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Integrated network, docking, and experimental validation of the dual anti-inflammatory and uricosuric actions of Artemisia vulgaris compounds 青蒿类化合物抗炎、尿双重作用的整合网络、对接及实验验证
Pub Date : 2025-10-25 DOI: 10.1016/j.prmcm.2025.100712
Pham Thi Nhat Trinh , Dang Thi Le Hang , Nguyen Ngoc Phuong Uyen , Tran Nguyen Minh An , Le Xuan Tien , Le Tien Dung
In Traditional Chinese Medicine (TCM), mugwort (Artemisia vulgaris) is documented as the primary material for moxibustion, prepared as moxa floss (ai rong, 艾绒), moxa cones (ai zhu, 艾炷), and moxa sticks (ai tiao, 艾条) to warm the channels and regulate qi–blood [6–8]. We therefore investigated A. vulgaris compounds for multi-target anti-gout relevance, anchored in these TCM indications.
Network pharmacology and molecular docking prioritized A. vulgaris phytochemicals against gout-related targets, followed by in-vitro validation in LPS-challenged RAW 264.7 macrophages.
Of 62 compounds, 52 met drug-likeness and intersected 277 gout genes. A flavonoid (AV52) showed strong predicted binding to PTGS2/XO, and artemisinin (AV46) to urate transporters (SLC22A12/ABCG2). Experimentally, AV46 reduced IL-6/TNF-α and nitrite while preserving IL-10. IL-10 showed a small, non-monotonic change at 6.25 µM (p < 0.05) that was not reproduced at adjacent doses, suggesting limited biological relevance, while overall IL-10 was preserved alongside reductions in IL-6 and TNF-α.
Framed within TCM practice of moxibustion and warming/qi–blood-regulating indications, these data support a lead–anchor concept (AV52 anti-inflammatory/XO; AV46 uricosuric-anti-inflammatory) warranting further in-vivo and formulation studies for TCM-relevant applications.
A. vulgaris phytochemicals demonstrate complementary potential against gout-related inflammation and urate handling within a TCM use-case anchored to mugwort preparations (moxa floss/cones/sticks). AV46 showed experimental activity consistent with predictions, while AV52 requires bench confirmation. These results motivate focused biochemical, transporter, pharmacokinetic, and in-vivo evaluations to support translation into Chinese preparation - compatible applications.
在中医中,艾草(Artemisia vulgaris)被记载为艾灸的主要原料,制成艾牙线(艾蓉,绒)、艾球茎(艾朱,炷)和艾条(艾条,),以温经、调气血[6-8]。因此,我们研究了寻常草化合物的多靶点抗痛风相关性,锚定在这些中医适应症中。网络药理学和分子对接优先考虑了A. vulgaris植物化学物质对痛风相关靶点的作用,随后在lps挑战的RAW 264.7巨噬细胞中进行了体外验证。62个化合物中,52个与药物相似,并与277个痛风基因交叉。类黄酮(AV52)与PTGS2/XO结合,青蒿素(AV46)与尿酸转运蛋白(SLC22A12/ABCG2)结合。实验表明,AV46降低IL-6/TNF-α和亚硝酸盐,同时保留IL-10。IL-10在6.25µM (p < 0.05)时表现出小的非单调变化,在相邻剂量下没有重现,表明有限的生物学相关性,而IL-10总体上与IL-6和TNF-α的减少保持一致。在中医艾灸和温热/气血调节适应症的框架下,这些数据支持了一个铅锚概念(AV52抗炎/XO; AV46抗尿-抗炎),为中医相关应用的进一步体内和配方研究提供了依据。在艾草制剂(艾牙线/艾锥/艾棒)的中医用例中,vulgaris植物化学物质显示出对抗痛风相关炎症和尿酸处理的互补潜力。AV46的实验活动与预测一致,而AV52则需要实验验证。这些结果激发了集中的生化,转运体,药代动力学和体内评价,以支持翻译成中国制剂兼容的应用。
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引用次数: 0
Mechanistic insights into the neuroprotective effects of Radix Astragali (Huang Qi): Bridging Traditional Chinese Medicine and modern pharmacology 黄芪神经保护作用的机理研究:中医与现代药理学的桥梁
Pub Date : 2025-10-24 DOI: 10.1016/j.prmcm.2025.100711
Rizwan Ahmad , Chhavi Verma , Sandeep Kumar , Vishal Kumar , Darakhshan Gazala Bari , Saurabh Sharma , Shadab Ali , Shamim Shamim

Introduction

Radix Astragali, a major herb in Traditional Chinese Medicine, has traditionally been used to strengthen vital energy and promote blood circulation. Recent research has revealed its neuroprotective potential in disorders such as ischemic stroke, Alzheimer’s disease, and traumatic brain injury.

Methods

This review evaluates recent preclinical and clinical studies on the neuroprotective effects of Radix Astragali and its active components, including astragaloside four, flavonoids, polysaccharides, terpenoids, alkaloids, and amino acids. Peer-reviewed scientific literature was analyzed and interpreted within the context of Traditional Chinese Medicine principles.

Results

Radix Astragali exhibits multiple neuroprotective actions, including antioxidant, anti-inflammatory, anti-apoptotic, and immune-regulating effects. Astragaloside IV regulates critical signaling pathways, including phosphoinositide 3-kinase/protein kinase B, mitogen-activated protein kinase, and nuclear factor-κB, thereby supporting neuronal survival and reducing oxidative damage. Flavonoids and polysaccharides enhance synaptic plasticity, nerve regeneration, and cerebral blood flow. These findings are consistent with Traditional Chinese Medicine concepts of replenishing vital energy and stimulating blood flow in neurological disorders.

Discussion

Radix Astragali exemplifies the integration of Traditional Chinese Medicine and modern neuropharmacology. However, clinical translation remains limited due to challenges in standardization, potential herb drug interactions, and insufficient large-scale clinical validation. Future studies should emphasize pharmacokinetics, synergistic formulations, and biomarker-based personalized neurotherapy to ensure safe and effective clinical application.
黄芪是一种重要的中药,传统上被用来增强元气,促进血液循环。最近的研究表明,它在缺血性中风、阿尔茨海默病和创伤性脑损伤等疾病中具有神经保护作用。方法综述了近年来黄芪及其有效成分黄芪甲苷、黄酮类、多糖、萜类、生物碱和氨基酸等神经保护作用的临床前和临床研究。同行评议的科学文献在中医原理的背景下进行分析和解释。结果黄芪具有抗氧化、抗炎、抗凋亡、免疫调节等多种神经保护作用。黄芪甲苷调节磷酸肌苷3-激酶/蛋白激酶B、丝裂原活化蛋白激酶、核因子-κB等关键信号通路,支持神经元存活,减少氧化损伤。黄酮类化合物和多糖增强突触可塑性、神经再生和脑血流量。这些发现与传统中医在神经系统疾病中补充元气和刺激血液流动的概念是一致的。黄芪是中医与现代神经药理学相结合的典范。然而,由于标准化、潜在的中草药相互作用和大规模临床验证不足的挑战,临床翻译仍然有限。未来的研究应强调药代动力学、协同配方和基于生物标志物的个性化神经治疗,以确保安全有效的临床应用。
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引用次数: 0
Therapeutic modulation of unfolded protein response by biochemic tissue salts in alcohol- and acetaminophen-induced liver cirrhosis 生物化学组织盐对酒精和对乙酰氨基酚诱导的肝硬化中未折叠蛋白反应的治疗调节
Pub Date : 2025-10-21 DOI: 10.1016/j.prmcm.2025.100710
Debabrata Dash, Raj Kumar Koiri

Introduction

Alcohol-associated liver disease (ALD) is a major global public health problem with chronic alcohol use responsible for a large proportion of alcohol-attributed fatalities. The combined exposure to acetaminophen raises the level of hepatotoxicity. The unfolded protein response (UPR) is one of the key cellular processes stimulated following liver injury but whose regulation under dual alcohol and acetaminophen treatment is ill defined. While Natrum sulphuricum (NS) and Natrum phosphoricum (NP) are Western biochemic homeopathic tissue salts, mineral salts and allied compounds have been traditionally used in Traditional Chinese Medicine (TCM) for the upkeep of liver and digestive functions. The present study was aimed at ascertaining hepatoprotective action of NS and NP through modulation of UPR signaling in chemically induced liver cirrhosis rat model.

Methods: Wistar albino rats were divided at random into five groups

control, alcohol control, liver cirrhosis, LC+NS, and LC+NP. Liver cirrhosis was induced by chronic oral treatment with alcohol and acetaminophen. NS and NP were given orally for four weeks following induction. Liver tissues were taken for molecular analysis, and expression of a few of the major UPR-related genes and proteins were quantified by quantitative RT-PCR and Western blotting.

Results

Both acetaminophen and alcohol coexposures significantly dysregulated UPR markers, suggesting endoplasmic reticulum stress and altered proteostasis. NP and NS treatment restored levels of key UPR components, suggesting therapeutic protein-folding mechanism modulation.

Conclusions

NS and NP showed hepatoprotective action through UPR signaling modulation and reduction of protein-misfolding stress in chemically induced liver cirrhosis. These results are preliminary scientific basis to explore mineral-based compounds in new and traditional medicine settings, including their theoretical significance to TCM approaches to the prevention of liver disease.
酒精相关性肝病(ALD)是一个主要的全球公共卫生问题,慢性酒精使用导致很大比例的酒精相关死亡。对乙酰氨基酚的联合暴露会提高肝毒性水平。未折叠蛋白反应(UPR)是肝损伤后刺激的关键细胞过程之一,但其在酒精和对乙酰氨基酚双重治疗下的调控尚不明确。虽然Natrum sulphuricum (NS)和Natrum phospicum (NP)是西方生物化学顺势疗法的组织盐,但矿物盐和相关化合物一直被传统地用于中医(TCM)中,以维持肝脏和消化功能。本研究旨在确定NS和NP通过调节UPR信号通路在化学诱导肝硬化大鼠模型中的保肝作用。方法:将Wistar白化大鼠随机分为对照组、酒精对照组、肝硬化组、LC+NS组和LC+NP组。慢性口服酒精和对乙酰氨基酚治疗导致肝硬化。诱导后口服NS和NP 4周。取肝组织进行分子分析,采用定量RT-PCR和Western blotting方法定量检测部分主要的uprr相关基因和蛋白的表达。结果对乙酰氨基酚和酒精共同暴露均显著失调UPR标记,提示内质网应激和蛋白质平衡改变。NP和NS治疗恢复了关键UPR成分的水平,提示治疗性蛋白折叠机制的调节。结论sns和NP通过调节UPR信号通路,减少化学诱导肝硬化的蛋白错误折叠应激,发挥保护肝脏的作用。这些结果为探索矿物质化合物在新医学和传统医学中的应用提供了初步的科学依据,包括它们对中医预防肝病的理论意义。
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引用次数: 0
To explore the scientific connotation of Fuyang therapy for liver cancer based on mitochondrial function 探讨基于线粒体功能的肝癌复阳疗法的科学内涵
Pub Date : 2025-10-20 DOI: 10.1016/j.prmcm.2025.100709
Yang Wang , Bugao Zhou , Shanshan Li , Linxin Zheng , Bohan Cai , Huiyu Wang , Sili Li , Yuhan Lin , Yanhe Xu

Background

Liver cancer poses a serious threat to human health,and research into its pathogenesis and exploration of treatment strategies have always been major focuses in the medical field.Recent studies have indicated that mitochondrial dysfunction plays a promoting role in the progression of liver cancer,primarily manifested through disruptions in energy metabolism,decreased mitochondrial outer membrane permeability, and dysregulation of calcium ion homeostasis. In traditional Chinese medicine (TCM), “Yang deficiency and Yin excess” is considered the core pathogenesis of liver cancer, and the fundamental treatment principle of “Fuyang Guben” (supporting Yang and reinforcing the root) has been proposed. The mechanism of action may be associated with the improvement of mitochondrial function, however modern research in this area remains relatively limited.

Methods

Through theoretical analysis and comprehensive literature review, this paper elucidates the theoretical basis of Fuyang therapy for liver cancer from the perspective of TCM theory,summarizes the specific roles of mitochondrial function in the progression of liver cancer, and systematically reviews recent advances in modern mechanistic research on how Fuyang therapy inhibits the occurrence and development of liver cancer by regulating mitochondrial function.

Results

Fuyang therapy can improve mitochondrial function from multiple perspectives,including restoring energy metabolism,regulating membrane permeability, and maintaining calcium homeostasis,thereby inhibiting the proliferation and progression of liver cancer cells.Existing experimental and clinical studies have preliminarily verified the potential efficacy of Fuyang-based formulas in anti-liver cancer treatments and their regulatory mechanisms involving mitochondrial function-related pathways.

Conclusion

Fuyang therapy demonstrates both theoretical rationality and experimental support in the treatment of liver cancer.Its anti-liver cancer effects are achieved through the improvement of mitochondrial function,providing new insights for the formulation of TCM-based treatments and mechanistic research on liver cancer.
肝癌严重威胁人类健康,其发病机制的研究和治疗策略的探索一直是医学界关注的焦点。近期研究表明,线粒体功能障碍在肝癌的进展中起促进作用,主要表现为能量代谢紊乱、线粒体外膜通透性降低、钙离子稳态失调。在中医中,“阳虚阴虚”被认为是肝癌的核心病机,并提出了“扶阳固本”(扶阳补根)的基本治疗原则。其作用机制可能与线粒体功能的改善有关,但在这方面的现代研究相对有限。方法通过理论分析和综合文献综述,从中医理论角度阐述阜阳疗法治疗肝癌的理论基础,总结线粒体功能在肝癌进展中的具体作用,系统综述阜阳疗法通过调节线粒体功能抑制肝癌发生发展的现代机制研究最新进展。结果复阳疗法可从恢复能量代谢、调节细胞膜通透性、维持钙稳态等多个角度改善线粒体功能,从而抑制肝癌细胞的增殖和进展。现有的实验和临床研究已经初步验证了阜阳方抗肝癌的潜在疗效及其涉及线粒体功能相关通路的调控机制。结论扶阳法治疗肝癌具有理论合理性和实验依据。其抗肝癌作用是通过改善线粒体功能实现的,为肝癌中药治疗方案的制定和机制研究提供了新的见解。
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引用次数: 0
The role of Traditional Chinese medicinal plants in the management of fibromyalgia: A review 中药在纤维肌痛治疗中的作用综述
Pub Date : 2025-10-18 DOI: 10.1016/j.prmcm.2025.100707
Kaniga Pandi, Binoy Varghese Cheriyan, Kunal R. Kataria

Introduction

Fibromyalgia is a chronic, multifactorial disorder characterized by widespread musculoskeletal pain, fatigue, sleep disturbances, and cognitive impairments, substantially reducing quality of life. Conventional pharmacological therapies, including analgesics, antidepressants, and anticonvulsants, provide only partial relief and are often associated with adverse effects. This highlights the need for safer and more effective alternatives. Traditional Chinese Medicine (TCM) has a long history of managing chronic pain conditions through medicinal plants, which may offer therapeutic benefits in fibromyalgia.

Methods

A systematic literature search was performed across PubMed, Scopus, Web of Science, and CNKI databases using predetermined inclusion and exclusion criteria. The focus was on studies reporting the phytochemical composition, pharmacological actions, and clinical outcomes of TCM medicinal plants relevant to fibromyalgia.

Results

Several plants with potential therapeutic effects were identified, including Panax ginseng (Ren Shen), Corydalis yanhusuo (Yan Hu Suo), Salvia miltiorrhiza (Dan Shen), and Astragalus membranaceus (Huang Qi). Their bioactive compounds, ginsenosides, tetrahydropalmatine, salvianolic acids, ferulic acid, and astragalosides, exert multimodal actions. These include modulation of neurotransmitter pathways, reduction of pro-inflammatory cytokines, antioxidative activity, and improvement of mitochondrial function. Preclinical studies demonstrate analgesic, anti-fatigue, and neuroprotective effects, while limited clinical evidence suggests improvements in pain, sleep, and overall well-being.

Discussion

Although preliminary findings are promising, current evidence is limited by small sample sizes, heterogeneous herbal formulations, and lack of standardized dosing regimens. Well-designed, large-scale randomized controlled trials are essential to validate efficacy, establish safety profiles, and support the integration of TCM herbal therapies into evidence-based fibromyalgia management.
纤维肌痛是一种慢性、多因素疾病,以广泛的肌肉骨骼疼痛、疲劳、睡眠障碍和认知障碍为特征,严重降低生活质量。传统的药物治疗,包括镇痛药、抗抑郁药和抗惊厥药,只能部分缓解,而且往往伴有不良反应。这突出表明需要更安全、更有效的替代方案。中医(TCM)通过药用植物治疗慢性疼痛的历史悠久,这可能为纤维肌痛提供治疗益处。方法采用预定的纳入和排除标准,对PubMed、Scopus、Web of Science、CNKI等数据库进行系统文献检索。重点是报道与纤维肌痛相关的中药植物的化学成分、药理作用和临床结果的研究。结果鉴定出几种具有潜在治疗作用的植物,包括人参、延胡索、丹参和黄芪。它们的生物活性化合物,人参皂苷、四氢巴马汀、丹酚酸、阿魏酸和黄芪甲苷,发挥多种作用。这些包括神经递质通路的调节、促炎细胞因子的减少、抗氧化活性和线粒体功能的改善。临床前研究表明具有镇痛、抗疲劳和神经保护作用,而有限的临床证据表明可以改善疼痛、睡眠和整体健康。尽管初步发现很有希望,但目前的证据受到样本量小、草药配方不均匀以及缺乏标准化给药方案的限制。精心设计的大规模随机对照试验对于验证疗效、建立安全性、支持将中药疗法整合到循证纤维肌痛治疗中至关重要。
{"title":"The role of Traditional Chinese medicinal plants in the management of fibromyalgia: A review","authors":"Kaniga Pandi,&nbsp;Binoy Varghese Cheriyan,&nbsp;Kunal R. Kataria","doi":"10.1016/j.prmcm.2025.100707","DOIUrl":"10.1016/j.prmcm.2025.100707","url":null,"abstract":"<div><h3>Introduction</h3><div>Fibromyalgia is a chronic, multifactorial disorder characterized by widespread musculoskeletal pain, fatigue, sleep disturbances, and cognitive impairments, substantially reducing quality of life. Conventional pharmacological therapies, including analgesics, antidepressants, and anticonvulsants, provide only partial relief and are often associated with adverse effects. This highlights the need for safer and more effective alternatives. Traditional Chinese Medicine (TCM) has a long history of managing chronic pain conditions through medicinal plants, which may offer therapeutic benefits in fibromyalgia.</div></div><div><h3>Methods</h3><div>A systematic literature search was performed across PubMed, Scopus, Web of Science, and CNKI databases using predetermined inclusion and exclusion criteria. The focus was on studies reporting the phytochemical composition, pharmacological actions, and clinical outcomes of TCM medicinal plants relevant to fibromyalgia.</div></div><div><h3>Results</h3><div>Several plants with potential therapeutic effects were identified, including <em>Panax ginseng</em> (Ren Shen), <em>Corydalis yanhusuo</em> (Yan Hu Suo), <em>Salvia miltiorrhiza</em> (Dan Shen), and <em>Astragalus membranaceus</em> (Huang Qi). Their bioactive compounds, ginsenosides, tetrahydropalmatine, salvianolic acids, ferulic acid, and astragalosides, exert multimodal actions. These include modulation of neurotransmitter pathways, reduction of pro-inflammatory cytokines, antioxidative activity, and improvement of mitochondrial function. Preclinical studies demonstrate analgesic, anti-fatigue, and neuroprotective effects, while limited clinical evidence suggests improvements in pain, sleep, and overall well-being.</div></div><div><h3>Discussion</h3><div>Although preliminary findings are promising, current evidence is limited by small sample sizes, heterogeneous herbal formulations, and lack of standardized dosing regimens. Well-designed, large-scale randomized controlled trials are essential to validate efficacy, establish safety profiles, and support the integration of TCM herbal therapies into evidence-based fibromyalgia management.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"17 ","pages":"Article 100707"},"PeriodicalIF":0.0,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145417335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ameliorative effects of traditional Chinese medicine formula NRICM101 on periodontal inflammation: In vitro and in vivo 中药方剂NRICM101对牙周炎症的改善作用:体外和体内研究
Pub Date : 2025-10-17 DOI: 10.1016/j.prmcm.2025.100708
Fang-Wei Lin , Yann-Jen Chen , Hui-Rong Cheng , Chi-Tsung Wu , Hsien-Chung Chiu

Introduction

Taiwan Chingguan Yihau (NRICM101) is a novel anti-inflammatory traditional Chinese medicine formula developed in 2020 for COVID-19 pandemic. This study aimed to evaluate the effect of NRICM101 on periodontal inflammation, using human gingival fibroblasts (HGFs) exposed to Porphyromonas gingivalis lipopolysaccharide (Pg LPS) and rat models of ligature-induced periodontitis.

Methods

In vitro, HGFs were stimulated with Pg LPS and NRICM101. Cell viability and the expression of pro-inflammatory cytokines, including interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and IL-1β were measured using MTS assay and reverse transcription quantitative polymerase chain reaction (RT-qPCR). In vivo, Sprague-Dawley rats were divided into control, ligature placement, and NRICM101 treatment groups. Ligature placement was performed at day one and oral administration of NRICM101 (50 or 100 mg/kg body weight/day) or saline began one day prior to ligation and the following days. On day 8, the rats were sacrificed, periodontal tissue specimens were analyzed using microcomputed tomography (Micro-CT) imaging, RT-qPCR, and immunohistochemical (IHC) staining to evaluate the effects of the treatments.

Results

NRICM101 reduced HGFs viability above 1.0 mg/mL, while Pg LPS caused similar effects at concentrations above 1.0 μg/mL. Co-treatment with Pg LPS (0.5–1.0 μg /mL) and NRICM101 (0.1–0.5 mg/mL) showed no cytotoxicity. In vivo, NRICM101 attenuated alveolar bone loss and significantly decreased IL-6, TNF-α, and partially IL-1β expression, as confirmed by micro-CT, RT-qPCR, and IHC analyses.

Discussion

This study demonstrates that NRICM101 exerts protective anti-inflammatory effects in both cellular and animal models of periodontitis. It suppressed pro-inflammatory cytokine expression in HGFs and mitigated alveolar bone loss in ligature-induced periodontitis rats. The effects on IL-6 and TNF-α were pronounced, while the partial reduction of IL-1β may reflect additional regulatory mechanisms such as inflammasome activation, which warrants further investigation. These findings indicate that NRICM101 reduces inflammation without cytotoxicity and supports its potential application in managing chronic periodontal inflammation.
台湾青观益口(NRICM101)是2020年针对新冠肺炎大流行研发的新型抗炎中药配方。本研究旨在通过暴露于牙龈卟啉单胞菌脂多糖(Pg LPS)的人牙龈成纤维细胞(HGFs)和结痂性牙周炎大鼠模型,评估NRICM101对牙周炎症的影响。方法体外用Pg LPS和NRICM101刺激hgf。采用MTS法和逆转录定量聚合酶链反应(RT-qPCR)检测细胞活力和促炎细胞因子,包括白细胞介素-6 (IL-6)、肿瘤坏死因子-α (TNF-α)和IL-1β的表达。在体内,Sprague-Dawley大鼠分为对照组、结扎组和NRICM101治疗组。在结扎的第一天进行结扎,并在结扎前一天和之后的几天开始口服NRICM101(50或100 mg/kg体重/天)或生理盐水。第8天处死大鼠,采用显微计算机断层扫描(Micro-CT)成像、RT-qPCR和免疫组化(IHC)染色对牙周组织标本进行分析,评价治疗效果。结果snricm101在1.0 mg/mL以上可降低hgf活力,Pg LPS在1.0 μg/mL以上可降低hgf活力。Pg LPS (0.5 ~ 1.0 μg /mL)与NRICM101 (0.1 ~ 0.5 mg/mL)共处理无细胞毒性。显微ct、RT-qPCR和免疫组化分析证实,在体内,NRICM101可减轻牙槽骨丢失,并显著降低IL-6、TNF-α和部分IL-1β的表达。本研究表明,NRICM101在牙周炎细胞和动物模型中均具有保护性抗炎作用。抑制HGFs中促炎细胞因子的表达,减轻结扎性牙周炎大鼠牙槽骨丢失。对IL-6和TNF-α的影响是明显的,而IL-1β的部分减少可能反映了其他的调节机制,如炎性体激活,这需要进一步的研究。这些发现表明,NRICM101可以减少炎症而不产生细胞毒性,并支持其在治疗慢性牙周炎症方面的潜在应用。
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引用次数: 0
Integrating traditional chinese medicine and modern pharmacology: The role of Jiang Huang (curcumin) in cardiovascular health 中西医结合:姜黄在心血管健康中的作用
Pub Date : 2025-10-17 DOI: 10.1016/j.prmcm.2025.100706
Rufaida Wasim , Sumaiya Azmi , Asad Ahmad

Introduction

: Cardiovascular diseases (CVDs) remain the leading global cause of morbidity and mortality, driven by mechanisms such as oxidative stress, endothelial dysfunction, inflammation, and lipid imbalance. Curcumin, the principal bioactive constituent of Curcuma longa (turmeric), has long been used in Traditional Chinese Medicine (TCM) to improve circulation and alleviate stasis. Modern pharmacological evidence suggests it may offer cardiovascular protection.

Methods

: This review synthesises findings from preclinical models, clinical studies, and molecular investigations of curcumin in CVD, alongside traditional perspectives from TCM for integrative context.

Results

: Experimental studies reveal that curcumin reduces oxidative stress, downregulates NF-κB and pro-inflammatory cytokines, enhances nitric oxide bioavailability, and inhibits vascular smooth muscle proliferation. In animal models, it decreases myocardial infarct size, attenuates hypertrophy, and improves ventricular function. Clinical trials report improvements in blood pressure, endothelial function, lipid regulation, and inflammatory biomarkers among individuals at cardiovascular risk. However, outcomes remain inconsistent due to variability in study design, small sample sizes, heterogeneous formulations, and limited duration of follow-up. TCM perspectives on promoting blood flow and reducing stasis align with curcumin’s observed effects on vascular remodeling and atherosclerosis.

Discussion

: Curcumin is a safe, pleiotropic compound with growing evidence for adjunctive use in CVD management. Its poor oral bioavailability remains a key limitation, highlighting the need for novel formulations. Well-designed, larger clinical trials are essential to establish efficacy and bridge traditional knowledge with modern cardiovascular therapeutics.
心血管疾病(cvd)仍然是全球发病率和死亡率的主要原因,由氧化应激、内皮功能障碍、炎症和脂质失衡等机制驱动。姜黄素(Curcuma longa,姜黄)是姜黄的主要生物活性成分,长期以来一直被用于促进血液循环和化瘀。现代药理学证据表明,它可能对心血管有保护作用。方法:本文综述了姜黄素在心血管疾病中的临床前模型、临床研究和分子研究的发现,并结合传统中医观点进行了综合研究。结果:实验研究表明姜黄素可降低氧化应激,下调NF-κB和促炎细胞因子,提高一氧化氮的生物利用度,抑制血管平滑肌增殖。在动物模型中,它能减小心肌梗死面积,减轻肥厚,改善心室功能。临床试验报告了心血管风险个体的血压、内皮功能、脂质调节和炎症生物标志物的改善。然而,由于研究设计的可变性、小样本量、异质配方和随访时间有限,结果仍然不一致。中医对活血化瘀的看法与姜黄素对血管重构和动脉粥样硬化的影响一致。讨论:姜黄素是一种安全的、多效性的化合物,越来越多的证据表明姜黄素在心血管疾病治疗中的辅助使用。其较差的口服生物利用度仍然是一个关键的限制,突出了对新配方的需求。精心设计、规模更大的临床试验对于建立疗效和将传统知识与现代心血管治疗联系起来至关重要。
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引用次数: 0
Laiyang pear cough syrup relieves cough through the PI3K-AKT pathway 莱阳梨止咳糖浆通过PI3K-AKT通路缓解咳嗽
Pub Date : 2025-10-12 DOI: 10.1016/j.prmcm.2025.100702
Haoling Liu , Yiying Zhao , Yige Zhao , Kairui Gao , Yawen Xue , Dongyue Ma , Jia Liu , Zhenquan Liu , Wenyan Sun

Objective

To predict the mechanism of action of Laiyang Pear Cough Syrup in treating cough by using network pharmacology, molecular docking technology and the predicted key pathways in animal experiments.

Methods

Chemical components of each medicinal flavor were collected and screened from TCMSP and other databases to establish a database of the components of Laiyang Pear Cough Syrup. Cough-related targets were obtained from TTD and other databases. A Venn diagram of the components targets and cough targets was drawn to prelim determine the potential targets of the active ingredients of Laiyang Pear Cough Syrup in the treatment of cough. A PPI network was constructed and key targets were screened. The data were into Cytoscape 3.10.1 software, and a "active component-disease target" network was constructed, and key components were screened. The screened targets were subjected to GO enrichment analysis and KEGG pathway enrichment analysis. Molecular docking verification between key targets and core active ingredients was conducted using AutoDock Tools 1.5.6 software. A citric acid-induced guinea pig cough model was established. The cough latency and cough frequency were measured in the control and treatment groups, and the PI3K-AKT pathway predicted by network pharmacology was validated via Western blot analysis.

Results

43 active chemical components, 76 common targets, 591 GO biological processes, and 159 KEGG signaling pathways were screened out. The active components of Laiyang Pear Cough Syrup in the treatment of cough may be quercetin, stigmasterol, and luteolin, and the key may be IL-6, TNF, AKT1, IL-1β, and PTGS2, which mainly regulate the PI3K/AKT pathway to relieve cough. Molecular docking revealed that luteolin, quercetin, and stigmasterol as the key active ingredients in Laiyang Pear Cough Syrup bind to AKT1 with high affinities, displaying docking scores of −8.1, −8.0, and −7.7 kcal mol−1. These results indicate that the compounds may function as potent agonists to activate the PI3K-AKT signaling pathway. Laiyang Pear Cough Syrup can significantly prolong the cough latency period and reduce the number of coughs (compared with the control group, P < 0.01 or 0.05), and down-regulate the expression of PI3K, p-PI3K, AKT, p-AKT proteins.

Conclusion

Laiyang Pear Cough Syrup can relieve cough through a variety of components, targets and pathways. Regulating the PI3K-AKT pathway may be its main mechanism of action.
目的应用网络药理学、分子对接技术及动物实验预测的关键通路,预测莱阳梨止咳糖浆治疗咳嗽的作用机制。方法从TCMSP等数据库中收集和筛选莱阳梨止咳糖浆各药用香料的化学成分,建立莱阳梨止咳糖浆成分数据库。从TTD和其他数据库获得咳嗽相关靶标。绘制成分靶点与咳嗽靶点的维恩图,初步确定莱阳梨止咳糖浆有效成分治疗咳嗽的潜在靶点。构建PPI网络,筛选关键靶点。将数据导入Cytoscape 3.10.1软件,构建“活性组分-疾病靶点”网络,筛选关键组分。筛选的靶点进行GO富集分析和KEGG途径富集分析。利用AutoDock Tools 1.5.6软件对关键靶点与核心活性成分进行分子对接验证。建立了柠檬酸致豚鼠咳嗽模型。检测对照组和治疗组的咳嗽潜伏期和咳嗽频率,并通过Western blot分析验证网络药理学预测的PI3K-AKT通路。结果共筛选出43种活性化学成分、76种常见靶点、591种氧化石墨烯生物过程和159种KEGG信号通路。莱阳梨止咳糖浆治疗咳嗽的有效成分可能是槲皮素、豆甾醇和木犀草素,关键成分可能是IL-6、TNF、AKT1、IL-1β和PTGS2,主要通过调节PI3K/AKT通路缓解咳嗽。分子对接发现,莱阳梨止咳糖浆的关键活性成分木犀草素、槲皮素和豆甾醇与AKT1具有高亲和力,对接得分分别为−8.1、−8.0和−7.7 kcal mol−1。这些结果表明,这些化合物可能作为有效的激动剂激活PI3K-AKT信号通路。莱阳梨止咳糖浆能显著延长咳嗽潜伏期,减少咳嗽次数(与对照组比较,P <; 0.01或0.05),下调PI3K、P -PI3K、AKT、P -AKT蛋白的表达。结论莱阳梨止咳糖浆可通过多种成分、靶点和途径起到止咳作用。调节PI3K-AKT通路可能是其主要作用机制。
{"title":"Laiyang pear cough syrup relieves cough through the PI3K-AKT pathway","authors":"Haoling Liu ,&nbsp;Yiying Zhao ,&nbsp;Yige Zhao ,&nbsp;Kairui Gao ,&nbsp;Yawen Xue ,&nbsp;Dongyue Ma ,&nbsp;Jia Liu ,&nbsp;Zhenquan Liu ,&nbsp;Wenyan Sun","doi":"10.1016/j.prmcm.2025.100702","DOIUrl":"10.1016/j.prmcm.2025.100702","url":null,"abstract":"<div><h3>Objective</h3><div>To predict the mechanism of action of Laiyang Pear Cough Syrup in treating cough by using network pharmacology, molecular docking technology and the predicted key pathways in animal experiments.</div></div><div><h3>Methods</h3><div>Chemical components of each medicinal flavor were collected and screened from TCMSP and other databases to establish a database of the components of Laiyang Pear Cough Syrup. Cough-related targets were obtained from TTD and other databases. A Venn diagram of the components targets and cough targets was drawn to prelim determine the potential targets of the active ingredients of Laiyang Pear Cough Syrup in the treatment of cough. A PPI network was constructed and key targets were screened. The data were into Cytoscape 3.10.1 software, and a \"active component-disease target\" network was constructed, and key components were screened. The screened targets were subjected to GO enrichment analysis and KEGG pathway enrichment analysis. Molecular docking verification between key targets and core active ingredients was conducted using AutoDock Tools 1.5.6 software. A citric acid-induced guinea pig cough model was established. The cough latency and cough frequency were measured in the control and treatment groups, and the PI3K-AKT pathway predicted by network pharmacology was validated via Western blot analysis.</div></div><div><h3>Results</h3><div>43 active chemical components, 76 common targets, 591 GO biological processes, and 159 KEGG signaling pathways were screened out. The active components of Laiyang Pear Cough Syrup in the treatment of cough may be quercetin, stigmasterol, and luteolin, and the key may be IL-6, TNF, AKT1, IL-1β, and PTGS<sub>2</sub>, which mainly regulate the PI3K/AKT pathway to relieve cough. Molecular docking revealed that luteolin, quercetin, and stigmasterol as the key active ingredients in Laiyang Pear Cough Syrup bind to AKT1 with high affinities, displaying docking scores of −8.1, −8.0, and −7.7 kcal mol<sup>−1</sup>. These results indicate that the compounds may function as potent agonists to activate the PI3K-AKT signaling pathway. Laiyang Pear Cough Syrup can significantly prolong the cough latency period and reduce the number of coughs (compared with the control group, <em>P</em> &lt; 0.01 or 0.05), and down-regulate the expression of PI3K, p-PI3K, AKT, p-AKT proteins.</div></div><div><h3>Conclusion</h3><div>Laiyang Pear Cough Syrup can relieve cough through a variety of components, targets and pathways. Regulating the PI3K-AKT pathway may be its main mechanism of action.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"17 ","pages":"Article 100702"},"PeriodicalIF":0.0,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145321065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Role of traditional Chinese medicine in combating metabolic disorders: A systematic review 中医药在对抗代谢紊乱中的作用:系统综述
Pub Date : 2025-10-11 DOI: 10.1016/j.prmcm.2025.100703
Arpan Pathak , Mohit Agrawal , Pranshul Sethi , Kantrol Kumar Sahu , Monika Sharma , Hema Chaudhary , Devesh Kumar , Thakur Gurjeet Singh , Mohit Kumar

Introduction

Metabolic disorders, including type 2 diabetes, obesity, hyperuricemia, and MASLD, are increasing worldwide, and conventional therapies often have limited efficacy. Traditional Chinese Medicine (TCM), with its multi-targeted approach, shows promise as a complementary strategy.

Methods

A systematic literature search was conducted in PubMed and CNKI (1966–2024) using predefined keywords related to TCM, metabolic disorders, clinical trials, and mechanisms. Eligible studies were screened and synthesized according to PRISMA guidelines to evaluate pharmacological pathways and therapeutic outcomes.

Results

Numerous TCM studies, including those on berberine, ginsenosides, bavachinin, and resveratrol, as well as formulations such as Shenge Formula, Huangqin Decoction, and Zibu Piyin Formula, have demonstrated the ability to regulate AMPK, PPARα, SIRT1, PI3K/Akt, and NF-κB signalling pathways. These interventions improve insulin resistance, lipid metabolism, inflammation, oxidative stress, and hepatic steatosis, with most findings derived from in vitro and in vivo studies.

Conclusion

TCM holds significant therapeutic potential for managing a spectrum of metabolic disorders through multi-target interventions that act on multiple interconnected biological systems. While preclinical and some clinical data support the efficacy and safety of TCM, further well-designed randomized clinical trials and integrated omics-based research are necessary to elucidate precise mechanisms, standardize formulations, and validate long-term outcomes. Integration of TCM into modern metabolic therapy may offer novel strategies for personalized and holistic healthcare.
代谢性疾病,包括2型糖尿病、肥胖、高尿酸血症和MASLD,在世界范围内正在增加,而常规治疗通常疗效有限。传统中医(TCM)以其多目标的方法,显示出作为一种补充战略的希望。方法系统检索PubMed和中国知网(CNKI) 1966-2024年的相关文献,检索关键词为中医、代谢紊乱、临床试验和机制。根据PRISMA指南筛选和合成符合条件的研究,以评估药理学途径和治疗结果。结果大量的中药研究,包括小檗碱、人参皂苷、巴伐克苷、白藜芦醇,以及神格方、黄芩汤、补补补饮等方剂,已经证明其具有调节AMPK、ppr α、SIRT1、PI3K/Akt和NF-κB信号通路的能力。这些干预措施改善了胰岛素抵抗、脂质代谢、炎症、氧化应激和肝脂肪变性,大多数发现来自体外和体内研究。结论中医药通过作用于多个相互关联的生物系统的多靶点干预,在管理一系列代谢紊乱方面具有显著的治疗潜力。虽然临床前和一些临床数据支持中药的疗效和安全性,但需要进一步精心设计的随机临床试验和基于组学的综合研究来阐明确切的机制,规范配方,并验证长期结果。中医与现代代谢疗法的结合可能为个性化和整体医疗保健提供新的策略。
{"title":"Role of traditional Chinese medicine in combating metabolic disorders: A systematic review","authors":"Arpan Pathak ,&nbsp;Mohit Agrawal ,&nbsp;Pranshul Sethi ,&nbsp;Kantrol Kumar Sahu ,&nbsp;Monika Sharma ,&nbsp;Hema Chaudhary ,&nbsp;Devesh Kumar ,&nbsp;Thakur Gurjeet Singh ,&nbsp;Mohit Kumar","doi":"10.1016/j.prmcm.2025.100703","DOIUrl":"10.1016/j.prmcm.2025.100703","url":null,"abstract":"<div><h3>Introduction</h3><div>Metabolic disorders, including type 2 diabetes, obesity, hyperuricemia, and MASLD, are increasing worldwide, and conventional therapies often have limited efficacy. Traditional Chinese Medicine (TCM), with its multi-targeted approach, shows promise as a complementary strategy.</div></div><div><h3>Methods</h3><div>A systematic literature search was conducted in PubMed and CNKI (1966–2024) using predefined keywords related to TCM, metabolic disorders, clinical trials, and mechanisms. Eligible studies were screened and synthesized according to PRISMA guidelines to evaluate pharmacological pathways and therapeutic outcomes.</div></div><div><h3>Results</h3><div>Numerous TCM studies, including those on berberine, ginsenosides, bavachinin, and resveratrol, as well as formulations such as Shenge Formula, Huangqin Decoction, and Zibu Piyin Formula, have demonstrated the ability to regulate AMPK, PPARα, SIRT1, PI3K/Akt, and NF-κB signalling pathways. These interventions improve insulin resistance, lipid metabolism, inflammation, oxidative stress, and hepatic steatosis, with most findings derived from <em>in vitro and in vivo</em> studies.</div></div><div><h3>Conclusion</h3><div>TCM holds significant therapeutic potential for managing a spectrum of metabolic disorders through multi-target interventions that act on multiple interconnected biological systems. While preclinical and some clinical data support the efficacy and safety of TCM, further well-designed randomized clinical trials and integrated omics-based research are necessary to elucidate precise mechanisms, standardize formulations, and validate long-term outcomes. Integration of TCM into modern metabolic therapy may offer novel strategies for personalized and holistic healthcare.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"17 ","pages":"Article 100703"},"PeriodicalIF":0.0,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145321496","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Therapeutic potential of flavonoid-enriched Chinese medicinal herbs in atherosclerosis, hypertension, myocardial infarction, and heart failure 富含类黄酮的中草药对动脉粥样硬化、高血压、心肌梗死和心力衰竭的治疗潜力
Pub Date : 2025-10-01 DOI: 10.1016/j.prmcm.2025.100701
Dharshini Jaisankar, Suruthi Ramamoorthy, Jubilee Ramasamy

Introduction

CVDs such as atherosclerosis, hypertension, myocardial infarction, and heart failure, are the top cause of death worldwide. Due to the challenges with traditional therapies, interest in complementary treatments has increased. Research has found that TCM and its herbal constituents, rich in flavonoids, appear to have a positive effect on cardiovascular health due to several underlying mechanisms.

Methods

This review provides an overview of current clinical and experimental research on flavonoid-rich Chinese medicinal plants. The database includes PubMed, Scopus, Web of Science, and CNKI. Details include various cardiovascular diseases (CVD) types and their mechanism of action (including antioxidant, anti-inflammation, enhancement of endothelial function, and stabilization of mitochondria). It also features studies of several compounds in preclinical models and clinical trials, including quercetin and baicalin as key representatives. Significant portion pathways are PI3K/AKT, NF-κB, Nrf2/HO-1, eNOS and AMPK/mTOR. The comparative table highlights plants, pharmaceutical targets, and the impact of diseases.

Result

Evidence suggests that flavonoids from Chinese medicinal plants have a wide-ranging cardio-protective effect, regardless of the CVD model. The compounds possess potent antioxidant, anti-inflammatory, endothelial-enhancing, and lipid-regulatory effects. While recent clinical studies indicate improvements in blood pressure, lipid profiles, myocardial resilience, and endothelial function, results remain inconsistent due to small sample size, differences in extract composition, and variation in trial design.

Discussion

The use of Chinese medicinal herbs enriched in flavonoids can provide effective multi-pathway intervention against complex pathophysiological mechanisms, making them a valuable resource for cardiovascular therapy. Despite the obvious translational potential, shortcomings like poor bioavailability, phytochemical variability, and limited clinical trials are significant. These limitations continue to hinder clinical translation, and addressing them will be critical for broder therapeutic adoption. Future research should focus on improving the formulation, facilitating clinical standardization, and developing systems-level pharmacology to enable evidence-based use of flavonoid therapies in modern cardiovascular medicine.
心血管疾病,如动脉粥样硬化、高血压、心肌梗死和心力衰竭,是全世界最主要的死亡原因。由于传统疗法的挑战,对补充疗法的兴趣增加了。研究发现,中药及其富含类黄酮的草药成分似乎对心血管健康有积极的影响,这是由于几种潜在的机制。方法综述了近年来富含类黄酮的中药材的临床和实验研究进展。数据库包括PubMed、Scopus、Web of Science和CNKI。详细内容包括各种心血管疾病(CVD)类型及其作用机制(包括抗氧化、抗炎症、增强内皮功能和稳定线粒体)。以槲皮素和黄芩苷为主要代表,对几种化合物进行了临床前模型和临床试验研究。PI3K/AKT、NF-κB、Nrf2/HO-1、eNOS和AMPK/mTOR通路占显著比例。比较表突出了植物、药物靶点和疾病的影响。结果有证据表明,无论心血管疾病模型如何,中草药类黄酮都具有广泛的心脏保护作用。这些化合物具有有效的抗氧化、抗炎、内皮增强和脂质调节作用。虽然最近的临床研究表明血压、血脂、心肌恢复力和内皮功能有所改善,但由于样本量小、提取物成分不同以及试验设计的差异,结果仍然不一致。富含黄酮类化合物的中草药可对复杂的病理生理机制提供有效的多途径干预,是心血管治疗的宝贵资源。尽管有明显的转化潜力,但生物利用度差、植物化学变异性和有限的临床试验等缺点是显著的。这些限制继续阻碍临床转化,解决它们对于更广泛的治疗采用至关重要。未来的研究应着眼于改进黄酮类药物的处方,促进临床标准化,发展系统级药理学,使黄酮类药物在现代心血管医学中的循证应用成为可能。
{"title":"Therapeutic potential of flavonoid-enriched Chinese medicinal herbs in atherosclerosis, hypertension, myocardial infarction, and heart failure","authors":"Dharshini Jaisankar,&nbsp;Suruthi Ramamoorthy,&nbsp;Jubilee Ramasamy","doi":"10.1016/j.prmcm.2025.100701","DOIUrl":"10.1016/j.prmcm.2025.100701","url":null,"abstract":"<div><h3>Introduction</h3><div>CVDs such as atherosclerosis, hypertension, myocardial infarction, and heart failure, are the top cause of death worldwide. Due to the challenges with traditional therapies, interest in complementary treatments has increased. Research has found that TCM and its herbal constituents, rich in flavonoids, appear to have a positive effect on cardiovascular health due to several underlying mechanisms.</div></div><div><h3>Methods</h3><div>This review provides an overview of current clinical and experimental research on flavonoid-rich Chinese medicinal plants. The database includes PubMed, Scopus, Web of Science, and CNKI. Details include various cardiovascular diseases (CVD) types and their mechanism of action (including antioxidant, anti-inflammation, enhancement of endothelial function, and stabilization of mitochondria). It also features studies of several compounds in preclinical models and clinical trials, including quercetin and baicalin as key representatives. Significant portion pathways are PI3K/AKT, NF-κB, Nrf2/HO-1, eNOS and AMPK/mTOR. The comparative table highlights plants, pharmaceutical targets, and the impact of diseases.</div></div><div><h3>Result</h3><div>Evidence suggests that flavonoids from Chinese medicinal plants have a wide-ranging cardio-protective effect, regardless of the CVD model. The compounds possess potent antioxidant, anti-inflammatory, endothelial-enhancing, and lipid-regulatory effects. While recent clinical studies indicate improvements in blood pressure, lipid profiles, myocardial resilience, and endothelial function, results remain inconsistent due to small sample size, differences in extract composition, and variation in trial design.</div></div><div><h3>Discussion</h3><div>The use of Chinese medicinal herbs enriched in flavonoids can provide effective multi-pathway intervention against complex pathophysiological mechanisms, making them a valuable resource for cardiovascular therapy. Despite the obvious translational potential, shortcomings like poor bioavailability, phytochemical variability, and limited clinical trials are significant. These limitations continue to hinder clinical translation, and addressing them will be critical for broder therapeutic adoption. Future research should focus on improving the formulation, facilitating clinical standardization, and developing systems-level pharmacology to enable evidence-based use of flavonoid therapies in modern cardiovascular medicine.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"17 ","pages":"Article 100701"},"PeriodicalIF":0.0,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145268679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Pharmacological Research - Modern Chinese Medicine
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