- Open Access
Metabolic regulations of a decoction of Hedyotis diffusa in acute liver injury of mouse models
© The Author(s) 2017
- Received: 25 October 2017
- Accepted: 14 December 2017
- Published: 20 December 2017
Dysfunctional metabolisms are contributed to LPS/GALN-induced hepatitis. However, whether Hedyotis diffusa (HD) employs metabolic strategies against hepatitis is unknown.
We use the cytokines expression, levels of serum alanine transaminase and aspartate transaminase, survival and histological analysis to measure the effect of decoction of HD on acute severe hepatitis of mouse induced by LPS/GALN. Meanwhile, we utilize GC/MS-based metabolomics to characterize the variation of metabolomes.
The present study shows the relieving liver damage in HD decoction-treated mice. Metabolic category using differential metabolites indicates the lower percentage of carbohydrates in LPS/GALN + HD group than LPS/GALN group, revealing the value of carbohydrate metabolism in HD decoction-administrated mouse liver. Further pathway enrichment analysis proposes that citrate cycle, galactose metabolism, and starch and sucrose metabolism are three important carbohydrate metabolisms that involve in the protective effect of decoction of HD during acute hepatitis. Furthermore, other important enrichment pathways are biosynthesis of unsaturated fatty acids, alanine, aspartate and glutamate metabolism, and arginine and proline metabolism. Fatty acids or amino acids involved in above-mentioned pathways are also detected in high loading distribution on IC01 and IC02, thereby manifesting the significance of these metabolites. Other key metabolites detect in ICA analysis were cholesterol, lactic acid and tryptophan.
The variation tendency of above-mentioned metabolites is totally consistent with the protective nature of decoction of HD. These findings give a viewpoint that HD decoction-effected metabolic strategies are linked to underlying mechanisms of decoction of HD and highlight the importance of metabolic mechanisms against hepatitis.
- Hedyotis diffusa
- Carbohydrate metabolism
The worldwide incidence of hepatocellular carcinoma (HCC), a major cause of human cancer death, has enhanced in recent years . Hepatocyte death that drives liver disease progression from hepatitis associated with a number of liver insults, including steatosis, hepatotoxins, viral infection, and autoimmune disease, are responsible for the development of HCC [2, 3]. These liver insults are related to the subsequent development of inflammation, fibrosis, and cirrhosis. Actually, inflammation, a syndrome responsive to pathogen infection or injury, is a hallmark of liver disease that may represent a cause of HCC development [3, 4]. Therefore, it is an urgent clinical challenge to develop new therapeutic interventions through targeting hepatic inflammation, which may ultimately provide therapeutic benefit for the treatment of HCC .
Hedyotis diffusa, a traditional Chinese herbal medicine that belongs to the Rubiaceae family and also known as Oldenlandia diffusa and Bai Hua She She Cao , is widely spread in South of China and other Asian countries. H. diffusa has been largely employed in the treatments of inflammation-involved diseases, such as bronchitis, arthritis, rheumatism, appendicitis, sore throat, urethral infection, contusions, and ulcerations . Accumulating evidence also proposes that H. diffusa is capable of controlling the liver, breast, lung, colon, brain and pancreatic cancers through promoting apoptosis of cancer cell and inhibiting tumor angiogenesis [7–11]. Moreover, the isolated splenocytes from H. diffusa extract-administrated leukemic mice manifest an improvement of T- and B- cell proliferation in vivo . Also, H. diffusa addition affects the levels of cell markers (CD3, CD11b, and CD19) in white blood cell, enhances macrophage phagocytosis, and increases the cytotoxic activities of NK cells in normal Balb/c mice . All above-mentioned studies show that H. diffusa has anti-inflammatory, anti-cancer and immunomodulatory activities. Actually, recent papers coincidentally demonstrate that inflammatory process, cancer development and progression, and immune response have strong inter-relationship with metabolism happened in host cells [14–17]. Currently, only one paper focuses on metabolic alterations of H. diffusa in tumor-bearing rat . The underlying metabolic mechanisms related to H. diffusa-involved activities need to be elaborated further, and the metabolic activities of this herb in liver inflammation is unknown.
Metabolomics is a powerful new technology studying metabolic processes, identifying crucial biomarkers responsible for metabolic characteristics, and revealing metabolic mechanisms. Analysis of the key metabolites in various samples has become a meaningful part of improving the diagnosis, prognosis, and therapy of diseases . Gas chromatography/mass spectrometry (GC–MS), liquid chromatography–mass spectrometry (LC–MS) and nuclear magnetic resonance (NMR) are three most common analytical technologies in metabolomics investigation . While each technology has its own unique advantages and disadvantages, GC–MS is specifically becoming for the analyses of volatile compounds and thus is widely applied [21–23]. Here, we report the use of GC–MS combined with multivariate statistical tools to exploit, among the differential metabolites, key metabolites and important pathways as biomarkers capable of differentiating LPS/GALN treatment from the treatment of decoction of H. diffusa plus LPS/GALN in the liver metabolome.
Animals and experimental design
Adult female mice (C57BL/6, pathogen-free), weighing 24 ± 2 g from the same litters, were reared in an environmentally controlled breeding room (temperature: 20 ± 2 °C, humidity: 60 ± 5%, 12 h dark/light cycle), and in cages fed with sterile water and dry pellet diets. They were maintained in accordance with internationally accepted principles for laboratory animal use. All work was conducted in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Institutional Animal Care (Animal Welfare Assurance Number: IS06). The Minimum Standards of Reporting Checklist (Additional file 1) contained details of the experimental design, and statistics, and resources used in this study.
According to the previous study , murine model of acute hepatitis was induced by combined injection of LPS (50 g/kg) and D-GALN (1.2 g/kg). Mice were randomly separated into 3 groups (n = 26 per group). The control and model groups were injected intraperitoneally with 200 μL of saline twice a day ; the treatment group received the 200 μL of decoction of H. diffusa (5 g/kg) twice a day . Three days after injection, the mice in both model and treatment groups were challenged intraperitoneally by LPS/GALN. Twelve hours later, six mice in each group were euthanized by decapitation, and blood and livers were collected for following studies. The remaining 20 mice in each group were observed for 20 days to examine their survival.
Preparation of a decoction of H. diffusa
According the previous procedure , 100 g of dried H. diffusa were cut into 1–1.5 mm pieces and crushed using a mortar and pestle, and then boiled with 1 L of deionised water for 1 h. After cooling, the decoction was centrifuged at 3000 rpm for 20 min, and filtered through a 0.45 μm filter. The filtrate was evaporated in vacuum (EYELA N-1001, Tokyo, Japan) and a dry residue was recovered. Finally, the total residue was reconstituted in saline and the final volume of extract is 100 mL (equal to 1.0 g raw material/mL).
The liver sample was fixed in 4% paraformaldehyde overnight at room temperature, then embedded in paraffin, sliced into 5-μm sections. For histological analysis, paraffin sections were stained with hematoxylin and eosin (H&E). The morphologic criteria used to determine the degree of necrosis included portal inflammation, hepatocellular necrosis, inflammatory cell infiltration, and loss of cell architecture. The pathological changes were evaluated in nonconsecutive, randomly chosen 200× histological fields.
Quantitative RT-PCR assay
For quantitative RT-PCR assay, RNA was isolated from mouse livers using the TRIzol reagent according to the manufacturer’s instructions. 2 µg of total RNA was provided to generate the first-strand cDNAs by using commercially available kits (Applied Biosystems). All subsequent PCR reactions were carried out using the 7 Universal PCR Master Mix (Applied Biosystems). PCR primers of mouse CXCL1 were 5′-TCGTCTTTCATATTGTATGGTCAAC-3′ and 5′-CGAGACGAGACCAGGAGAAA C-3′. The primers for mouse TNFα were 5′-CATCTTCTAAAATTCGAGTGACAA-3′ and 5′-TGGGAGTAGACAAGGTACAACCC-3′. The real-time PCR primers for mouse IL-1β were 5′-ACAGATGAAGTGCTCCTTCCA-3′ and 5′-GTCGGAGATTCGTAGCTGGAT-3′. The real-time PCR primers for mouse MIP-2 were 5′-CCCCCTGGTTCAGAAAATCATC-3′ and 5′-AACTCTCAGACAGCGAGGCACATC-3′. The primers for the mouse housekeeping gene GAPDH were 5′-TTCACCACCATGGAGAAGGC-3′ and 5′-GGCATGGACTGTGGTCATGA-3′ and were used as a control.
Measurement of cytokines in liver
Concentrations of TNF-α, IL-1β, IL-6, and MCP-1 in liver were measured through mouse-specific enzyme-linked immunosorbent assay (ELISA) kits (NeoBioscience, Shenzhen, China). Each analysis was carried out according to the manufacturer’s instruction, and the concentrations of cytokines were determined according to the standard curves.
Measurement of serum alanine transaminase and aspartate transaminase activities
Blood samples were centrifuged at 1500g for 20 min at 4 °C, and alanine transaminase (ALT) and aspartate transaminase (AST) activities in serum were measured by commercial kits from Randox Laboratories (UK).
Extraction of metabolites in mouse liver
For the metabolomics investigation, the extraction of total metabolites in mouse liver was performed according a procedure described previously . Briefly, 1 g of liver tissue was homogenized and dissolved for 1 min in 1 mL of methanol at 4 °C. The homogenates were centrifuged at 12,000×g for 10 min at 4 °C. 300 μL of supernatant was transferred to a GC sampling vial containing ribitol (10 μL, 0.1 mg/mL), an internal standard, and then dried in a vacuum centrifuge concentrator before the subsequent derivatization.
Derivatization and GC–MS analysis
Prior to GC–MS analysis, deriving liver samples was required. After drying samples, 80 μL of methoxamine/pyridine hydrochloride (20 mg/mL) was added to induce oximation for 1.5 h at 37 °C and then 80 μL of MSTFA, a derivatization reagent (Sigma), was mixed and reacted with the liver sample for additional 0.5 h at 37 °C. By centrifuging, 1 μL of supernatant derivative was added to a tube and analyzed using GC–MS (Trace DSQ II, Thermo Scientific). The separation conditions of GC–MS consisted of an initial temperature of 70 °C (5 min) with a uniform increase to 270 °C at a speed of 2 °C/min (5 min); 0.5 μL sample volume, splitless injection; injection temperature, 270 °C; interface temperature, 270 °C; ion source (EI) temperature, 30 °C; ionization voltage, 70 eV; quadrupole temperature, 150 °C; carrier gas, highly pure helium; velocity, 1.0 mL/min; and full scan way, 60–600 m/z.
Statistical and bioinformatics analysis
The data of liver metabolome were collected using Thermo Foundation 1.0.1. The sum abundance value was employed for normalizing the resulting data matrix, and then the computed abundance of metabolites was centered for each tissue sample on their median value and scaled by their inter-quartile range (IQR) to decline between-sample variation [25, 26]. The significant analysis of microarray (SAM), a permutation-based hypothesis testing method for the analysis of proteomic and metabolomic data [27, 28], was applied to analyze the differential metabolites. Independent component analysis (ICA) was chosen as the pattern recognition method . Statistical significance between groups was determined with the unpaired two-tailed Student t test. All data were analyzed by Prism (GraphPad Software, Inc.), and P values less than 0.05 and 0.01 were deemed as two significant levels.
Decoction of H. diffusa (HD) attenuates the acute inflammation in hepatitis mouse
Metabolomic profiling of mouse liver
Decoction of HD varied the metabolomic profiling of liver in LPS/GALN-injected mice
Metabolic categories of these differential metabolites in abundance were explored further. They presented analogous varying percentage in the two groups, ranking lipids > carbohydrates > amino acids > nucleotides, but relative higher percentage of lipids and amino acid, and lower carbohydrates were discovered in the LPS/GALN + HD than the LPS/GALN groups (Fig. 3c). Figure 3d visualized the numbers of up-regulated and down-regulated metabolites in these categories. HD reduced the numbers of up-regulated and down-regulated carbohydrates caused by LPS/GALN, and up-regulated lipids and down-regulated amino acid in LPS/GALN group were declined after HD administration. These data reveal that decoction of HD might provide a helpful response through a change in metabolome.
Differential enriched pathways responsible for the helpful response induced by HD
Among these pathway, two were uniquely related to the relief of liver damage, which were arginine and proline metabolism, and starch and sucrose metabolism (Fig. 4b). Metabolites enriched in the starch and sucrose metabolism were all decreased. Although all metabolites enriched in biosynthesis of unsaturated fatty acids had higher abundance in LPS/GALN and LPS/GALN + HD groups in contrast to control group, abundance of most metabolites in LPS/GALN + HD group were lower than LPS/GALN group. In other words, HD was capable of reducing the abundance of these up-regulated metabolites enriched in biosynthesis of unsaturated fatty acids in LPS/GALN-treated liver. These metabolites included eicosenoic acid, palmitic acid, stearic acid, eicosanoic acid, oleic acid, arachidonic acid and linoleic acid. More importantly, some of metabolites in alanine, aspartate and glutamate metabolism, arginine and proline metabolism, and galactose metabolism were reversal between LPS/GALN and LPS/GALN + HD groups. These metabolites included glutamine and myo-inositol, and were all declined in LPS/GALN group and augmented in LPS/GALN + HD group. Besides, l-alanine enriched in alanine, aspartate and glutamate metabolism and citrulline enriched in arginine and proline metabolism was only boosted, and urea enriched in arginine and proline metabolism was only reduced in LPS/GALN + HD group. Moreover, three of four metabolites (oxoglutaric acid, fumaric acid and isocitrate), which were enriched in citrate cycle and showed higher abundance in LPS/GALN group, had the similar metabolic levels between control and LPS/GALN + HD groups. Meanwhile, remaining metabolite, succinic acid, had a lower abundance in LPS/GALN + HD group, when compared to the LPS/GALN group. Collectively, these results indicated that biosynthesis of unsaturated fatty acids, alanine, aspartate and glutamate metabolism, arginine and proline metabolism and citrate cycle might be significantly related to the HD decoction-induced benefit for hepatitis mouse.
Identification of crucial metabolites using ICA analysis
The finding of current metabolic category shows that LPS/D/GALN + HD have a lower percentage of carbohydrates than LPS/GALN group (Fig. 3c, d), subsequent pathway enrichment analysis further make clear that citrate cycle, galactose metabolism, and starch and sucrose metabolism are able to be involved in the metabolic activities of HD. Among these, citrate cycle is more striking because two metabolites (oxoglutaric acid and isocitrate) are down-regulated but others (succinic acid and fumaric acid) are up-regulated after LPS/GALN treatment (Fig. 6). Consistent with this, previous study show the down-regulation of isocitrate, and up-regulation of succinic acid and fumaric acid in LPS-treated mice . In fact, recent papers demonstrate that LPS stimulates a profound metabolic transition to aerobic glycolysis through phosphatidyl inositol 3′-kinase/Akt pathway and inhibits mitochondrial oxidative phosphorylation, an action that have an indispensable connection with citrate cycle [33, 34]. Succinic acid is an inflammatory signal that activate IL-1β through stabilizing the hypoxia-inducible factor-1α (HIF-1α) . Similarly, fumaric acid also have a function in HIF stability and fumaric acid up-regulation can be recognized as a tumor-promoting event . Given that the lower abundance of succinic acid and fumaric acid are found in LPS/D/GALN + HD group than that in LPS/D/GALN group, thus a becoming possibility is that modulation of succinic acid and fumaric acid concentrations and following HIF-dependent cytokine production partly explains how decoction of HD possesses strong host protection in liver damage. Other interesting carbohydrates are d-glucose and myo-inositol enriched by pathway analysis (Fig. 4b), and lactic acid detected by ICA analysis (Fig. 5c). In patients, glucose metabolism is abnormal when the liver cell damage occurs , and the higher level of lactic acid in LPS/GALN group can be explained by the acceleration of aerobic glycolysis [33, 34]. After HD decoction treatment, the abundance of d-glucose and lactic acid is almost equal to the control group, indicating that maintaining the normal glucose metabolism and glycolysis is the potential metabolic mechanisms to relieve the acute hepatitis. It has been reported that myo-inositol plays an important role in immunity system [25, 37]. However, the detailed meaning of myo-inositol elevated by decoction of HD still needs to be studied in future.
Combining current pathway enrichment analysis with ICA analysis, the shared lipid-related metabolites are palmitic acid (PA), stearic acid (SA), oleic acid (OA), linoleic acid (LA), eicosanoic acid (EA) and arachidonic acid (AA). We know that PA (16:0), stearic acid (18:0), OA (18:1) and LA (18:2) are capable of stimulating TLR4 signaling to produce an inflammatory response , which may eventually contribute to acute severe hepatitis . Other lipid-related metabolites are AA and cholesterol, which also have an excellent action in inducing the severe inflammation . These metabolites were up-regulated by LPS/GALN treatment but decoction of HD down-regulated these metabolites, indicating that decoction of HD has an anti-inflammatory action through declining the abundance of lipids including PA, SA, OA, LA, AA and cholesterol (Fig. 6).
For amino acid metabolisms, alanine, aspartate and glutamate metabolism, and arginine and proline metabolism, cyanoamino acid metabolism, and nitrogen metabolism are enriched by pathway analysis. In these pathway, l-alanine, l-glutamine, citrulline, glycine and serine are involved (Fig. 6). l-Alanine, a significant energy substrate for cell, is beneficial for supporting gluconeogensis and leucocyte metabolism through unknown mechanism . l-Glutamine is known to support the anti-inflammatory response through various signal pathways [42–44]. Serine and glycine are two potent antioxidants that scavenge free radicals, thereby playing an essential role in anti-oxidative defense of liver cell [45, 46]. There is also in vivo evidence that glycine blunts the production of TNFα and reduces inflammatory reactions [47, 48]. When compared to the LPS/GALN group, the boosted level of l-alanine, l-glutamine, glycine and serine found in LPS/GALN + HD group indicates that the high level of these amino acids is benefit for the alleviation of acute severe hepatitis. Citrulline and nitric oxide (NO) are produced by the metabolic response of l-arginine through NO synthase (NOS) and l-arginine also can generate urea and ornithine through arginase [23, 49]. The boosted citrulline and declined urea in LPS/GALN + HD revealed that NO may be involved in the protective effect of HD decoction on acute severe hepatitis, which certainly requires to be determined in further investigation. In addition, tryptophan is a high loading in differentiating LPS/GALN + HD from LPS/GALN. Tryptophan metabolism is increased during inflammation or stimulation by LPS or certain cytokines . Most of tryptophan in mammals is oxidized along kynurenine pathway and kynurenine promotes carcinogenesis by acting on the aryl hydrocarbon receptor . Thus inhibiting tryptophan metabolism is a possible metabolic mechanisms for HD decoction-induced protection.
The current study uses GC/MS-based metabolomics to characterize variation of metabolomes in response to LPS/GALN and HD decoction treatment before LPS/GALN. Metabolic category using differential metabolites showed the lower percentage of carbohydrate in LPS/GALN + HD group than LPS/GALN group, revealing that carbohydrates metabolism may play an important role in HD-treated mice to combat liver damage. Subsequent pathway enrichment analysis further find out that citrate cycle, galactose metabolism, and starch and sucrose metabolism are three important carbohydrate metabolisms that involve in the protective effect of decoction of HD during acute severe hepatitis. Thus, these findings provide a viewpoint that underlying mechanisms of decoction of HD are connected to the metabolic strategies and highlight the value of metabolic strategies against hepatitis.
Designed the experiments: HZY, MD, FLW. Performed the experiments: MD, FLW, ZCZ, GMX. Analyzed the data: MD, FLW, ZCZ, HJC. Wrote the paper: MD, FLW, HZY. All authors read and approved the final manuscript.
The authors declare that they have no competing interests
Availability of data and materials
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Ethics approval and consent to participate
Prior to commencement of the study, ethical approval was obtained from the ethics committee of Institutional Animal Care (Animal Welfare Assurance Number: IS06).
This work was sponsored by Grants from State Administration of Traditional Chinese Medicine (JDZX2015173).
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