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Innovation theory, technical methods and industrial application of quality marker of traditional Chinese medicine 中药质量标识创新理论、技术方法及产业化应用
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.12.001
Tiejun Zhang , Gang Bai , Changxiao Liu
Quality marker (Q-Marker) of traditional Chinese medicine (TCM) is a new concept of TCM quality research. Since it was proposed in 2016, it has aroused wide response from the industry and has become an innovative theory and technical method leading the quality research and quality control of TCM. This paper summarized the core connotation, theoretical basis and innovative value of Q-Marker, proposed the technical strategies and paths of the Q-Marker research, and showed the prospect of its application in the TCM industry. The paper provides references for TCM quality research, quality evaluation, quality control and scientific supervision and has important significance for promoting the quality standard and quality control level of TCM.
中药质量标记(Q-Marker)是中药质量研究的一个新概念。自2016年提出以来,引起了业界的广泛反响,已成为引领中医药质量研究和质量控制的创新理论和技术方法。本文总结了Q-Marker的核心内涵、理论基础和创新价值,提出了Q-Marker研究的技术策略和路径,并对Q-Marker在中药行业的应用前景进行了展望。为中药质量研究、质量评价、质量控制和科学监管提供参考,对提高中药质量标准和质量控制水平具有重要意义。
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引用次数: 0
Review of Astragalus membranaceus polysaccharides: Extraction process, structural features, bioactivities and applications 黄芪多糖研究进展:提取工艺、结构特征、生物活性及应用
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.09.004
Hongyue Tian , Lingzhuo An , Pengwang Wang , Xuemin Zhang , Wenyuan Gao , Xia Li
Astragalus membranaceus possesses the function of enhancing immunity, protecting the liver, diuretic, anti-aging, anti-stress, anti-hypertensive, and more extensive antibacterial effects. Polysaccharides, one kind of the major active ingredients of A. membranaceus, are considered to be responsible for their versatile use. Now, a systematic summary of research progress and prospects of polysaccharides from A. membranaceus polysaccharides (AMPs) is necessary to facilitate their further study and application. In this review, the optimal extraction methods, structural features, biological activities, and applications of AMPs were emphasized. The structure–activity relationships are also analyzed and elucidated. Solvent, ultrasonic, microwave, enzyme-assisted, ultra-high pressure, and combined methods have been used to extract AMPs. Among them, solvent extraction is the most commonly used method because it is simple and easy to operate, but the efficiency needs to be improved further. The ultra-high pressure method is the most efficient but has a low economic return. AMPs exhibited various bioactivities, including immunomodulation, antitumor, and antidiabete. The structure–activity relationships revealed that different structure configurations, chain conformations, and physical properties would have different bioactivities. However, the new method for purification of certain polysaccharides, detailed structure–activity relationships (SAR), mechanisms of bioactivities, and quality control of AMPs need to be extensively investigated.
黄芪具有增强免疫力、保护肝脏、利尿、抗衰老、抗应激、降压等功能,并具有更广泛的抗菌作用。多糖是黄芪的一种主要活性成分,被认为是其用途广泛的原因。现在,有必要系统地总结一下黄芪多糖(AMPs)的研究进展和前景,以促进其进一步的研究和应用。本文就抗菌肽的最佳提取方法、结构特点、生物活性及其应用进行了综述。并对其构效关系进行了分析和阐明。溶剂法、超声波法、微波法、酶辅助法、超高压法以及多种方法的联合提取都已被广泛采用。其中,溶剂萃取是最常用的方法,因其操作简便,但效率有待进一步提高。超高压法效率最高,但经济效益较低。amp具有多种生物活性,包括免疫调节、抗肿瘤和抗糖尿病。构效关系表明,不同的结构构型、链的构象和物性具有不同的生物活性。然而,某些多糖的纯化新方法、详细的构效关系(SAR)、生物活性机制和amp的质量控制需要进行广泛的研究。
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引用次数: 0
Metabolome and transcriptome association study reveals biosynthesis of specialized benzylisoquinoline alkaloids in Phellodendron amurense 代谢组学和转录组学关联研究揭示了黄柏中特异性苯基异喹啉生物碱的生物合成
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.11.003
Tingxia Liu , Wanran Zhang , Sijia Wang , Ya Tian , Yifan Wang , Ranran Gao , Shilin Chen , Wei Sun , Wei Ma , Zhichao Xu

Objective

Benzylisoquinoline alkaloids (BIAs) have pharmacological functions and clinical use. BIAs are mainly distributed in plant species across the order Ranunculales and the genus Phellodendron from Sapindales. The BIA biosynthesis has been intensively investigated in Ranunculales species. However, the accumulation mechanism of BIAs in Phellodendron is largely unknown. The aim of this study is to unravel the biosynthetic pathways of BIAs in Phellodendron amurens.

Methods

The transcriptome and metabolome data from 18 different tissues of P. amurense were meticulously sequenced and subsequently subjected to a thorough analysis. Weighted gene co-expression network analysis (WGCNA), a powerful systems biology approach that facilitates the construction and subsequent analysis of co-expression networks, was utilized to identify candidate genes involved in BIAs biosynthesis. Following this, recombinant plasmids containing candidate genes were expressed in Escherichia coli, a widely used prokaryotic expression system. The purpose of this genetic engineering endeavor was to express the candidate genes within the bacteria, thereby enabling the assessment of the resultant enzyme activity.

Results

The synonymous substitutions per synonymous site for paralogs indicated that at least one whole genome duplication event has occurred. The potential BIA biosynthetic pathway of P. amurense was proposed, and two PR10/Bet v1 members, 14 CYP450s, and 33 methyltransferases were selected as related to BIA biosynthesis. One PR10/Bet v1 was identified as norcoclaurine synthase, which could catalyze dopamine and 4-hydroxyphenylacetaldehyde into (S)-norcoclaurine.

Conclusion

Our studies provide important insights into the biosynthesis and evolution of BIAs in non-Ranunculales species.
目的探讨苯基异喹啉生物碱的药理作用及临床应用。偏倚主要分布在毛茛目和柏属植物中。对毛茛属植物BIA的生物合成进行了深入的研究。然而,黄柏中BIAs的积累机制在很大程度上是未知的。本研究旨在揭示黄柏中BIAs的生物合成途径。方法对18个不同组织的金银花转录组和代谢组数据进行测序和分析。加权基因共表达网络分析(Weighted gene co-expression network analysis, WGCNA)是一种功能强大的系统生物学方法,可促进共表达网络的构建和后续分析,该方法被用于识别参与BIAs生物合成的候选基因。随后,含候选基因的重组质粒在大肠杆菌中表达,大肠杆菌是一种广泛使用的原核表达系统。这项基因工程的目的是在细菌中表达候选基因,从而能够评估所得酶的活性。结果每个同源位点的同义替换表明至少发生了一次全基因组重复事件。提出了紫金花潜在的BIA生物合成途径,并筛选出2个PR10/Bet v1成员、14个cyp450和33个甲基转移酶与BIA生物合成相关。其中一个PR10/ betv1被鉴定为去甲氯氨合酶,该酶能催化多巴胺和4-羟基苯乙醛生成(S)-去甲氯氨合酶。结论本研究为非毛茛属植物的生物合成和进化提供了重要的见解。
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引用次数: 0
A comprehensive review of phytochemical approaches in treatment of acute myeloid leukemia: Associated pathways and molecular mechanisms 植物化学治疗急性髓系白血病的综合综述:相关途径和分子机制
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.11.010
Mouvanal Sajana , T.S. Gopenath , Basalingappa M. Kanthesh
Acute myeloid leukemia (AML) is a type of cancer that affects the blood and bone marrow. This review conducts a thorough analysis of AML, addressing its genetic modification. The examination extends to the current therapeutic approaches employed for AML, shedding light on their efficacy and the notable side effects experienced by patients undergoing these treatments, leading to a low overall survival rate. Therefore, exploring alternative treatments, such as phytochemicals, is necessary. Furthermore, the review explores the complex landscape of phytochemicals, categorizing them based on their diverse properties, which include alkaloids, phenols, terpenoids, organo-sulfur compounds, and other compounds, including quinones, and elucidating their mechanisms of action. Special emphasis is placed on their involvement in critical signaling pathways, with a particular focus on how these phytochemicals impact AML when evaluated across a spectrum of cell lines. This in-depth exploration aims to uncover potential targets within the molecular landscape of AML where phytochemicals can exert their therapeutic effects. The review investigates the potential role of plant-derived phytochemicals as adjunctive therapies for AML. This exploration encompasses the identification of specific phytochemicals that exhibit promising anti-leukemic properties and evaluates their potential in clinical settings. Beyond conventional treatments, the review explores the integration of complementary and alternative medicine as a holistic approach to managing AML. The examination encompasses the synergy between conventional therapies and alternative interventions, exploring how these combined strategies may enhance overall therapeutic outcomes and mitigate side effects. From a forward-looking perspective, the overarching goal is to contribute to the evolving landscape of AML treatment by considering innovative approaches that harness the therapeutic potential of phytochemicals, both independently and in conjunction with established medical interventions.
急性髓性白血病(AML)是一种影响血液和骨髓的癌症。本综述对AML进行了深入的分析,解决其基因修饰问题。这项研究扩展到目前用于AML的治疗方法,揭示了它们的疗效和接受这些治疗的患者所经历的显著副作用,导致总生存率低。因此,探索替代疗法,如植物化学物质,是必要的。此外,本文还探讨了植物化学物质的复杂格局,根据它们的不同性质对它们进行了分类,包括生物碱、酚类、萜类、有机硫化合物和其他化合物,包括醌类,并阐明了它们的作用机制。特别强调它们在关键信号通路中的参与,特别关注这些植物化学物质如何在细胞系光谱中评估时影响AML。这项深入的探索旨在揭示AML分子景观中的潜在靶点,其中植物化学物质可以发挥其治疗作用。这篇综述探讨了植物源性植物化学物质作为AML辅助治疗的潜在作用。这一探索包括鉴定具有抗白血病特性的特定植物化学物质,并评估其在临床环境中的潜力。除了常规治疗之外,该综述还探讨了补充和替代医学作为治疗AML的整体方法的整合。检查包括传统疗法和替代干预之间的协同作用,探索这些联合策略如何提高整体治疗效果并减轻副作用。从前瞻性的角度来看,总体目标是通过考虑利用植物化学物质的治疗潜力的创新方法,无论是独立的还是与现有的医疗干预措施相结合,为AML治疗的不断发展做出贡献。
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引用次数: 0
Promotion of chronic wound healing by plant-derived active ingredients and research progress and potential of plant polysaccharide hydrogels 植物源性活性成分对慢性伤口愈合的促进作用及植物多糖水凝胶的研究进展与潜力
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.11.005
Ru Yan , Yanhong Wang , Weinan Li , Jialin Sun
Wound healing is a complex biochemical process. The use of herbal medicine in wound healing not only carries forward the wisdom of traditional medicine, with its anti-inflammatory and immune-regulating effects, but also reflects the direction of modern biopharmaceutical technology, such as its potential in developing new biomaterials like hydrogels. This article first outlines the inherent structural properties of healthy skin, along with the physiological characteristics related to chronic wounds in patients with diabetes and burns. Subsequently, the article delves into the latest advancements in clinical and experimental research on the impact of active constituents in herbal medicine on wound tissue regeneration, summarizing existing studies on the mechanisms of various herbal medicines in the healing of diabetic and burn wounds. Finally, the paper thoroughly examines the application and mechanisms of plant polysaccharide hydrogels containing active herbal compounds in chronic wound healing. The primary objective is to provide valuable resources for the clinical application and development of herbal medicine, thereby maximizing its therapeutic potential. It also represents the continuation of traditional medical wisdom, offering new possibilities for advancements in regenerative medicine and wound care.
伤口愈合是一个复杂的生化过程。在伤口愈合中使用草药不仅传承了传统医学的智慧,具有抗炎和免疫调节的作用,而且反映了现代生物制药技术的方向,例如它在开发水凝胶等新型生物材料方面的潜力。本文首先概述了健康皮肤的固有结构特性,以及与糖尿病和烧伤患者慢性伤口相关的生理特征。随后,本文深入探讨了中药有效成分对创面组织再生影响的临床和实验研究的最新进展,总结了各种中药对糖尿病创面和烧伤创面愈合机制的现有研究。最后,本文对植物多糖水凝胶在慢性伤口愈合中的应用及其机制进行了深入探讨。主要目的是为草药的临床应用和开发提供宝贵的资源,从而最大限度地发挥其治疗潜力。它也代表了传统医学智慧的延续,为再生医学和伤口护理的进步提供了新的可能性。
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引用次数: 0
Cerbera odollam fruit extracts enhance anti-cancer activity of sorafenib in HCT116 and HepG2 cells 山竹果提取物增强索拉非尼对HCT116和HepG2细胞的抗癌活性
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.11.007
Supawadee Parhira , Orakot Simanurak , Khemmachat Pansooksan , Julintorn Somran , Apirath Wangteeraprasert , Zhihong Jiang , Liping Bai , Pranee Nangngam , Dumrongsak Pekthong , Piyarat Srisawang
<div><h3>Objective</h3><div>While higher therapeutic doses of toxic cardiac glycosides derived from <em>Cerbera odollam</em> are frequently employed in cases of suicide or homicide, ongoing research is investigating the potential anticancer properties of low-concentration extracts obtained from the fruits of <em>C. odollam</em>. The present study aimed to determine the enhanced anticancer effects and minimize potential side effects of combining extracts from <em>C. odollam</em> fruits from Thailand with sorafenib against HCT116 and HepG2 cells.</div></div><div><h3>Methods</h3><div>The dried powder of fresh green fruits of <em>C. odollam</em> was fractionated, and its phytochemical contents, including total cardiac glycosides, phenolics, flavonoids, and triterpenoids, were quantified. The cytotoxic effects of these fractions were evaluated against HCT116 and HepG2 cells using the MTT assay. The fractions showing the most significant response in HCT116 and HepG2 cells were subsequently combined with sorafenib to examine their synergistic effects. Apoptosis induction, cell cycle progression, and mitochondrial membrane potential (MMP) were then assessed. The underlying mechanism of the apoptotic effect was further investigated by analyzing reactive oxygen species (ROS) generation and the expression levels of antioxidant proteins.</div></div><div><h3>Results</h3><div>Phytochemical analysis showed that <em>C. odollam</em>-ethyl acetate fraction (COEtOAc) was rich in cardiac glycosides, phenolics, and flavonoids, while the dichloromethane fraction (CODCM) contained high levels of triterpenoids and saponins. Following 24 h treatment, HCT116 showed the most significant response to COEtOAc, while HepG2 responded well to CODCM with IC<sub>50</sub> values of (42.04 ± 16.94) μg/mL and (123.75 ± 14.21) μg/mL, respectively. Consequently, COEtOAc (20 μg/mL) or CODCM (30 μg/mL), both administered at sub-IC<sub>50</sub> concentrations, were combined with sorafenib at 6 μmol/L for HCT116 cells and 2 μmol/L for HepG2 cells, incubated for 24 h. This combination resulted in a significant suppression in cell viability by approximately 50%. The combination of treatments markedly enhanced apoptosis, diminished MMP, and triggered G<sub>0</sub>/G<sub>1</sub> phase cell cycle arrest compared to the effects of each treatment administered individually. Concurrently, increased formation of ROS and decreased expression of the antioxidant enzymes superoxide dismutase 2 and catalase supported the proposed mechanism of apoptosis induction by the combination treatment. Importantly, the anticancer effect demonstrated a specific targeted action with a favorable safety profile, as evidenced by HFF-1 cells displaying IC<sub>50</sub> values 2–3 times higher than those of the cancer cells.</div></div><div><h3>Conclusion</h3><div>Utilizing sub-IC<sub>50</sub> concentrations of COEtOAc or CODCM in combination with sorafenib can enhance targeted anticancer effects beyond those achieved with
目的:虽然高剂量的毒心苷常用于自杀或杀人,但正在进行的研究正在调查从蛇耳草果实中获得的低浓度提取物的潜在抗癌特性。本研究旨在确定泰国大黄果提取物与索拉非尼联合使用对HCT116和HepG2细胞的增强抗癌作用,并减少潜在的副作用。方法对鲜青果干粉进行分馏,定量测定其总苷、酚类、黄酮类、三萜等植物化学成分的含量。使用MTT法评估这些组分对HCT116和HepG2细胞的细胞毒性作用。在HCT116和HepG2细胞中表现出最显著反应的部分随后与索拉非尼联合观察其协同作用。然后评估细胞凋亡诱导、细胞周期进展和线粒体膜电位(MMP)。通过分析活性氧(ROS)的产生和抗氧化蛋白的表达水平,进一步探讨了凋亡效应的潜在机制。结果植物化学分析表明,大黄草乙酸乙酯部位(COEtOAc)含有丰富的心苷、酚类物质和类黄酮,二氯甲烷部位(CODCM)含有高含量的三萜和皂苷。处理24 h后,HCT116对COEtOAc的反应最为显著,HepG2对CODCM的IC50值分别为(42.04±16.94)μg/mL和(123.75±14.21)μg/mL。因此,COEtOAc (20 μg/mL)或CODCM (30 μg/mL)均以低于ic50浓度给药,与HCT116细胞(6 μmol/L)和HepG2细胞(2 μmol/L)的索拉非尼联合孵育24小时。这种联合对细胞活力的抑制作用约为50%。与单独治疗相比,联合治疗显著增强了细胞凋亡,减少了MMP,并引发了G0/G1期细胞周期阻滞。同时,ROS的形成增加,抗氧化酶超氧化物歧化酶2和过氧化氢酶的表达降低,支持了联合处理诱导细胞凋亡的机制。重要的是,HFF-1细胞的IC50值比癌细胞高2-3倍,证明了其抗癌作用具有良好的安全性。结论使用低于ic50浓度的COEtOAc或CODCM联合索拉非尼治疗可提高靶向抗癌效果,同时减轻副作用。未来的研究将集中在提取和表征活性成分,特别是心脏苷,以提高从有毒植物中提取的抗癌化合物的治疗潜力。
{"title":"Cerbera odollam fruit extracts enhance anti-cancer activity of sorafenib in HCT116 and HepG2 cells","authors":"Supawadee Parhira ,&nbsp;Orakot Simanurak ,&nbsp;Khemmachat Pansooksan ,&nbsp;Julintorn Somran ,&nbsp;Apirath Wangteeraprasert ,&nbsp;Zhihong Jiang ,&nbsp;Liping Bai ,&nbsp;Pranee Nangngam ,&nbsp;Dumrongsak Pekthong ,&nbsp;Piyarat Srisawang","doi":"10.1016/j.chmed.2024.11.007","DOIUrl":"10.1016/j.chmed.2024.11.007","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;div&gt;While higher therapeutic doses of toxic cardiac glycosides derived from &lt;em&gt;Cerbera odollam&lt;/em&gt; are frequently employed in cases of suicide or homicide, ongoing research is investigating the potential anticancer properties of low-concentration extracts obtained from the fruits of &lt;em&gt;C. odollam&lt;/em&gt;. The present study aimed to determine the enhanced anticancer effects and minimize potential side effects of combining extracts from &lt;em&gt;C. odollam&lt;/em&gt; fruits from Thailand with sorafenib against HCT116 and HepG2 cells.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;The dried powder of fresh green fruits of &lt;em&gt;C. odollam&lt;/em&gt; was fractionated, and its phytochemical contents, including total cardiac glycosides, phenolics, flavonoids, and triterpenoids, were quantified. The cytotoxic effects of these fractions were evaluated against HCT116 and HepG2 cells using the MTT assay. The fractions showing the most significant response in HCT116 and HepG2 cells were subsequently combined with sorafenib to examine their synergistic effects. Apoptosis induction, cell cycle progression, and mitochondrial membrane potential (MMP) were then assessed. The underlying mechanism of the apoptotic effect was further investigated by analyzing reactive oxygen species (ROS) generation and the expression levels of antioxidant proteins.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;Phytochemical analysis showed that &lt;em&gt;C. odollam&lt;/em&gt;-ethyl acetate fraction (COEtOAc) was rich in cardiac glycosides, phenolics, and flavonoids, while the dichloromethane fraction (CODCM) contained high levels of triterpenoids and saponins. Following 24 h treatment, HCT116 showed the most significant response to COEtOAc, while HepG2 responded well to CODCM with IC&lt;sub&gt;50&lt;/sub&gt; values of (42.04 ± 16.94) μg/mL and (123.75 ± 14.21) μg/mL, respectively. Consequently, COEtOAc (20 μg/mL) or CODCM (30 μg/mL), both administered at sub-IC&lt;sub&gt;50&lt;/sub&gt; concentrations, were combined with sorafenib at 6 μmol/L for HCT116 cells and 2 μmol/L for HepG2 cells, incubated for 24 h. This combination resulted in a significant suppression in cell viability by approximately 50%. The combination of treatments markedly enhanced apoptosis, diminished MMP, and triggered G&lt;sub&gt;0&lt;/sub&gt;/G&lt;sub&gt;1&lt;/sub&gt; phase cell cycle arrest compared to the effects of each treatment administered individually. Concurrently, increased formation of ROS and decreased expression of the antioxidant enzymes superoxide dismutase 2 and catalase supported the proposed mechanism of apoptosis induction by the combination treatment. Importantly, the anticancer effect demonstrated a specific targeted action with a favorable safety profile, as evidenced by HFF-1 cells displaying IC&lt;sub&gt;50&lt;/sub&gt; values 2–3 times higher than those of the cancer cells.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;Utilizing sub-IC&lt;sub&gt;50&lt;/sub&gt; concentrations of COEtOAc or CODCM in combination with sorafenib can enhance targeted anticancer effects beyond those achieved with","PeriodicalId":9916,"journal":{"name":"Chinese Herbal Medicines","volume":"17 1","pages":"Pages 108-126"},"PeriodicalIF":4.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
TPMGD: A genomic database for the traditional medicines in Pakistan TPMGD:巴基斯坦传统医药基因组数据库
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.03.004
Rushuang Xiang , Huihua Wan , Wei Sun , Baozhong Duan , Weiqian Chen , Xue Cao , Sifan Wang , Chi Song , Shilin Chen , Yan Wang , Atia-tul Wahab , M. Iqbal Choudhary , Xiangxiao Meng

Objective

In Pakistan, traditional medicines are an important component of the medical system, with numerous varieties and great demands. However, due to the scattered resources and the lack of systematic collection and collation, adulteration of traditional Pakistani medicine (TPM) is common, which severely affects the safety of their medicinal use and the import and export trades. Therefore, it is urgent to systematically organize and unify the management of TPM and establish a set of standards and operable methods for the identification of TPM.

Methods

We collected and organized the information on 128 TPMs with regard to their medicinal parts, efficacy, usage, and genetic material, based on Pakistan Hamdard Pharmacopoeia of Eastern Medicine: Pharmaceutical Codex. The genetic information of TPM is summarized from national center for biotechnology information (NCBI) and global pharmacopoeia genome database (GPGD). Furthermore, we utilized bioinformatics technology to supplement the chloroplast genome (cp-genome) data of 12 TPMs. To build the web server, we used the Linux + Apache + MySQL + PHP (LAMP) system and constructed the webpage on a PHP: Hypertext Preprocessor (PHP) model view controller (MVC) framework.

Results

We constructed a new genomic database, the traditional Pakistani medicine genomic database (TPMGD). This database comprises five entries, namely homepage, medicinal species, species identification, basic local alignment search tool (BLAST), and download. Currently, TPMGD contains basic profiles of 128 TPMs and genetic information of 102 TPMs, including 140 cytochrome c oxidase subunit I (COI) sequences and 119 mitochondrial genome sequences from Bombyx mori, 1 396 internal transcribed spacer 2 (ITS2) sequences and 1 074 intergenic region (psbA-trnH) sequences specific to 92 and 83 plant species, respectively. Additionally, TPMGD includes 199 cp-genome sequences of 82 TPMs.

Conclusion

TPMGD is a multifunctional database that integrates species description, functional information inquiry, genetic information storage, molecular identification of TPM, etc. The database not only provides convenience for TPM information queries but also establishes the scientific basis for the medication safety, species identification, and resource protection of TPM.
目的在巴基斯坦,传统药物是医疗体系的重要组成部分,品种众多,需求量大。然而,由于资源分散,缺乏系统的收集和整理,传统巴基斯坦药掺假现象普遍存在,严重影响了传统巴基斯坦药的药用安全和进出口贸易。因此,系统地组织统一对TPM的管理,建立一套TPM识别的标准和可操作的方法迫在眉睫。方法根据巴基斯坦汉达德东药药典(药典)对128种中药的药用部位、疗效、用法、遗传物质等资料进行收集整理。从国家生物技术信息中心(NCBI)和全球药典基因组数据库(GPGD)中总结了TPM的遗传信息。此外,我们利用生物信息学技术对12种TPMs的叶绿体基因组(cp-genome)数据进行了补充。为了构建web服务器,我们使用了Linux + Apache + MySQL + PHP (LAMP)系统,并在PHP: Hypertext Preprocessor (PHP) model view controller (MVC)框架上构建了网页。结果构建了一个新的基因组数据库——巴基斯坦传统医学基因组数据库(TPMGD)。该数据库包括主页、药用物种、物种鉴定、基本本地比对检索工具(BLAST)和下载五个条目。目前,TPMGD包含128个TPMs的基本图谱和102个TPMs的遗传信息,包括家蚕140个细胞色素c氧化酶亚基I (COI)序列和119个线粒体基因组序列,以及92种和83种植物特有的1 396个内部转录间隔物2 (ITS2)序列和1 074个基因间区(psbA-trnH)序列。此外,TPMGD包括82个TPMs的199个cp基因组序列。结论tpmgd是一个集TPM物种描述、功能信息查询、遗传信息存储、分子鉴定等功能于一体的多功能数据库。该数据库不仅为TPM信息查询提供了便利,而且为TPM用药安全、品种鉴定、资源保护等工作奠定了科学依据。
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引用次数: 0
Material basis revelation of anti-hepatoma effect of Huachansu (Cinobufacini) through down-regulation of thymidylate synthase 通过下调胸苷酸合成酶揭示华蟾素抗肝癌作用的物质基础
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.04.002
Qi Wu, Qimei Chen, Jingyi Yang, Jiayu Zhang, Ailin Yang
<div><h3>Objective</h3><div>Hepatocellular carcinoma (HCC) is a leading cause of mortality worldwide. Huachansu (Cinobufacini) is active extract isolated from the dry skin of <em>Bufo Bufo gargarizans</em>. It has now been widely used in clinical treatment of cancer, this study is to clarify the material basis of down-regulation of thymidylate synthase (TYMS) induced by Huachansu.</div></div><div><h3>Methods</h3><div>Our study utilized UPLC-MS/MS to identify major bioactive components from Huachansu. Cell Counting Kit 8 (CCK-8) assay and clone formation assay were used to examine the cell viability of tumor cells. TYMS and γ-H2AX level were detected by using quantitative real-time RT-PCR and/or western blotting. Small interfering RNA (siRNA) transfection was used to explore whether inhibition of TYMS could enhance the suppressive effect of Huachansu on cell growth of HCC cells.</div></div><div><h3>Results</h3><div>In our study, firstly, we identify 21 major bioactive components from Huachansu. CCK-8 assay results showed that Huachansu and its bioactive bufadienolides (Bufalin, Bufotalin, Cinobufotalin, Desacetylcinobufagin, Arenobufagin, Telocinobufagin, and Resibufogenin) significantly inhibited the proliferation of HepG2 and SK-HEP-1 cells in a dose- and time-dependent manner. Further molecular mechanistic investigation demonstrates that Huachansu significantly suppresses thymidylate synthase (TYMS), the enzyme which provides the sole de novo source of thymidylate for DNA synthesis. The inhibition of TYMS could lead to cell-cycle block and DNA damage of HCC cells. Furthermore, we identified that Huachansu markedly increased γ-H2AX expression, which indicated the presence of DNA damage. Moreover, we confirmed that transfection of cells with small interfering RNA specific to TYMS could increase the suppressive effects of Huachansu on the HCC cells proliferation. Quantitative RT-PCR analysis showed that Huachansu treatment had no effect on the transcription level of TYMS. Furthermore, proteasomal inhibitor MG132 could block TYMS inhibition induced by Huachansu, and concomitant administration of protein synthesis inhibitor cycloheximide (CHX) with Huachansu could further suppress the protein level of TYMS, indicating that Huachansu promotes proteasome-dependent degradation of TYMS in liver cancer cells. More importantly, the bioactive bufadienolides of Huachansu such as Bufalin, Bufotalin, Cinobufotalin, Desacetylcinobufagin, Arenobufagin, Telocinobufagin, and Resibufogenin could also significantly restrain the protein level of TYMS, revealing the material basis of inhibition of TYMS exposed to Huachansu. 5-Fluorouracil (5-FU) is a TYMS inhibitor, we also evaluate the effects of the combined treatment of Huachansu with 5-FU, the results show that interactions between Huachansu and 5-FU are synergistic or antagonistic. Thus, in clinical, attention should be paid to the dosage of Huachansu in combination with 5-FU.</div></div><div><h3>Conclusion</h3>
目的肝细胞癌(HCC)是世界范围内死亡的主要原因。花蟾素是从蟾蜍干皮中提取的活性提取物。目前已广泛应用于临床治疗癌症,本研究旨在阐明花脓素诱导胸苷酸合成酶(TYMS)下调的物质基础。方法采用超高效液相色谱-质谱联用技术对花参素的主要生物活性成分进行鉴定。采用细胞计数试剂盒8 (CCK-8)法和克隆形成法检测肿瘤细胞的细胞活力。采用实时荧光定量RT-PCR和/或western blotting检测TYMS和γ-H2AX水平。采用小干扰RNA (Small interfering RNA, siRNA)转染,探讨抑制TYMS是否能增强花脓素对HCC细胞生长的抑制作用。结果在本研究中,首先鉴定出花参素中21种主要活性成分。CCK-8检测结果显示,花参素及其生物活性蟾毒二烯内酯(蟾毒苷、蟾毒苷、蟾毒苷、去乙酰蟾毒苷、arennobufagin、Telocinobufagin和Resibufogenin)对HepG2和SK-HEP-1细胞的增殖有明显的抑制作用,且呈剂量依赖性和时间依赖性。进一步的分子机制研究表明,花参素显著抑制胸腺苷酸合成酶(TYMS),该酶是DNA合成中胸腺苷酸的唯一来源。TYMS的抑制可导致肝癌细胞周期阻滞和DNA损伤。此外,我们发现花参素显著增加了γ-H2AX的表达,这表明存在DNA损伤。此外,我们证实用TYMS特异性小干扰RNA转染细胞可以增强花脓素对HCC细胞增殖的抑制作用。定量RT-PCR分析显示,花参素处理对TYMS的转录水平没有影响。此外,蛋白酶体抑制剂MG132可阻断花脉素诱导的TYMS抑制,蛋白合成抑制剂环己亚胺(cycloheximide, CHX)与花脉素合用可进一步抑制TYMS的蛋白水平,表明花脉素促进肝癌细胞中蛋白酶体依赖性的TYMS降解。更重要的是,花参素中具有生物活性的蟾毒素二烯内酯如蟾毒灵、蟾毒灵、蟾毒灵、去乙酰蟾毒素、阿仑蟾毒素、远凝蟾毒素、瑞蟾毒素等也能显著抑制TYMS的蛋白水平,揭示了花参素对TYMS抑制的物质基础。5-氟尿嘧啶(5-FU)是一种TYMS抑制剂,我们还对花参素与5-FU联合治疗的效果进行了评价。结果表明,花脉素与5-FU之间存在增效或拮抗作用。因此,在临床上应注意花喘素与5-FU合用的剂量。结论花参素通过蛋白酶体依赖性降解TYMS抑制人肝癌细胞生长并诱导DNA损伤,生物活性丁二烯内酯是花参素下调TYMS的物质基础。
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引用次数: 0
Traditional Chinese herbal medicine in European Union: State of art, challenges, and future perspectives focusing on Italian market 欧盟的传统中草药:意大利市场的现状、挑战和未来展望
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2024.11.008
Anna Rita Bilia , Rebecca Ballerini , Liping Qu , Mei Wang
Traditional Chinese herbal medicine (TCM) has been used in China for thousands of years as an integral part of the healthcare system.The use of botanical products deriving from plants from TCM has become very spread and rooted in European Union (EU), generating a manufacturing industry of pronounced size, in particular the segment of food supplements, but recently also medical devices and cosmetics based on plants from TCM, especially in Italy. Only seven Herbal Medicinal Products (HMP) based on plants from TCM are present in EU besides more than 100 monographs on TCM plants are present in the European Pharmacopoeia. Indeed, the number of herbal monographs of European Medicine Agency (EMA) which report the main data on safety and efficacy of medicinal plants from TCM are very limited and this could be a reason for the limited number of HMP based on herbal drugs used in TCM. It is clear that those botanicals based on TCM but not classified as HMP can represent a sort of “borderline” products. Very likely, they are present on the European market because of the simpler authorization when compared with HMP. Some examples of these categories (food supplements and medical devices) containing plants from TCM and marketed in Italy are reported in this review. Consequently, it is urgent the need to clarify their categorization, also fundamental for the consumer protection. It is imperative the establishment of EU quality standards and official registration for Chinese herbal medicinal products, even if they are marketed as food supplements, medicinal devices or cosmetics because the international quality standards International Organization for Standardization Technical Committee 249-Traditional Chinese Medicine (ISO/TC249) can harmonize the quality control and promote the trading internationally. Governmental organizations together with companies producing TCM should work together to accelerate the legislation of laws pertaining to TCM, and generate an environment where TCM does not just continue to exist but truly develop.
传统的中草药(TCM)在中国已经使用了数千年,是医疗保健系统的一个组成部分。从中药植物中提取的植物产品的使用已经非常广泛,并扎根于欧盟(EU),产生了一个规模显著的制造业,特别是食品补充剂领域,但最近也有基于中药植物的医疗器械和化妆品,特别是在意大利。欧盟目前只有7种基于中药植物的草药产品(HMP),而欧洲药典中有100多部关于中药植物的专著。事实上,欧洲药品管理局(EMA)报告中医药用植物安全性和有效性主要数据的草药专著数量非常有限,这可能是中医中使用的基于草药的HMP数量有限的原因。很明显,那些以中医为基础但未被归类为HMP的植物药可以代表一种“边缘”产品。很有可能,它们在欧洲市场上的存在是因为与HMP相比,它们的授权更简单。本文报道了在意大利销售的含有中药植物的这些类别(食品补充剂和医疗器械)的一些例子。因此,明确其分类是迫切需要的,也是消费者保护的基础。欧盟对中草药产品的质量标准和正式注册是势在必行的,即使它们是作为食品补充剂,医疗器械或化妆品销售,因为国际质量标准国际标准化组织技术委员会249-中药(ISO/TC249)可以协调质量控制,促进国际贸易。政府部门和中药生产企业应共同努力,加快中医药相关法律的立法,营造中医药不是继续存在,而是真正发展的环境。
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引用次数: 0
Qishen Granule protects against myocardial ischemia by promoting angiogenesis through BMP2-Dll4-Notch1 pathway 芪参颗粒通过BMP2-Dll4-Notch1途径促进血管生成,对心肌缺血具有保护作用
IF 4.7 4区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.chmed.2023.12.007
Yiqin Hong , Hui Wang , Hanyan Xie , Xinyi Zhong , Xu Chen , Lishuang Yu , Yawen Zhang , Jingmei Zhang , Qiyan Wang , Binghua Tang , Linghui Lu , Dongqing Guo

Objective

Therapeutic angiogenesis has become a promising approach for treating ischemic heart disease (IHD). The present study aims to investigate the effects of Qishen Granule (QSG) on angiogenesis in myocardial ischemia (MI) and the potential mechanism.

Methods

In vivo study was conducted on rat model of myocardial infarction. QSG was performed daily at a dose of 2.352 g/kg for four weeks. Cardiac function was assessed by echocardiogram and pro-angiogenic effects were evaluated by Laser Doppler and CD31 expression. Oxygen-glucose deprivation (OGD) was applied in cultured human umbilical vein endothelial cells (HUVECs). Cell viability, wound healing and tube formation assay were used to test functions of HUVECs. ELISA and Western blots were used to assess protein expressions of bone morphogenetic protein 2-delta-like 4-notch homolog 1 (BMP2-Dll4-Notch1) signaling pathway.

Results

The results showed that QSG improved heart function, cardiac blood flow and microvessel density in myocardial ischemic rats. In vitro, QSG protected HUVECs by promoting the cell viability and tube formation. QSG upregulated bone morphogenetic protein-2 (BMP2) and downregulated delta-like 4 (Dll4) and notch homolog 1 (Notch1) expressions both in rats and HUVECs.

Conclusion

QSG protected against MI by promoting angiogenesis through BMP2-Dll4-Notch1 pathway. BMP2 might be a promising therapeutic target for IHD.
目的治疗性血管生成已成为治疗缺血性心脏病(IHD)的一种很有前途的方法。本研究旨在探讨芪肾颗粒(QSG)对心肌缺血血管生成的影响及其可能机制。方法采用大鼠心肌梗死模型进行体内研究。每日进行QSG,剂量为2.352 g/kg,持续4周。超声心动图评价心功能,激光多普勒和CD31表达评价促血管生成作用。采用氧糖剥夺法(OGD)培养人脐静脉内皮细胞(HUVECs)。采用细胞活力、创面愈合和成管实验检测HUVECs的功能。ELISA和Western blots检测骨形态发生蛋白2-delta-样4-notch同源物1 (BMP2-Dll4-Notch1)信号通路的蛋白表达。结果大鼠心功能、心脏血流及微血管密度均有明显改善。在体外,QSG通过促进细胞活力和试管形成来保护HUVECs。QSG上调骨形态发生蛋白2 (BMP2),下调delta-like 4 (Dll4)和notch同源物1 (Notch1)在大鼠和huvec中的表达。结论芪多糖通过BMP2-Dll4-Notch1通路促进血管生成,对心肌梗死具有保护作用。BMP2可能是IHD的一个有希望的治疗靶点。
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引用次数: 0
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Chinese Herbal Medicines
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