	2.78
	8	101.78 ± 4.32	4.24	2.87	3.80
	40	101.76 ± 4.50	4.42	4.24	2.14
N-phe	1800	100.29 ± 4.32	4.31	4.72	3.07
	2500	98.97 ± 4.13	4.17	3.71	3.18
	12500	92.24 ± 5.12	5.55	5.95	1.09
L-Try	4500	97.33 ± 3.25	3.34	3.75	0.71
	6000	95.45 ± 4.12	4.32	4.22	3.35
	30000	94.89 ± 4.77	5.03	4.22	4.00
L-Kyn	37	99.61 ± 4.66	4.68	5.00	2.98
	50	102.43 ± 4.15	4.05	4.41	1.73
	250	99.76 ± 4.11	4.12	4.15	2.09
5-HTP	300	102.45 ± 4.51	4.40	3.98	3.65
	400	95.20 ± 8.80	9.24	7.50	6.16
	2000	101.77 ± 8.11	7.97	7.89	7.36
CA	1.5	99.88 ± 3.70	3.70	3.83	1.47
	2	97.00 ± 3.19	3.29	2.97	2.47
	10	96.76 ± 5.30	5.48	4.17	5.22
GSH	1500	101.91 ± 4.65	4.56	5.19	1.45
	2000	96.05 ± 3.98	4.14	4.63	0.89
	10000	97.51 ± 5.88	6.03	4.45	2.45
GSSG	750	99.64 ± 3.97	3.98	4.43	1.56
	1000	100.8 ± 6.45	6.40	7.23	4.89
	5000	98.39 ± 4.54	4.61	3.90	3.80

L-Leu: L-leucine; 5-HT: 5-Hydroxytryptamine; N-phe: N-phenylacetylglycine; L-Try: L-tryptophan; L-Kyn: L-kynurenine; 5-HTP: 5-hydroxytryptophan; CA: Cholic acid; GSH: Glutathione; GSSG: Glutathione oxidized.

Table 4 Recovery of the developed ultra performance liquid chromatography-tandem mass spectrometry method (n = 6).

Ingredient	Baseline (ng/mL)	Spiked (ng/mL)	Recovery %
L-Leu	1000	250	92.53 ± 7.13
		500	93.42 ± 11.52
		750	87.53 ± 9.59
5-HT	8	2	85.37 ± 9.79
		4	90.52 ± 13.47
		6	93.05 ± 10.16
N-phe	2500	625	94.54 ± 12.15
		1250	89.46 ± 6.54
		1875	86.72 ± 8.19
L-Try	6000	1500	93.04 ± 13.23
		3000	85.42 ± 7.12
		4500	91.16 ± 12.25
L-Kyn	50	12.5	90.48 ± 6.18
		25	85.30 ± 10.42
		37.5	86.20 ± 6.13
5-HTP	2	0.5	91.49 ± 5.36
		1	94.64 ± 7.46
		1.5	93.58 ± 5.15
CA	400	100	91.83 ± 12.12
		200	93.29 ± 8.62
		300	90.22 ± 7.28
GSH	1000	250	88.17 ± 6.33
		500	91.16 ± 6.15
		750	90.85 ± 9.81
GSSG	2000	500	91.15 ± 10.08
		1000	93.92 ± 12.15
		1500	89.27 ± 10.92

L-Leu: L-leucine; 5-HT: 5-Hydroxytryptamine; N-phe: N-phenylacetylglycine; L-Try: L-tryptophan; L-Kyn: L-kynurenine; 5-HTP: 5-hydroxytryptophan; CA: Cholic acid; GSH: Glutathione; GSSG: Glutathione oxidized.

Metabolic analysis: Analysis of 92 metabolites was achieved by UPLC-QTRAP-LC-MS/MS. NEM was used to improve the stability of GSH. Twenty-four differential metabolites in the serum (normal control group vs model control group and F-G groups vs model control group) were confirmed according to statistical analysis (Table 5).

Table 5 Serum metabolites in CCl₄-induced acute liver injury in rats (n = 8).

Metabolite	Model group	Control group	FG group
L-leucine	431.1 ± 54.32	331.4 ± 48.78d	393.5 ± 53.83
N-phenylacetylglycine	5.350 ± 0.938	1.417 ± 0.351d	2.915 ± 0.496b,d
L-tryptophan	17.96 ± 3.014	14.63 ± 2.724c	17.05 ± 2.679a
L-kynurenine	6.270 ± 0.729	3.948 ± 0.450d	6.646 ± 1.214b
Cholic acid	1.342 ± 0.230	0.047 ± 0.004d	1.001 ± 0.124b,d
GSH	2.562 ± 0.433	0.991 ± 0.285d	2.317 ± 0.632b
GSSG	0.108 ± 0.016	0.021 ± 0.002d	0.051 ± 0.009b,d
lactate	257.8 ± 32.57	230.8 ± 37.30	185.3 ± 31.52b,d
Choline	3.548 ± 0.539	2.639 ± 0.451	2.802 ± 0.413
(E)-butenedioic acid	163.6 ± 18.57	79.48 ± 8.625d	87.82 ± 10.55d
Hypoxanthine	0.052 ± 0.003	0.021 ± 0.002d	0.022 ± 0.003d
Carnitine	23.55 ± 5.024	13.52 ± 1.370d	20.05 ± 1.323b
Phenylalanine	289.5 ± 37.51	165.6 ± 23.76d	261.4 ± 32.33b
Uric acid	4.523 ± 0.863	2.769 ± 0.474d	2.927 ± 0.488d
Hippuric acid	95.58 ± 16.47	65.78 ± 13.92d	76.53 ± 16.92d
Citric acid	11.86 ± 1.531	15.62 ± 2.437d	13.51 ± 2.002
Pantothenic acid	7.852 ± 0.953	4.602 ± 0.560d	4.831 ± 0.693d
Uridine	19.37 ± 2.772	6.816 ± 0.829d	17.53 ± 2.503b
Glucosamine-1-phosphate	0.025 ± 0.005	0.017 ± 0.004c	0.020 ± 0.004
8-OH-dG	0.008 ± 0.001	0.007 ± 0.001c	0.007 ± 0.001c
C16:1 Lyso PC	3.215 ± 0.491	4.813 ± 0.503d	6.293 ± 1.337b,d
C16:0 Lyso PC	13.37 ± 2.434	16.62 ± 3.027	18.39 ± 3.316c
C18:1 Lyso PC	16.837 ± 2.392	23.699 ± 4.427d	26.647 ± 4.339a,d
C18:0 LysoPC	11.42 ± 1.130	18.332 ± 1.833d	16.66 ± 2.603a,d

^aP < 0.05.

^bP < 0.01 compared with the negative control group.

^cP < 0.05.

^dP < 0.01 compared with the model control group. GSH: Glutathione; GSSG: Glutathione oxidized.

Partial Least-Squares Discriminant Analysis (PLS-DA) (Figure 2) was performed on the data matrix of the variation in individual metabolites in Table 4. The results showed that the samples of the negative control group, model control group, and F-G groups were distributed in different areas and could be separated completely, but samples of the same group had the tendency to aggregate (Figure 2A). The results showed that the difference in all metabolites between the negative control group and the model control group was significant, indicating that the contents of these 24 metabolites were significantly changed in acute liver injury induced by CCl₄. The difference in all metabolites between the F-G groups and the model control group was also significant, indicating that the administration of the F-G extract could cause a significant reduction in the metabolite contents in the serum of rats with acute liver injury induced by CCl₄, which could cause a significant change in the metabolic network. In the PLS-DA plot, samples of the F-G groups were closer to those of the negative control group than those of the model control group, indicating a significant difference in the metabolite contents in rats with liver injury compared to those in the negative control group after treatment with F-G. P-test analysis (Figure 2B) showed that there was no overfitting of the separation model between groups.

Figure 2 Serum metabolites in rats. A: Partial Least-Squares Discriminant Analysis; B: P-test analysis. M: Model control group; N: Negative control group; F-G: Fuzi-Gancao group.

Combined with the variable importance in the projection (VIP) value based on PLS-DA, it was shown that the metabolites with a VIP value greater than 1.0 contributed greatly to the difference before and after treatment with the F-G extract and were the key metabolites. There were 14 key metabolites in the model control group vs the negative control group (Table 6) and 13 key metabolites in the F-G groups vs the model control group (Table 7). Ten common metabolites, namely, GSSG, cholic acid, N-phenylacetylglycine, hippuric acid, uric acid, hypoxanthine, (E)-butenedioic acid, pantothenic acid, C16:1 LPC, and C18:0 LPC, were observed.

Table 6 Variable importance in the projection values of serum metabolites and effects of CCl₄ on their changes (model group vs negative group).

Var ID (primary)	M1-VIP	Variation trend
GSSG	1.19631	↑↑
Cholic acid	1.18964	↑↑
Uridine	1.18609	↑↑
N-phenylacetylglycine	1.16986	↑↑
Hypoxanthine	1.13469	↑↑
(E)-butenedioic acid	1.1299	↑↑
GSH	1.12862	↑↑
C18:0LPC	1.12325	↓↓
Pantothenic acid	1.08663	↑↑
Carnitine	1.08264	↑↑
Phenylalanine	1.07794	↑↑
Hippuric acid	1.06083	↑↑
C16:1LPC	1.05866	↓↓
Uric acid	1.01621	↑↑
C18:1LPC	0.943612	↓↓
L-kynurenine	0.919692	↑
L-leucine	0.90164	↑↑
Glucosamine-1-phosphate	0.893372	↑
Citric acid	0.866932	↓↓
L-tryptophan	0.842517	↑
8-OH-dG	0.711595	↑
Lactate	0.704198	NS
Choline	0.639509	NS
C16:0LPC	0.514772	NS

↑ represents a P value ≤ 0.05 for the increase in mean content; ↑↑ represents a P value ≤ 0.01 for the increase in mean content; ↓ represents a P value ≤ 0.05 for the mean content decrease; ↓↓ represents a P value ≤ 0.01 for the mean content decrease; NS: The mean concentrations of metabolites in the model group were not statistically significant; GSSG: Glutathione oxidized; GSH: Glutathione; VIP: Variable importance in the projection.

Table 7 Variable importance in the projection values of serum metabolites and effects of Fuzi-Gancao on their changes (Fuzi-Gancao group vs model group).

Var ID (primary)	M1-VIP	Variation trend
Hypoxanthine	1.37706	↓↓
GSSG	1.36516	↓↓
Pantothenic acid	1.28548	↓↓
C18:1LPC	1.27880	↑↑
C16:1LPC	1.25881	↑↑
N-phenylacetylglycine	1.22022	↓↓
Lactate	1.21835	↓↓
Hippuric acid	1.21598	↓↓
Uric acid	1.21291	↓↓
(E)-butenedioic acid	1.21107	↓↓
Cholic acid	1.17091	↓↓
C18:0LPC	1.15078	↑↑
C16:0LPC	1.00088	↑
Choline	0.906949	NS
L-kynurenine	0.893225	↑↑
Uridine	0.810356	NS
8-OH-dG	0.777736	NS
Citric acid	0.633654	NS
GSH	0.512313	NS
L-leucine	0.497685	NS
Carnitine	0.447434	NS
Phenylalanine	0.427897	NS
Glucosamine-1-phosphate	0.312245	NS
L-tryptophan	0.0800812	NS

↑ represents a P value ≤ 0.05 for the increase in mean content; ↑↑ represents a P value ≤ 0.01 for the increase in mean content; ↓ represents a P value ≤ 0.05 for the mean content decrease; ↓↓ represents a P value ≤ 0.01 for the mean content decrease; NS: No statistically significant change in the mean concentration of metabolites in the Fuzi-Gancao group; GSSG: Glutathione oxidized; GSH: Glutathione; VIP: Variable importance in the projection.

Pathway analysis: Metaboanalyst software was used to analyze the metabolic mechanism. Metabolic pathway differences between the negative control group and model control group and between the model control group and F-G group were analyzed by topological and enrichment analyses to confirm the important metabolic pathway effects of F-G in acute liver injury induced by CCl₄.

The results indicated that the primary bile acid biosynthesis pathway was the most important metabolic pathway affected in the model control group vs the negative control group (Figure 3A). Other pathways, such as pyrimidine metabolism, glutathione metabolism, glutamate metabolism, and phenylalanine metabolism, are also affected by CCl₄. The pantothenate and CoA biosynthesis, primary bile acid biosynthesis, and pyruvate metabolism pathways were significantly affected by the administration of the F-G extract (Figure 3B).

Figure 3 Metabolic pathway analysis of serum in rats. A: Negative control group vs model control group; B: Fuzi-Gancao group vs model control group.

Bile acids analysis

Method validation: The calibration curve of each standard was plotted on the concentrations of 11 bile acids and the ratio of the peak area of each component to that of the internal standard with weighted (1/x) least square linear regression. The calibration curves of the 11 analytes exhibited a good linearity (Table 8).

Table 8 Standard curve, R², and concentration range of 11 bile acids in serum.

Compound	Standard curve	R²	Range (ng/mL)
CDCA	Y = 0.0235X - 0.0056	0.9981	2.5-1000
UDCA	Y = 0.0013X + 0.2156	0.9972	1.25-500
GCA	Y = 0.0164X + 1.1577	0.9956	1.25-500
GDCA	Y = 0.0025X + 0.833	0.9982	1.25-500
TCA	Y = 0.0198X - 0.0113	0.9953	1.25-500
TUDCA	Y = 0.0332X + 0.0023	0.9985	2.5-1000
TCDCA	Y = 0.0306X + 0.00422	0.9923	2.5-1000
GCDCA	Y = 0.0133X - 0.00324	0.9915	2.5-1000
GLCA	Y = 0.0018X + 0.00242	0.9931	2.5-1000
DCA	Y = 0.0076X + 0.00614	0.9956	2.5-1000
CA	Y = 0.0916X - 0.00465	0.9987	2.5-1000

CDCA: Chenodeoxycholic acid; UDCA: Ursodeoxycholic acid; GCA: Glycocholic acid; GDCA: Glycochenodeoxycholic acid; TCA: Taurocholic acid; TUDCA: Taurocholic acid; GCDCA: Glycochenodeoxycholic acid; GLCA: Glycinic acid; DCA: Deoxycholic acid; CA: Cholic acid.

The intraday precision of QC samples with three concentrations of bile acids ranged from 1.20% to 6.57%, the interday precision ranged from 2.10% to 6.35%, and the recovery of each analyte was greater than 80% (Table 9). Eleven bile acid analytes exhibited good stability (short-term stability, long-term stability, freeze-thaw stability, and postpreparation stability) (Table 10). All the analytical values of the 11 analytes had satisfactory results within the acceptable criteria.

Table 9 Precision, accuracy, and recovery of bile acids in serum samples (n = 6, mean ± SD).

Compound	Concentration (ng/mL)	Recovery (%)	Intraday		Interday
			Accuracy (%)	Precision (%)	Accuracy (%)	Precision (%)
CA	2.5	90.12 ± 2.16	96.44 ± 2.05	4.26	91.83 ± 3.32	5.03
	500	88.21 ± 5.34	91.65 ± 4.14	3.60	94.42 ± 4.55	4.36
	2000	85.60 ± 7.22	92.11 ± 4.11	5.42	94.54 ± 8.35	6.00
GLCA	1.25	91.52 ± 5.51	92.13 ± 2.97	5.71	98.48 ± 2.22	3.75
	250	86.74 ± 7.12	87.31 ± 1.92	4.23	93.42 ± 3.67	5.40
	1000	90.48 ± 3.31	91.55 ± 5.31	6.13	89.24 ± 4.63	4.57
GDCA	1.25	88.54 ± 2.93	90.67 ± 6.87	6.22	88.55 ± 3.87	3.28
	250	98.43 ± 1.26	97.24 ± 7.86	6.38	101.53 ± 2.54	2.76
	1000	95.56 ± 4.01	89.34 ± 2.65	2.81	89.23 ± 6.25	6.16
GCDCA	1.25	96.02 ± 3.11	93.24 ± 3.78	6.30	89.32 ± 4.32	3.19
	250	90.13 ± 3.42	97.43 ± 2.82	5.03	88.54 ± 4.75	2.10
	1000	89.32 ± 3.13	86.53 ± 4.27	2.96	89.52 ± 3.63	3.28
GCA	1.25	80.87 ± 3.83	99.31 ± 5.19	4.18	89.42 ± 1.71	2.32
	250	91.43 ± 6.38	101.33 ± 2.23	2.59	112.53 ± 5.76	2.29
	1000	92.43 ± 2.14	88.76 ± 1.46	1.20	89.16 ± 3.46	3.09
TCA	2.5	84.77 ± 2.38	103.55 ± 1.27	1.50	98.24 ± 2.14	5.51
	500	86.92 ± 4.96	89.04 ± 6.42	5.53	95.33 ± 2.86	3.82
	2000	81.34 ± 1.84	88.57 ± 4.85	4.77	97.81 ± 3.08	4.50
CDCA	1.25	80.33 ± 3.23	94.33 ± 4.62	4.39	90.49 ± 4.83	5.18
	250	86.34 ± 2.45	92.33 ± 4.93	3.70	91.49 ± 7.39	4.49
	1000	84.62 ± 3.21	92.33 ± 6.03	5.58	92.77 ± 4.83	6.18
DCA	1.25	95.54 ± 2.17	94.67 ± 4.93	5.88	104.21 ± 7.22	3.87
	250	82.56 ± 4.32	106.33 ± 7.37	4.36	99.31 ± 5.66	5.57
	1000	94.45 ± 5.34	101.33 ± 5.77	6.31	89.83 ± 4.53	4.71
UDCA	1.25	83.32 ± 1.43	91.67 ± 4.62	6.41	93.43 ± 4.63	3.38
	250	88.13 ± 5.94	95.33 ± 4.73	6.57	92.12 ± 4.49	2.84
	1000	85.26 ± 3.01	94 ± 4.58	2.90	91.79 ± 5.74	6.35
TCDCA	1.25	86.04 ± 3.36	93.67 ± 5.86	6.49	92.77 ± 4.83	3.28
	250	87.98 ± 3.11	94.67 ± 4.93	5.18	89.83 ± 4.53	2.17
	1000	83.72 ± 2.19	91.67 ± 4.62	3.05	92.77 ± 7.36	3.38
TUDCA	1.25	87.17 ± 4.61	94.67 ± 7.51	4.31	96.69 ± 9.82	2.39
	250	87.41 ± 4.09	98.67 ± 10.02	2.66	98.33 ± 8.33	2.36
	1000	99.06 ± 3.56	100.33 ± 8.5	1.23	92.45 ± 4.53	3.18

CDCA: Chenodeoxycholic acid; UDCA: Ursodeoxycholic acid; GCA: Glycocholic acid; GDCA: Glycochenodeoxycholic acid; TCA: Taurocholic acid; TUDCA: Taurocholic acid; GCDCA: Glycochenodeoxycholic acid; GLCA: Glycinic acid; DCA: Deoxycholic acid; CA: Cholic acid.

Table 10 Stability of bile acid standards in serum samples (n = 6, mean ± SD).

Compound	Concentration (ng/mL)	Concentration (mean ± SD)
		Initial	Freeze-thaw	Short-term	Long-term	Post-preparation
CA	2.5	2.35 ± 0.17	2.3 ± 0.16	2.56 ± 0.18	2.33 ± 0.17	2.52 ± 0.08
	500	495.43 ± 12.15	485.52 ± 11.91	538.93 ± 13.22	511.98 ± 12.56	505.09 ± 5.54
	2000	2080.38 ± 101	2038.77 ± 98.98	2263.03 ± 109.87	2149.88 ± 104.38	2194.52 ± 99.16
GLCA	1.25	1.24 ± 0.14	1.22 ± 0.13	1.17 ± 0.15	1.21 ± 0.14	1.25 ± 0.14
	250	247.1 ± 10.76	242.15 ± 10.55	258.79 ± 11.71	255.35 ± 11.12	250.24 ± 10.9
	1000	979.04 ± 40.32	959.46 ± 39.51	985 ± 43.86	1011.75 ± 41.66	991.52 ± 40.83
GDCA	1.25	1.27 ± 0.05	1.24 ± 0.05	1.24 ± 0.06	1.19 ± 0.06	1.26 ± 0.08
	250	240.43 ± 3.98	235.62 ± 3.9	261.54 ± 4.33	248.46 ± 4.12	249.32 ± 5.42
	1000	975.71 ± 45.93	956.19 ± 45.01	1061.38 ± 49.96	1008.31 ± 47.46	1035.03 ± 14.83
GCDCA	1.25	1.27 ± 0.06	1.23 ± 0.08	1.36 ± 0.08	1.21 ± 0.09	1.21 ± 0.08
	250	243.49 ± 4.03	242.1 ± 19.01	237.25 ± 18.63	263.35 ± 20.68	250.18 ± 19.64
	1000	988.14 ± 46.51	1047.04 ± 49.29	1026.1 ± 48.31	1108.97 ± 53.62	1082.02 ± 50.94
GCA	1.25	1.19 ± 0.03	1.27 ± 0.03	1.27 ± 0.03	1.22 ± 0.03	1.21 ± 0.04
	250	237.1 ± 1.93	232.35 ± 1.9	257.91 ± 2.1	245.02 ± 2	244.16 ± 1.88
	1000	982.38 ± 30.18	962.73 ± 29.58	1068.63 ± 32.83	1015.2 ± 31.19	1014.36 ± 44.06
TCA	2.5	2.25 ± 0.17	2.21 ± 0.16	2.45 ± 0.18	2.33 ± 0.17	2.42 ± 0.08
	500	492.1 ± 28.22	482.25 ± 27.65	535.3 ± 30.69	508.54 ± 29.16	494.76 ± 23.69
	2000	2013.71 ± 105.21	1973.43 ± 103.1	2190.51 ± 114.44	2080.99 ± 108.72	2142.85 ± 26.09
CDCA	1.25	1.19 ± 0.1	1.28 ± 0.1	1.23 ± 0.11	1.24 ± 0.1	1.22 ± 0.08
	250	232.1 ± 6.9	227.45 ± 6.77	252.47 ± 7.51	239.85 ± 7.14	236.41 ± 5.54
	1000	1010.38 ± 39.44	990.17 ± 38.65	1099.09 ± 42.91	1044.13 ± 40.76	1057.77 ± 46.98
DCA	1.25	1.13 ± 0.03	1.15 ± 0.06	1.18 ± 0.13	1.23 ± 0.13	1.24 ± 0.14
	250	236.33 ± 13.65	229.67 ± 21.36	233 ± 10.15	244.65 ± 10.66	247.1 ± 10.76
	1000	967.67 ± 15.82	947.67 ± 106.82	1031 ± 115.66	982.55 ± 53.41	979.04 ± 40.32
UDCA	1.25	1.22 ± 0.06	1.19 ± 0.06	1.23 ± 0.07	1.26 ± 0.07	1.28 ± 0.07
	250	252.1 ± 6.9	247.05 ± 6.77	244.23 ± 7.51	250.52 ± 7.14	257.07 ± 5.54
	1000	931.71 ± 85.92	971.43 ± 120.15	958.15 ± 108.46	940.89 ± 109.04	1061.11 ± 99.16
TCDCA	1.25	1.22 ± 0.06	1.25 ± 0.06	1.28 ± 0.07	1.22 ± 0.06	1.19 ± 0.06
	250	251.76 ± 3.11	246.73 ± 3.05	273.87 ± 3.39	260.17 ± 3.22	261.73 ± 2.5
	1000	1013.71 ± 69.97	993.43 ± 68.57	1102.71 ± 76.11	1047.58 ± 72.31	1057.77 ± 99.16
TUDCA	1.25	1.22 ± 0.02	1.2 ± 0.02	1.23 ± 0.03	1.26 ± 0.02	1.27 ± 0.03
	250	249.1 ± 6.47	244.11 ± 6.34	270.97 ± 7.04	257.42 ± 6.68	259.14 ± 8.46
	1000	977.04 ± 18.84	957.5 ± 18.46	1062.83 ± 20.49	1009.69 ± 19.47	1006.1 ± 26.09

CDCA: Chenodeoxycholic acid; UDCA: Ursodeoxycholic acid; GCA: Glycocholic acid; GDCA: Glycochenodeoxycholic acid; TCA: Taurocholic acid; TUDCA: Taurocholic acid; GCDCA: Glycochenodeoxycholic acid; GLCA: Glycinic acid; DCA: Deoxycholic acid; CA: Cholic acid.

Bile acids analysis: Liver injury induced by CCl₄ in rats could reduce bile secretion and rapidly alter the distribution of bile acid stores, resulting in a significant increase in serum bile acid concentrations. The results indicated that the contents of 11 analytes (CDCA, DCA, UDCA, GLCA, GLCA, GCDCA, GDCA, GCA, TCDCA, TUDCA, and TCA) in the serum of the model control group, compared with the negative control group, were significantly increased (P < 0.01), and the contents of the 11 bile acids in the serum of the F-G groups were decreased in a dose-dependent manner (Figure 4).

Figure 4 Bile acids in rats (n = 6, mean ± SD). ^aP < 0.05, ^bP < 0.01 for each treatment group and model control group, respectively; ^cP < 0.05, ^dP < 0.01 for the model control group and normal control group, respectively.

PLS-DA analysis was performed using a data matrix on the effect of F-G on serum bile acid levels in rats with CCl₄ induced acute liver injury. As seen from the PLS-DA analysis (Figure 5A), the samples of the negative control group and model control group are distributed in different areas and far away from each other and can be completely separated from each other. The content differences of bile acids between the negative control group and model control group were significant. At the same time, the samples of the F-G group (10 g/kg) were partially overlapping those of the model control group, but with increasing dose, the samples of the mid-dose and high-dose F-G groups (20 g/kg and 30 g/kg) were clearly separated from those of the model control group, indicating that the dose-dependent relationship between the bile acid level and the dose of F-G extract was apparent in the overall analysis. P-test analysis showed that there was no overfitting of the between-group separation model (Figure 5B).

Figure 5 Bile acids in rats. A: Partial Least-Squares Discriminant Analysis; B: P-test analysis.

DISCUSSION

Analysis of 24 differential metabolites by UPLC-QTRAP-LC-MS/MS showed that CCl₄ could affect a variety of metabolic pathways, such as primary bile acid biosynthesis, glutathione metabolism, pyrimidine metabolism, and phenylalanine metabolism. The F-G extract could affect the metabolic pathways of pantothenic acid and CoA biosynthesis, primary bile acid biosynthesis, and pyruvate biosynthesis. The primary bile acid synthesis pathway was the most important common pathway affected by CCl₄ and the F-G extract. Subsequently, a UPLC-QQQ-LC-MS/MS method was established for the simultaneous quantitative detection of 11 bile acids, and the regulatory mechanism of the F-G extract on bile acids in the prevention of acute liver injury induced by CCl₄ was obtained.

Since the content of different bile acids varied greatly in the serum, we first used the relative variation in each bile acid for analysis. This analysis evaluated the relative changes in bile acids for each group based on their primary contents (1.0) in the negative control group (Table 11). Free and conjugated bile acids are the two bile acid types in the liver and blood. CA, CDCA, and DCA are the main free bile acids, and bile acids conjugated with glycine or taurine compose the combined bile acids. In this study, a relatively higher increase in taurine-conjugated bile acids, except TCA, was observed in the model control group than in the negative control group (TUDCA, 6.00; TCDCA, 3.24), whereas the increase in glycine conjugated bile acids, except GDCA, was relatively low (GLCA, 1.61; GCDCA, 1.74; GCA, 1.30). Taurine possessed protective effects on hepatocellular injury and apoptosis. When hepatocellular injury occurs, the body can regulate the compensatory increase in taurine and further increase the content of taurine-conjugated bile acids[36]. The content of taurine conjugated bile acids was significantly decreased after treatment with the F-G extract in a dose-dependent manner.

Table 11 Ratio of bile acids in each experimental group to corresponding composition of negative control group.

Bile acid	Negative	Model	Positive	FGL	FGM	FGH
CA	1.00	2.57	1.38	2.16	1.92	1.40
GLCA	1.00	1.61	1.08	1.45	1.17	1.15
GDCA	1.00	4.45	2.43	3.53	2.78	2.14
GCDCA	1.00	1.74	1.18	1.85	1.28	1.09
GCA	1.00	1.30	1.25	1.22	1.16	1.12
TCA	1.00	1.99	1.11	1.90	1.37	1.31
CDCA	1.00	4.12	2.08	3.76	2.90	2.03
UDCA	1.00	5.68	3.17	4.87	3.72	3.62
TUDCA	1.00	6.00	3.08	4.73	4.13	3.87
TCDCA	1.00	3.24	1.57	2.92	2.63	2.03
DCA	1.00	5.16	2.40	4.48	3.84	2.95

CDCA: Chenodeoxycholic acid; UDCA: Ursodeoxycholic acid; GCA: Glycocholic acid; GDCA: Glycochenodeoxycholic acid; TCA: Taurocholic acid; TUDCA: Taurocholic acid; GCDCA: Glycochenodeoxycholic acid; GLCA: Glycinic acid; DCA: Deoxycholic acid; CA: Cholic acid.

Bile acids exhibit different hydrophilic and hydrophobic properties according to their chemical structure. Hydrophobic bile acids can lyse cell membrane lipids, exhibiting “decontamination”, resulting in hepatocellular necrosis. Therefore, the accumulation of hydrophobic bile acids in the liver is a major and important cause of liver injury. UDCA is a nontoxic hydrophilic bile acid. Taurine conjugated bile acids (TCA, TCDCA, and TDCA) and glycine conjugated bile acids (GLCA, GDCA, GCDCA, and GCA) exhibit low toxicity due to some hydrophobicity, while CA, CDCA, and DCA are free and hydrophobic bile acids that show strong hepatotoxicity. DCA is one of the most toxic bile acids. The accumulation of DCA in the liver or blood leads to mitochondrial destruction, cell membrane rupture, and the production of reactive oxygen species in hepatocytes, leading to apoptosis and necrosis[36,37]. In this study, three hydrophobic components, CA, CDCA, and DCA, were significantly increased in the model control group, showing a positive correlation with the toxic effects reported[38]. The F-G extract can promote the binding of CA, CDCA, and DCA to taurine and glycine to reduce the accumulation of free CA, CDCA, and DCA in vivo, thus preventing acute liver injury induced by CCl₄.

When acute liver injury was caused by CCl₄ in rats, the hepatocytes were damaged, and the activities of cholesterol 7α-hydroxylase and cholesterol 12α-hydroxylase in hepatocytes were decreased, resulting in decreased CA and CDCA produced by cholesterol synthesis. However, due to impaired hepatic uptake of bile acids, the uptake of these two bile acids in the enterohepatic circulation is greatly reduced, resulting in a significant increase in the concentrations of bile acids in the serum. In this study, CA and CDCA were significantly increased in the model control group, showing liver damage and leading to bile acid malabsorption in the hepatoenteric circulation. The F-G extract decreased the contents of CA and CDCA in serum in a dose-dependent manner, indicating that the F-G extract could repair liver injury, improve enterohepatic circulation, and promote the absorption of CA and CDCA, exhibiting almost the same pharmacological effect as silybin.

CONCLUSION

In this study, the effects of F-G extract in preventing acute liver injury induced by CCl₄ have been assayed. The F-G extract decreases the adhesion between the lobules and the mucosa, reduces the bleeding point on the surface of the liver, effectively decreases ALT and AST in a rat model of acute liver injury in a dose-dependent manner, and reduces hepatocellular swelling, inflammatory cell infiltration, blood stasis, hepatic steatosis, and other pathological changes in rats.

ARTICLE HIGHLIGHTS

Research background

Fuzi (Radix aconiti lateralis)-Gancao (Radix glycyrrhizae) (F-G) is often used in the treatment of liver diseases such as hepatitis and liver failure.

Research motivation

This study can clarify the bile acid mechanism of F-G in the treatment of liver injury, and establish a complete bile acid spectrum research method, so as to provide reference for future research.

Research objectives

To study the molecular mechanism and action mechanism of F-G in the treatment of liver injury, and to provide a theoretical basis for the clinical research of F-G.

Research methods

An ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous determination of 92 metabolites from multiple pathways was established to explore the protective metabolic mechanism of F-G in serum on the liver.

Research results

A UPLC-MS/MS method for simultaneous determination of 11 bile acids was established to analyze the regulatory mechanism of F-G in serum. F-G decreased the contents of 11 bile acids in the serum in a dose-dependent manner.

Research conclusions

F-G could promote the conjugation of free bile acids to glycine and taurine, reduce the accumulation of free bile acids in the liver, regulate the compensatory degree of taurine, and decrease the content of taurine conjugated bile acids.

Research perspectives

The research group will continue to study the effect of bile acid metabolism regulation on molecular regulation in the body.