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Table of Content

    01 July 2023, Volume 32 Issue 6
    Original articles
    The structure and antiproliferative activity of the inclusion complex of neoandrographolide/β-cyclodextrin
    Yancong Zhao, Li Wang, Jingjing Zeng, Jinghua Li
    2023, 32(6):  427-434.  DOI: 10.5246/jcps.2023.06.036
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    In the present study, the inclusion complex of neoandrographolide and β-cyclodextrin (β-CD) was studied by experimental and theoretical methods. The inclusion complex of neoandrographolide/β-CD was prepared by the saturated solution method. The equilibrium constant of the inclusion complex was determined by UV-vis spectra. The structure of the complex was characterized by DTA, FT-IR, and molecular modeling techniques. All these results indicated that neoandrographolide could enter the cavity of β-CD to form an inclusion complex, and the neoandrographolide/β-CD inclusion complex exhibited different spectroscopic features and properties from neoandrographolide. The molar rate of the inclusion complex was 1:1. The five-membered lactone ring of the neoandrographolide molecule was inserted into the cavities of β-CD from the wider edge. The calculated equilibrium constant of the complex was 489.9918 mol/L. The in-vitro antiproliferative activity of neoandrographolide was significantly improved through the inclusion complexation process. Taken together, the inclusion complexation process was a successful method that could be used in the pharmaceutical industry.

    Oyster peptide ameliorates hepatic fibrosis through the NF-κB/iNOS signaling pathway
    Kaixiang Deng, Jingzhou Peng, Meiquan Zhang, Huijuan Lin, Xiaohua Wang, Daoxing He, Junming Zhu, Mingguang Chen, Jin Huang
    2023, 32(6):  435-445.  DOI: 10.5246/jcps.2023.06.037
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    In the present study, we found that oyster peptide (OP) could ameliorate hepatic fibrosis through the NF-κB/iNOS signaling pathway. A total of 50 male Sprague-Dawley rats were randomly divided into five groups by the random digital table method: control group, model group, low-dose (0.5 g/kg) OP group, medium-dose (1.0 g/kg) OP group, and high-dose (2.0 g/kg) OP group, with 10 rats in each group. The rat model of hepatic fibrosis was established by subcutaneous injection of 50% carbon tetrachloride (CCl4). In OP therapy groups, the expressions of collagen I, collagen III, and TGF-β1 in the liver with CCl4-induced hepatic fibrosis were significantly lower than those in the model group (P < 0.05). OP could down-regulate the expressions of NF-κB and iNOS in the liver tissue of rats with hepatic fibrosis. Collectively, OP ameliorated hepatic fibrosis, possibly through the NF-κB/iNOS signaling pathway.

    Discussion on the potential target and mechanism of Dachaihu Decoction in treating hyperlipidemia based on network pharmacology
    Huan Yan, Jian Wang, Hao Fu, Min Yang, Miao Qu, Zhie Fang
    2023, 32(6):  446-459.  DOI: 10.5246/jcps.2023.06.038
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    To explore the potential targets and related signaling pathways of Dachaihu Decoction in treating hyperlipidemia, we obtained the active ingredients of the decoction by searching the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) for eight Chinese herbal ingredients, namely Radix Bupleuri, Radix Scutellariae, Radix Paeoniae Alba, Rhizoma Pinelliae, Fructus Aurantii Immaturus, Ginger, Jujube, and Rhubarb. To obtain the disease target for hyperlipidemia, we searched the English keyword “hyperlipidemia” and compared and analyzed the drug target of Dachaihu Decoction with the target of hyperlipidemia disease through an online website. We then identified the intersection between the two as the target of Dachaihu Decoction for treating hyperlipidemia. We conducted a topological analysis to screen the key effective components of Dachaihu Decoction for treating hyperlipidemia based on their degree value. Then, the gene targets of Dachaihu Decoction for hyperlipidemia were imported into the String platform to identify the key interaction modules in the PPI network. We also used the cytohubba plug-in to screen the key genes of these modules. The online database platform DAVID was utilized to perform enrichment and analysis of the key module genes with the highest number of genes and scores. The study yielded 116 active ingredients and 294 targets as the drug targets of Dachaihu Decoction. Furthermore, a total of 1349 disease-related gene targets were obtained from the CTD database, OMIM database, and TCMIP platform. After comparing the drug targets of Dachaihu Decoction with the targets related to hyperlipidemia, a total of 168 targets were found to be involved in the treatment of hyperlipidemia by Dachaihu Decoction. Using the MCODE plug-in in Cytoscape software, eight key protein modules were identified in the PPI network. Further analysis of the first key module revealed the top 15 hub genes which may play important roles in the pharmacological effects of Dachaihu Decoction for treating hyperlipidemia. To further understand the underlying mechanism, GO function annotation and KEGG pathway enrichment analysis were performed for the genes included in the key modules using the DAVID database. Based on the GO function annotation, the biological process (BP) of the key module genes was mainly related to the positive regulation of transcription from the RNA polymerase II promoter, the negative regulation of apoptosis, and the response to drugs. The cellular component (CC) was mainly located in the extracellular space, extracellular area, and pits. The molecular function (MF) was mainly focused on enzyme binding, cytokine activity, and protein binding. The KEGG pathway enrichment analysis showed that the key module genes were involved in several signaling pathways, including the hepatitis B signaling pathway, TNF signaling pathway, tumor-related signaling pathway, and PI3K-AKT signaling pathway. These pathways are known to be associated with inflammation, apoptosis, and cell growth, which are all critical processes in the development of hyperlipidemia. In conclusion, it appeared that Dachaihu Decoction could potentially be effective in the treatment of hyperlipidemia by regulating the expression of key genes, such as MMP9 and MAPK2, as well as the PI3K-AKT and TNF signaling pathways.

    Mangiferin alleviates cardiac inflammatory injury in spontaneously hypertensive rats by inhibiting the MCP-1/CCR2 signaling pathway
    Xiaoqin Hu, Xuefei Ding, Jiagang Deng, Erwei Hao, Zhengcai Du, Bei Zhou, Xuewen Zeng
    2023, 32(6):  460-472.  DOI: 10.5246/jcps.2023.06.039
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    Hypertension is a low-grade inflammation state of the disease and often complicated by inflammation of the heart. Mangiferin (MGF), which is a natural glucosyl xanthone, has a strong anti-inflammatory activity. However, the effects of MGF on cardiac inflammatory injury in hypertension remain unclear. In the present study, we investigated the protective effects and mechanisms of MGF on cardiac inflammatory injury in spontaneously hypertensive rats (SHRs). Briefly, 10-week-old male SHRs and 10-week-old male normotensive Wistar-Kyoto (WKY) rats were used. MGF was used in SHRs at doses of 10, 20, and 40 mg/kg for 8 weeks consecutively. The systolic blood pressure (SBP) level was measured, and the cardiac tissues were collected for morphology, immunohistochemistry, ELISA, Western blotting analysis, and real-time reverse transcription PCR (RT-PCR) analysis. The results showed that the SBP level was increased significantly in the model group compared with the control group both before and after intragastric administration, the SHRs increased the SBP level spontaneously, and all doses of MGF showed no significant effect on the SBP level. Cardiac histomorphology showed that there was an apparent inflammatory injury in the model group. MGF significantly inhibited this injury. Meanwhile, MGF significantly inhibited the increased abundance of IL-6 and TNF-α in SHRs. Furthermore, MGF also significantly inhibited the increased expressions of MCP-1 and CCR2 at the protein and mRNA levels in SHRs. In conclusion, this study demonstrated that MGF did not decrease the SBP level of SHRs. However, MGF had a protective effect on cardiac inflammatory injury in SHRs, which might be mediated partly by inhibiting the expression of the MCP-1/CCR2 signaling pathway.

    Cidofovir inhibits human adenovirus type 55 infection in vitro
    Wenbo Wang, Mengke Wang, Zonghai Hu, Jie Xiong, Yuan Liu
    2023, 32(6):  473-477.  DOI: 10.5246/jcps.2023.06.040
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    Human adenovirus type 55 (HAdV-55) can usually cause acute respiratory diseases. Unfortunately, there is no available specific antiviral drug. In the present study, 14 nucleotide analogs were screened for their anti-HAdV-55 activities in vitro. The results suggested that cidofovir could inhibit HAdV-55 infection in HEp-2 cells, providing strong evidence for further research on treating HAdV-55 infection.

    The in vitro antioxidant activities of the ethanol extract and its different polar fractions from Ephedra saxatilis Royle ex Florin in Tibet
    Han Wang, Fanglong Li, Aga Er-bu, Xiaoxia Liang, Geng Sang, Car Rangnanjia
    2023, 32(6):  478-486.  DOI: 10.5246/jcps.2023.06.041
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    In the present study, we aimed to investigate the in vitro antioxidant activity of the ethanol extract and its polar extracts from Ephedra saxatilis Royle ex Florin in Tibet. The chemical constituents were first screened by the preliminary phytochemical methods. The contents of total polyphenols and total flavonoids were identified by the Folin-Ciocalteu method and colorimetric method of the aluminum chloride method, respectively. Furthermore, their antioxidant activities were investigated by the DPPH method, ABTS method, hydroxyl radical scavenging, and reduction powder method. The preliminary phytochemical screening showed that the polyphenols, glycosides, flavonoids, and saponins existed in ethanol extract, and the chemical composition in different polar extracts varied, among which the contents of polyphenols and flavonoids were highest in the ethyl acetate part, followed by the dichloromethane part, exhibiting best antioxidant capacity. Both the ethyl acetate and dichloromethane parts from Ephedra saxatilis Royle ex Florin exhibited better antioxidant activities than BHT, which was associated with the high contents of polyphenols and flavonoids.

    Drug administration and clinical pharmacy column
    Analysis of 365 illogical prescriptions for parenteral feeding from a hospital's intravenous drug dispensing center
    Juntao Fu, Chunjie Nie, Min Li, Jia Li, Shuzhang Du
    2023, 32(6):  487-493.  DOI: 10.5246/jcps.2023.06.042
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    abstract

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    The research group of Prof. Yanxing Jia has made important progress in the field of total synthesis of natural product
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    2023, 32(6):  503-504. 
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    State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University Health Science Center
    2023, 32(6):  512-512. 
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