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Chinmedomics: a potent tool for the evaluation of traditional Chinese medicine efficacy and identification of its active components

Abstract

As an important part of medical science, Traditional Chinese Medicine (TCM) attracts much public attention due to its multi-target and multi-pathway characteristics in treating diseases. However, the limitations of traditional research methods pose a dilemma for the evaluation of clinical efficacy, the discovery of active ingredients and the elucidation of the mechanism of action. Therefore, innovative approaches that are in line with the characteristics of TCM theory and clinical practice are urgently needed. Chinmendomics, a newly emerging strategy for evaluating the efficacy of TCM, is proposed. This strategy combines systems biology, serum pharmacochemistry of TCM and bioinformatics to evaluate the efficacy of TCM with a holistic view by accurately identifying syndrome biomarkers and monitoring their complex metabolic processes intervened by TCM, and finding the agents associated with the metabolic course of pharmacodynamic biomarkers by constructing a bioinformatics-based correlation network model to further reveal the interaction between agents and pharmacodynamic targets. In this article, we review the recent progress of Chinmedomics to promote its application in the modernisation and internationalisation of TCM.

Introduction

Traditional Chinese Medicine (TCM) has become an important part of medical science with a long history and rich clinical experience [1]. Due to its characteristics of fewer side effects, natural growth, and multi-target effects than synthetic drugs, TCM has recently attracted the attention of many medical researchers [2]. It has made prominent contributions to modern medicine, the most successful example being artemisinin extracted from Artemisia annua L. for the treatment of malaria, for which Tu Youyou was awarded the 2015 Nobel Prize in Physiology or Medicine [3]. During these years, herbal formulas have proven effective for patients with COVID-19 in improving cure rates, shortening the course of the disease, delaying disease progression, and reducing mortality [4]. However, despite its significant intervention effect on diseases, the active ingredients and mechanism of most TCM formulas are still unclear due to the lack of methods that are consistent with TCM theory and practice. Thus, the exploration of new scientific strategies, the study of the mechanisms of action of TCM, the scientific interpretation of the connotations of TCM, and the understanding of its biological basis have become urgent clinical challenges.

In recent decades, many research methods have been proposed to reveal the active ingredients and molecular mechanism of TCM against diseases, such as TCM network pharmacology [5], TCM system pharmacology [6], and Fangjiomics [7]. These methods build bridges between herbal compounds and disease targets by searching databases to screen for active compounds. However, whether the selected compounds can be absorbed into serum and exert their bioactivities still needs further verification. In addition, many disease targets have been obtained by previous methods, how to lock core therapeutic targets and key pathways from numerous disease targets has become an important issue [8, 9].

We are introducing an emerging integrated research strategy called Chinmedomics to address these issues [10]. It uses serum pharmacochemistry of TCM to obtain active ingredients, and then further associates these ingredients with identified disease/symptom biomarkers to clarify the pharmacodynamic substance basis and mechanism of action under the premise of effective treatment of diseases. In 2015, Nature commented that Chinmedomics has built a linguistic bridge between TCM and modern medicine, which is of great significance for fully understanding the efficacy of TCM, enhancing the social value of TCM clinical experience, and promoting the academic progress of TCM [11]. At present, Chinmedomics has been widely accepted at home and abroad and has been widely applied in disease/syndrome diagnosis, biomarker discovery, efficacy evaluation, active ingredients discovery, and solving other problems of modern TCM. In the following chapters of this paper, we introduce the application and analytical techniques of Chinmedomics in these areas.

Background and development of chinmedomics theory formation

Active ingredients in TCM and natural products have long been an interesting research hotspot. Initially, the determination of active ingredients from herbal medicine, such as berberine [12], glycyrrhizic acid [13], tanshinone IIA [14], etc., relies on standardized procedures including extraction, isolation, purification, qualitative analysis, quantitative analysis, derivatization, and pharmacological activity studies [15]. Subsequently, the emergence of new approaches is improving the efficiency of screening for novel functional botanicals. For example, a luciferase-based high-throughput screening (HTS) assay can speed up the drug discovery process by reducing the number of replicate leads [16]. With the continuous deepening understanding of the active ingredients of TCM, it has been found that studying the behavior of herbal ingredients in vivo is a crucial link for screening active ingredients, so in the 1990s, Professor Wang proposed the serum pharmacochemistry of TCM [17,18,19]. This approach utilizes a combination of high-throughput techniques to analyze and characterize herbal components absorbed into serum, and shows comprehensive superiority in explaining drug changes in vivo and in vitro, as well as drug-drug interactions [20].

The ambiguity of the nature of the disease/syndrome limits the clarification of the mechanism of action of drugs. Fortunately, metabolomics provides an important basis for clarifying the nature of the symptoms and clinical diagnosis of diseases by providing new insights into the pathology of diseases through the confirmation and analysis of biomarkers [21]. For example, using this method, Lv et al. identified and validated 5 metabolites as indicators for the diagnosis of pancreatic cancer, which have higher accuracy and specificity in accurately diagnosing pancreatic cancer than traditional biomarkers [22]. Multifactorial diseases, such as metabolic syndrome and coronary heart disease, are often caused by multiple underlying pathological mechanisms, and advanced metabolomics has helped us gain a comprehensive understanding of the biological processes and pathogenesis of these diseases [23, 24].

Multidisciplinary integration is essential to fully understand disease and drug mechanisms. Chinmedomics, a new and standardized research approach, has been proposed and established [10]. Based on the metabolomics and serum pharmacochemistry of TCM, this strategy also introduces systems biology, molecular biology and bioinformatics, and forms a multi-omics and multidisciplinary systematic research method to study the efficacy of herbal formulas and discover the active ingredients of TCM. The basic framework is shown in Fig. 1. First, we classify syndromes or diseases according to clinical diagnosis, and use high-throughput, high-sensitivity analysis techniques to analyze the metabolic profiles of metabolites in various biospecimens, comprehensively identify and discover the syndromes/diseases biomarkers and their functions by searching bioinformatics platform and related databases [25, 26]. Second, based on the clinical significance of biomarkers, we accurately analyze disease states and objectively evaluate therapeutic efficacy by analyzing recall biomarkers after intervention with TCM. Thirdly, herbal components are analyzed qualitatively and quantitatively for their absorption and metabolism in serum, and under the premise of ensuring therapeutic efficacy, compounds in TCM are screened for activity through in vitro or in vivo experiments to identify compounds with pharmacological effects, and compounds in TCM are separated, purified, and identified using chromatography, mass spectrometry, and other methods of chemical analysis, and the mechanism of action of TCM on living organisms is further determined through biological experiments, such as gene expression, proteomics etc., to study the mechanism of action of Chinese medicines on living organisms and further determine the bioactive components. Comprehensive characterization of in vivo properties. Finally, a multi-dimensional correlation analysis network model was constructed by mathematical model, which integrated various biomarkers, active ingredients, multiple biochemical factors, and complex clinical phenotypes, so as to elucidate the therapeutic mechanism of active ingredients at different levels. Chinmedomics describes "what happened in TCM ingredients" in vivo, thus it has a more reliable ability to evaluate the efficacy and discover the active ingredients of TCM and is a feasible strategy for the modernization of TCM.

Fig. 1
figure 1

The basic research framework of Chinmedomics

The analytical technologies of chinmedomics

Chinmedomics applies modern high-throughput and sensitive chromatography-mass spectrometry (LC–MS, GC–MS) and nuclear magnetic resonance (NMR) techniques to characterize herbal constituents and metabolites in various bio-samples, given the complexity and diversity of the biological matrix [27]. In addition, for the structural identification of chemical compounds, the combined strategy of NMR and LC–MS has also been applied [28, 29]. Recently, new mass spectrometry imaging technology has been increasingly utilized to investigate diseases, particularly in the case of cancer [30, 31]. It can visualize the location and quantity of biomarkers in cells and tissues. This allows for the monitoring of biomarker dynamics in disease progression and the observation of molecular interactions between biomarkers and active ingredients of TCM at various stages of the disease [32]. All of these analytical techniques can separate hundreds to thousands of chemical compounds in complex mixtures and display them as spectra or chromatograms, which contain thousands of unique peaks and complex overlapping peaks [33].And the MS/MS spectra obtained via mass spectrometry are compared with the database's reference compounds to achieve accurate identification. Therefore, it is necessary to utilize extensive databases comprising reference mass and NMR spectra of pure compounds to ascertain the corresponding compounds for each peak in such spectra. Databases including the Human Metabolome Database [34], Metlin [26], Birmingham Metabolite Library NMR database [35], MassBank [36], and LipidMaps [37] are frequently employed for the purpose of annotating and identifying metabolite signatures, cloud-based computing and database advancements have tackled the issues associated with data analysis and sharing [38]. ChemSpider [39] and PubChem [40] are widely utilized chemical composition databases that encompass molecular structure, physicochemical properties, and spectral information. Additionally, newer databases like mzCloud and mzCompound have been created to supplement retrieval [41].

Correlation measures the association between variables. The relationship between biomarkers and active ingredients is the most frequently studied linear association of two continuous variables. Their relationship can be established through bioinformatics algorithms including weighted correlation network analysis (WGCNA) [42], PCMS [43], and several prediction software packages (GGally, ggcor, corrplot) that offer information on both the strength and direction of a relationship [44]. The complex relationship between disease phenotypes, biomarkers, and active ingredients requires multivariate association analysis. The R package is capable of integrating these variables together [45, 46]. To gain a comprehensive understanding of the disease-related biological network system, we performed a metabolic pathway search and network topology analysis using biomarkers as core nodes. These biomarkers can be visualized through MetPA, regularized partial correlation network, and Cytoscape, allowing us to identify and elucidate all nodes and their corresponding functions in the correlation network [47,48,49]. In Chinmedomics, the correlation analysis principles dictate that the focus should be on retaining core metabolic targets that are closely related to pathogenic links of syndromes and diseases. Additionally, there should be emphasis on retaining the key targets and pathways that have significant regulatory potential, along with herbal ingredients that are correlated with many targets. Lastly, it is important to retain the key phenotypic characteristics reflected by the core targets. These methods of multidimensional network association analysis simplify the complexity of biological networks and enhance the readability of network information.

The main application of chinmedomics

Clarifying the efficacy and active ingredients of herbal medicines is crucial in constructing a modernized TCM system. Achieving this goal often requires sufficient prior knowledge in understanding the pathogenesis of the disease and the complex interactions of active compounds with their biological targets in physiological and pathological states, which is also one of the bottlenecks of TCM study [50,51,52]. Yet it is noteworthy that Chinmedomics offers a potent strategy for diagnosing diseases/syndromes, evaluating the efficacy of TCM, and discovering active ingredients. Furthermore, Chinmedomics has been applied to studies on active ingredients for over 10 years. This includes discovering quality markers of TCM, elucidating the mechanisms of reducing toxicity and improving efficiency of herbal formulas, and developing new herbal medicines/formulas, as depicted in Fig. 2.

Fig. 2
figure 2

The application of Chinmedomics in the diagnosis of syndromes/diseases, evaluation of efficacy of herbal medicines/formulas, discovery of active ingredients, discovery of quality markers of TCM, elucidation of mechanisms to reduce toxicity and improve efficiency of herbal formulas, and development of new herbal medicines/formulas

Diagnosis of syndromes/diseases

Accurately identifying symptomatic status is a prerequisite for effective treatment. However, current diagnosis of syndromes and diseases remains highly experience-based, relying on four diagnostic methods: inspection, palpation, percussion, and auscultation [53]. This diagnostic pattern has been historically summarized based on logical reasoning and empirical experience. Therefore, it may be perceived as subjective and ambiguous to some extent, leading to differences in diagnoses due to variations in the experiences and manual evaluations of different practitioners [54]. Achieving reproducibility and accuracy of diagnosis is particularly challenging when the syndrome is in the early stages of development or in transition [55]. With the advancement of molecular biology and systems biology, Chinmedomics utilizes metabolomics as a central approach to offer standardized, scientific, objective, and computerized diagnosis for common syndromes and diseases.

Several investigations based on Chinmedomics have been conducted to achieve precise diagnosis of various syndromes and diseases, including Jaundice Syndrome [56], Liver-Depression and Spleen-Deficiency Syndrome [57], and Alzheimer's Disease [58], displayed in Table 1. Jaundice Syndrome (JS) will serve as an example to introduce Chinmedomics' accurate diagnosis pattern [56]. JS is a frequently occurring and life-threatening illness that presents diagnostic and prognostic challenges due to the low sensitivity of clinically available indicators. In a study by Wang Xijun et al., Chinmedomics was used to analyze the urine metabolic characteristics of JS patients, namely Yang Huang and Yin Huang, resulting in the identification of 44 biomarkers, such as dimethyl guan (purine) glycoside, indole glutamine, corticosterone tetrol-3-glucosidic acid, and pregnanediol-3-glucosidic acid, among others. The metabolic pathways of JS were elucidated for the first time from a metabolic perspective. These pathways predominantly encompassed ketone body synthesis and degradation, alanine, aspartate and glutamate metabolism, tryptophan metabolism, and arginine and proline metabolism. Utilizing the automatic scaling method of MetaboAnalyst, these metabolic features can differentiate JS patients from healthy individuals with ease. Furthermore, we accomplished the differentiation and typing for JS and its subcategories, namely Yang Huang and Yin Huang, utilizing Chinmedomics. We identified 40 biomarkers linked primarily to tryptophan metabolism, vitamin B6 metabolism, arginine, and proline metabolism for Yang Huang, and 49 biomarkers predominantly associated with cysteine and methionine metabolism and primary bile acid biosynthesis for Yin Huang. As a contemporary omics method for scrutinizing syndromes and diseases, Chinmedomics has accurately interpreted the microscopic biological characteristics of JS, enabling an unbiased and standardized diagnosis of JS and its subtypes.

Table 1 The application of Chinmedomics in the diagnosis of syndromes/diseases

Efficacy evaluation of herbal medicines/herbal formulas

Western medicine is often seen as a strictly scientific field, while TCM incorporates a variety of philosophical and medical approaches [68, 69]. TCM views the body as a complex and dynamic system, highlighting the importance of balance and harmonious interaction with the ever-changing environment in maintaining health. Disease is viewed as a result of internal disharmony or imbalance in bodily functions and interactions [69]. Furthermore, TCM incorporates therapeutic principles such as Zang-Fu organs, Five-Elements, and the Meridian system, among other approaches. However, these approaches are often viewed as too abstract and criticized by Westerners for their lack of standardization. To determine the effectiveness of these theories [70], an objective evaluation is required. To enhance the reputation of TCM in modern healthcare, it is necessary to prove its efficacy scientifically while preserving its unique framework and strengths. Chinmedomics is a theoretical system that aims to bridge the gap between the East and the West, as well as ancient and modern approaches to medicine. Its goal is to measure the functional output of small molecule metabolites that interact with environmental factors in highly complex biological systems, to reflect the overall biochemical effects of patients after consuming herbal medicine [71]. Due to its consistent fundamental concept with TCM dynamic theories, the Chinmedomics strategy is becoming feasible in understanding the efficacy of TCM.

Chinmedomics has conducted many studies to evaluate the efficacy of herbal formulas, as shown in Table 2, with technical abbreviations explained throughout. This chapter presents the use of Liu Wei Di Huang Wan (LW) as an example to treat kidney yin deficiency [72]. LW is a well-known herbal formula that tonifies kidney yin and includes Radix Rehmanniae Preparata, Fructus Macrocarpii, Rhizoma Dioscoreae Oppositae, Poria, Rhizoma Alismatis, and Cortex Moutan Radicis. The writing avoids biased or emotional language with a clear and objective tone, and adheres to academic conventions for structure, format, and language. The first three herbs are referred to as "Sanbu" (SB) as they help tonify the kidneys, liver, and spleen. The remaining herbs, called "Sanxie" (SX), weaken the effects of excessive nourishment and contribute towards maintaining the The SB and SX are involved in maintaining kidney essence balance. Wang Xijun and colleagues discovered that LW has the potential to enhance kidney function in humans by regulating various metabolic pathways such as glucose, amino acids, and lipids, as well as intestinal flora. They replicated a rat model based on kidney yin deficiency biomarkers to evaluate LW's therapeutic efficacy. By quantifying biomarkers, analyzing metabolic networks, and identifying 20 pharmacodynamic biomarkers, LW's effectiveness was confirmed. The interventions primarily pertained to inhibiting the tryptophan-kynurenine metabolic pathway and stabilizing lysine metabolism, leading to heightened protein absorption and nutritional utilization. Additionally, improved tRNA to transport amino acids facilitated protein biosynthesis and biological functions, thereby providing ample nutritional supplementation for addressing kidney yin deficiency. Notably, the experimental rats demonstrated normal food and water consumption. Additionally, enhancements in glucose metabolism and the tricarboxylic acid cycle have adequately supplied mitochondria with energy to uphold kidney function homeostasis, as evidenced by blood biochemical analyses. This investigation replicated clinical findings and introduced a fresh methodology for merging clinical and experimental research. Additionally, we compared the call-back rates of pharmacodynamic biomarkers in positive and negative modes among different groups. The findings indicated that the SB group had a stronger regulatory effect than the SX group. Nonetheless, neither of these groups alone could fully express the overall efficacy of LW, which explains the significance of their synergistic combination.

Table 2 The application of Chinmedomics in the evaluation of the efficacy of herbal medicines/herbal formulas

Discovery of the active ingredients of TCM

TCM comprises natural medicinal plants, which serve as pivotal sources of modern drugs. Notably, natural products or their derivatives account for approximately 45% of FDA-approved drugs [81]. The application of TCM in drug development has transpired for decades. However, the progress in exploring and utilizing TCM in modern times has been limited by the dearth of high-performance research strategies that are well-suited for studying how TCM treats diseases [82]. The biochemical process by which TCM mitigates diseases can be understood as involving multilateral molecular interactions between effective compounds and dysregulated molecules [32]. To precisely qualify and quantify the two fundamental elements in disease progression and therapeutics, Chinmedomics is an innovative strategy for understanding biological systems. It can identify pharmacodynamic biomarkers and associated functional metabolic pathways with priority capability while comprehensively characterizing herbal compounds in vivo. Moreover, it precisely recognizes active ingredients that are highly related to the metabolic process of pharmacodynamic biomarkers.

Thus far, Chinmedomics has been utilized to reveal the molecular mechanisms of classical herbal formulas for treating illnesses and identify their active constituents, as demonstrated in Table 3. The analysis of the active constituents in Yin-Chen-Hao-Tang (YCHT), which treats cholestatic jaundice, serves as an example of the research methodology employed in Chinmedomics [83]. YCHT is a herbal formula that is often used to treat cholestatic jaundice. It was first documented in the Treatise on Febrile Diseases penned by Zhongjing Zhang during the Eastern Han Dynasty. YCHT consists of Rheum officinale Baill, Artemisia capillaries Thunb., and Gardenia jasminoides Ellis. Technical terms are explained on first use, and the language used is objective and precise, avoiding ornamental and biased language. The text adheres to proper academic writing principles, such as being grammatically correct, using a formal register, and employing a clear and logical structure. Citations are used consistently, and the appropriate formatting features are used. Metabolomics analysis was initially conducted on serum samples from patients and mice afflicted with cholestatic jaundice. Following comparisons of metabolic profiles and changes in metabolite content with healthy individuals or mice, 11 and 13 potential biomarkers were identified in patients and mice, respectively. Of note, multiple biomarkers were found to be shared between the two groups. The pathway analysis revealed that lipid metabolism and bile acid metabolism were the principal pathological mechanisms underlying cholestatic jaundice in mice and patients alike. However, YCHT administration improved cholestatic jaundice and primarily regulated the bile acid metabolism pathway. Bias has been avoided. Bile acid-related enzymes, including FXR, ABCC3 and UGT1A1, were activated while CYP7A1 was inhibited. Further modulation was observed in four core biomarkers, including bilirubin, biliverdin, bilirubin glucuronide, and taurocholic acid. Technical term abbreviations were explained upon first use. The language is formal, objective, value-neutral, and grammatically correct. The structure is logical, and causal connections are clearly established. American spelling, grammar, and style have been followed throughout. Validation experiments indicate that metabolite clusters with these four core metabolites are capable of distinguishing jaundice patients from healthy subjects. This demonstrates the importance of YCHT-improved metabolites for patients with jaundice. Furthermore, we detected 26 prototype compounds and 3 metabolic compounds in the serum of patients as well as 33 prototype compounds and 3 metabolic compounds in mice. Subsequently, we created a biological network consisting of herbal ingredients, pharmacodynamic biomarkers, and metabolic enzymes. Finally, the metabolic profile of eight components, namely geniposide, scoparone, isorhamnetin, quercetin, naringenin, rhein, chlorogenic acid, and kaempferol, is linked to the metabolic targets of disease recovery. These components are regarded as the active ingredients of YCHT, which is used to treat cholestatic jaundice.

Table 3 The Application of Chinmedomics in Discovering Active Ingredients of TCM

Discovery of quality markers in herbal formulas/herbal medicines

As the uncertainties about the quality of herbal medicines are an obstacle to their modernization, the establishment of a standardized and systematic quality evaluation system is a national strategy to ensure the safety and efficacy of herbal medicines and facilitate their development [91]. TCM comprises various chemical components with diverse structures and content [92,93,94]. Currently, the primary methods for evaluating the quality of TCM involve chemical qualitative identification and index component detection, which follow the basic mode of evaluating foreign plant drugs [91]. In addition, phytochemical fingerprint analysis is an advanced quality control method that provides a comprehensive overview of herbal medicine [95, 96]. However, a major drawback of the compounds detected is their potential lack of absorption or pharmacological activity, rendering their content insufficient for evaluating the efficacy of TCM [97]. Therefore, it is of great significance to establish a new quality control strategy for TCM based on their biological effects. Interestingly, Professor Liu's concept of Q-marker also highlights effectiveness as a critical criterion for evaluating TCM quality [98]. The theory of Q-marker reveals that the active ingredients identified by Chinmindomics are capable of reflecting TCM's effectiveness while simultaneously screening efficacy-related Q-markers. Recently, Wang et al. learned that Chinmendomics has successfully discovered Q-markers pertaining to herbal medicines and formulas, including Xiyangshen (Pawajc quinquefolium L.), Shengmai San, and Sijunzi Decoction. This discovery has comprehensively resolved the technical challenges associated with uncovering and confirming TCM's Q-markers [66, 85, 99].

Explanation of the mechanism of herbal formulas to reduce toxicity and increase efficacy

Herbal formulas are usually composed of several medicinal herbs according to the compatibility principles of TCM to achieve the basic purpose of reducing toxicity and increasing efficacy [100]. For example, when Dahuang (Rheum palmatum L.) is used together with Fuzi (Aconitum carmichaeli Debx.), the acidic compounds in Dahuang tend to bind with the toxic alkaloids in Fuzi and form insoluble salts, ultimately reducing the toxicity of Fuzi [101, 102]. In addition, the components of Danggui (Angelica sinensis (Oliv.) Diels) in Dangguibuxue decoction are shown to enhance the activity of astragaloside IV derived from Huangqi (Astragalus membranaceus (Fisch.) Bge.) in vivo, thus increasing the elevation of "Qi" and nourishing the "Blood" effect of the whole formula [103, 104]. However, due to the difficulty of expressing the TCM compatibility theory of most herbal formulas in modern scientific language, the application of some classical herbal formulas, especially those containing toxic Chinese medicines, has been limited [105]. The ban on the sale of Yunnan Baiyao prescription (YNBY) containing the controversial Caowu (Aconiti Kusnezoffii Radix.) is a well-known example. In order to explore the compatibility theory of YNBY, we used Chinmedomics to study the pharmacological mechanism of Caowu and YNBY. The results showed that YNBY administration within one treatment cycle showed no obvious toxicity, and 5 of the 13 toxic biomarkers of Caowu could be adjusted to a normal state. Importantly, 7 alkaloids in the active ingredients of YNBY for the treatment of blood stasis syndrome are derived from Caowu [106,107,108]. Chinmedomics not only scientifically proves the safety of YNBY, but also provides a powerful detection tool for elucidating the mechanism of reducing toxicity and enhancing the efficacy of TCM compatibility theory.

Discovery and popularization of new herbal medicinal parts and herbal ingredients

The discovery and development of new drugs with definite efficacy is one of the most important scientific activities contributing to human health and well-being [109]. The proposal and application of Chinmedomics has facilitated the process of new drug discovery. The original medicinal parts of Ciwujia (Acanthopanax senticosus Harms) are dried roots and rhizomes or stems, which are widely used to treat various diseases [110, 111]. Recently, Wang et al. found that Ciwujia leaves and fruits are effective in modulating multiple metabolic pathways and enhancing immune function, and have completed the identification of the active ingredients of Ciwujia leaves intervening acute promyelocytic leukemi with Chinmedomics [76, 112, 113].

The first isolation of morphine monomer from poppy initiated the search for natural plant compounds [114]. Subsequently, artemisinin, quinine and paclitaxel are all single compounds with significant activity obtained by isolation and purification from specific TCM with significant efficacy and clinical validation [115,116,117]. Using Chinmendomics strategy, our team has also found some active ingredients with significant efficacy in herbal medicines and herbal formulas, such as 6,7-dimethoxy coumarin and geniposide of YCHT, which showed good hepatoprotective effects by regulating primary acid biosynthesis, amino acid metabolism and glucose conversion, etc. [118,119,120,121]. Schisandrin of Shengmaisan could play an important role in ameliorating Alzheimer's disease by restoring multiple metabolites, and its pharmacokinetic study illustrated the characteristics of rapid absorption and a relatively long period of high concentration in serum [85, 122]. In addition, the proposal of Chinmedomics can systematically solve the problem of promoting new drugs and make them widely accepted by the medical community as soon as possible. The Wenxin Formula is a new herbal formula summarized by Chinese medicine experts based on years of clinical experience [123]. Our team adopted the Chinmedomics strategy to understand and elucidate the molecular interaction mode and mechanism of action of Wenxin Formula in the treatment of heart disease, which has increased the acceptance of this herbal formula [90].

Summary and outlook

The modernization and globalization of TCM have become an overwhelming trend, supported by the development and innovation of TCM research strategies. Chinmedomics is proposed in the context of emphasizing the development of TCM and is a powerful tool for interpreting herbal medicines. It covers two of the most important elements in the clinical application of TCM-diseases and herbal formulas, and demonstrates innovative insights in exploring efficacy, elucidating mechanisms of action, and discovering TCM lead compounds. In addition, Chinmedomics has made significant breakthroughs in the field of TCM drug quality evaluation and new drug discovery, which is also an important reason for the prosperous development of Chinmedomics.

Accurate identification of herbal constituents and biomarkers is a prerequisite for the discovery of active compounds and disease targets, and further elucidation of therapeutic mechanisms [124]. Therefore, the development of sufficient chemical reference substances to establish a high-quality and comprehensive TCM and disease big data information platform, including molecular properties, structural characteristics, and ionic fragments of compounds with different energy collisions, is necessary to realize a multi-parameter reference component identification system. Due to the increasing demand for TCM, quality assessment has become a global concern. The chemical composition of TCM has been extensively studied and analyzed using modern analytical technologies. However. A single analytical technique has certain limitations. It is not sufficient to judge the quality of TCM based on the characteristics of its constituents alone. Therefore, fusion technologies that combine multiple sources of information can be incredibly useful in TCM research, allowing us to understand the relationship between herbal samples in multiple aspects using data from different analytical instruments [125]. In addition, the application of computational bioinformatics models, such as probabilistic models and deep learning models, simplifies complex TCM data to some extent and makes them easy to understand [126]. However, these computational models may not show good agreement with the complete and unified essence of TCM. Therefore, there is an urgent need to construct a multidimensional association computational model with the characteristics of TCM, including from clinical trials to basic research of TCM, from symptom phenotype to molecular basis, from characterization of TCM components to their transformation and target sites in vivo.

The exploration of systems biology-driven multi-omics and the maturity of gene interference technology and sequencing technology could not only play an important role in the discovery of new drug targets and the molecular mechanisms of TCM in various diseases, but also make it possible to conduct multi-faceted and multi-angle verification studies of biomarkers and drug components, and promote the mutual transformation of experiments and clinical trials [127,128,129,130]. In conclusion, with the emergence of new analytical techniques and the integrated application of multiple disciplines, the Chinmedomics strategy can be continuously refined and developed, which will undoubtedly trigger the research paradigm shift in the efficacy evaluation and drug discovery of TCM and realize the modernization and globalization of TCM.

Availability of data and materials

Data availability is not applicable to this article as no new data were created or analyzed in this study.

Abbreviations

TCM:

Traditional Chinese medicine

NMR:

Nuclear magnetic resonance

References

  1. Lin Y, et al. Computer especially AI-assisted drug virtual screening and design in traditional Chinese medicine. Phytomedicine. 2022;107: 154481.

    Article  CAS  PubMed  Google Scholar 

  2. Liu Z, et al. A novel transfer learning model for traditional herbal medicine prescription generation from unstructured resources and knowledge. Artif Intell Med. 2022;124: 102232.

    Article  PubMed  Google Scholar 

  3. Tu Y. The discovery of artemisinin (qinghaosu) and gifts from Chinese medicine. Nat Med. 2011;17(10):1217–20.

    Article  CAS  PubMed  Google Scholar 

  4. Huang K, et al. Traditional Chinese Medicine (TCM) in the treatment of COVID-19 and other viral infections: efficacies and mechanisms. Pharmacol Ther. 2021;225: 107843.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Li S, et al. Traditional Chinese medicine network pharmacology: theory, methodology and application. Chin J Nat Med. 2013;11(2):110–20.

    Article  ADS  PubMed  Google Scholar 

  6. Ru J, et al. TCMSP: a database of systems pharmacology for drug discovery from herbal medicines. J Cheminform. 2014;6:13.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Wang Z, et al., Fangjiomics: in search of effective and safe combination therapies. J Clin Pharmacol, 2011. 51(8): p. 1132–1151.

  8. Wu J, et al. Integrated metabonomics and network pharmacology to reveal the action mechanism effect of Shaoyao decoction on ulcerative colitis. Drug Des Dev Ther. 2022;16:3739–76.

    Article  CAS  Google Scholar 

  9. Qu S-Y, et al. Analysis of antidepressant activity of Huang-Lian Jie-Du decoction through network pharmacology and metabolomics. Front Pharmacol. 2021;12:619288.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Wang X-J. Methodology for systematic analysis of in vivo efficacy material base of traditional Chinese medicine–Chinmedomics. Zhongguo Zhong Yao Za Zhi. 2015;40(1):13–7.

    Google Scholar 

  11. X W. Inside view. Nature, 2015; 528(7582).

  12. Habtemariam S. Berberine pharmacology and the gut microbiota: a hidden therapeutic link. Pharmacol Res. 2020;155: 104722.

    Article  CAS  PubMed  Google Scholar 

  13. Tan D, et al. Glycyrrhizic acid and its derivatives: promising candidates for the management of type 2 diabetes mellitus and its complications. Int J Mol Sci. 2022;23(19):10988.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Zhang X, et al. Tanshinone IIA protects against heart failure post-myocardial infarction via AMPKs/mTOR-dependent autophagy pathway. Biomed Pharmacother. 2019;112: 108599.

    Article  CAS  PubMed  Google Scholar 

  15. Zhu H, et al. Gastrodia elata blume polysaccharides: a review of their acquisition, analysis, modification, and pharmacological activities. Molecules. 2019;24(13):2436.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Yu Y, et al. Ononin, sec-O-β-d-glucosylhamaudol and astragaloside I: antiviral lead compounds identified via high throughput screening and biological validation from traditional Chinese medicine Zhongjing formulary. Pharmacol Res. 2019;145: 104248.

    Article  CAS  PubMed  Google Scholar 

  17. He Y, et al. Metabolic profiling and pharmacokinetic studies of Baihu-Guizhi decoction in rats by UFLC-Q-TOF–MS/MS and UHPLC-Q-TRAP-MS/MS. Chin Med. 2022;17(1):117.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Tang C, et al. Pharmacodynamics, network pharmacology, and pharmacokinetics of Chinese medicine formula 9002A in the treatment of Alzheimer’s disease. Front Pharmacol. 2022;13:849994.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Wang XJ. Progress and Future Development of Serum Pharmacochemistry of Traditional Chinese Medicine. Zhongguo Zhong Yao Za Zhi. 2006; 31(10): p. 789–92, 835

  20. Ma FX, et al. Research progress of serum pharmacochemistry of traditional Chinese medicine. Zhongguo Zhong Yao Za Zhi. 2017;42(7):1265–70.

    PubMed  Google Scholar 

  21. Zhang A-H, et al. Metabolomics in diabetes. Clin Chim Acta. 2014;429:106–10.

    Article  ADS  CAS  PubMed  Google Scholar 

  22. Luo X, et al. Metabolomics identified new biomarkers for the precise diagnosis of pancreatic cancer and associated tissue metastasis. Pharmacol Res. 2020;156: 104805.

    Article  CAS  PubMed  Google Scholar 

  23. Wu Q, et al. Multi-stage metabolomics and genetic analyses identified metabolite biomarkers of metabolic syndrome and their genetic determinants. eBioMedicine. 2021;74:103707.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Talmor-Barkan Y, et al. Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease. Nat Med. 2022;28(2):295–302.

    Article  CAS  PubMed  Google Scholar 

  25. Wishart DS, et al. HMDB 5.0: the human metabolome database for 2022. Nucleic Acids Res. 2022;50(D1):D622–31.

    Article  CAS  PubMed  Google Scholar 

  26. Guijas C, et al. METLIN: a technology platform for identifying knowns and unknowns. Anal Chem. 2018;90(5):3156–64.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Li T, et al. High-throughput chinmedomics strategy discovers the quality markers and mechanisms of wutou decoction therapeutic for rheumatoid arthritis. Front Pharmacol. 2022. https://doi.org/10.3389/fphar.2022.854087.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Yao C-L, et al. Global profiling combined with predicted metabolites screening for discovery of natural compounds: characterization of ginsenosides in the leaves of Panax notoginseng as a case study. J Chromatogr A. 2018;1538:34–44.

    Article  CAS  PubMed  Google Scholar 

  29. Hamade K, et al. NMR and LC-MS-based metabolomics to study osmotic stress in Lignan-deficient flax. Molecules. 2021;26(3):767.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Wang J, et al. Spatial metabolomics identifies distinct tumor-specific subtypes in gastric cancer patients. Clin Cancer Res. 2022;28(13):2865–77.

    Article  CAS  PubMed  Google Scholar 

  31. He MJ, et al. Comparing DESI-MSI and MALDI-MSI mediated spatial metabolomics and their applications in cancer studies. Front Oncol. 2022;12: 891018.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Wang T, et al. Functional metabolomics innovates therapeutic discovery of traditional Chinese medicine derived functional compounds. Pharmacol Ther. 2021;224: 107824.

    Article  CAS  PubMed  Google Scholar 

  33. Wishart DS. Metabolomics for investigating physiological and pathophysiological processes. Physiol Rev. 2019;99(4):1819–75.

    Article  CAS  PubMed  Google Scholar 

  34. Wishart DS, et al. HMDB 4.0: the human metabolome database for 2018. Nucleic Acids Res. 2018;46(D1):D608–17.

    Article  CAS  PubMed  Google Scholar 

  35. Ludwig C, et al. Birmingham Metabolite Library: a publicly accessible database of 1-D 1H and 2-D 1H J-resolved NMR spectra of authentic metabolite standards (BML-NMR). Metabolomics. 2011;8(1):8–18.

    Article  Google Scholar 

  36. Horai H, et al. MassBank: a public repository for sharing mass spectral data for life sciences. J Mass Spectrom. 2010;45(7):703–14.

    Article  ADS  CAS  PubMed  Google Scholar 

  37. Fahy E, et al. Update of the LIPID MAPS comprehensive classification system for lipids. J Lipid Res. 2009;50:S9–14.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Rinschen MM, et al. Identification of bioactive metabolites using activity metabolomics. Nat Rev Mol Cell Biol. 2019;20(6):353–67.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Editorial: ChemSpider--a tool for Natural Products research. Nat Prod Rep, 2015. 32(8): p. 1163–4.

  40. Kim S, et al. PubChem in 2021: new data content and improved web interfaces. Nucleic Acids Res. 2020;2020:D1388–95.

    Google Scholar 

  41. González-Gaya B, et al. Suspect screening workflow comparison for the analysis of organic xenobiotics in environmental water samples. Chemosphere. 2021;274: 129964.

    Article  PubMed  Google Scholar 

  42. Langfelder P, Horvath S. WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics. 2008;9(1):559.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Zhang AH, et al. Chinmedomics: a new strategy for research of traditional Chinese medicine. Zhongguo Zhong Yao Za Zhi. 2015;40(4):569–76.

    PubMed  Google Scholar 

  44. Schober P, Boer C, Schwarte LA. Correlation coefficients: appropriate use and interpretation. Anesth Analg. 2018;126(5):1763–8.

    Article  PubMed  Google Scholar 

  45. Vuckovic D, et al. MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studies. Bioinformatics. 2015;31(16):2754–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Yan Q, et al. KMgene: a unified R package for gene-based association analysis for complex traits. Bioinformatics. 2018;34(12):2144–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Höltge J, et al. A cross-country network analysis of adolescent resilience. J Adolesc Health. 2021;68(3):580–8.

    Article  PubMed  Google Scholar 

  48. Shannon P, et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003;13(11):2498–504.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Xia J, Wishart DS. MetPA: a web-based metabolomics tool for pathway analysis and visualization. Bioinformatics. 2010;26(18):2342–4.

    Article  CAS  PubMed  Google Scholar 

  50. Zhou X, et al. The signaling pathways of traditional Chinese medicine in promoting diabetic wound healing. J Ethnopharmacol. 2022;282: 114662.

    Article  CAS  PubMed  Google Scholar 

  51. Li W, et al. A novel drug combination of mangiferin and cinnamic acid alleviates rheumatoid arthritis by inhibiting TLR4/NFκB/NLRP3 activation-induced pyroptosis. Front Immunol. 2022;13:912933.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Wang Y, et al. Methodology and applications for multimodal identification of active constituents of traditional Chinese medicine. Zhongguo Zhong Yao Za Zhi. 2020;45(1):1–6.

    PubMed  Google Scholar 

  53. Schroeder M, et al. Comparison of four diagnostic criteria for invasive pulmonary aspergillosis—a diagnostic accuracy study in critically ill patients. Mycoses. 2022;65(8):824–33.

    Article  PubMed  Google Scholar 

  54. Zhang Q, Zhou J, Zhang B. Computational traditional Chinese medicine diagnosis: a literature survey. Comput Biol Med. 2021;133: 104358.

    Article  PubMed  Google Scholar 

  55. Kang H, et al. Integrating clinical indexes into four-diagnostic information contributes to the traditional Chinese medicine (TCM) syndrome diagnosis of chronic hepatitis B. Sci Rep. 2015;5(1):9395.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Wang X, et al. Urine metabolomics analysis for biomarker discovery and detection of jaundice syndrome in patients with liver disease. Mol Cell Proteom. 2012;11(8):370–80.

    Article  Google Scholar 

  57. Zhang A, et al. Exploratory urinary metabolic biomarkers and pathways using UPLC-Q-TOF-HDMS coupled with pattern recognition approach. Analyst. 2012;137(18):4200.

    Article  ADS  CAS  PubMed  Google Scholar 

  58. Gao H-L, et al. High-throughput lipidomics characterize key lipid molecules as potential therapeutic targets of Kaixinsan protects against Alzheimer’s disease in APP/PS1 transgenic mice. J Chromatogr B. 2018;1092:286–95.

    Article  CAS  Google Scholar 

  59. Zhang A, et al. High resolution metabolomics technology reveals widespread pathway changes of alcoholic liver disease. Mol BioSyst. 2016;12(1):262–73.

    Article  CAS  PubMed  Google Scholar 

  60. Zhang H-L, et al. High-throughput lipidomics reveal mirabilite regulating lipid metabolism as anticancer therapeutics. RSC Adv. 2018;8(62):35600–10.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  61. Wu X-H, et al. High-throughput metabolomics used to identify potential therapeutic targets of Guizhi Fuling Wan against endometriosis of cold coagulation and blood stasis. RSC Adv. 2018;8(34):19238–50.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  62. Liu C, et al. Lipidomic characterisation discovery for coronary heart disease diagnosis based on high-throughput ultra-performance liquid chromatography and mass spectrometry. RSC Adv. 2018;8(2):647–54.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  63. Sun H, et al. Exploring potential biomarkers of coronary heart disease treated by Jing Zhi Guan Xin Pian using high-throughput metabolomics. RSC Adv. 2019;9(20):11420–32.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  64. Zhao Q, et al. Chinmedomics facilitated quality-marker discovery of Sijunzi decoction to treat spleen qi deficiency syndrome. Front Med. 2019;14(3):335–56.

    Article  ADS  PubMed  Google Scholar 

  65. Fang H, et al. High-throughput metabolomics reveals the perturbed metabolic pathways and biomarkers of Yang Huang syndrome as potential targets for evaluating the therapeutic effects and mechanism of geniposide. Frontiers of Medicine. 2020;14(5):651–63.

    Article  PubMed  Google Scholar 

  66. Zhang N, et al. Effects of radix scrophulariae on hyperthyroidism assessed by metabonomics and network pharmacology. Front Pharmacol. 2021;12:727735.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Zhang Q, et al. UPLC-G2Si-HDMS untargeted metabolomics for identification of Yunnan Baiyao’s metabolic target in promoting blood circulation and removing blood stasis. Molecules. 2022;27(10):3208.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Ma Y, Sun S, Peng C-K. Applications of dynamical complexity theory in traditional Chinese medicine. Front Med. 2014;8(3):279–84.

    Article  PubMed  Google Scholar 

  69. Ma Y, et al. Traditional Chinese medicine: potential approaches from modern dynamical complexity theories. Front Med. 2016;10(1):28–32.

    Article  PubMed  Google Scholar 

  70. Li-Ling J. Human Phenome based on traditional Chinese medicine–a solution to congenital syndromology. Am J Chin Med. 2003;31:991–1000.

    Article  PubMed  Google Scholar 

  71. Ren J-L, et al. Efficacy evaluation, active ingredients, and multitarget exploration of herbal medicine. Trends Endocrinol Metab. 2023;34(3):146–57.

    Article  CAS  PubMed  Google Scholar 

  72. Zhang T, et al. Current trends and innovations in bioanalytical techniques of metabolomics. Crit Rev Anal Chem. 2015;46(4):342–51.

    Article  PubMed  Google Scholar 

  73. Wang P, et al. Thyroxine and reserpine-induced changes in metabolic profiles of rat urine and the therapeutic effect of Liu Wei Di Huang Wan detected by UPLC-HDMS. J Pharm Biomed Anal. 2010;53(3):631–45.

    Article  CAS  PubMed  Google Scholar 

  74. Sun H, et al. UPLC-G2Si-HDMS untargeted metabolomics for identification of metabolic targets of Yin-Chen-Hao-Tang used as a therapeutic agent of dampness-heat jaundice syndrome. J Chromatogr B. 2018;1081–1082:41–50.

    Article  Google Scholar 

  75. Lu S, et al. Characterizing serum metabolic alterations of Alzheimer’s disease and intervention of Shengmai-San by ultra-performance liquid chromatography/electrospray ionization quadruple time-of-flight mass spectrometry. Food Funct. 2017;8(4):1660–71.

    Article  CAS  PubMed  Google Scholar 

  76. Zhou X-H, et al. Novel chinmedomics strategy for discovering effective constituents from ShenQiWan acting on ShenYangXu syndrome. Chin J Nat Med. 2016;14(8):561–81.

    CAS  PubMed  Google Scholar 

  77. Kong L, et al. Chinmedomics strategy for elucidating the pharmacological effects and discovering bioactive compounds from keluoxin against diabetic retinopathy. Front Pharmacol. 2022;13: 728256.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  78. Li T, et al. High throughput metabolomics explores the mechanism of Jigucao capsules in treating Yanghuang syndrome rats using ultra-performance liquid chromatography quadrupole time of flight coupled with mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2022;1194: 123185.

    Article  CAS  PubMed  Google Scholar 

  79. Li H-Y, et al. Therapeutic effect and mechanism of Si-Miao-Yong-An-Tang on thromboangiitis obliterans based on the urine metabolomics approach. Front Pharmacol. 2022;13:827733.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  80. He Y, et al. Metabolomics analysis coupled with UPLC/MS on therapeutic effect of jigucao capsule against dampness-heat jaundice syndrome. Front Pharmacol. 2022;13:822193.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  81. Patridge E, et al. An analysis of FDA-approved drugs: natural products and their derivatives. Drug Discovery Today. 2016;21(2):204–7.

    Article  CAS  PubMed  Google Scholar 

  82. Jung H, Lim Y, Kim E-K. Therapeutic phytogenic compounds for obesity and diabetes. Int J Mol Sci. 2014;15(11):21505–37.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Xiong H, et al. A clinical and animal experiment integrated platform for small-molecule screening reveals potential targets of bioactive compounds from a herbal prescription based on the therapeutic efficacy of yinchenhao tang for jaundice syndrome. Engineering. 2021;7(9):1293–305.

    Article  CAS  Google Scholar 

  84. Wang X, et al. Pattern recognition approaches and computational systems tools for ultra performance liquid chromatography-mass spectrometry-based comprehensive metabolomic profiling and pathways analysis of biological data sets. Anal Chem. 2011;84(1):428–39.

    Article  PubMed  Google Scholar 

  85. Zhang A-H, et al. Identifying quality-markers from Shengmai San protects against transgenic mouse model of Alzheimer’s disease using chinmedomics approach. Phytomedicine. 2018;45:84–92.

    Article  CAS  PubMed  Google Scholar 

  86. Wang X-J, et al. Rapid discovery of quality-markers from Kaixin San using chinmedomics analysis approach. Phytomedicine. 2019;54:371–81.

    Article  PubMed  Google Scholar 

  87. Wei W-F, et al. Targets and effective constituents of ZhiziBaipi decoction for treating damp-heat jaundice syndrome based on chinmedomics coupled with UPLC-MS/MS. Front Pharmacol. 2022. https://doi.org/10.3389/fphar.2022.857361.

    Article  PubMed  PubMed Central  Google Scholar 

  88. Kong L, et al. Chinmedomics strategy for elucidating the pharmacological effects and discovering bioactive compounds from keluoxin against diabetic retinopathy. Front Pharmacol. 2022;13:728256.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Yan GI, et al. An effective method for determining the ingredients of Shuanghuanglian formula in blood samples using high-resolution LC–MS coupled with background subtraction and a multiple data processing approach. J Sep Sci. 2013;36(19):3191–9.

    Article  CAS  PubMed  Google Scholar 

  90. Wang Z-W, et al. Discovery of Q-markers of Wenxin formula based on a chinmedomics strategy. J Ethnopharmacol. 2022;298: 115576.

    Article  CAS  PubMed  Google Scholar 

  91. Wu X, et al. Quality markers based on biological activity: a new strategy for the quality control of traditional Chinese medicine. Phytomedicine. 2018;44:103–8.

    Article  CAS  PubMed  Google Scholar 

  92. Yu Y, Yao C, Guo D-A. Insight into chemical basis of traditional Chinese medicine based on the state-of-the-art techniques of liquid chromatography−mass spectrometry. Acta Pharm Sinica B. 2021;11(6):1469–92.

    Article  CAS  Google Scholar 

  93. Liang J, et al. A dynamic multiple reaction monitoring method for the multiple components quantification of complex traditional Chinese medicine preparations: Niuhuang Shangqing pill as an example. J Chromatogr A. 2013;1294:58–69.

    Article  CAS  PubMed  Google Scholar 

  94. Ren J-L, et al. Analytical strategies for the discovery and validation of quality-markers of traditional Chinese medicine. Phytomedicine. 2020;67: 153165.

    Article  CAS  PubMed  Google Scholar 

  95. Lu H, et al. Quantitative and chemical fingerprint analysis for the quality evaluation of platycodi radix collected from various regions in China by HPLC coupled with chemometrics. Molecules. 2018;23(7):1823.

    Article  PubMed  PubMed Central  Google Scholar 

  96. Dou Z, et al. Quality evaluation of rhubarb based on qualitative analysis of the HPLC fingerprint and UFLC–Q-TOF–MS/MS combined with quantitative analysis of eight anthraquinone glycosides by QAMS. Biomed Chromatogr. 2021;35(6):e5074.

    Article  CAS  PubMed  Google Scholar 

  97. Wang L, et al. A bio-activity guided in vitro pharmacokinetic method to improve the quality control of Chinese medicines, application to Si Wu Tang. Int J Pharm. 2011;406(1–2):99–105.

    Article  CAS  PubMed  Google Scholar 

  98. Liu Chang-xiao CS-l, Xiao Xiao-He, Zhang Tie-Jun, Hou Wen-bin, Liao Mao-Liang. A new concept on quality marker of Chinese materia medica: quality control for Chinese medicinal products. Chin Tradit Herbal Drugs. 2016; 47: p. 1443–1457

  99. Xiong H, et al. Discovery of quality-marker ingredients of Panax quinquefolius driven by high-throughput chinmedomics approach. Phytomedicine. 2020;74: 152928.

    Article  CAS  PubMed  Google Scholar 

  100. Zhang J-H, et al. Efficacy-oriented compatibility for component-based Chinese medicine. Acta Pharmacol Sin. 2015;36(6):654–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  101. Duan X, Pei M, Pei X. Compatability chemistry of acid-alkaline pair medicine of dahuang and Fuzi in Dahuang Fuzi decoction. Zhongguo Zhong Yao Za Zhi. 2009;34(17):2167–71.

    CAS  PubMed  Google Scholar 

  102. Li Y, et al. The effects of Rheum palmatum L. on the pharmacokinetic of major diterpene alkaloids of Aconitum carmichaelii Debx. in rats. Eur J Drug Metabol Pharmacokinet. 2016;42(3):441–51.

    Article  ADS  Google Scholar 

  103. Wang H, et al. Synergistic promotion of blood vessel regeneration by astragaloside IV and ferulic acid from electrospun fibrous mats. Mol Pharm. 2013;10(6):2394–403.

    Article  ADS  CAS  PubMed  Google Scholar 

  104. Zhou M, et al. Recent pharmaceutical evidence on the compatibility rationality of traditional Chinese medicine. J Ethnopharmacol. 2017;206:363–75.

    Article  PubMed  Google Scholar 

  105. Zhang X, et al. Quantification of promoting efficiency and reducing toxicity of traditional Chinese medicine: a case study of the combination of Tripterygium wilfordii hook. f. and Lysimachia christinae hance in the treatment of lung cancer. Front Pharmacol. 2022. https://doi.org/10.3389/fphar.2022.1018273.

    Article  PubMed  PubMed Central  Google Scholar 

  106. Wang 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(52):683.

    Article  MathSciNet  PubMed  PubMed Central  Google Scholar 

  107. Ren J-L, et al. Network pharmacology combined with metabolomics approach to investigate the protective role and detoxification mechanism of Yunnan Baiyao formulation. Phytomedicine. 2020;77: 153266.

    Article  CAS  PubMed  Google Scholar 

  108. Yang B, et al. Study on absorbed components of Aconitum kusnezoffii under Yunnan Baiyao compatibility in effect of activating blood circulation and removing blood stasis. Zhongguo Zhong Yao Za Zhi. 2019;44(15):3349–57.

    PubMed  Google Scholar 

  109. Xiong L, et al. Aberrant enhancer hypomethylation contributes to hepatic carcinogenesis through global transcriptional reprogramming. Nat Commun. 2019;10(1):335.

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  110. Takahashi Y, et al. Prophylactic and therapeutic effects of acanthopanax senticosus harms extract on murine collagen-induced arthritis. Phytother Res. 2014;28(10):1513–9.

    Article  PubMed  PubMed Central  Google Scholar 

  111. Miyazaki S, et al. Anxiolytic effects of acanthopanax senticosus HARMS occur via regulation of autonomic function and activate hippocampal BDNF–TrkB signaling. Molecules. 2018;24(1):132.

    Article  PubMed  PubMed Central  Google Scholar 

  112. Yingzhi Zhang AZ, Zhang Ying, Sun H, Meng X, Yan G, Wang X. Application of ultra-performance liquid chromatography with time-of-flight mass spectrometry for the rapid analysis of constituents and metabolites from the extracts of acanthopanax senti. Pharmacogn. 2015. https://doi.org/10.4103/0973-1296.177902.

    Article  Google Scholar 

  113. Han Y, et al. High-throughput ultra high performance liquid chromatography combined with mass spectrometry approach for the rapid analysis and characterization of multiple constituents of the fruit ofAcanthopanax senticosus(Rupr. et Maxim.) Harms. J Sep Sci. 2017;40(10):2178–87.

    Article  MathSciNet  CAS  PubMed  Google Scholar 

  114. Klockgether-Radke AP. Sertürner and the discovery of morphine 200 years of pain therapy with opioids. Anasthesiol Intensivmed Notfallmed Schmerzther. 2002;37:244–9.

    Article  CAS  PubMed  Google Scholar 

  115. Shi Q, et al. Discovery and repurposing of artemisinin. Frontiers of Medicine. 2022;16(1):1–9.

    Article  ADS  MathSciNet  CAS  PubMed  PubMed Central  Google Scholar 

  116. Achan J, et al. Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria. Malar J. 2011;10:144.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  117. Zhu L, Chen L. Progress in research on paclitaxel and tumor immunotherapy. Cell Mol Biol Lett. 2019;24:40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  118. Sun H, et al. High-throughput chinmedomics strategy for discovering the quality-markers and potential targets for Yinchenhao decoction. Phytomedicine. 2019;54:328–38.

    Article  CAS  PubMed  Google Scholar 

  119. Lv H, et al. Pharmacokinetic studies of a Chinese triple herbal drug formula. Phytomedicine. 2008;15(11):993–1001.

    Article  CAS  PubMed  Google Scholar 

  120. Fang H, et al. Insight into the metabolic mechanism of scoparone on biomarkers for inhibiting Yanghuang syndrome. Sci Rep. 2016. https://doi.org/10.1038/srep37519.

    Article  PubMed  PubMed Central  Google Scholar 

  121. Wölfl S, et al. Metabolomics and proteomics annotate therapeutic properties of geniposide: targeting and regulating multiple perturbed pathways. PLoS One. 2013;8(8): e71403.

    Article  ADS  Google Scholar 

  122. Lu SW, et al. Ultra-performance liquid-chromatography with tandem mass spectrometry for rapid analysis of pharmacokinetics, biodistribution and excretion of schisandrin after oral administration of Shengmaisan. Biomed Chromatogr. 2013;27(12):1657–63.

    Article  CAS  PubMed  Google Scholar 

  123. Cao HX, Zong WJ, Li JX. Effect of Wenxin prescription on G1/S cell cycle transformation in atherosclerosis rats. Chin J Exp Tradit Med Formul. 2021;27(20):38–45.

    Google Scholar 

  124. Li L, Zhang L, Yang CC. Multi-target strategy and experimental studies of traditional chinese medicine for Alzheimer’s disease therapy. Curr Top Med Chem. 2016;16(5):537–48.

    Article  CAS  PubMed  Google Scholar 

  125. Ding R, et al. Quality assessment of traditional Chinese medicine based on data fusion combined with machine learning: a review. Crit Rev Anal Chem. 2023. https://doi.org/10.1080/10408347.2023.2189477.

    Article  PubMed  Google Scholar 

  126. Chu X, et al. Quantitative knowledge presentation models of traditional Chinese medicine (TCM): A review. Artif Intell Med. 2020;103:101810.

    Article  PubMed  Google Scholar 

  127. Chen D-Q, et al. Identification of serum metabolites associating with chronic kidney disease progression and anti-fibrotic effect of 5-methoxytryptophan. Nat Commun. 2019;10(1):1476.

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  128. He Y-Y, et al. Spermine promotes pulmonary vascular remodelling and its synthase is a therapeutic target for pulmonary arterial hypertension. Eur Respir J. 2020;56(5):00522–2020.

    Article  Google Scholar 

  129. Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev. 2009;10:57–63.

    Article  CAS  Google Scholar 

  130. Ullah I, et al. Multi-omics approaches in colorectal cancer screening and diagnosis, recent updates and future perspectives. Cancers. 2022;14(22):5545.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We would like to thank the reviewers for taking the time and effort necessary to review the manuscript. In addition, the thorough and helpful suggestions of all research staff in the article revision must be acknowledged.

Funding

This study was supported by the National Natural Science Foundation of China (81830110) and the Heilongjiang Province key research and development plan (2022ZX02C04).

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Mengmeng Wang and Fengting Yin analyzed the data and wrote the manuscript. Ling Kong, Le Yang, Hui Sun, Ye Sun, Guangli Yan, Ying Han, Xijun Wang revised the manuscript. All authors have read and agreed to the published version of the manuscript.

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Correspondence to Hui Sun or Xijun Wang.

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Mengmeng Wang, Fengting Yin, Ling Kong, Le Yang, Hui Sun, Ye Sun, Guangli Yan, Ying Han, and Xijun Wang declare that they have no competing interests.

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Wang, M., Yin, F., Kong, L. et al. Chinmedomics: a potent tool for the evaluation of traditional Chinese medicine efficacy and identification of its active components. Chin Med 19, 47 (2024). https://doi.org/10.1186/s13020-024-00917-x

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