- Open Access
Application of metabolomics in toxicity evaluation of traditional Chinese medicines
Chinese Medicine volume 13, Article number: 60 (2018)
Traditional Chinese medicines (TCM) have a long history of use because of its potential complementary therapy and fewer adverse effects. However, the toxicity and safety issues of TCM have drawn considerable attention in the past two decades. Metabolomics is an “omics” approach that aims to comprehensively analyze all metabolites in biological samples. In agreement with the holistic concept of TCM, metabolomics has shown great potential in efficacy and toxicity evaluation of TCM. Recently, a large amount of metabolomic researches have been devoted to exploring the mechanism of toxicity induced by TCM, such as hepatotoxicity, nephrotoxicity, and cardiotoxicity. In this paper, the application of metabolomics in toxicity evaluation of bioactive compounds, TCM extracts and TCM prescriptions are reviewed, and the potential problems and further perspectives for application of metabolomics in toxicological studies are also discussed.
Traditional Chinese medicines (TCM) have been used for the treatment of a variety of diseases for thousands of years in China since they are relatively inexpensive, widely available and have reliable therapeutic efficacy [1,2,3]. Accompanying with hot discussions on development of multidrug therapy for multi-gene diseases, TCM are receiving increasing attention worldwide because it is well accepted that TCM exert their curative effects via multiple components on multiple targets in clinic [4,5,6].
Many people believe that TCM are safe because they derive from natural origin. However, this belief has been greatly challenged in recent years. In fact, the toxicity and safety issues of TCM has aroused increasing concern to international community, such as identification of plant materials, preparation method, and the potential to interact with other herbal medicines and conventional drugs [7,8,9,10]. Moreover, the traditional safety assessment methods may not accurately assess safety knowledge of TCM due to the complexity of its constituents and action mechanisms.
Systems biology is a biology-based interdisciplinary field of study that focuses on complex interactions within biological systems, using a holistic approach to biological research . Indeed, the holistic properties of systems biology are in agreement with TCM theory in nature [12, 13]. The omics approaches, such as genomics, transcriptomics, proteomics and metabolomics, have greatly facilitated the systematic study of complex systems, especially TCM and herbal medicines [14,15,16].
Metabolomics, first put forward by professor Nicholson in 1999 , is defined as systematically qualitative and quantitative analysis of metabolites in a given organism or biological sample. It allows the quantitative measurement of large numbers of low-molecular-weight (< 1 kDa) endogenous metabolites, including lipids, amino acids, peptides, nucleic acids, organic acids, vitamins, and carbohydrates, which play important roles in biological systems and represent attractive candidates to understand phenotypes [18,19,20]. Metabolomics is suitable for observing abnormal changes of endogenous metabolites before the appearance of physiological or pathological damages. As a systemic approach, metabolomics adopts a “top-down” strategy to reflect the function of organisms from terminal symptoms of metabolic network and understand metabolic changes of a complete system caused by interventions in a holistic context .
Recently, metabolomics has been widely applied to the modern researches of TCM including theory of TCM, syndrome, efficacy and toxicity since the metabolome represents the physiological or pathological status of organisms [22,23,24,25]. It was deemed that metabolomic analysis is an efficacious and noninvasive method to evaluate toxicity of TCM and explore toxicity mechanisms through correlations of physiological changes and metabolic changes [26, 27]. In this review, we summarized the metabolomics analytical techniques widely used in the study of TCM, and focusing on the application of metabolomics in the toxicological evaluation of TCM.
Metabolomic technology and data analysis
Modern metabolomic technologies allow for qualitative and quantitative measurement of a vast number of metabolites in complex biological systems. The main analytical techniques in metabolomics, which have widespread applications in the assessments of efficacy and toxicology of TCM, are proton nuclear magnetic resonance spectroscopy (1H NMR) and mass spectrometry (MS) .
1H NMR is a non-destructive technique, which provides high-throughput and automated analysis of crude extracts, and quantitatively detects different metabolites in different groups, as well as offers structural information . The advantages of 1H NMR in metabolomic analysis include simple and nondestructive sample preparation, fast analysis rate, and non-selective judgment. However, 1H NMR fails to obtain valid data when the concentrations of metabolites in complex sample are quite low . Therefore, in most cases, MS is preferred in metabolomic analysis because of its advantages of unparalleled sensitivity, high resolution and structural specificity . In practical applications, MS requires combining with different separation techniques such as gas chromatography (GC–MS), liquid chromatography (LC–MS), capillary electrophoresis (CE–MS) and ultra-performance liquid chromatography (UPLC-MS) for a pre-separation. GC–MS is particularly suitable for the detection of thermally stable volatile metabolites. Hence, the application range of GC–MS is limited as most non-volatile metabolites cannot be analyzed directly . Compared to GC–MS, the utilization of LC–MS is more frequent in metabolomic analysis, LC can isolate different kinds of metabolites in a complex system and MS can provide structural information to help to identify metabolites. LC–MS can provide more details of submerged portions than 1H NMR, and can detected molecules with different proper polarity . The ability of LC–MS to analyze various kinds of metabolites depends on the ionization source and the chromatographic method that is used to separate a complex mixture of analytes. Nowadays, two-dimensional LC method has been successfully applied in metabolomic analysis of TCM and due to its enhanced selectivity, peak capacity and high resolution compared with one-dimensional LC . Normally, the selection of metabolomic technology depends on the research purpose and the properties of samples. In fact, due to the large number and the wide concentration range of metabolites, and the complexity of TCM, integrated metabolomic approaches have been frequently used to provide sensitive, accurate and reliable results .
Sample preparation, including its source, storage and extraction, has significant effects on the results of metabolomic analysis. Plasma, serum, urine and tissue are usually biological samples in metabolomic analysis . To decrease the changes of potential metabolites in metabolomic samples, biological samples usually can be restored in − 80 °C. For 1H NMR analysis, the change of pH and ionic strength caused by the change of the chemical shift is the primary problem, and the addition of pH buffer during the sample extraction can solve the problem . Compared with 1H NMR, the samples extraction for MS-based metabolomics are more complicated. For LC–MS analysis, biological samples are complex and contain various endogenous and exogenous acidic, basic, and neutral compounds with high polarity. The samples usually require to be centrifuged and diluted with deionized water before metabolomic analysis . For GC–MS analysis, most potential biomarkers in biological samples are high polar and nonvolatile, thus the samples must be derivatized before analysis .
Data analysis are crucial since the data matrix generated in metabolomic study is generally large and complex. Data preprocessing is the first step of metabolomic data analysis. The main objective of data preprocessing is to transform the data in such way that the samples in the dataset are more comparable in order to ease and improve the data analysis . 1H NMR data preprocessing usually includes baseline correction, alignment, binning, normalization and scaling . For MS data preprocessing, many softwares such as MetAlign, MZmine and XCMS have been developed to process raw data . Multivariate statistical methods are professional approaches for analyzing and maximizing information retrieval from complex metabolomic data. The multivariate statistical methods can be classified into two groups, namely unsupervised methods and supervised methods. Unsupervised methods mainly include principal component analysis (PCA), hierarchical cluster analysis (HCA), K-means and statistical total correlation spectroscopy. PCA can summarize the information in an experimental data set using a small number of orthogonal latent variables obtained by searching the direction of maximum variance in the data set. However, PCA does not always extract hidden information that explains system behavior. Supervised methods, such as partial least squares discriminant analysis (PLS-DA), orthogonal partial least squares discriminant analysis (OPLS-DA), quadratic discriminant analysis and linear discriminant analysis can reveal the most important factors of variability characterizing the metabolomic datasets . The commonly used softwares for metabolomic multivariate statistical analysis are Shimadzu Class-VP software and SIMCA-P software. The identification of metabolites and the pathway analysis of metabolites are also essential components of metabolomic data analysis. The updating commercial software is crucial for identifying potential metabolites, while accurate mass, isotopic pattern, fragments information, and available biochemical databases are also necessary. Presently, a number of metabolites databases such as Human Metabolome Database (HMDB), Kyoto Encyclopedia of Genes and Genomes (KEGG), Biochemical Genetic and Genomic (BiGG), ChemSpider and PubChem Compound, are emerging and have been applied in the identification of metabolites and biomarkers. For metabolic pathway analysis, KEGG, Ingenuity Pathway Analysis, Cytoscape and Reactome Pathway Database are commonly used databases and softwares. The flowchart of typical metabolomic experiment including sample preparation, metabolomic technology, data analysis and pathway analysis is shown in Fig. 1.
Metabolomics in toxicity evaluation of TCM
Metabolomic analysis is an effectively and noninvasive method for evaluating toxicology of TCM and exploring toxicity mechanisms through correlations of physiological changes and metabolic changes. The metabolomic researches on hepatotoxicity, nephrotoxicity, cardiotoxicity and other toxicity induced by bioactive compounds, TCM extracts and TCM prescriptions were summarized in Tables 1, 2, 3 and 4, respectively.
Metabolomics in hepatotoxicity evaluation of TCM
Metabolomics is a useful tool to evaluate toxicity and identify toxicological biomarkers of bioactive compounds from TCM. Triptolide, a bioactive diterpenoid compound isolated from Tripterygium wilfordii, exhibits diverse biological activities such as anti-inflammatory, immune-modulatory and anti-proliferative activities . However, the further clinical research and application of triptolide is confined by its severe toxicity on the liver, kidney and reproductive systems . Zhao et al. developed a LC–MS based metabolomic method to investigate the hepatotoxicity of triptolide in mice. Mice were administered triptolide by gavage to establish the acute liver injury model. Metabolomic results showed that a total of thirty metabolites were significantly changed by triptolide treatment and the abundance of twenty-nine metabolites was correlated with toxicity. Pathway analysis indicated that the mechanism of triptolide induced hepatotoxicity was related to alterations in multiple metabolic pathways, including glutathione metabolism, tricarboxylic acid cycle, purine metabolism, glycerophospholipid metabolism, taurine and hypotaurine metabolism, pantothenate and coenzyme A biosynthesis, pyrimidine metabolism and amino acid metabolism . Recently, another LC–MS based metabolomic approach was developed to discover hepatotoxic and nephrotoxic potential biomarkers of triptolide. The metabolic profiles of liver, kidney and plasma were characterized by HPLC Q/TOF MS. The metabolite profiles of the liver, kidney and plasma of toxic and therapeutically dosed mice showed significant differences. Two toxic markers, mono-hydroxylated metabolite of triptolide, tri-hydroxylated and dehydrogenated metabolite of triptolide, were detected both in mice plasma and human liver microsomes following incubation with triptolide. The two metabolites could be potential diagnosis markers for hepatotoxicity and nephrotoxicity induced by triptolide . The metabolomic analysis could provide an integral understanding of the mechanism of the hepatotoxicity, and it may be useful for further prediction and diagnosis of liver injury during clinical use of triptolide.
Compared with the limited applications in toxicity evaluation of bioactive compounds, metabolomics was widely applied to toxicity evaluation of the TCM extracts. Dioscorea bulbifera Rhizome, the dried root of Dioscorea bulbifera L., has been known to have many bioactivities such as anti-tumor, anti-bacterial, anti-feedant, anti-fungal and anti-salmonella . However, experimental studies and clinical reports indicated that Dioscorea bulbifera Rhizome could cause toxicity, particularly in the liver . A multisample integrated metabolomic strategy was employed to precisely describe the status and mechanism of hepatotoxicity induced by Dioscorea bulbifera Rhizome. Comparison of metabolomic profiles of rat plasma, urine, and feces by GC–MS, a total of fifty-five metabolites distributed in 33 metabolic pathways were identified. Correlation network analysis revealed that the hub metabolites of hepatotoxicity were mainly associated with amino acid metabolism, bile acid metabolism, purine metabolism, pyrimidine metabolism, lipid metabolism and energy metabolism . In another study, liver toxicity induced by Dioscorea bulbifera Rhizome was investigated by 1H NMR. The metabolomic results revealed that the levels of taurine, creatine, betaine, dimethylglycine, acetate, glycine were elevated, whereas, the levels of succinate, 2-oxoglutarate, citrate, hippurate and urea were reduced. With molecular function analysis of these changed metabolites, the hepatotoxicity of Dioscorea bulbifera Rhizome was involved in hepatic mitochondrial injury .
Xanthii Fructus is the mature fruit with involucres of Xanthium sibirium Patr. and widely used for the treatment of sinusitis, headache, rheumatism, and skin itching . Xue et al. performed an integrated metabolomic study using 1H NMR combined with multivariate statistical analysis to elucidate the hepatotoxicity of Xanthii Fructus. When rats were treated with Xanthii Fructus at 30.0 g/kg, the hepatotoxicity was reflected in the changes observed in serum biochemical profiles and by the histopathological examination of the liver. The results demonstrated that atractyloside, carboxyatractyloside and 40-desulphate-atractyloside were the major hepatotoxicity constituents in Xanthii Fructus. Moreover, the hepatotoxicity of Xanthii Fructus mainly associated with mitochondrial inability, fatty acid metabolism, and some amino acids metabolism . The urinary metabolic perturbations associated with toxicity induced by Xanthii Fructus were also studied using UPLC–MS. The results showed that the metabolic characters in Xanthii Fructus treated rats were perturbed in a dose dependent manner and ten metabolites including 6-hydroxy-5-methoxyindole glucuronide/5-hydroxy-6-methoxyindole glucuronide, 4,6-dihydroxyquinoline, 3-methyldioxyindole, phenylalanine, indoxyl sulfate, hippuric acid, uridine, l-phenylalanyl-l-hydroxyproline, sebacic acid, and arachidonic acid were preliminarily identified as potential toxicity biomarkers .
Polygoni Multiflori Radix, the dried root of Polygonum multiflorum Thunb, is commonly used to prevent or treat non-alcoholic fatty liver disease, hyperlipidemia or related hepatic diseases in clinic. Currently, several clinical cases associated with hepatotoxicity of Polygoni Multiflori Radix including toxic hepatitis and acute hepatitis have been reported . Xia et al. used an untargeted metabolomic strategy to investigate the chronic hepatotoxicity induced by Polygoni Multiflori Radix in rats. Ten potential endogenous metabolites including glycine, 13-eicosenoic acid, lactic acid, octadecanoic acid, proline, 2-furoic acid, cholesterol, alanine, docosahexaenoic acid, and lysine were identified. The ten potential biomarkers were involved in three metabolic pathways, amino acid metabolism, fatty acid metabolism and oxidative injury. The results indicated that Polygoni Multiflori Radix-induced liver damage is dosage dependent and disruption in amino acid and energy metabolism might lead to subsequent oxidative damage in the liver of rats .
Realgar, an ore crystal containing more than 90% tetra-arsenic tetrasulfide, has been used for the treatment of carbuncles, boils, insect-and snake-bites, intestinal parasitosis, convulsive epilepsy and psoriasis . As an arsenical, realgar is known as a poison and paradoxically as a therapeutic agent. Using a combined LC–MS and 1H NMR based metabolomic approach, Huang et al. investigated the hepatotoxicity induced by realgar in rats. Thirty-six potential biomarkers were discovered, and these metabolites were distributed in citric acid cycle, tryptophan metabolism, and porphyrin metabolism. Glycine and serine were proposed as key metabolites related to realgar-induced disturbance . In another study, a 1H NMR-based metabolomic approach was employed to investigate the subchronic hepatotoxicity of realgar on mice. The change trends of metabolites in urine and plasma from mice subchronic exposed to realgar are similar to those acute exposed to realgar, which indicate the acute and sub-chronic toxic mechanisms of realgar are same. The disturbed metabolic pathways include energy metabolism, amino acids metabolism and gut bacteria metabolism .
Metabolomics in nephrotoxicity evaluation of TCM
Aristolochic acid is a mixture of structural-related nitrophenanthrene carboxylic acid derivatives existed in Aristolochia, Bragantia and Asarum genus, such as Aristolochiae Fructus, Stephaniae tetrandrae Radix and Asari Ridix et Rhizoma . Aristolochic acid is a toxicant that can cause a common and rapidly progressive interstitial nephropathy called aristolochic acid nephropathy. The pathophysiology and underlying mechanisms of the aristolochic acid nephropathy have been studied using metabolomic approach by different analysis methods. Hu et al. employed a GC–MS based metabolomic technique to analyze urinary metabolites in aristolochic acid treated rats. Eight metabolites were selected as potential metabolic biomarkers including methylsuccinic acid, nicotinamide, 3-hydroxyphenylacetic acid, citric acid, creatinine, uric acid, glycolic acid, and gluconic acid. The identified metabolites suggested that the pathways of energy metabolism, gut microbiota, and purine metabolism were associated with aristolochic acid induced nephrotoxicity . In another LC–MS based urinary metabolomic study, the results suggested that the nephrotoxicity of aristolochic acid could be characterized via systemic disturbance of metabolic network including tricarboxylic acid cycle, gut microflora metabolism, amino acid metabolism, purine metabolism and bile acid biosynthesis, which were partly consistent with the results of GC–MS based metabolomic study .
Strychni Semen, the dried ripe seeds of Strychnos nux-vomica Linn., was commonly used to relieve rheumatism, induce analgesia, remove stasis, clear heat, and alleviate swelling in China . However, the clinical applications of Strychni Semen is limited by its severe toxicity, especially nephrotoxicity. Fan et al. established a 1H NMR based metabolomic method to evaluate the toxicity induced by Strychni Semen. The results indicated that Strychni Semen induced disruptions in glycolysis, lipid and amino acid metabolism, and the toxic effects were aggravated in liver and kidney tissues as dosing time was prolonged . A cell metabolomic strategy was also developed to investigate the nephrotoxicity of Strychni Semen. A total of 10 biomarkers and 24 related metabolic pathways were screened. The possible mechanisms of Strychni Semen nephrotoxicity might be cellular component disruption, oxidative damage, metabolic waste accumulation and the disturbance of energy and ion transport systems . Metabolomics could be an efficient means to elucidate the mechanism of Strychni Semen-induced nephrotoxicity and might contribute to investigation of possible nephrotoxic mechanisms of other TCM.
Arisaematis Rhizoma, the dried rhizomes of Arisaema erubescens Schott, Arisaema heterophyllum BI. and Arisaema amurense Maxim., has been widely used due to its various effects including analgesic, sedative, stomachic, anticoagulant, antiemetic, anti-inflammatory and antitumor activities . A 1H NMR based metabolomic approach complemented with serum chemistry and histopathology has been applied to investigate the nephrotoxicity of Arisaematis Rhizoma. The results indicated that thirteen metabolites in urine and six metabolites in serum were significantly altered, suggesting disturbances in energy metabolism, perturbation of the gut microflora environment, membrane damage, folate deficiency and injury of kidneys produced by Arisaematis Rhizoma .
Pharbitidis Semen, the dried mature seeds of Pharbitis nil (L.) Choisy or Pharbitis purpurea (L.) Voigt, is widely used for treatment of edema, simple obesity and lung fever in China and some east Asian countries. Several animal and clinical studies have reported the nephrotoxicity of Pharbitidis Semen . Recently, a LC–MS based metabolomic approach was employed to delineate the comprehensive mechanism of nephrotoxicity induced by Pharbitidis Semen. The results indicated that certain metabolic pathways, such as lysophosphatidylcholines formation and sphingolipids cycle were accelerated . Ma et al. performed another LC–MS based urinary metabolomics to investigate the nephrotoxicity induced by Pharbitidis Semen. The results indicated that ethanol extract of Pharbitidis Semen should be responsible for the nephrotoxicity and eight metabolites were identified. According to the identified metabolites, the underlying regulations of Pharbitidis Semen perturbed metabolic pathways were amino acid metabolism, citric acid cycle and bile acid metabolism .
Alismatis Rhizoma, the dried rhizome of Alisma orientale (Sam.) Juz., has been widely used as diuretic, antinephrolithic, hypolipidemic, antiatherosclerotic, antidiabetic and anti-inflammatory in China . However, overdose or long-term usage of Alismatis Rhizoma can cause nephrotoxicity. Yu et al. employed a LC–MS based metabolomic approach to investigate the nephrotoxicity of Alismatis Rhizoma in rats. The results indicated that significant changes in thirteen metabolite biomarkers were detected in the urine after treatment of Alismatis Rhizoma. The metabolomic method could discriminate the extract treated rats from the control rats on days 60, 120, and 180 after treatment. While serious organic renal damage was not observed on histopathology until day 180. The results indicated that LC–MS based metabolomic analysis is an useful tool for predicting the chronic nephrotoxicity induced by Alismatis Rhizoma .
Metabolomics in cardiotoxicity evaluation of TCM
Periplocin, a digitalis-like cardiac glycoside from Periplocae Cortex, has been used widely in clinic for its cardiotonic, anti-inflammatory and anti-tumor effects . To evaluate the cardiotoxicity of periplocin, Li et al. reported an UPLC Q/TOF MS method to reveal the metabolic profiles on neonatal rat cardiomyocytes exposed to periplocin. Eleven biomarkers associated with cardiotoxicity including carnitine, acetylcarnitine, lysoPC, proline, glutamic acid, pyroglutamic acid, leucine, pantothenic acid, tryptophan, indoleacrylic acid and citric acid were identified. The metabolic pathway analysis indicated that these metabolites were associated with amino acid metabolism, energy metabolism and sphingolipid metabolism, which contributes to the cardiotoxicity mechanism of periplocin .
Herbal medicines derived from Aconitum species, including Aconiti kusnezoffii Radix, Aconiti Radix and Aconiti Lateralis Preparata Radix have a long history of clinical use. These herbs have been shown to exhibit biological effects on various diseases, including rheumatic fever, painful joints, bronchial asthma, gastroenteritis, collapse, syncope, diarrhea, edema and tumors. Modern research revealed that Aconitum herbs have potent toxicity, and Aconitum alkaloids are not only the active ingredients but also toxic components . Aconitine, mesaconitine, and hypaconitine are the main Aconitum alkaloids derived from Aconiti lateralis Radix praeparata, the lateral root of Aconitum carmichaelii Debx. These alkaloids have analgesic, antipyretic, and local anesthetic activities and have beneficial effects against rheumatosis and rheumatoid arthritis. But the strong toxicity and the narrow margin between therapeutic and toxic doses limited clinical application of the Aconitum alkaloids. Sun et al. investigated the metabolic changes in rats caused by the aconitine, mesaconitine, and hypaconitine using 1H NMR and GC–MS. Compared with control group, the results revealed larger deviations in the aconitine and mesaconitine groups and smaller deviations in hypaconitine group, illustrating the different toxicity mechanisms of these alkaloids. Metabolomic analysis indicated that most of the metabolic biomarkers were related to tricarboxylic acid cycle .
Aconiti kusnezoffii Radix, the root of Aconitum kusnezoffii Reichb., was reported to induce toxicity to heart and central nervous system . Recently, Yan et al. proposed a UPLC Q/TOF MS based metabolomic approach to characterize the phenotypically biochemical perturbations and potential mechanisms of Aconiti kusnezoffii Radix-induced toxicity. The urinary metabolomics revealed serious toxicity to heart and liver. Thirteen metabolites were identified and validated as phenotypic toxicity biomarkers of Aconiti kusnezoffii Radix. These biomarkers were responsible for pentose and glucuronate interconversions, tryptophan metabolism, amino sugar and nucleotide sugar metabolism, taurine and hypotaurine metabolism, ascorbate and aldarate metabolism, fructose and mannose metabolism, and starch and sucrose metabolism .
The potential cardiotoxicity of Aconiti Radix (the mother roots of Aconitum carmichaelii Debx) was frequently reported because of its narrow therapeutic window. A metabolomic method was performed to characterize the potential mechanisms of Aconiti Radix-induced cardiotoxicity by UPLC Q/TOF MS. Seventeen biomarkers were identified in urinary samples, which were associated with pentose and glucuronate interconversions, alanine, aspartate, and glutamate metabolism . Meanwhile, the levels of the identified toxicity biomarkers were modulated to the normal ranges by Glyeyrrhizae Radix, Paeoniae Alba Radix and Zingiberis Rhizoma. The results indicated that these three compatible herbal medicines could be the effective detoxifying substances against the toxicity of Aconiti Radix .
Aconiti Lateralis Radix Praeparata, the lateral or daughter root of Aconitum carmichaelii Debx, has a potential cardiotoxicity with a relatively narrow margin of safety. Wang et al. reported a LC–MS metabolomic approach to investigate and compare the metabolic changing of Aconiti Lateralis Radix Praeparata, Aconiti Radix and the processed products. The data demonstrated that both Aconiti Lateralis Radix Praeparata and Aconiti Radix could lead to serious cardiotoxicity in a time- and dose-dependent manner. Sphingolipid metabolism, aminoacyl-tRNA biosynthesis and tryptophan metabolism mainly contributed to the toxicity of Aconiti Lateralis Radix Praeparata and Aconiti Radix . Cai et al. further employed a lipidomics strategy to explore the cardiotoxic mechanisms of Aconiti Lateralis Radix Praeparata and find out potential tissue-specific biomarkers by HPLC Q/TOF MS. Fourteen lipid metabolites, which are primarily involved in phospholipid metabolism, sphingolipid metabolism, saturated fatty acid oxidation and unsaturated fatty acid peroxidation, were identified and considered as the potential biomarkers of the cardiotoxicity induced by Aconiti Lateralis Radix Praeparata .
Pinelliae Rhizoma, the dried tuber of Pinellia ternata (Thunb.) Breit., is commonly used for treatment of cough, vomiting, infection and inflammation . Zhang et al. proposed a UPLC Q/TOF MS metabolomic approach to elucidate the toxicity of Pinelliae Rhizoma extract in rats. The results indicated that oral administration of Pinelliae Rhizoma did not induce obvious liver and kidney toxicity, but caused certain cardiotoxicity. The identified seven endogenous metabolites indicated the perturbations of phospholipid metabolism, amino acid metabolism and carnitine metabolism in Pinelliae Rhizoma treated rats . According to the TCM theory, processing can reduce the toxicity of Pinelliae Rhizoma. Using the metabolomic approach, Su et al. investigated the mechanisms of raw Pinelliae Rhizoma induced toxicity and toxicity-reducing effect of processing. Consistent with the above report, the metabolomic results also indicated that raw Pinelliae Rhizoma could cause cardiotoxicity. Inhibition of mTOR signaling and activation of the TGF-β pathway contributed to raw Pinelliae Rhizoma-induced cardiotoxicity, and free radical scavenging might be responsible for the toxicity-reducing effect of processing .
Metabolomics in other toxicity evaluation of TCM
In addition to the above-mentioned hepatotoxicity, nephrotoxicity and cardiotoxicity, reproduction toxicity of triptolide is also the main obstacle for its clinical applications. Ma et al. developed a GC–MS based metabolomic approach to evaluate the mechanism of triptolide-induced reproductive toxicity in male mice and identify potential biomarkers for the early detection of spermatogenesis dysfunction. The results indicated that the testicular toxicity of triptolide may be caused by abnormal lipid and energy metabolism in testis via down-regulation of peroxisome proliferator-activated receptor mediated .
Cinnabar, a traditional mineral medicine containing more than 96% mercuric sulfide, has been used as a sedative and soporific for more than 2000 years. It was reported that cinnabar can impact central nervous system and cause neurotoxicity through blood–brain barrier . Wei et al. investigated the neurotoxicity of cinnabar in rats by 1H NMR based metabolomics combined with multivariate pattern recognition. The metabolite variations induced by cinnabar were characterized by increased levels of glutamate, glutamine, myo-inositol, and choline, as well as decreased levels of γ-amino-n-butyrate, taurine, N-acetylaspartate and N-acetylaspartylglutamate in tissue extracts of the cerebellum and cerebrum. The results indicated that cinnabar induced glutamate excitotoxicity, neuronal cell loss, osmotic state changes, membrane fluidity disruption, and oxidative injury in the brain .
Kunsui Radix, the dried root of Euphorbia kansui T. N. Liou ex T. P. Wang, was widely used for treatment of edema, ascites, and asthma . The clinical application of Kunsui Radix is greatly restricted since it can induce toxic symptoms such as stomachache, diarrhea, dehydration and respiratory failure. The metabolites responsible for the toxicity of Kunsui Radix were evaluated by 1H NMR based metabolomics. The toxicity of Kunsui Radix accumulated with dosing time, and persisted even when treatment was stopped. The metabolomic results revealed that the levels of alanine, lactate, taurine, betaine, hippurate, phenylalanine and glucose were increased, while the levels of succinate, citrate, glycine, creatine and creatinine were decreased. The corresponding biochemical pathways alterations included inhibited tricarboxylic acid cycle, increased anaerobic glycolysis, and perturbed amino acids metabolism .
Coptidis Rhizome has been used as a heat-clearing and detoxifying agent in China for 2000 years. Coptidis Rhizome is relatively safe in normal dosage, but an extensive dosage can cause side effects such as diarrhea. A combination of 1H NMR and GC–MS based metabolomic approach was applied to discover the endogenous metabolites which related to the diarrheal induced by Coptidis Rhizome. In the study, twelve marker metabolites from 1H NMR and eight from GC–MS were identified, among those metabolites, hippurate, acetate, alanine, glycine and glutamate were likely to break the balance of gut microbiota, whereas, lactate and 2-ketoisovalerate were associated with energy metabolism .
TCM is generally used in the form of prescriptions (the combination of several different herbal medicines). The bioactive constituents and fundamental mechanisms of most TCM prescriptions remain unclear due to the complex components of remedies. Metabolomics could provide a holistic view and deeper insight into the efficacy and toxicity of TCM prescriptions. It might also be a promising approach to investigate the detoxification of Chinese medicines and reasonable combination of TCM prescriptions. Niuhuang Jiedu Tablet, composed of Realgar, Bovis Calculus Artificialis, Borneolum Synthcticum, Gypsum Fibrosum, Rhei Radix et Rhizoma, Scutellariae Radix, Platycodonis Radix and Glycyrrhizae Radix et Rhizoma, is an effective TCM prescription used for treatment of acute tonsillitis, pharyngitis, periodontitis and mouth ulcer . In the prescription, significant level of realgar is a potentially toxic element. Xu et al. proposed a 1H NMR based metabolomic approach to investigate the toxicity of realgar after being counterbalanced by other herbal medicines in Niuhuang Jiedu Tablet. The results showed that it was more secure and much less toxic for counterbalanced realgar in Niuhuang Jiedu Tablet. The effective material bases of toxicity alleviation to realgar were Rhei Radix et Rhizoma, Scutellariae Radix, Platycodonis Radix and Glycyrrhizae Radix et Rhizoma, which regulated energy metabolism, choline metabolism, amino acid metabolism and gut flora disorder affected by realgar exposure .
Zhusha Anshen Wan, composed of cinnabar, Coptidis Rhizoma, Angelicae Sinensis Radix, Rehmanniae Radix, Glycyrrhizae Radix et Rhizoma, is a widely used TCM prescription for sedative therapy. Cinnabar is the chief component of Zhusha Anshen Wan and possesses certain toxicity. A metabolomic analysis suggested that Zhusha Anshen Wan may be more secure and much less toxic than cinnabar alone, and the four combined herbal medicines of Zhusha Anshen Wan had the effects of protecting from the toxicity induced by cinnabar alone .
Shuanghuanglian injection, composed of Lonicerae japonicae Flos, Scutellariae Radix and Forsythiae Fructus suspensa, is a commonly used TCM preparation with known antimicrobial properties . It was reported that the adverse drug reactions of Shuanghuanglian injection occurred in approximately 2.22–2.56% after clinical exposure and the main adverse drug reactions were hypersensitive response, hemolytic anemia, haematuria and jaundice. The toxicological effects of Shuanghuanglian injection after intravenous administration in Beagle dogs were investigated by a 1H NMR-based metabolomic approach. The results revealed increases in serum choline, phosphocholine, ketone body and lactate, but decreases in trimethylamine N-oxide, taurine, leucine, valine, glycine and glutamine, and these findings may underlie the toxicity mechanisms of Shuanghuanglian injection .
Conclusions and perspectives
In recent years, metabolomics analysis has increased markedly in efficacy, quality control, action of mechanism, and active components discovery of TCM. Meanwhile, the toxicity of TCM have attracted a wide range of concerns and aroused many toxicity studies on TCM. Nevertheless, there is no standard and objective basis for TCM toxicity evaluation and no standard for safety assessment up to now, which seriously hinders the toxicological researches of TCM. As a systemic approach, metabolomics focuses on the analysis of global metabolites and their functions in the biological system. It allows quantitative measurement of large numbers of low-molecular endogenous metabolites involved in metabolic pathways, and thus reflects fundamental metabolism status of body. The systematic study of metabolomics is in agreement with TCM theory and may be the best approach to fit the holistic concept of TCM. Therefore, metabolomic analysis is a suitable tool to systematically evaluate toxicity, find potential biomarkers and explore the toxicological mechanisms of TCM.
Despite its potential and advantages, there are still great challenges for the metabolomic applications on toxicology of TCM. Firstly, high sensitivity of metabolites to various genetic and environmental factors might lead to difficult interpretation of data analysis. Secondly, there are still substantial shortcomings for the existing metabolomic techniques to analyze the full spectrum of metabolites. Thirdly, it is difficult to establish relationships between metabolomic results with genomics, proteomics and clinical data. Although there are still many challenges for the development of metabolomics in toxicity evaluation and it is a long way to get it into clinical application, we believe that the comprehensive metabolomic approach is a potentially powerful tool to evaluate toxicology and explore toxicological mechanisms of TCM. It is expectable that with the development of various analytical techniques, metabolomics will play an increasingly critical role in TCM toxicology research and be beneficial to the modernization of TCM.
traditional Chinese medicines
- 1H NMR:
proton nuclear magnetic resonance spectroscopy
gas chromatography–mass spectrometry
liquid chromatography–mass spectrometry
capillary electrophoresis–mass spectrometry
ultra-performance liquid chromatography
ultra-performance liquid chromatography–mass spectrometry
principal component analysis
hierarchical cluster analysis
partial least squares discriminant analysis
orthogonal partial least squares discriminant analysis
human metabolome database
Kyoto Encyclopedia of Genes and Genomes
biochemical genetic and genomic
- HPLC Q/TOF MS:
high performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry
- UPLC Q/TOF MS:
ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry
Cheung F. TCM: made in China. Nature. 2011;480:S82–3.
Chan K, Zhang H, Lin ZX. An overview on adverse drug reactions to traditional Chinese medicines. Br J Clin Pharmacol. 2015;80:834–43.
Lin AX, Chan G, Hu Y, Ouyang D, Ung COL, Shi L, et al. Internationalization of traditional chinese medicine: current international market, internationalization challenges and prospective suggestions. Chin Med. 2018;13:9.
Wang L, Zhou GB, Liu P, Song JH, Liang Y, Yan XJ, et al. Dissection of mechanisms of Chinese medicinal formula Realgar-Indigo naturalis as an effective treatment for promyelocytic leukemia. Proc Natl Acad Sci USA. 2008;105:4826–31.
Li P, Qi LW, Liu EH, Zhou JL, Wen XD. Analysis of chinese herbal medicines with holistic approaches and integrated evaluation models. Trends Analyt Chem. 2008;27:66–77.
Liu P, Yang H, Long F, Hao HP, Xu X, Liu Y, et al. Bioactive equivalence of combinatorial components identified in screening of an herbal medicine. Pharm Res. 2014;31:1788–800.
Liu SH, Chuang WC, Lam W, Jiang Z, Cheng YC. Safety surveillance of traditional Chinese medicine: current and future. Drug Saf. 2015;38:117–28.
Jeong TY, Park BK, Cho JH, Kim YI, Ahn YC, Son CG. A prospective study on the safety of herbal medicines, used alone or with conventional medicines. J Ethnopharmacol. 2012;143:884–8.
Zheng RS, Wang WL, Tan J, Xu H, Zhan RT, Chen WW. An investigation of fungal contamination on the surface of medicinal herbs in China. Chin Med. 2017;12:2.
Ouedraogo M, Baudoux T, Stévigny C, Nortier J, Colet JM, Efferth T, et al. Review of current and “omics” methods for assessing the toxicity (genotoxicity, teratogenicity and nephrotoxicity) of herbal medicines and mushrooms. J Ethnopharmacol. 2012;140:492–512.
Kitano H. Systems biology: a brief overview. Science. 2002;295:1662–4.
Zhang A, Sun H, Wang P, Han Y, Wang X. Future perspectives of personalized medicine in traditional Chinese medicine: a systems biology approach. Complement Ther Med. 2012;20:93–9.
Wang X, Zhang A, Sun H, Wang P. Systems biology technologies enable personalized traditional Chinese medicine: a systematic review. Am J Chin Med. 2012;40:1109–22.
Uzuner H, Bauer R, Fan TP, Guo DA, Dias A, El-Nezami H, et al. Traditional Chinese medicine research in the post-genomic era: good practice, priorities, challenges and opportunities. J Ethnopharmacol. 2012;140:458–68.
Dong L, Xu J, Zhang L, Yang J, Liao B, Li X, et al. High-throughput sequencing technology reveals that continuous cropping of American ginseng results in changes in the microbial community in arable soil. Chin Med. 2017;12:18.
Suo T, Wang H, Li Z. Application of proteomics in research on traditional Chinese medicine. Expert Rev Proteomics. 2016;13:873–81.
Nicholson JK, Lindon JC, Holmes E. Metabonomics: understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data. Xenobiotica. 1999;29:1181–9.
Wood PL. Mass spectrometry strategies for clinical metabolomics and lipidomics in psychiatry, neurology, and neuro-oncology. Neuropsychopharmacology. 2014;39:24–33.
Gu H, Du J, Carnevale Neto F, Carroll PA, Turner SJ, Chiorean EG, et al. Metabolomics method to comprehensively analyze amino acids in different domains. Analyst. 2015;140(8):2726–34.
Liu LY, Zhang HJ, Luo LY, Pu JB, Liang WQ, Zhu CQ, et al. Blood and urinary metabolomic evidence validating traditional chinese medicine diagnostic classification of major depressive disorder. Chin Med. 2018;13:53.
Holmes E, Loo RL, Stamler J, Bictash M, Yap IK, Chan Q, et al. Human metabolic phenotype diversity and its association with diet and blood pressure. Nature. 2008;453:396–400.
Zhang AH, Sun H, Qiu S, Wang XJ. Recent highlights of metabolomics in chinese medicine syndrome research. Evid Based Complement Alternat Med. 2013;2013:402159.
Dai M, Wang F, Zou Z, Xiao G, Chen H, Yang H. Metabolic regulations of a decoction of Hedyotis diffusa in acute liver injury of mouse models. Chin Med. 2017;12:35.
Wang M, Chen L, Liu D, Chen H, Tang DD, Zhao YY. Metabolomics highlights pharmacological bioactivity and biochemical mechanism of traditional Chinese medicine. Chem Biol Interact. 2017;273:133–41.
Tang JF, Li WX, Zhang F, Li YH, Cao YJ, Zhao Y, et al. Discrimination of Radix Polygoni Multiflori from different geographical areas by UPLC-QTOF/MS combined with chemometrics. Chin Med. 2017;12:34.
Shi J, Cao B, Wang XW, Aa JY, Duan JA, Zhu XX, et al. Metabolomics and its application to the evaluation of the efficacy and toxicity of traditional Chinese herb medicines. J Chromatogr B Analyt Technol Biomed Life Sci. 2016;1026:204–16.
Lao YM, Jiang JG, Yan L. Application of metabonomic analytical techniques in the modernization and toxicology research of traditional Chinese medicine. Br J Pharmacol. 2009;157:1128–41.
Zhang A, Sun H, Wang P, Han Y, Wang X. Modern analytical techniques in metabolomics analysis. Analyst. 2012;137:293–300.
Nagana Gowda GA, Raftery D. Recent advances in NMR-based metabolomics. Anal Chem. 2017;89:490–510.
Markley JL, Brüschweiler R, Edison AS, Eghbalnia HR, Powers R, Raftery D, et al. The future of NMR-based metabolomics. Curr Opin Biotechnol. 2017;43:34–40.
Ernst M, Silva DB, Silva RR, Vêncio RZ, Lopes NP. Mass spectrometry in plant metabolomics strategies: from analytical platforms to data acquisition and processing. Nat Prod Rep. 2014;31:784–806.
Naz S, Moreira dos Santos DC, García A, Barbas C. Analytical protocols based on LC–MS, GC–MS and CE–MS for nontargeted metabolomics of biological tissues. Bioanalysis. 2014;6:1657–77.
Chaleckis R, Meister I, Zhang P, Wheelock CE. Challenges, progress and promises of metabolite annotation for LC–MS-based metabolomics. Curr Opin Biotechnol. 2018;55:44–50.
Li Z, Chen K, Guo MZ, Tang DQ. Two-dimensional liquid chromatography and its application in traditional Chinese medicine analysis and metabonomic investigation. J Sep Sci. 2016;39:21–37.
Yan Y, Du C, Li Z, Zhang M, Li J, Jia J, et al. Comparing the antidiabetic effects and chemical profiles of raw and fermented chinese Ge-Gen-Qin-Lian decoction by integrating untargeted metabolomics and targeted analysis. Chin Med. 2018;13:54.
Vuckovic D. Current trends and challenges in sample preparation for global metabolomics using liquid chromatography-mass spectrometry. Anal Bioanal Chem. 2012;403:1523–48.
Gil RB, Lehmann R, Schmitt-Kopplin P, Heinzmann SS. 1H NMR-based metabolite profiling workflow to reduce inter-sample chemical shift variations in urine samples for improved biomarker discovery. Anal Bioanal Chem. 2016;408:4683–91.
Sitnikov DG, Monnin CS, Vuckovic D. Systematic assessment of seven solvent and solid-phase extraction methods for metabolomics analysis of human plasma by LC–MS. Sci Rep. 2016;6:38885.
Tong K, Li ZL, Sun X, Yan S, Jiang MJ, Deng MS, et al. Metabolomics approach reveals annual metabolic variation in roots of Cyathula officinalis Kuan based on gas chromatography–mass spectrum. Chin Med. 2017;12:12.
Martínez-Arranz I, Mayo R, Pérez-Cormenzana M, Mincholé I, Salazar L, et al. Enhancing metabolomics research through data mining. J Proteomics. 2015;127:275–88.
Smolinska A, Blanchet L, Buydens LM, Wijmenga SS. NMR and pattern recognition methods in metabolomics: from data acquisition to biomarker discovery: a review. Anal Chim Acta. 2012;750:82–97.
Eliasson M, Rännar S, Madsen R, Donten MA, Marsden-Edwards E, Moritz T, et al. Strategy for optimizing LC–MS data processing in metabolomics: a design of experiments approach. Anal Chem. 2012;84:6869–76.
Gromski PS, Muhamadali H, Ellis DI, Xu Y, Correa E, Turner ML, et al. A tutorial review: metabolomics and partial least squares-discriminant analysis–a marriage of convenience or a shotgun wedding. Anal Chim Acta. 2015;879:10–23.
Li XJ, Jiang ZZ, Zhang LY. Triptolide: progress on research in pharmacodynamics and toxicology. J Ethnopharmacol. 2014;155:67–79.
Wang Z, Qu L, Li M, Zhang J. Identification of hepatotoxic and nephrotoxic potential markers of triptolide in mice with delayed-type hypersensitivity. J Pharm Biomed Anal. 2018;160:404–14.
Zhao J, Xie C, Mu X, Krausz KW, Patel DP, Shi X, et al. Metabolic alterations in triptolide-induced acute hepatotoxicity. Biomed Chromatogr. 2018;32:e4299.
Mbiantcha M, Kamanyi A, Teponno RB, Tapondjou AL, Watcho P, Nguelefack TB. Analgesic and Anti-Inflammatory Properties of Extracts from the Bulbils of Dioscorea bulbifera L. var sativa (Dioscoreaceae) in Mice and Rats. Evid Based Complement Alternat Med. 2011;2011:912935.
Zhao DS, Wu ZT, Li ZQ, Wang LL, Jiang LL, Shi W, et al. Liver-specific metabolomics characterizes the hepatotoxicity of Dioscorea bulbifera rhizome in rats by integration of GC–MS and 1H-NMR. J Ethnopharmacol. 2018;226:111–9.
Zhao DS, Jiang LL, Fan YX, Wang LL, Li ZQ, Shi W, et al. Investigation of dioscorea bulbifera rhizome-induced hepatotoxicity in rats by a multisample integrated metabolomics approach. Chem Res Toxicol. 2017;30:1865–73.
Liu Y, Huang R, Liu L, Peng J, Xiao B, Yang J, et al. Metabonomics study of urine from Sprague-Dawley rats exposed to Huang-yao-zi using (1)H NMR spectroscopy. J Pharm Biomed Anal. 2010;52:136–41.
Han T, Li HL, Zhang QY, Han P, Zheng HC, Rahman K, et al. Bioactivity-guided fractionation for anti-inflammatory and analgesic properties and constituents of Xanthium strumarium L. Phytomedicine. 2007;14(12):825–9.
Xue LM, Zhang QY, Han P, Jiang YP, Yan RD, Wang Y, et al. Hepatotoxic constituents and toxicological mechanism of Xanthium strumarium L. fruits. J Ethnopharmacol. 2014;152:272–82.
Lu F, Cao M, Wu B, Li XZ, Liu HY, Chen DZ, et al. Urinary metabonomics study on toxicity biomarker discovery in rats treated with Xanthii Fructus. J Ethnopharmacol. 2013;149:311–20.
Liu Y, Wang Q, Yang J, Guo X, Liu W, Ma S, et al. Polygonum multiflorum Thunb.: a review on chemical analysis, processing mechanism, quality evaluation, and hepatotoxicity. Front Pharmacol. 2018;9:364.
Xia XH, Yuan YY, Liu M. The assessment of the chronic hepatotoxicity induced by Polygoni Multiflori Radix in rats: a pilot study by using untargeted metabolomics method. J Ethnopharmacol. 2017;203:182–90.
Liu J, Lu Y, Wu Q, Goyer RA, Waalkes MP. Mineral arsenicals in traditional medicines: orpiment, realgar, and arsenolite. J Pharmacol Exp Ther. 2008;326:363–8.
Huang Y, Tian Y, Li G, Li Y, Yin X, Peng C, et al. Discovery of safety biomarkers for realgar in rat urine using UFLC-IT-TOF/MS and 1H NMR based metabolomics. Anal Bioanal Chem. 2013;405:4811–22.
Huo T, Fang Y, Zhao L, Xiong Z, Zhang Y, Wang Y, et al. 1HNMR-based metabonomic study of sub-chronic hepatotoxicity induced by realgar. J Ethnopharmacol. 2016;192:1–9.
Michl J, Ingrouille MJ, Simmonds MS, Heinrich M. Naturally occurring aristolochic acid analogues and their toxicities. Nat Prod Rep. 2014;31:676–93.
Hu X, Shen J, Pu X, Zheng N, Deng Z, Zhang Z, et al. Urinary time- or dose-dependent metabolic biomarkers of aristolochic acid-induced nephrotoxicity in rats. Toxicol Sci. 2017;156(1):123–32.
Zhao YY, Tang DD, Chen H, Mao JR, Bai X, Cheng XH, et al. Urinary metabolomics and biomarkers of aristolochic acid nephrotoxicity by UPLC-QTOF/HDMS. Bioanalysis. 2015;7:685–700.
Tang HB, Cai HL, Li HD, Zhang LJ, Li XL, Tang JH, et al. HPLC-DAD method for comprehensive quality control of Semen Strychni. Pharm Biol. 2013;51(11):1378–83.
Fan Y, Liu S, Chen X, Feng M, Song F, Gao X. Toxicological effects of Nux Vomica in rats urine and serum by means of clinical chemistry, histopathology and 1H NMR-based metabonomics approach. J Ethnopharmacol. 2018;210:242–53.
Gu L, Hou P, Zhang R, Liu Z, Bi K, Chen X. An analytical strategy to investigate Semen Strychni nephrotoxicity based on simultaneous HILIC-ESI-MS/MS detection of Semen Strychni alkaloids, tyrosine and tyramine in HEK 293t cell lysates. J Chromatogr B Analyt Technol Biomed Life Sci. 2016;1033–1034:157–65.
Huang CF, Yang RS, Liu SH, Hsieh PC, Lin-Shiau SY. Evidence for improved neuropharmacological efficacy and decreased neurotoxicity in mice with traditional processing of Rhizoma Arisaematis. Am J Chin Med. 2011;39:981–98.
Dong G, Wang J, Guo P, Wei D, Yang M, Kong L. Toxicity assessment of Arisaematis Rhizoma in rats by a (1)H NMR-based metabolomics approach. Mol BioSyst. 2015;11:407–17.
Tian LQ, Zhang ZL, Zhang BS. Research on the pharmacology, toxicity and clinical application of morning glory seed. Chin J Nat Med. 2004;3:146–7.
Ma C, Bi K, Su D, Ji W, Zhang M, Fan X, et al. Serum and kidney metabolic changes of rat nephrotoxicity induced by Morning Glory Seed. Food Chem Toxicol. 2010;48:2988–93.
Ma C, Bi K, Zhang M, Su D, Fan X, Ji W, et al. Metabonomic study of biochemical changes in the urine of Morning Glory Seed treated rat. J Pharm Biomed Anal. 2010;53:559–66.
Zhang LL, Xu W, Xu YL, Chen X, Huang M, Lu JJ. Therapeutic potential of Rhizoma Alismatis: a review on ethnomedicinal application, phytochemistry, pharmacology, and toxicology. Ann N Y Acad Sci. 2017;1401:90–101.
Yu Y, Ma C, Bi K, Yang G, Xie P, Wang J, et al. A metabonomic analysis of urine from rats treated with rhizoma alismatis using ultra-performance liquid chromatography/mass spectrometry. Rapid Commun Mass Spectrom. 2011;25:2633–40.
Li Y, Li J, Zhou K, He J, Cao J, An M, et al. A review on phytochemistry and pharmacology of Cortex Periplocae. Molecules. 2016;21:E1702.
Li A, Guo X, Xie J, Liu X, Zhang Z, Li Y, et al. Validation of biomarkers in cardiotoxicity induced by Periplocin on neonatal rat cardiomyocytes using UPLC-Q-TOF/MS combined with a support vector machine. J Pharm Biomed Anal. 2016;123:179–85.
Nyirimigabo E, Xu Y, Li Y, Wang Y, Agyemang K, Zhang Y. A review on phytochemistry, pharmacology and toxicology studies of Aconitum. J Pharm Pharmacol. 2015;67:1–19.
Sun B, Li L, Wu S, Zhang Q, Li H, Chen H, et al. Metabolomic analysis of biofluids from rats treated with Aconitum alkaloids using nuclear magnetic resonance and gas chromatography/time-of-flight mass spectrometry. Anal Biochem. 2009;395:125–33.
Sui Z, Li Q, Zhu L, Wang Z, Lv C, Liu R, et al. An integrative investigation of the toxicity of Aconiti kusnezoffii radix and the attenuation effect of its processed drug using a UHPLC-Q-TOF based rat serum and urine metabolomics strategy. J Pharm Biomed Anal. 2017;145:240–7.
Yan Y, Zhang A, Dong H, Yan G, Sun H, Wu X, et al. Toxicity and detoxification effects of herbal Caowu via ultra performance liquid chromatography/mass spectrometry metabolomics analyzed using pattern recognition method. Pharmacogn Mag. 2017;13:683–92.
Dong H, Zhang A, Sun H, Wang H, Lu X, Wang M, et al. Ingenuity pathways analysis of urine metabolomics phenotypes toxicity of Chuanwu in Wistar rats by UPLC-Q-TOF-HDMS coupled with pattern recognition methods. Mol BioSyst. 2012;8:1206–21.
Dong H, Yan GL, Han Y, Sun H, Zhang AH, Li XN, et al. UPLC-Q-TOF/MS-based metabolomic studies on the toxicity mechanisms of traditional Chinese medicine Chuanwu and the detoxification mechanisms of Gancao, Baishao, and Ganjiang. Chin J Nat Med. 2015;13:687–98.
Wang X, Wang H, Zhang A, Lu X, Sun H, Dong H, et al. Metabolomics study on the toxicity of aconite root and its processed products using ultra-performance liquid-chromatography/electrospray-ionization synapt high-definition mass spectrometry coupled with pattern recognition approach and ingenuity pathways analysis. J Proteome Res. 2012;11:1284–301.
Cai Y, Gao Y, Tan G, Wu S, Dong X, Lou Z, et al. Myocardial lipidomics profiling delineate the toxicity of traditional Chinese medicine Aconiti Lateralis radix praeparata. J Ethnopharmacol. 2013;147:349–56.
Wu J, Cheng Z, He S, Shi J, Liu S, Zhang G, et al. Pinelliae rhizoma, a toxic chinese herb, can significantly inhibit CYP3A activity in rats. Molecules. 2015;20:792–806.
Zhang ZH, Zhao YY, Cheng XL, Dai Z, Zhou C, Bai X, et al. General toxicity of Pinellia ternata (Thunb.) Berit. in rat: a metabonomic method for profiling of serum metabolic changes. J Ethnopharmacol. 2013;149:303–10.
Su T, Tan Y, Tsui MS, Yi H, Fu XQ, Li T, et al. Metabolomics reveals the mechanisms for the cardiotoxicity of Pinelliae Rhizoma and the toxicity-reducing effect of processing. Sci Rep. 2016;6:34692.
Ma B, Qi H, Li J, Xu H, Chi B, Zhu J, et al. Triptolide disrupts fatty acids and peroxisome proliferator-activated receptor (PPAR) levels in male mice testes followed by testicular injury: a GC–MS based metabolomics study. Toxicology. 2015;336:84–95.
Liu J, Shi JZ, Yu LM, Goyer RA, Waalkes MP. Mercury in traditional medicines: is cinnabar toxicologically similar to common mercurials? Exp Biol Med. 2008;233:810–7.
Li X, Pei F, Wei L, Zhang P, Wu Y, Xue R. H-1 NMR-based metabolomics and neurotoxicity study of cerebrum and cerebellum in rats treated with cinnabar, a traditional chinese medicine. OMICS. 2015;19:490–8.
Shen J, Kai J, Tang Y, Zhang L, Su S, Duan JA. The chemical and biological properties of Euphorbia kansui. Am J Chin Med. 2016;44:253–73.
Tang B, Ding J, Wu F, Chen L, Yang Y, Song F. 1H NMR-based metabonomics study of the urinary biochemical changes in Kansui treated rat. J Ethnopharmacol. 2012;141:134–42.
Zhou Y, Liao Q, Lin M, Deng X, Zhang P, Yao M, et al. Combination of 1H NMR- and GC–MS-based metabonomics to study on the toxicity of Coptidis Rhizome in rats. PLoS ONE. 2014;9:e88281.
Xu W, Wang H, Chen G, Li W, Xiang R, Zhang X, et al. A metabolic profiling analysis of the acute toxicological effects of the realgar (As2S2) combined with other herbs in Niuhuang Jiedu Tablet using 1H NMR spectroscopy. J Ethnopharmacol. 2014;153:771–81.
Xu W, Wang H, Chen G, Li W, Xiang R, Pei Y. 1H NMR-based metabonomics study on the toxicity alleviation effect of other traditional Chinese medicines in Niuhuang Jiedu tablet to realgar (As2S2). J Ethnopharmacol. 2013;148:88–98.
Wang H, Bai J, Chen G, Li W, Xiang R, Su G, et al. A metabolic profiling analysis of the acute hepatotoxicity and nephrotoxicity of Zhusha Anshen Wan compared with cinnabar in rats using 1H NMR spectroscopy. J Ethnopharmacol. 2013;146:572–80.
Tang Y, Wang Z, Huo C, Guo X, Yang G, Wang M, et al. Antiviral effects of Shuanghuanglian injection powder against influenza A virus H5N1 in vitro and in vivo. Microb Pathog. 2018;121:318–24.
Yan G, Zhao Y, Deng P, Lv L, Wang Y, Bu Q, et al. Investigation of toxicological effects of Shuanghuanglian injection in Beagle dogs by metabonomic and traditional approaches. Exp Biol Med. 2010;235:1356–64.
LD, LG and LW drafted the manuscript. CMZ, QY and YGZ collected and analyzed relevant literatures. EHL conceived and designed the review. All authors read and approved the final manuscript.
The authors greatly appreciate financial support from the National Key Research and Development Program of China (2017YFC1701105 and 2017YFC1701103), National Natural Science Foundation of China (81673569, 81803685, 81803697), National Modern Agricultural Industrial Park of China (NO. njf  110), a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions, Natural Science Foundation of Hebei Province (H2018205185, H2018423032) and Research Foundation of Hebei Provincial Administration of Traditional Chinese Medicine (2018108).
The authors declare that they have no competing interests.
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National Key Research and Development Program of China (2017YFC1701105 and 2017YFC1701103), National Natural Science Foundation of China (81673569, 81803685, 81803697), National Modern Agricultural Industrial Park of China (NO. njf  110), a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions, Natural Science Foundation of Hebei Province (H2018205185, H2018423032), Research Foundation of Hebei Provincial Administration of Traditional Chinese Medicine (2018108).
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Duan, L., Guo, L., Wang, L. et al. Application of metabolomics in toxicity evaluation of traditional Chinese medicines. Chin Med 13, 60 (2018). https://doi.org/10.1186/s13020-018-0218-5
- Traditional Chinese medicines
- Toxicity mechanisms