Volume 14,Issue 2,2022 Table of Contents

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  • 1  Chinese herbal medicines will illuminate the post-epidemic era
    Dacheng Hao
    2022, 14(2). DOI: 10.1016/j.chmed.2022.03.005
    [Abstract](335) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    In less than 20 years since the beginning of 21th century, there have been many major outbreaks of SARS, avian influenza, H1N1 flu, Ebola virus, and COVID-19 in the world one after another. These epidemics have caused huge losses of human life and property. Meanwhile, tumors, diabetes, cardiovascular and cerebrovascular diseases, mental diseases and diseases with unknown etiology that were rare in the past have now become common diseases in society. Coupled with the outbreak of major epidemics, they have posed a huge threat to human health and even survival. How to minimize and/or eliminate these threats? The traditional application and modern research of traditional Chinese medicine (TCM) give us a lot of inspiration. This issue has ushered in several excellent papers to continuously spotlight the exciting progress of Chinese herbal medicines in human health and diseases. Both Rosa and Tetrastigma belong to the Eudicots clade Rosids, which possess astounding biodiversity and chemodiversity, followed by highly diverse bioactivities. Their traditional uses and pharmacological activities have been elaborated in two comprehensive reviews (Wang et al., 2022; Zhang et al., 2022a); extracts and compounds of both genera showed the following activities: Antineoplastic and anti-cancer, anti-inflammatory, antioxidant, hepatoprotective, blood sugar regulatory/antidiabetic, antibacterial, antiviral, and cardiovascular protection, and others. Possibly due to the distinct chemical composition, these genera also have some differences in bioactivities, e.g., flavonoids of Rosa displayed the nervous system protection, Rosa also had the anti-aging and hypolipidemic properties, while Tetrastigma showed the analgesic activity. The studies of these pharmacological activities are booming (Gu et al., 2022; Zhang et al., 2022b), as they are aimed at the current common and frequently occurring diseases, including epidemic and pandemic diseases. Promisingly, both Rosa and Tetrastigma had no toxic effect in human subjects, which is especially validated by their long-term uses in folk medicine. Notwithstanding, the drug metabolism and pharmacokinetic studies of both genera, as well as other taxonomic groups with abundant medicinal phytometabolites, should be strengthened to further expound the absorption, distribution, metabolism, excretion and toxicity attributes of botanical extracts and phytometabolites; Q-markers of herbal products (Liu, 2021; Liu et al., 2018) derived from them should also be developed to maximize their health-promoting and therapeutic effects. The specialized metabolites of medicinal plants induced by ecological/environmental factors vary greatly, but meanwhile the specific biosynthetic pathways and related phytometabolites, and even therapeutic efficacy, may have some phylogenetic signals, which is suggested by pharmacophylogeny investigations (Hao et al., 2022). The metabolomic studies of medicinal genera should be further expanded to collect compound information as completely as possible, so as to analyze the correlation between specialized metabolites and molecular phylogeny qualitatively and quantitatively. After superimposing phylogenetic background, the dominance of a specific type of phytometabolites could be found in the specific part of phylogenetic tree, and the evolutionary trajectory of chemodiversity could be revealed, which has important guiding significance for the discovery and development of new/alternative phytomedicine resources. Many phytometabolites are phylogenetically conserved, and their abundance in different taxonomic groups is highly variable; e.g., indole alkaloids are reported in Tetrastigma instead of Rosa (Wang et al., 2022; Zhang et al., 2022a), the ursane-type triterpenoids are abundant in the latter rather than the former, while diterpenoids are trivial in both genera. In addition, the correlation between geographical distributions and therapeutic compounds should also be taken into account to assess the resource value of any taxonomic groups. We could find that some local species which were lately diverged have more diverse specialized metabolites as compared with widespread species firstly diverged, or vice versa. The genetic background and environmental pressure jointly shape the unique metabolome of each taxonomic group. With the explosive increase of the identified compounds in recent years (Gu et al., 2022), we are more confident in the systematic study of variation pattern of chemodiversity in the taxonomic group of interest in the light of evolution. These studies will promote the vitality of TCM supply chain and the sustainable development of Chinese herbal medicine industry.
    2  Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020
    Xiaojie Gu Dacheng Hao Peigen Xiao
    2022, 14(2). DOI: 10.1016/j.chmed.2022.03.004
    [Abstract](940) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Traditional Chinese medicines (TCMs) have continued to be a treasure trove. The study of chemodiversity and versatility of bioactivities has always been an important content of pharmacophylogeny. There is amazing progress in the discovery and research of natural components with novel structures and significant bioactivities in 2020. In this paper we review 271 valuable natural products, including terpenoids, steroids, flavonoids, phenylpropanoids, phenolics, nitrogen containing compounds and essential oil, etc., isolated and identified from TCMs published in journals of Chinese Traditional and Herbal Drugs (Zhong Cao Yao) and Chinese Herbal Medicines (CHMs), and focus on their structures, source organisms, and relevant bioactivities, paying special attention to structural characteristics of novel compounds and newly revealed pharmacological properties of known compounds. It is worth noting that natural products with antitumor activity still constitute the primary object of research. Among the reported compounds, two new triterpenoids, i.e., ursolic acid 3-O-β-cis-caffeate and mollugoside E, display remarkable cytotoxicity against PC-9 and HL-60 cell lines, respectively. Three known phenolic compounds, i.e., pyoluteorin, 4-hydroxy-3-methoxy cinnamaldehyde and 3,7-dimethoxy-5-hydroxy-1,4-phenanthrenequinone, exhibit significant cytotoxicity against multiple cell lines. Numerous studies on the free radical scavenging activity of reported compounds are currently underway. In vitro, three known phenolic compounds, i.e., 3,4-O-dicaffeoylquinic acid methyl ester, 3,4,5-O-tricaffeoylquinic acid methyl ester and arbutin, had more considerable antioxidant activities than vitamin C. The anti-inflammatory, anti-diabetic, hypolipidemic, neuroprotective and antimicrobial activities of isolated compounds are also encouraging. The structural characteristics and bioactivities of TCM compounds highlighted here reflect the enormous progress of CHM research in 2020 and will play a positive role in the future drug discovery and development. According to pharmacophylogeny, the phylogenetic distribution of compounds with different natures and flavors can be explored, with view to better mining TCM resources.
    3  Chemical constituents and pharmacological activities of medicinal plants from Rosa genus
    Yansheng Wang a b Yanmin Zhao c Xinnan Liu a Jingyang Li c Jingze Zhang b Dailin Liu a b
    2022, 14(2). DOI: 10.1016/j.chmed.2022.01.005
    [Abstract](607) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    The genus Rosa (Rosaceae family) includes about 200 species spread in the world, and this genus shows unique advantages in medicine and food. To date, several scholars concentrated on compounds belonging to flavonoids, triterpenes, tannins, polysaccharide, phenolic acids, fatty acids, organic acids, carotenoids, vitamins. Pharmacological effects such as antineoplastic and anti-cancer properties, anti-inflammatory, antioxidant, liver protection, regulate blood sugar, antimicrobial activity, antiviral activity, as well as nervous system protection and cardiovascular protection were wildly reported. This article reviews the chemical constituents, pharmacological effects, applications and safety evaluations of Rosa plants, which provides a reference for the comprehensive utilization of medicine and food resources and gives a scientific basis for the development of medicinal plants of the genus Rosa.
    4  Genus Tetrastigma: A review of its folk uses, phytochemistry and pharmacology
    Lizhi Zhanga Bin Lia Mengyun Wanga Haotian Lina Yilin Penga Xudong Zhoua Caiyun Penga Jixun Zhana b Wei Wanga
    2022, 14(2). DOI: 10.1016/j.chmed.2022.03.003
    [Abstract](817) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    The genus Tetrastigma belongs to the Vitaceae family and contains over 100 species. This paper reviewed folk uses, chemical constituents, pharmacological activities, and clinical applications of the medicinal plants in the genus Tetrastigma. In addition, the paper also discussed the current problems for the further studies. Up to now, more than 240 compounds were reported from the genus Tetrastigma, covering 74 flavonoids, 14 terpenoids, 19 steroids, 21 phenylpropanoids, 14 alkaloids and others constituents. Among them, flavonoids are the major and the characteristic chemical constituents in this genus. Modern pharmacological studies and clinical practice showed that the extracts and chemical constituents of Tetrastigma species possessed wide pharmacological activities including antitumor, antioxidative, hepatoprotective, antiviral, anti-inflammatory, and analgesic activities. The information summarized in this paper provided valuable clues for discovering new drug for further research and an incentive to expand the research of genus Tetrastigma.
    5  Molecular mechanisms of isoflavone puerarin against cardiovascular diseases: What we know and where we go
    Weida Qina b Jianghong Guoa Wenfeng Goua Shaohua Wua b
    2022, 14(2). DOI: 10.1016/j.chmed.2021.12.003
    [Abstract](853) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Puerarin (Pue), known as a phytoestrogen, has salient bioactivities and is promising against cardiovascular diseases. This article summarizes the underlying molecular mechanisms of Pue in treating cardiovascular diseases, especially regulating the intracellular signal transduction, influencing ion channels, modulating the expression of microRNA, and impacting on the autophagy, which are mainly involved in the inflammatory signaling pathways, fatty acid/lipid metabolism, oxidative stress, apoptosis, and the like. The protective effect of Pue against cardiovascular diseases mainly involves attenuating the myocardial injury and decreasing the myocardial fibrosis, improving the myocardial ischemia/reperfusion injury, as well as inhibiting the myocardial hypertrophy and atherosclerosis. The molecular mechanisms of Pue’s cardiovascular protective effects for the first time and comment on the state-of-the-art research methods and principles of Pue’s regulation of small molecules were reviewed, so as to provide the rationale for its basic research and clinical applications.
    6  Curcumin's prevention of inflammation-driven early gastric cancer and its molecular mechanism
    Wensen Zhang Na Cui Jin Ye Bingyou Yang Yanping Sun Haixue Kuang
    2022, 14(2). DOI: 10.1016/j.chmed.2021.11.003
    [Abstract](442) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Worldwide, gastric cancer is the second leading cause of cancer deaths and the fifth most common malignant tumor. Gastric cancer is believed to be caused by a variety of factors, such as genetics, epigenetics, and environmental influences. Among the pathogenic factors, inflammation has been considered as one of the main risk factors for gastric cancer. There are currently limited ways to prevent gastric cancer. Although the combined application of aspirin and non-steroidal anti-inflammatory drugs can reduce the risk, it has great side effects and can easily cause gastric perforation or gastric bleeding. Therefore, an alternative plan is urgently needed. Curcumin is the yellow pigment in the rhizome of the plant turmeric. Current studies have found that curcumin has a protective effect on gastric mucosal damage caused by non-steroidal anti-inflammatory drugs, gastric mucosal damage in rats, and gastric mucosal damage caused by stress bleeding and Helicobacter pylori infection. Curcumin shows significant anti-inflammatory and anti-cancer activities by regulating DNA methylation, histone modification, nuclear factor erythrocyte 2 related factor 2 and other related signal pathways. In this article, the latest evidence of curcumin for epigenetic changes in gastric cancer and its potential contribution to gastric cancer were discussed.
    7  6,6′-bieckol induces apoptosis and suppresses TGF-β-induced epithelial-mesenchymal transition in non-small lung cancer cells
    Yong-xin Li Man Liu Kun-long Yang Jun Tian
    2022, 14(2). DOI: 10.1016/j.chmed.2021.11.003
    [Abstract](692) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: In this study, the aim was to investigate the inhibitory effect of 6,6′-bieckol on the migration and epithelial-mesenchymal transition (EMT) of non-small cell lung cancer (NSCLC) cells, and explore its potential molecular mechanisms. Methods: Cell migration was measured using a CCK8, wound healing, and transwell migration assay. Apoptosis was determined using an Annexin V/propidium iodide staining. Western blotting and immunofluorescence were used to examine the expression level of apoptosis-related proteins and EMT marker proteins. Results: The results showed that 6,6′-bieckol inhibited migration and induced apoptosis of NSCLC cells. Furthermore, 6,6′-bieckol had significantly up-regulated the E-cadherin and down-regulated Snail1 and Twist1 transcriptional levels. 6,6′-Bieckol might inhibit TGF-β-induced EMT by down-regulating Snail1 and Twist1 and up-regulating E-cadherin in lung cancer cells. Conclusion: It was suggested that 6,6′-bieckol has the potential to be developed as a therapeutic candidate for lung cancer.
    8  Extracts of Portulaca oleracea promote wound healing by enhancing angiology regeneration and inhibiting iron accumulation in mice
    Jinglin Guoa Juan Pengb Jing Hana Ke Wangc Ruijuan Sia Hui Shana Xiaoying Wanga Ju Zhanga
    2022, 14(2). DOI: 10.1016/j.chmed.2021.09.014
    [Abstract](877) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: To investigate the role of Portulaca oleracea (POL) in promoting revascularization and re-epithelization as well as inhibiting iron aggregation and inflammation of deep tissue pressure injury (DTPI). Methods: The hydroalcoholic extract of POL (P) and aqueous phase fraction of POL (PD) were prepared based on maceration and liquid-liquid extraction. The number of new blood vessels and VEGF-A expression level were assessed using H&E stain and Western blot on injured muscle to examine the role of POL different extracts in vascularization. The iron distribution and total elemental iron of injured muscle were detected using laser ablation inductively coupled plasma mass spectrometry (ICP-MS) and Perls' stainning to determine whether POL extracts can inhibit the iron accumulation. Besides, the ability of POL extracts to promote wound healing by combining re-epithelization time, inflammation degree and collagen deposition area were comprehensively evaluated. Results: In vitro, we observed a significant increase in HUVEC cell viability, migration rate and the number of the tube after P and PD treatment (P < 0.05). In vivo, administration of P and PD impacted vascularization and iron accumulation on injured tissue, evident from more new blood vessels, higher expression of VEGF-A and decreased muscle iron concentration of treatment groups compared with no-treatment groups (P < 0.05). Besides, shorter re-epithelization time, reduced inflammatory infiltration and distinct collagen deposition were associated with administration of P and PD (P < 0.05). Conclusion: POL extract administration groups have high-quality wound healing, which is associated with increased new blood vessels, collagen deposition and re-epithelization, along with decreased iron accumulation and inflammatory infiltration. Our results suggest that that POL extract is beneficial to repair injured muscle after ischemia-reperfusion, highlighting the potential of POL in the DTPI treatment.
    9  Network pharmacology analysis to explore mechanism of Three Flower Tea against nonalcoholic fatty liver disease with experimental support using high-fat diet-induced rats
    Peixuan Wua Shufei Lianga Yanping Hea Rui Lva Bendong Yanga Meng Wanga Chao Wanga Yong Lic Xinhua Songa b Wenlong Suna b
    2022, 14(2). DOI: 10.1016/j.chmed.2022.03.002
    [Abstract](779) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: Nonalcoholic fatty liver disease (NAFLD) has become a common chronic liver disease that is harmful to human health. Moreover, there is currently no FDA-approved first-line drug for the treatment of nonalcoholic steatohepatitis (NASH) or NAFLD. Traditional Chinese medicine (TCM) is widely used to ameliorate liver diseases, such as the traditional ancient recipe called Three Flower Tea (TFT), which consists of double rose (Rosa rugosa), white chrysanthemum (Chrysanthemum morifolium), and Daidaihua (Citrus aurantium). However, the mechanisms of the action of TFT are not clear. Therefore, this study aimed to elucidate the mechanisms of TFT against NAFLD in high-fat diet (HFD)-induced rats. Methods: This study utilized bioinformatics and network pharmacology to establish the active and potential ingredient-target networks of TFT. Furthermore, a protein-protein interaction (PPI) network was constructed, and enrichment analysis was performed to determine the key targets of TFT against NAFLD. Furthermore, an animal experiment was conducted to evaluate the therapeutic effect and confirm the key targets of TFT against NAFLD. Results: A total of 576 NAFLD-related genes were searched in GeneCards, and under the screening criteria of oral bioavailability (OB) ≥ 30% and drug-likeness (DL) ≥ 0.18, a total of 19 active ingredients and 210 targets were identified in TFT. Network pharmacology analysis suggested that 55 matching targets in PPIs were closely associated with roles for NAFLD treatment. Through the evaluation of network topology parameters, four key central genes, PPARγ, SREBP, AKT, and RELA, were identified. Furthermore, animal experiments indicated that TFT could reduce plasma lipid profiles, hepatic lipid profiles and hepatic fat accumulation, improve liver function, suppress inflammatory factors, and reduce oxidative stress. Through immunoblotting and immunofluorescence analysis, PPARγ, SREBP, AKT, and RELA were confirmed as targets of TFT in HFD-induced rats. Conclusion: In summary, our results indicated that TFT could prevent and treat NAFLD via multiple targets, including lipid accumulation, antioxidation, insulin sensitivity, and inflammation.
    10  Exploration of Hanshi Zufei prescription for treatment of COVID-19 based on network pharmacology
    Xinrui Li a Zishuai Wen a Mingdong Si a Yuxin Jia a Huixian Liu a Yuguang Zheng a b c Donglai Ma a b c
    2022, 14(2). DOI: 10.1016/j.chmed.2021.09.013
    [Abstract](790) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: Network pharmacology combines drug and disease targets with biological information networks based on the integrity and systematicness of the interactions between drugs and disease targets. This study aims to explore the molecular basis of Hanshi Zufei formula for treatment of COVID-19 based on network pharmacology and molecular docking techniques. Methods: Using TCMSP, the chemical constituents and molecular targets of Atractylodis Rhizoma, Citri Reticulatae Pericarpium, Magnoliae Officinalis Cortex, Pogostemonis Herba, Tsaoko Fructus, Ephedrae Herba, Notopterygii Rhizoma et Radix, Zingiberis Rhizoma Recens, and Arecae Semen were investigated. The predicted targets of novel coronavirus were screened using the NCBI and GeneCards databases. To further screen the drug-disease core targets network, the corresponding target proteins were queried using multiple databases (Biogrid, DIP, and HPRD), a protein interaction network graph was constructed, and the network topology was analyzed. The molecular docking studies were also performed between the network’s top 15 compounds and the coronavirus (SARS-CoV-2) 3CL hydrolytic enzyme and angiotensin conversion enzyme II (ACE2). Results: The herb-active ingredient-target network contained nine drugs, 86 compounds, and 49 drug-disease targets. Gene ontology (GO) enrichment analysis resulted in 1566 GO items (P < 0.05), among which 1438 were biological process items, 35 were cell composition items, and 93 were molecular function items. Fourteen signal pathways were obtained by enrichment screening of the KEGG pathway database (P < 0.05). The molecular docking results showed that the affinity of the core active compounds with the SARS-CoV-2 3CL hydrolase was better than for the other compounds. Conclusion: Several core compounds can regulate multiple signaling pathways by binding with 3CL hydrolase and ACE2, which might contribute to the treatment of COVID-19.
    11  Functional and binding studies of gallic acid showing platelet aggregation inhibitory effect as a thrombin inhibitor
    Yu-xin Zhanga Xing Wangb Bi-nan Lua Yan-bin Gaob Yan-ling Zhangc Ya-tong Lib Hong-juan Niua Lu Fana Zong-ran Panga Yan-jiang Qiaoc
    2022, 14(2). DOI: 10.1016/j.chmed.2021.09.001
    [Abstract](829) [HTML](0) [PDF 0.00 Byte](0)
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    Objective: This study was devoted to identifying natural thrombin inhibitors from traditional Chinese medicine (TCM) and evaluating its biological activity in vitro and binding characteristics. Methods: A combination strategy containing molecular docking, thrombin inhibition assay, surface plasmon resonance (SPR) and molecular dynamics simulation were applied to verify the study result. Results: Gallic acid was confirmed as a direct thrombin inhibitor with IC50 of 9.07 μmol/L and showed a significant inhibitory effect on thrombin induced platelet aggregation. SPR-based binding studies demonstrated that gallic acid interacted with thrombin with a KD value of 8.29 μmol/L. Molecular dynamics and binding free energy analysis revealed that thrombin-gallic acid system attained equilibrium rapidly with very low fluctuations, the calculated binding free energies was ?14.61 kcal/mol. Ala230, Glu232, Ser235, Gly258 and Gly260 were the main amino acid residues responsible for thrombin inhibition by gallic acid, providing a mechanistic basis for further optimization. Conclusion: This study proved that gallic acid is a direct thrombin inhibitor with platelet aggregation inhibitory effect, which could provide a basis for the follow-up research and development for novel thrombin inhibitors.
    12  Preparation and pharmacokinetics in vivo of linarin solid dispersion and liposome
    Yingying Huang a Lihua Xu a Fangping Zhang a Yang Liu a b Yunyu Wang a Fangfeng Meng a Shuang Li a Xintao Cheng a Yuefeng Bi a b
    2022, 14(2). DOI: 10.1016/j.chmed.2021.12.004
    [Abstract](724) [HTML](0) [PDF 0.00 Byte](0)
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    Objective: The current investigation aimed to determine the appropriate dosage form by comparing solid dispersion and liposome to achieve the purpose of improving the solubility and bioavailability of linarin. Methods: Linarin solid dispersion (LSD) and linarin liposome (LL) were developed via the solvent method and the thin film hydration method respectively. The Transwell chamber model of Caco-2 cells was established to evaluate the absorption of drug. The pharmacokinetics of linarin, LSD and LL in rats after ig administration were carried out by high performance liquid chromatography (HPLC) method. Results: The solubility of LSD and LL was severally 3.29 times and 3.09 times than that of linarin. The permeation coefficients of LSD and LL were greater than 10-6, indicating that the absorption of LSD and LL were both better than linarin. The bioavailability of the LSD was 3.363 times higher than that of linarin, and the bioavailability of LL was 0.9886 times higher than that of linarin. Conclusion: The linarin was more suitable for making solid dispersion to enhance its solubility and bioavailability.
    13  Difference analysis of different parts of chicory based on HPLC fingerprint and multi-component content determination
    Mengzhen Yana b Zhenling Zhanga b c Yanze Liud
    2022, 14(2). DOI: 10.1016/j.chmed.2021.01.006
    [Abstract](897) [HTML](0) [PDF 0.00 Byte](0)
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    Objective: To establish HPLC fingerprints of different parts of chicory stems, leaves, roots, flowers and seeds, and compare the similarities and differences of chemical components in different parts, so as to provide a scientific basis for the comprehensive utilization of chicory. Methods: To establish the HPLC fingerprint of chicory, the chromatographic column was chosen with Agilent ZORBAX Eclipse XDB-C18, the mobile phase was methanol (A) - 0.2% formic acid (B), the flow rate was 1 mL/min, the column temperature was 30 °C, and the detection wavelength was 254 nm. The Similarity Evaluation System of Chromatographic Fingerprint of Traditional Chinese Medicine (2012 Edition) was used to evaluate the similarity of different parts of decoction pieces, and the determination method of multi-component content was established based on fingerprint identification chromatographic peaks, and the determination results were analyzed. Results: The HPLC fingerprinting method of chicory was established. Sixteen chromatographic peaks were identified and 10 of them were identified as: caftaric acid (1), esculin (2), chlorogenic acid (3), esculetin (4), caffeic acid (5), cichoric acid (8), hyperoside (11), rutin (12), isochlorogenic acid C (14) and luteolin (16). The similarity of different parts was 0.084?0.701. At the same time, the total content of detected chemical components was ranked as flower > leaf > stem > root > seed. Roots did not contain caftaric acid, rutin, and luteolin, flowers did not contain luteolin, and seeds did not contain caftaric acid, cichoric acid, and luteolin. The content of cichoric acid in leaves was the most, and esculin in flowers was the most. Conclusion: The results of HPLC fingerprint and multi-component content determination revealed the similarity and difference of different parts of chicory from chemical composition, indicating that there were certain differences in different parts of chicory. The established HPLC fingerprinting method can provide a reference for quality control and evaluation of different parts of the chicory.
    14  Quantitative determination of multi-class bioactive constituents for quality control of Yiqi Jiangzhi Granules
    Shaobo Guo Shaowei Hu Lijuan Jiang Xiaohe Chen Wei Zhang Yanyan Jiang Bin Liu
    2022, 14(2). DOI: 10.1016/j.chmed.2022.03.001
    [Abstract](449) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: To establish a reliable and sensitive method for evaluating quality of Yiqi Jiangzhi Granules (YQJZG). Methods: Ultra performance liquid chromatography electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS) was employed for simultaneous determination of eight marker components. Separation was performed on an AQUITY UPLC? HSS T3 column, the mobile phase consisted of acetonitrile as the organic phase and 0.1% (volume percentage) formic acid as the aqueous. Eight marker components, ginsenoside Rg1 (GRg1), ginsenoside Re (GRe), ginsenoside Rb1 (Gb1), typhaneoside (TEO), isorhamnetin-3-O-neohespeidoside (IN), hesperidin (HPD), aurantio-obtusin-6-O-β-D-glucoside (AG) and curcumin (CCM), were detected by multiple reaction monitoring (MRM) mode. The Chinese Pharmacopoeia (2020 edition) was regarded as the guidance document for this method validation. Results: The method showed good linearity (R2 ≥ 0.9990). The relative standard deviation (RSD) values for the instrument precision, intermediate precision and repeatability were less than 2.91%, 2.88%, and 3.54%, respectively. The average recovery varied from 91.08% to 103.89%, with RSD below 3.81%. Sample solutions were found to be stable within 24 h at 4 °C (RSD < 2.85%). Eight marker components were successfully determined from three batches of YQJZG. Conclusion: The proposed UPLC-ESI-MS/MS method was found to be simple, fast and sensitive, and can be used for the routine quality assessment of YQJZG. Simultaneously, this method may provide a new and powerful tool of quality control for other traditional Chinese medicine analogous formulae.
    15  Cathayanalactone G and other constituents from leaves and twigs of Callicarpa cathayana
    Shuang Gong Bin Cheng Tiantian Sun Xiaoli Li Xinxin Liang Yuan Wang Xiaochang Dai Weilie Xiao
    2022, 14(2). DOI: 10.1016/j.chmed.2021.05.006
    [Abstract](443) [HTML](0) [PDF 0.00 Byte](0)
    Abstract:
    Objective: To study the chemical constituents from the leaves and twigs of Callicarpa cathayana. Methods: The chemical constituents were isolated and purified by column chromatography on silica gel, MCI gel CHP 20P/P120, Sephadex LH-20, and HPLC. The structures of the compounds were determined by HR-ESI-MS, 1D and 2D NMR data. Results: A total of 24 compounds were isolated from the 85% methanol extract of leaves and twigs of C. cathayana. They were identified as cathayanalactone G (1), a new diterpene, and 23 known compounds as patagonic acid (2), (-)-16-hydroxycledroda-3,13-dien-16,15-olide-18-oic acid (3), 15-methoxypatagonic acid (4), oleanolic acid (5), ursolic acid (6), siaresinolic acid (7), pomolic acid (8), α-amyrin (9), tormentic acid (10), lupeol (11), 5,7-dihydroxy-3,4'-dimethoxyflavone (12), 5,4'-dihydroxy-3,7,3'-dimethoxyfla-vone (13), 5-hydroxy-3,6,7,4'- tetramethoxyflavone (14), salvigenin (15), kaemferol (16), astragalin (17), pinoresinol 4-O-β-D-glucopyranoside (18), paulownin (19), β-sitosterol (20), β-sitosterol β-D-glucopyranoside (21), 5-hydroxy-coumarin (22), isocopoletin (23), and 4-hydroxycinnamic acid (24). Conclusion: Compound 1 is a new labdane diterpene. Compounds 10, 13, 16 and 17 are isolated from the genus Callicarpa for the first time. Compounds 7, 8, 9, 12, 14, 23 and 24 are reported from C. cathayana for the first time.
    16  Three new triterpenoid saponins from Aralia echinocaulis
    Mengyun Yan Yajia Sun Ling Ding Jiuxu Sun Jingzhu Song Wenbin Zhou
    2022, 14(2). DOI: 10.1016/j.chmed.2022.02.002
    [Abstract](626) [HTML](0) [PDF 0.00 Byte](0)
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    Objective: To study the active ingredients in the root bark of Aralia echinocaulis. Methods: Three triterpenoid saponins were separated from the 70% ethanol extracts and purified by column chromatography and their structures were determined by spectroscopic analysis. Compound 1 and 3 were evaluated for antioxidant activity by the in vitro DPPH free radical scavenging ability and the protective effect of OH- induced DNA oxidative damage. Results: Compound 1 was a new type of triterpenoid saponin, named as echinocaulisaglycone 3-O-β-D-glucopyranoside (echinocaulisaponin A), and it had good antioxidant activity. Compound 2 was similar to compound 1, named as 1-hydroxyl-echinocaulisaglycone 3-O-β-D-glucopyranoside (echinocaulisaponin B). Compound 3 was also a new type of triterpenoid saponin, named as echinocaulisaglycone II 3-O-α-L-arabinopyranosyl-(1”→4’)-β-D-glucopyranosiduronic acid (echinocaulisaponin C), and its antioxidant activity was weaker than compound 1. Conclusion: In this study, three new compounds were discovered and two of them were carried out in vitro anti-oxidation studies, laying the foundation for further research on the treatment of related diseases (cardiovascular disease, arthritis, age-related macular degeneration, etc.) through anti-oxidation or quenching free radical function.

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