Volume 17,Issue 4,2025 Table of Contents

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  • 1  Challenges of regenerative medicine: New strategies from traditional Chinese medicine
    Jiuhong?Kang
    2025, 17(4):609-610. DOI: https://doi.org/10.1016/j.chmed.2025.09.006
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    2  Natural compounds from traditional Chinese medicine regulating stem cell fate: Identification and therapeutic potential
    Zhigao?Zhao?a?b Yu?Ma?a Shizhe?Wang?a Mengyuan?Zhou?a Yang?Tian?a Li?Yang?b Jian?Gu?c Rui?Tan?a?b
    2025, 17(4):611-627. DOI: https://doi.org/10.1016/j.chmed.2025.05.002
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    The problems of uncontrolled stem cell differentiation and the limited number of cells available represent significant obstacles to the advancement of stem cell research in the medical field. It is therefore imperative to control the potential of stem cells and to develop effective methods to regulate stem cell fate. A number of natural products derived from TCM have been shown to provide valuable insights into the regulation of biological signals and epigenetic mechanisms in stem cells. Furthermore, the structural modification of these natural products by synthetic means promises to unlock a wealth of possibilities in the field of precision regenerative medicine. However, a systematic and comprehensive review of these natural products has yet to be conducted. This article presents an overview of the natural products that have been identified as regulating the fate of stem cells. It includes a discussion of the classification, mechanism of action, and current prospects for the application of these natural products as lead compounds. This provides valuable insights for the advancement of TCM modernization and internationalization, precision regenerative medicine involving natural products and stem cells, the discovery of green lead compounds, and the development of new drugs.
    3  Bioactive phytochemicals, pharmacological, and therapeutic potential of Dillenia indica: A comprehensive review of current research
    Lutfun?Nahar?a Emran?Habibi?b?c Chuanchom?Khuniad?c?d Kulyash?Kalieva?e Daijie?Wang?f Hesamoddin?Arabnozari?b Phanuphong?Chaiwut?g Sarita?Sangthong?g Tinnakorn?Theansungnoen?g Rajat?Nath?h Anupam Das?Talukdar?i Satyajit D.?Sarker?c
    2025, 17(4):628-642. DOI: https://doi.org/10.1016/j.chmed.2025.09.001
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    Dillenia indica, commonly known as “elephant apple”, is a tropical fruit-bearing tree with a rich history of medicinal use in traditional medicine across Southeast Asia and the Indian subcontinent. This review comprehensively examines current research on the pharmacological properties of D. indica, focusing on its diverse bioactive compounds, including flavonoids, tannins, saponins, and triterpenoids, which underpin its key biological activities such as antioxidant, anti-inflammatory, antimicrobial, anticancer, antidiabetic, and hepatoprotective properties. Flavonoids and tannins exhibit potent antioxidant activity, effectively scavenging free radicals and reducing oxidative stress; a mechanism implicated in metabolic disorders, cancer, and neurodegenerative diseases. Additionally, the plant demonstrates considerable anti-inflammatory effects by modulating key inflammatory pathways, including the inhibition of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6). Saponins and triterpenoids enhance its antimicrobial activity, supporting traditional uses for treating infections. Preclinical studies indicate that D. indica extracts can inhibit cancer cell proliferation and induce apoptosis in various cancer types, including breast, colorectal, and liver cancers. Furthermore, specific formulations may improve the bioavailability and targeted delivery of active constituents, thereby increasing therapeutic efficacy. Despite the promising findings in vitro and in vivo, there is a notable lack of well-designed clinical trials to validate these effects in humans. The plant is generally considered safe when consumed at recommended doses. However, excessive intake may lead to gastrointestinal discomfort and, in rare cases, hepatotoxicity. This review describes the therapeutic potential of D. indica as a natural agent while emphasizing the urgent need for comprehensive clinical trials, particularly those investigating pharmacodynamics profiles, to confirm its efficacy and safety.
    4  Decoding natural products for neuroprotection: Pathway networks and structural insights for drug development
    Suman?Ghosh?a? Ishita Debnath b Sobhanjan Bhunia c Sumit?Nandi?d Sumel?Ashique?e Aditi?Nayak?f Susmita?Mallick?g Souvik?Basak?g
    2025, 17(4):643-672. DOI: https://doi.org/10.1016/j.chmed.2025.09.005
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    Neurodegenerative diseases (NDs), including Alzheimer’s, Parkinson’s, Huntington’s, and amyotrophic lateral sclerosis, are progressive disorders marked by neuronal dysfunction and death, driven by pathological mechanisms such as oxidative stress, mitochondrial dysfunction, neuroinflammation, apoptosis, and protein misfolding. Despite scientific advances, current treatments remain largely palliative, underscoring the need for multitargeted therapeutic strategies. This narrative review synthesizes preclinical and clinical evidence to explore the neuroprotective potential of natural products, with a focus on their ability to modulate key molecular pathways implicated in NDs. A comprehensive literature search across Scopus, ScienceDirect, PubMed, MDPI, and Web of Science identified relevant studies. Bioactive compounds such as curcumin, resveratrol, ginsenosides, quercetin, and marine-derived molecules like fucoxanthin and phlorotannin demonstrated antioxidant, anti-inflammatory, anti-amyloidogenic, and mitochondrial-protective effects by modulating pathways including PI3K/Akt, NF-κB, and Nrf2/ARE, thereby mitigating neuronal damage and promoting cell survival. Natural products from diverse sources, including honey, ginseng, marine macroalgae, and cyanobacteria, exhibited broad-spectrum neuroprotective properties, with advances in nano-formulations improving bioavailability and brain penetration. Furthermore, emerging approaches such as gene-drug interaction studies and scaffold-based drug design offer promising avenues for enhancing clinical translation. While natural products provide a holistic, multitargeted approach to combat NDs, challenges related to bioavailability and therapeutic translation persist, necessitating future research that integrates advanced drug delivery systems, precision medicine, and synthetic modifications to develop innovative and effective treatment paradigms.
    5  Potential of Panax ginseng for bone health and osteoporosis management
    Wenjie?Fang Kaisong?Huang Jinlian?Hu
    2025, 17(4):673-684. DOI: https://doi.org/10.1016/j.chmed.2025.06.003
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    Panax ginseng is a medicinal and food-homologous herb with a long-standing reputation as a tonic. Extensive research has explored its potential in improving osteoporosis, a condition characterized by progressive bone loss that increases the risk of fractures. In this review, PubMed, Web of Science, Google Scholar, China National Knowledge Infrastructure, and Chinese Medical Journal Database are searched with no lower time limit up to August 2024. This review offers a comprehensive overview of how P. ginseng and its formulations can enhance bone health and alleviate osteoporosis. It also explores the signaling pathways influenced by compounds derived from P. ginseng in bone turnover. P. ginseng shows promise in regulating sex hormones, exerting antioxidant and anti-inflammatory effects, and enhancing bone turnover. It suppresses MAPKs and NF-κB pathways to inhibit bone resorption, while activating pathways like Wnt/β-catenin, AMPK, PI3K/Akt, and BMP/Smad to promote bone formation. In addition, this review describes the global production and trade of ginseng, the metabolism of P. ginseng after oral ingestion, and network pharmacology studies. Given its multi-target mechanisms, P. ginseng shows promise in the clinical management of osteoporosis. At doses below 10 g with sustained use (several months to one year), it may serve as a viable daily supplement for bone health maintenance. Furthermore, its synergistic interactions with conventional anti-osteoporosis drugs (e.g., bisphosphonates) could enhance therapeutic efficacy, positioning it as a complementary adjunct in clinical treatment regimens.
    6  Therapeutic potential and mechanisms of traditional Chinese medicine in regulating energy metabolism imbalance in heart failure
    Ailian Li a b Xuexi?Wang?b Ruoyu?Yang?b Jingping?Zhang?b Xiaotong?Jiang?b
    2025, 17(4):685-702. DOI: https://doi.org/10.1016/j.chmed.2025.07.002
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    Heart failure (HF) is a disease in which the heart fails to efficiently pump blood due to diminished cardiac function, which seriously affects the quality of life and prognosis of patients. In recent years, traditional Chinese medicine (TCM), as a national treasure of China, has been shown to regulate cardiac energy metabolism and has been widely used in the treatment of HF. This article summarised commonly used TCMs for the treatment of HF, mainly from the perspective of improving energy metabolism. The results showed that TCMs can enhance the cardiac energy supply and improve cardiac function by altering the heart’s preference for metabolic substrates, regulating the activity of key metabolic enzymes and the expression of related proteins, and attenuating impaired mitochondrial function. Among them, Astragali Radix (Huangqi in Chinese), Ginseng Radix et Rhizoma (Renshen in Chinese), Salviae Miltiorrhizae Radix et Rhizoma (Danshen in Chinese), and their extracts can exert significant cardioprotective effects. In addition, some TCM herbal formulas, such as Shengmai San and Zhenwu Tang, have been widely used in the treatment of HF. The application of these herbal extracts and formulas provides an effective option for the treatment of HF, but further studies are needed to clarify their mechanisms of action and clinical applications.
    7  NLRP3 inflammasome in acute lung injury: Cumulative evidence for traditional Chinese medicine and natural products
    Yiman?Liu? Junyu?Meng? Jia?Liu Fan?Zhang Chen?An Jian?Yang
    2025, 17(4):703-719. DOI: https://doi.org/10.1016/j.chmed.2025.06.002
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    Acute lung injury (ALI) and its more severe manifestation, acute respiratory distress syndrome (ARDS), continue to pose a substantial challenge for contemporary society. Having been linked to the processes of injury and inflammation, NLRP3 inflammasome is activated by various stimuli, including inhaled allergens, pathogens, and environmental pollutants, subsequently contributing to the dysfunction of the innate immune system. Understanding how the innate immune NLRP3 inflammasome is altered during ALI may facilitate the identification of new therapeutic targets. To further enrich the role of NLRP3 inflammasome in treating ALI with traditional Chinese Medicine (TCM), this review aims to thoroughly summarize the latest scientific research achievements on the effects of NLRP3 inflammasome in ALI, and the existing underlying therapeutic targets from TCM and natural products.
    8  Target deconvolution strategies in TCM: Bridging medicinal properties with therapeutic efficacies
    Yuanyuan?Hou Min?Jiang Gang?Bai
    2025, 17(4):720-723. DOI: https://doi.org/10.1016/j.chmed.2025.08.003
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    The discovery and characterization of molecular targets from traditional Chinese medicine (TCM) represents a paradigm shift in contemporary drug development. This approach systematically bridges empirical TCM knowledge with modern pharmacological principles, establishing a robust framework for rational drug design. Through integrative systems-chemical biology approaches, we can now mechanistically elucidate the therapeutic basis of TCM’s bioactive properties, facilitating the accelerated identification of both novel molecular targets and conserved pharmacological pathways. This multidisciplinary strategy significantly enhances drug development efficiency while advancing therapeutic innovation to address critical unmet medical needs. With the rapid advancement of next-generation target deconvolution technologies and AI-driven computational platforms, TCM is poised to make increasingly substantial contributions to modern pharmacotherapy.
    9  Rapid identification of Astragalus membranaceus processing with rice water based on intelligent color recognition and multi-source information fusion technology
    Dongmei?Guo?a?b? Yijing?Pan?a?b? Shunshun?Wang?a?b Kehong?Ming?a?b Qingjia?Chi?c Chunli?Wang?b?d Kang?Xu?a?b?e
    2025, 17(4):724-733. DOI: https://doi.org/10.1016/j.chmed.2025.01.006
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    Objective: This study seeks to optimize the processing parameters for Astragalus membranaceus with rice water (AM-RW), establish quality evaluation standards, and develop a rapid multilayer perceptron (MLP) model for classification. This model facilitates accurate identification of AM-RW at various processing stages, providing a scientific reference for the quality assessment of traditional Chinese medicine products. Methods: Optimization of AM-RW was achieved using a single-factor test and Box-Behnken design response surface methodology to determine the optimal process parameters. The Watershed Algorithm was applied to segment images of AM tablets, and the numpy and pandas libraries were used to collect color data from these tablets. The study also explored the correlation between R, G, B, and L color values and calycosin-7-glucoside content. A rapid classification model based on MLP was developed, utilizing color values, hardness values, and calycosin-7-glucoside content of AM-RW with various processing degrees. Results: The study identified the optimal parameters for AM-RW as 20 mL of rice water, a frying temperature of 180 °C, and a frying time of 7 min. The average color values for the best-processed products fell within the normal distribution range: R value (94.83 ± 8.57), G value (96.1 ± 19.37), B value (36.84 ± 5.93), and L value (89.55 ± 12.24). The rapid identification model using MLP demonstrated high accuracy and reliability, achieving an accuracy rate of 94% in the classification process. Conclusions: The response surface method effectively optimizes the precise processing parameters of AM-RW. Furthermore, the MLP-based model can accurately classify AM-RW with varying degrees of processing, providing a valuable reference for the expedited identification of processing quality in traditional Chinese medicine products.
    10  Effect of different drying degrees on content of various chemical components and in vitro bioactivity of Chrysanthemi Indici Flos
    Tao?Wang?a? Shuting?Dong?a?b? Qiaosheng?Guo?a Qingjun?Zou?a Feng?Yang?a
    2025, 17(4):734-743. DOI: https://doi.org/10.1016/j.chmed.2025.08.001
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    Objective: Chrysanthemi Indici Flos (CIF), the inflorescence of Chrysanthemum indicum L., is widely used in traditional Chinese medicine. Traditionally, the content of active components in Chinese medicinal materials often changes during processing. However, the variation patterns of main active components in CIF during drying remain largely unknown. This study aims to investigate the contents of multiple chemical components and in vitro bioactivity of CIF with different drying degrees, so as to provide an optimized scheme for its origin processing. Methods: Fresh CIF were dried at 60 °C to obtain samples with different water contents (80%WC, 60%WC, 40%WC, 20%WC and DS). HPLC was used to determine eight chemical components (chlorogenic acid, 3,5-O-dicaffeoylquinic acid, galuteolin, linarin, luteolin, naringenin, kaempferol and isorhamnetin). In vitro assays evaluated antioxidant activity (radical scavenging), anti-inflammatory activity (enzyme inhibition) and antibacterial activity (disk diffusion, MIC) against several strains. Results: Among eight chemical components, chlorogenic acid and linarin decreased significantly with drying, luteolin and kaempferol first increased then decreased (peaking at 40%WC), and naringenin was highest in 80%WC. HPLC fingerprint similarity was lowest (0.559) between 80%WC and DS samples. Antioxidant (Total reducing capacity/DPPH/ABTS/·OH IC50: 80%WC > DS) and anti-inflammatory (XOD/LOX IC50: 80%WC > DS) activities strengthened with drying. Extracts inhibited Staphylococcus aureus (MIC 1.560–3.125 mg/mL), Listeria monocytogenes (DS group inhibition zone larger) and Escherichia coli (MIC 3.125 mg/mL), but not Pseudomonas aeruginosa or Salmonella paratyphoid. Conclusion: Drying degree significantly affects CIF’s chemical profiles and in vitro bioactivities, with dry samples showing superior antioxidant/anti-inflammatory properties and specific antibacterial effects. These findings offer targeted guidance for optimizing primary processing parameters of CIF.
    11  Rhein alleviates renal interstitial fibrosis by inhibiting Smad3 phosphorylation in TGF-β/Smad signalling pathway
    Xiaoli Zheng a b Li?Wang?a?b? Yu?Cheng?c Hao?Lin?c Shundi?Liu?c Xinjiang?Chen?a Zheng?Xiang?a?b?c
    2025, 17(4):744-755. DOI: https://doi.org/10.1016/j.chmed.2025.07.003
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    Objective: The anthraquinone compound rhein (1,8-dihydroxy-3-carboxyanthraquinone), derived from Rhei Radix et Rhizoma (rhubarb, Dahuang in Chinese), exhibits notable anti-fibrotic effects. However, the mechanisms underlying these effects have not been fully elucidated. Suppressor of mothers against decapentaplegic 3 (Smad3) phosphorylation plays a crucial role in the canonical transforming growth factor-β (TGF-β)/Smad signalling pathway. In this study, we investigated the effect of rhein on the TGF-β/Smad signalling pathway in renal interstitial fibrosis (RIF). Methods: A unilateral ischaemia–reperfusion injury (UIRI) rat model was employed to simulate renal injury and assess the therapeutic effect of rhein in vivo. In vitro, TGF-β1-stimulated NRK-52E rat renal epithelial cells and HK-2 human proximal tubular epithelial cells were used to mimic fibrotic conditions. Rhein’s interaction with Smad3 was further explored using molecular docking and bio-layer interferometry assays. Additionally, Smad3 knockdown and overexpression studies were performed in HK-2 cells to elucidate the functional role of Smad3 in rhein-mediated anti-fibrotic activity. Results: Rhein treatment significantly improved renal function and reduced fibrosis in UIRI rats, primarily by inhibiting Smad3 phosphorylation. Rhein treatment mitigated aberrant remodelling and extracellular matrix accumulation in both NRK-52E and HK-2 cells and in the UIRI rat model. The anti-fibrotic effects of rhein were attenuated by Smad3 deficiency but enhanced by Smad3 overexpression in HK-2 cells. Conclusion: Rhein exerts its anti-fibrotic effects in renal interstitial fibrosis by targeting the TGF-β/Smad3 signaling pathway. Acting as a natural antagonist of Smad3, rhein offers promising potential for therapeutic development in renal fibrosis. These findings provide a new mechanistic insight for further clinical research and drug development.
    12  Ganoderic acid a derivative induces apoptosis of cervical cancer cells by inhibiting JNK pathway
    Mengchen?Wang?a?b?c?d? Qin?Han?a?b?c?d? Xuelian?Zhang?a?b?c?d Xi?Dong?a?b?c?d Jiadong?Ran?a?b?c?d Fei?Wei?a?b?c?d Yun?Luo?a?b?c?d Xiaobo?Sun?a?b?c?d
    2025, 17(4):756-767. DOI: https://doi.org/10.1016/j.chmed.2024.07.002
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    Objective: Ganoderic acid A can inhibit the proliferation and promotes the apoptosis of cancer cells. Surprisingly, the molecular mechanisms underlying the anti-cancer effects of ganoderic acid A still remain poorly defined. Ganoderic acid A derivative (GaAD19) is an effective ingredient obtained by structural modification of ganoderic acid A. The purpose of this study was to evaluate the anti-proliferation effect of GaAD19 on cervical cancer cells. Methods: Through the HeLa cervical cancer cell model, the drug target of GaAD19 was predicted using the SwissTargetPrediction database and molecular docking. Subsequently, computer analysis results were verified by a series of molecular biology experiments, such as flow cytometry, Western blot, immunocytochemical staining, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL), quantitative real time polymerase chain reaction (qPCR), and so on. Then, pathway agonists and inhibitors were used to investigate the mechanism of GaAD19. Finally, the mouse model of cervical cancer was established to evaluate the inhibitory effect of GaAD19 on tumor growth in U14 cervical cancer mice. Results: GaAD19 induced apoptosis and inhibited the growth of tumors. It also blocked the transition from the G1 to the S phase of the cell cycle. However, in the presence of a c-Jun N-terminal kinase (JNK)agonist, the effects of GaAD19 on the proliferation, apoptosis, and cell cycle transition of cancer cells were suppressed. Conclusion: This study showed that GaAD19 can play an anti-cervical cancer role by inhibiting the JNK signaling pathway. These results will be helpful in further exploring the mechanism of GaAD19 in the treatment of cervical cancer.
    13  Salvia miltiorrhiza water extract ameliorated cGAS-STING-mediated acute liver injury by blocking interaction between STING and TBK1
    Chengwei?Li?a?b?c?d? Ran?Xu?b?c? Manlin?Zhang?e? Simin?Chen?b?c Qing?Yao?b?c Congyang?Zheng?b?c Xianlin?Wang?b?c Xinru?Wen?b?c Xiaohe?Xiao?b?c?d Yinghao?Wang?a Zhaofang?Bai?a?b?c?d
    2025, 17(4):768-778. DOI: https://doi.org/10.1016/j.chmed.2025.01.002
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    Objective: To investigate the potential of Salvia miltiorrhiza water extract (SMWE) as a modulator of the cGAS-STING signaling pathway, which is implicated in the pathogenesis of immune and inflammatory disorders, and to elucidate its underlying mechanism of action through in vitro and in vivo experiments. Methods: The cGAS-STING signaling pathway was activated in bone marrow-derived macrophages (BMDMs), Tohoku hospital pediatrics-1 (THP-1) cells, and peripheral blood mononuclear cells (PBMCs). The effect of SMWE on the expression of phosphorylated interferon regulatory factor 3 (IRF3) and phosphorylated STING after aberrant activation of the cGAS-STING pathway was detected by immunoblotting. Subsequently, real-time quantitative PCR was performed to detect changes in the mRNA levels of interferon type I (IFN), interferon-stimulated genes and inflammatory factors. The effect of SMWE on STING oligomerisation and the interaction between STING, Tank Binding Kinase 1 (TBK1) and IRF3 was investigated by immunoblotting. A model of acute liver injury (ALI) caused by lipopolysaccharide/D-galactosamine (LPS/D-GaIN) was used to test the effects of SMWE on inflammation mediated by the cGAS-STING signaling cascade. Results: SMWE significantly inhibited the phosphorylation of STING and IRF3, thereby suppressing the activation of the cGAS-STING signaling pathway. It also stopped the cGAS-STING pathway from working by stopping the production of type I interferons and interferon-stimulated genes, like interferon-stimulated gene 15 (ISG15) and C-X-C motif chemokine ligand 10 (CXCL10). SMWE also reduced the production of pro-inflammatory cytokines, such as interleukin-6 (IL-6) and tumour necrosis factor-α (TNF-α). SMWE also significantly improved ALI resulting from LPS/D-GaIN by diminishing the hyperactivation of the cGAS-STING signalling pathway. Mechanistic analysis revealed that SMWE disrupted the interaction between STING and TBK1. Conclusion: SMWE is a potent modulator of aberrant activation of the cGAS-STING pathway and is able to prevent and treat LPS/D-GaIN-induced ALI by inhibiting activation of the cGAS-STING pathway.
    14  Human cytochrome P450 enzymes catalyze oxidative metabolism of pectolinarigenin to generate a more active Nrf2 agonist
    Peiqi?Liu?a?b? Yanyan?Deng?a? Dongzhu?Tu?a Jiahao?Gong?a Feng?Zhang?a Huixin?Liu?c Qian?Li?a Jing?Hu?d Guangbo?Ge?a
    2025, 17(4):779-789. DOI: https://doi.org/10.1016/j.chmed.2025.04.008
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    Objective: To characterize the oxidative metabolic pathway(s) of pectolinarigenin (PEC) and reveal the effect of PEC oxidative metabolism on its biological activities including peroxisome proliferator-activated receptors (PPAR) and nuclear factor erythroid 2-related factor 2 (Nrf2) agonist effects, as well as the anti-oxidative and hepatoprotective activities. Methods:The oxidative metabolites of PEC were identified by liquid chromatography-time of flight-mass spectrometry (LC-TOF-MS/MS). The key enzymes involved in oxidative metabolism of PEC were assigned by P450 reaction phenotyping assays and enzymatic kinetics assays. Luciferase reporter assays and western blotting analysis were used to evaluate the Nrf2 and PPAR agonist effects of PEC and its oxidative metabolites. The intracellular levels of total reactive oxygen species (ROS), mitochondrial membrane potential (MMP), lactate dehydrogenase (LDH) and glutathione (GSH) in acetaminophen (APAP)-challenged hepatocytes were also tested. Results:PEC could be readily metabolized to form two O-demethylated metabolites including hispidulin (HIS, 4′-O-demethylated PEC) and 6-O-demethylated PEC in human liver microsomes (HLM) in the presence of nicotinamide adenine dinucleotide phosphate (NADPH), while HIS was identified as the major oxidative metabolite of PEC. At least nine human cytochrome P450 enzymes (CYP) enzymes could catalyze PEC-4′-O-demethylation, while CYP1A2 and CYP2D6 showed the highest binding affinities and rapid metabolic clearance rates in the oxidative metabolism of PEC. Biological assays showed that PEC 4′-O-demethylation slightly decreased the PPAR agonist effects of PEC, while HIS showed more potent Nrf2 agonist effect. Compared with PEC, HIS showed more efficacious hepatoprotective effect against APAP-induced hepatocyte injury, evidenced by more potent ability to reduce intracellular ROS and LDH levels, as well as more effective ability to elevate the intracellular levels of both MPP and GSH in APAP-challenged hepatocytes. Conclusion:CYPs catalyze PEC-4′-O-demethylation to generate a more active Nrf2 agonist (HIS), which shows more efficacious hepatoprotective effects against APAP-induced hepatocyte injury.
    15  Jiaotaiwan activates serum SCFAs and upregulates cAMP-PKA-CREB-BDNF signaling pathway for antidepressant effects: A multicenter, randomized, controlled study
    Mengnan?Huang?a?b? Yuanyuan?He?a? Tong?Yang?a Lu?Yu?a Qina?Lei?a Lina?Gao?c Shan?Gao?a Lin?Li?a Chunquan?Yu?a
    2025, 17(4):790-797. DOI: https://doi.org/10.1016/j.chmed.2025.03.002
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    Objective:Jiaotaiwan (JTW) is a classic traditional Chinese medicine (TCM) prescription for treating depression, but its potential mechanisms are not fully understood. The aim of this study is to detect the levels of serum Short-chain fatty acids (SCFAs) and cyclic adenosine monophosphate (cAMP)-protein kinase A (PKA)-cAMP-response element binding protein (CREB)-brain derived neurotrophic factor (BDNF) signaling pathway, further revealing the scientific connotation of the antidepressant effect of JTW. Methods:In this multicenter, randomized, controlled study, 120 patients with depression were divided into the JTW (16.5 g/d) group, JTW (16.5 g/d) + selective serotonin reuptake inhibitors (SSRIs) group, and SSRIs group. Hamilton depression Scale-24 (HAMD-24) and Self-rating depression scale (SDS) were used for efficacy evaluation. Enzyme linked immunosorbent assay (ELISA) and reverse transcription-polymerase chain reaction (RT-PCR) were used to evaluate the expression levels of cAMP-PKA-CREB-BDNF signaling pathway. Serum SCFAs concentrations were analyzed using liquid chromatograph-mass spectrometer (LC-MS) targeted metabolomics. Results:After eight weeks of treatment, HAMD score and SDS score were significantly decreased in the three groups, and HAMD score in JTW + SSRIs group was significantly lower than that in SSRIs group. After treatment, the expression levels of cAMP-PKA-CREB-BDNF signaling pathway were significantly increased in the three group, with the JTW + SSRIs group showing more significant increase. After treatment, the levels of isobutyric, butyric, isovaleric, and valeric acids in the JTW + SSRIs groups were significantly higher than that before treatment, and the levels of isobutyric, and isovaleric acids in the JTW + SSRIs group was significantly higher than that in the JTW group and SSRIs groups. Conclusion:JTW can alleviate symptoms in patients with depression, and its antidepressant mechanism may be related to regulating serum SCFAs and cAMP-PKA-CREB-BDNF signaling pathway.
    16  Microbiota basis of antidepressant effects of Zhi-zi-chi Decoction: Lactobacillus rhamnosus and gut microbiota metabolism
    Jing?He?a?b? Zixin?Zhao?a?b? Ying?Ye?a?b Yujia?Zhai?c Dexun?Yu?a?b Fangyuan?Gao?d Jianlin?Wu?e Jun?Wen?a?b Tingting?Zhou?a?b
    2025, 17(4):798-807. DOI: https://doi.org/10.1016/j.chmed.2025.05.001
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    Objective: Zhi-zi-chi Decoction (ZZCD) is a classical antidepressant traditional Chinese medicine (TCM) formula. However, the microbiological basis of its antidepressant effects remains unclear. The objective of this study was to investigate the microbial basis of ZZCD. Methods: The bacteria that exhibit enhanced growth in ZZCD extracts were identified through in vitro culture. A depressed rat model was subsequently established to assess the antidepressant effects of the bacteria. A GC–MS-based metabolomics approach and molecular docking simulation were employed to investigate the potential mechanism of the antidepressant effects of the bacteria from the perspective of changes in the metabolic profile of the gut microbiota. Finally, the antioxidant effects of gut microbial metabolites following Lactobacillus rhamnosus treatment were validated through cellular experimentation. Results: ZZCD was able to promote the growth of L. rhamnosus. Furthermore, L. rhamnosus was demonstrated to increase the percentage of sucrose preference, reduce the immobility time in tail suspension and forced swimming tests, and alleviate depressive symptoms in rats. Additionally, L. rhamnosus was shown to alter the metabolic profile of gut microbiota. A total of six metabolites (ethanamin, butyric acid, 2-methylbutanoic acid, behenic acid, 3-methylvaleric acid and 1-hexadecanol) associated with depressive behavior in rats were identified. All six metabolites demonstrated the capacity to bind to kelch-like ECH-associated protein 1 (Keap 1) in molecular docking simulations. Gut microbial metabolites after L. rhamnosus treatment increased nuclear factor erythroid 2-related factor 2 (Nrf2) levels in HT22 cells. Conclusion: L. rhamnosus may be one of the microbial bases for the antidepressant effects of ZZCD. Its effects may be related to the regulation of gut microbiota metabolism and anti-oxidative stress.
    17  Exploring new therapeutic potential of five commonly used Pteris medicinal plants through pharmaphylogenomics and network pharmacology
    Yuwen?Guan?a?b Jilong?Cheng?a Qiuyue?Lv?a?b Xueping?Wei?a Baoping?Jiang?a?b Peigen?Xiao?a?b
    2025, 17(4):808-821. DOI: https://doi.org/10.1016/j.chmed.2024.09.003
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    Objective: This study investigates the novel medicinal potential of five commonly used Pteris genus plants, including Pteris cretica, P. multifida, P. wallichiana, P. semipinnata, and P. vittata, by analyzing their chloroplast genomes, chemical compositions, and pharmacological activities. Methods: We conducted a rigorous phylogenetic analysis of these five pteridophytes to elucidate their evolutionary relationships. Chemical constituents were subjected to network pharmacology analysis to investigate their potential medicinal properties. Protein–protein interaction (PPI) networks and compounds-disease target networks were constructed using Cytoscape 3.7.2. Functional annotations, including Gene ontology (GO) enrichment analysis and Kyoto encyclopedia of genes and genomes (KEGG) pathway analysis, were conducted by the Metascape platform. Finally, molecular docking simulations were carried out with AutoDock software to validate key findings. Results: Our study revealed a close phylogenetic relationship between P. cretica and P. multifida, with P. cretica exhibiting a higher enrichment score for COVID-19-related pathways. Network pharmacology analysis of P. cretica identified 21 compounds and 540 targets, including 69 associated with COVID-19. The potential therapeutic effects of P. cretica were linked to virus infection, inflammation, and immune response modulation. Core pathways included “coronavirus disease-COVID-19”, “JAK-STAT signaling pathway”, and “Toll-like receptor signaling pathway”. Molecular docking identified (22E)-5α,8α-epidioxyergosta-6,22-dien-3β-ol, notholaenic acid, 2β,15α-diol-ent-kaur-16-ene, and multikaurane A as vital compounds for COVID-19 treatment in P. cretica. Conclusion: This study highlights P. cretica as a potential candidate for COVID-19 prevention and treatment, identifying its key active components and mechanisms. These findings provide a scientific basis for further development of potential therapeutic agents based on P. cretica.
    18  Unveiling bioactive components in Sargassum fusiforme via phytochemical and biological evaluation: A heterogeneous information ensemble approach
    Yue?Zhu?a?b?c Yuting?Ai?d Jianfu?Zhou?e Xiaozhuan?Jia?a?b?c Shuying?Liu?f Bo?Zhu?f Yimin?Qin?f Jianping?Jiang?g?h Zhenzhong?Yang?a?b?c
    2025, 17(4):822-836. DOI: https://doi.org/10.1016/j.chmed.2025.08.002
    [Abstract](0) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: Sargassum fusiforme (SF), a brown algae, is a marine traditional Chinese medicine with nutritional value. However, studies on the bioactive components in SF are limited. The aim of this study is to investigate phytochemical and biological properties of SF from different geographical origins and botanical parts, as well as to explore bioactive components within SF. Methods: SF from different origins and botanical parts were collected for integrated phytochemical analyses using ultra-high performance liquid chromatography-tandem quadrupole time of flight mass spectrometry (UPLC-Q-TOF-MS), mass spectral molecular networking and liquid chromatography-single quadrupole mass spectrometry (LC-MSD), etc., followed by the systematic chemical profile evaluation. Subsequently, the glycolipid metabolism regulation and anticoagulation of SF were examined. Furthermore, the overall information acquired was assembled using multivariate analysis and machine learning to discover bioactive components. Results: A total of 123 compounds in SF were identified with the assistance of mass spectral molecular networking. The variations in the content of amino acids, fucoidan, alginate, phlorotannin, alkaloids, terpenoids, etc. were observed in SF from different origins and botanical parts. SF possessed the hypolipidemic, hypoglycemic and anticoagulant effects, and SF from Dongtou, Wenzhou, Zhejiang, was outstanding among origins in both phytochemical and biological evaluations. A heterogeneous information ensemble approach was adopted to discover the bioactive components in SF, namely 3-indoleacrylic acid, phlorotannin and fucoidan. Conclusion: This study evaluated the phytochemical and biological properties of SF, revealed the bioactive components using heterogeneous information and provided a reference for the rational consumption and further development of SF.
    19  Exploration of chemical components and Rac1-dependent anti-hepatic fibrosis mechanism by total flavonoids derived from Tetrastigma hemsleyanum
    Xin?Wu?a? Cuiwei?Chen?b? Hongyan?Zhang?b Keda?Lu?c Gang?Cao?a
    2025, 17(4):837-849. DOI: https://doi.org/10.1016/j.chmed.2024.12.003
    [Abstract](0) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: This study is mainly to elucidate the characteristic components, hepatoprotective effect, and the underlying anti-hepatic fibrosis molecular mechanism of the total flavonoids of Tetrastigma hemsleyanum Diels & Gilg (SYQTF). Methods: The components of SYQTF were confirmed based on global natural products social molecular networking (GNPS) as well as the hepatoprotective effect on CCl4-induced acute liver injury. Cell toxicity and viability, cell cycle, and apoptosis analyses were then performed to determine the effects of SYQTF in transforming growth factor-β1 (TGF-β1) (10 ng/mL)-induced HSC-T6 hepatic fibrosis cell model. Finally, the lentiviral particles to package recombinant Ras-related C3 botulinum toxin substrate 1 (Rac1) over-expression and Rac1 knockdown plasmids were transfected into TGF-β1-induced HSC-T6 cells to elucidate the mechanism of anti-hepatic fibrosis of SYQTF targeting Rac1, respectively. Results: Our findings demonstrated that 86 components in SYQTF were identified in MSE and FastDDA mode with the aid of GNPS. Moreover, S15-ZJ, the genuine functional food and medicinal materials of T. hemsleyanum, was significantly different from other regions by multivariate statistical methods based on progenesis QI. Remarkably, kaempferol-3-O-furananose7-O-rhamnosyl-glucoside, the highest response intensity in S15-ZJ, may act as the potential Q-marker of genuine functional food and medicinal materials of T. hemsleyanum in Zhejiang Province distinguished from other areas. In addition, the in vivo experiments revealed that SYQTF greatly alleviated CCl4-induced acute liver injury. Furthermore, SYQTF can reversible the activation and proliferation of HSC-T6 cells, block the cell cycle in the G0/G1 phase, and promote cell apoptosis. Remarkably, the study is the first to reveal that SYQTF exhibited the anti-hepatic fibrosis effect through targeting Rac1 in the hedgehog signaling pathway. Conclusion: Rac1 is an important signaling molecule for the activation of the hedgehog pathway in HSC-T6. Importantly, SYQTF exerted its anti-hepatic fibrosis effect by inhibiting the Rac1-hedgehog signaling pathway. Furthermore, kaempferol-3-O-furananose7-O-rhamnosyl-glucoside could be a potential Q-marker of T. hemsleyanum in Zhejiang Province distinguished from other areas.

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