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Targeting B-raf/MEK signaling in melanocytic carcinoma using HPLC-MS/MS characterized metabolites from Valeriana wallichii Rhizome 利用高效液相色谱-质谱联用技术对黑素细胞癌中B-raf/MEK信号通路进行表征
Pub Date : 2025-08-14 DOI: 10.1016/j.prmcm.2025.100674
Charushila V. Balikai , Raviraj M. Kulkarni , Kiran Thabaj , Shankar Gharge , Rohini S. Kavalapure , Shyam S. Desai
Valeriana wallichii (mǎ lù róng cǎo), a traditional medicinal herb native to southwestern China, holds promise as a source of novel anticancer agents. This study explores its therapeutic potential against A375 human melanoma cells through an integrated in silico, in vitro pharmacological approach. High-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) profiling of the ultrasonication-assisted hydroalcoholic extract identified key phytoconstituents, notably chlorogenic acid and quinic acid. Network pharmacology analysis linked these metabolites to critical signaling pathways involved in skin cancer progression, particularly the MAPK, PI3K-Akt, and Ras pathways. Target prediction and protein interaction networks further revealed modulation of key nodes such as BRAF and MEK. Molecular docking highlighted strong binding affinities of chlorogenic acid at the ATP-binding domains of both BRAF (CYS532, ASP594, LYS483, GLY534) and MEK (SER150, ALA95), with interaction energies comparable to reference inhibitors dabrafenib and DS03090629. Molecular dynamics simulations (100 ns) confirmed the stable occupation of these active sites by chlorogenic acid, supporting its potential as a dual BRAF/MEK inhibitor. ADME predictions revealed favorable drug-like properties for the major compounds. In vitro cytotoxicity assays on A375 melanoma cells demonstrated significant antiproliferative effects of the V. wallichii extract obtained via ultrasonication (IC₅₀ = 172.8 ± 1.07 μg/mL), with scanning electron microscopy indicating enhanced cell membrane disruption, likely due to improved bioactive extraction efficiency. Collectively, these findings underscore the potential of Valeriana wallichii rhizome metabolites, particularly chlorogenic acid, as multitargeted therapeutic agents in melanocytic carcinoma. This study provides scientific validation for the traditional use of V. wallichii in Chinese medicine and lays the groundwork for its development as a modern pharmacological intervention targeting BRAF/MEK signaling in skin cancer.
Valeriana wallichii (mjilù róng cǎo)是一种原产于中国西南部的传统草药,有望成为新型抗癌药物的来源。本研究通过集成的计算机体外药理学方法探索其对A375人黑色素瘤细胞的治疗潜力。高效液相色谱-串联质谱(HPLC-MS/MS)分析了超声辅助水醇提取物的主要植物成分,特别是绿原酸和奎宁酸。网络药理学分析将这些代谢物与参与皮肤癌进展的关键信号通路联系起来,特别是MAPK、PI3K-Akt和Ras通路。靶标预测和蛋白质相互作用网络进一步揭示了BRAF和MEK等关键节点的调节。分子对接显示,绿原酸在BRAF (CYS532、ASP594、LYS483、GLY534)和MEK (SER150、ALA95)的atp结合域具有很强的结合亲和力,其相互作用能与参比抑制剂dabrafenib和DS03090629相当。分子动力学模拟(100 ns)证实绿原酸稳定占据这些活性位点,支持其作为BRAF/MEK双抑制剂的潜力。ADME预测显示主要化合物具有良好的药物样性质。对A375黑色素瘤细胞的体外细胞毒性试验表明,通过超声波获得的V. wallichii提取物(IC₅₀= 172.8±1.07 μg/mL)具有显着的抗增殖作用,扫描电镜显示细胞膜破坏增强,可能是由于生物活性提取效率的提高。总的来说,这些发现强调了缬草根茎代谢物,特别是绿原酸作为黑色素细胞癌多靶点治疗药物的潜力。本研究为华里草的传统中药应用提供了科学验证,为其作为靶向BRAF/MEK信号通路的现代药物干预皮肤癌的研究奠定了基础。
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引用次数: 0
Hibiscus rosa-sinensis flower extract-mediated fabrication of zinc oxide nanoparticles, characterization and its antimicrobial activity 芙蓉花提取物介导氧化锌纳米颗粒的制备、表征及其抑菌活性
Pub Date : 2025-08-09 DOI: 10.1016/j.prmcm.2025.100673
Komal Thakur , Avneet Kaur

Introduction

Hibiscus rosa-sinensis commonly known as Zhū Jǐn Huā' (朱槿花) which is widely beings used in Traditional Chinese Medicine (TCM) in the form of herbal preparations and decoctions for the ailment of inflammations, skin infections, and gynecological disorders. Zhū Jǐn Huā' (朱槿花) is well known for its good phytochemicals composition including anthocyanins, flavonoids and other bioactive components making it a promising choice for linking traditional Chinese medical knowledge with modern nanotechnology.

Method

ZnO NPs (Zinc oxide nanoparticles) were fabricated following simple chemical precipitation method using aqueous flower extract (Hibiscus rosa-sinensis). Phytochemical screening of flower extract was done to identify bioactive components. Fabricated nanoparticles were characterized through Scanning Electron Microscopy (SEM), Transmission electron Microscopy (TEM), Energy Dispersive Spectroscopy (EDS), X-ray Diffraction (XRD), and Fourier-Transform Infrared Spectroscopy (FT-IR) to analyze their morphology, size, crystallinity, and elemental composition. Further, antimicrobial activity was evaluated against Escherichia coli and Rhizopus species.

Results

Phytochemical analysis of studied flower extract confirmed the presence of flavanone, coumarins, flavonoids, steroids, and anthocyanins in the flower extract. Characterization results demonstrated that the ZnO NPs were crystalline with an average size ranging from 7 to 14 nm, as revealed by XRD analysis. EDS confirmed the elemental composition of the nanoparticles. Antimicrobial assay observation indicates a good antibacterial and antifungal activity in fabricated ZnO NPs against E. coli and Rhizopus species, respectively.

Discussion

The present work revealed the successful green synthesis of ZnO NPs using H. rosa-sinensis flower extract and highlights the potential of its specific bioactive components documented in traditional Chinese medicine. The nanoparticles exhibited desirable properties with a good antimicrobial potential, suggesting their potential application in biomedical and environmental fields.
芙蓉(hibiscus rosa-sinensis),俗称zhu Jǐn花ā'(槿),广泛用于中药制剂和煎剂,用于炎症、皮肤感染和妇科疾病。花草Jǐn(槿)以其良好的植物化学成分而闻名,包括花青素、黄酮类化合物和其他生物活性成分,使其成为将传统中医知识与现代纳米技术联系起来的有希望的选择。方法以芙蓉花水提取物为原料,采用简单化学沉淀法制备氧化锌纳米粒子。对花提取物进行了植物化学筛选,以确定其生物活性成分。通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、能谱(EDS)、x射线衍射(XRD)和傅里叶变换红外光谱(FT-IR)对制备的纳米颗粒进行表征,分析其形貌、尺寸、结晶度和元素组成。此外,还对大肠杆菌和根霉进行了抑菌活性评价。结果花提取物的植物化学分析证实,花提取物中含有黄酮、香豆素、黄酮类化合物、类固醇和花青素。表征结果表明,ZnO纳米粒子呈结晶状,XRD分析表明ZnO纳米粒子的平均尺寸为7 ~ 14 nm。能谱仪证实了纳米颗粒的元素组成。抑菌实验结果表明,制备的氧化锌NPs分别对大肠杆菌和根霉具有良好的抑菌和抑菌活性。本研究揭示了用紫红花提取物成功绿色合成氧化锌NPs的方法,并强调了其在传统中药中具有特殊生物活性成分的潜力。纳米颗粒表现出良好的抗菌性能,在生物医学和环境领域具有潜在的应用前景。
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引用次数: 0
Neuroprotective potential of Hesperidin in Alcohol withdrawal syndrome: A preclinical study in Swiss albino mice 橙皮苷对酒精戒断综合征的神经保护作用:瑞士白化小鼠的临床前研究
Pub Date : 2025-08-08 DOI: 10.1016/j.prmcm.2025.100671
Ramsha Mehdiya , Zeenath Banu , M. Sumakanth
Background: Hesperidin (Chinese: 橙皮苷, Chéng pí gān) is a bioflavonoid primarily found in citrus fruits such as oranges and tangerines. It has been used for centuries in Traditional Chinese Medicine (TCM) as a key active component of Citri reticulatae Pericarpium (陈皮, Chénpí) and Aurantii fructus immaturus (枳实, Zhǐshí), which are traditionally employed to treat digestive disorders, circulatory problems, and respiratory ailments. These herbs are well-established in classical TCM formulations and have recently been included in Chinese guidelines for epidemic management, highlighting hesperidin’s broad therapeutic potential. Modern studies have demonstrated hesperidin’s strong antioxidant, anti-inflammatory, neuroprotective, and hepatoprotective effects. Owing to these properties, hesperidin has gained interest as a natural therapeutic candidate for neuropsychiatric conditions such as alcohol withdrawal syndrome (AWS). Accordingly, this study aimed to assess the efficacy of hesperidin in alleviating behavioral and biochemical alterations in a murine model of AWS.

Methods

Thirty male Swiss albino mice (n = 6 per group) were randomly divided into five groups. Four groups received a modified liquid diet (MLD) containing ethanol for 21 days to induce alcohol dependence, while the control group received an ethanol-free MLD. Upon ethanol withdrawal, mice were treated for 48 h with hesperidin (50 mg/kg or 100 mg/kg, orally) or diazepam (1 mg/kg, intraperitoneally), serving as the reference standard. Behavioral evaluations were conducted at 6th, 24th, and 48th h post-withdrawal using the elevated plus maze, open field test (for anxiety), forced swim and tail suspension tests (for depression), actophotometer (for locomotor activity), and hot plate and tail immersion tests (for nociception). Biochemical analyses included estimation of brain antioxidant enzymes such as, superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH), and liver enzymes like aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP).

Results

Hesperidin produced statistically significant improvements in anxiety- and depression-like behaviors, locomotor activity, nociceptive responses, brain antioxidant status, and hepatic enzyme levels compared to the ethanol withdrawal group.

Conclusion

Hesperidin alleviated behavioral, biochemical, and histopathological alterations associated with AWS in this study. Although the results indicate potential neuroprotective and hepatoprotective effects that may involve antioxidant mechanisms, these findings are preliminary. Comprehensive pharmacological and mechanistic studies are warranted to confirm its therapeutic relevance in AWS management.
背景:橙皮苷(中文:苷,pí gān)是一种生物类黄酮,主要存在于柑橘类水果中,如橙子和橘子。几个世纪以来,它一直被用于中医(TCM),作为柑橘皮(Chénpí)和枳实(枳嘟嘟的,Zhǐshí)的关键活性成分,传统上用于治疗消化系统疾病,循环系统问题和呼吸系统疾病。这些草药在经典的中医配方中得到了证实,最近已被纳入中国流行病管理指南,突出了橙皮苷广泛的治疗潜力。现代研究已经证明橙皮苷具有很强的抗氧化、抗炎、神经保护和肝脏保护作用。由于这些特性,橙皮苷作为神经精神疾病如酒精戒断综合征(AWS)的天然治疗候选者获得了兴趣。因此,本研究旨在评估橙皮苷减轻小鼠AWS模型行为和生化改变的功效。方法雄性瑞士白化小鼠30只,每组6只,随机分为5组。4组小鼠连续21天给予含乙醇的改良液体日粮(MLD)诱导酒精依赖,对照组小鼠连续21天给予不含乙醇的改良液体日粮。乙醇退出后,小鼠以橙皮苷(50 mg/kg或100 mg/kg,口服)或地西泮(1 mg/kg,腹腔注射)作为参比标准48 h。在戒断后第6、24和48小时进行行为评估,采用高架加迷宫、空地测试(焦虑测试)、强迫游泳和悬尾测试(抑郁测试)、视压计(运动活动测试)和热板和尾巴浸入测试(伤害感受测试)。生化分析包括脑抗氧化酶,如超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽(GSH),肝酶,如天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和碱性磷酸酶(ALP)。结果与乙醇戒断组相比,橙皮苷在焦虑和抑郁样行为、运动活动、伤害反应、大脑抗氧化状态和肝酶水平方面具有统计学意义的改善。结论橙皮苷减轻了与AWS相关的行为、生化和组织病理学改变。虽然结果表明潜在的神经保护和肝脏保护作用可能涉及抗氧化机制,但这些发现是初步的。全面的药理学和机制研究是必要的,以确认其治疗相关性的AWS管理。
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引用次数: 0
Aqueous extract of Hibiscus sabdariffa calyces offers neuroprotection against unpredictable chronic mild stress-induced neurobehavioral disorders and biochemical perturbations in male Swiss mice 芙蓉花萼水提物对瑞士雄性小鼠的慢性轻度应激性神经行为障碍和生化扰动具有神经保护作用
Pub Date : 2025-07-26 DOI: 10.1016/j.prmcm.2025.100665
Valiant Orodeh Adeoye , Abayomi Mayowa Ajayi , Peter Oghenebrorhie Orodeh , Joseph Chimezie , Love Enebeli , Paul Ademola Adeleke , Olatunde Owoeye , Solomon Umukoro

Introduction

Hibiscus sabdariffa (commonly known as roselle or Chinese rose tea) is widely known for its soothing effects, particularly during prolonged stress. In Traditional Chinese Medicine (TCM), it is valued for its therapeutic benefits, including antihypertensive, anti-inflammatory, and hepatoprotective effects. This study explores the neuroprotective potential of the aqueous extract of H. sabdariffa calyces (AEHS) in mitigating stress-induced neurobehavioral and biochemical changes in mice subjected to unpredictable chronic mild stress (UCMS).

Methods

Thirty male Swiss mice were randomly assigned to five groups (n = 6) and treated orally. Groups 1 (control) and 2 (UCMS-control) received distilled water, whereas group 3–5 received AEHS at doses of 50, 100, and 200 mg/kg, respectively. Group 2–5 were subjected to unpredictable chronic mild stress (UCMS) daily for 21 days. The neurobehavioral assessments including locomotor activity, memory, anxiety and depressive-like behaviors conducted on days 20 and 21. On day 22, blood glucose and serum corticosterone levels were analyzed alongside oxidative stress biomarkers, nitrites, pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6), and serotonin levels in the prefrontal cortex, amygdala, and hippocampus. The brain-derived neurotrophic factor (BDNF), nuclear factor kappa B (NF-κB), cyclic adenosine monophosphate (cAMP)-response element binding protein (CREB), and nuclear factor erythroid 2-related factor 2 (Nrf2) were evaluated. The enzymatic activities of acetylcholinesterase (AChE) and glutamic acid decarboxylase (GAD) as well as the histomorphological changes in the brain regions were also assessed.

Results

AEHS effectively modulated UCMS-induced neurobehavioral disorders, along with elevated blood glucose and plasma corticosterone levels. The extract mitigated UCMS-induced increases in malondialdehyde (MDA), nitrites, pro-inflammatory cytokines, NF-κB, and AChE. Additionally, AEHS restored the diminished levels of glutathione, catalase, superoxide dismutase, CREB, BDNF, Nrf2, serotonin, and GAD activity within the brain regions. Furthermore, AEHS ameliorated UCMS-induced histomorphological alterations in the brain.

Discussion/Conclusion

This study demonstrated that AEHS confers neuroprotection against chronic stress-induced neurobehavioral disorders, biochemical and histomorphological alterations by enhancing antioxidant defenses and modulating key signaling pathways, including BDNF, CREB, Nrf2 and NF-κB. These findings underscore the potential therapeutic applications of AEHS in mitigating chronic stress-related psychiatric disturbances within the framework of TCM.
芙蓉花茶(俗称玫瑰花茶或中国玫瑰花茶)因其舒缓作用而广为人知,特别是在长时间的压力下。在传统中医(TCM)中,它因其治疗益处而受到重视,包括抗高血压、抗炎和保护肝脏的作用。本研究探讨了沙达尼花萼水提物(AEHS)在缓解不可预测的慢性轻度应激(UCMS)小鼠应激诱导的神经行为和生化变化中的神经保护作用。方法30只雄性瑞士小鼠随机分为5组(n = 6),均给予口服治疗。1组(对照组)和2组(ucms -对照组)给予蒸馏水,3-5组分别给予剂量为50、100和200 mg/kg的AEHS。2 ~ 5组每天进行不可预测的慢性轻度应激(UCMS),持续21 d。在第20天和第21天进行神经行为评估,包括运动活动、记忆、焦虑和抑郁样行为。第22天,分析血糖和血清皮质酮水平以及氧化应激生物标志物、亚硝酸盐、促炎细胞因子(肿瘤坏死因子- α和白细胞介素-6)和前额皮质、杏仁核和海马中的血清素水平。检测脑源性神经营养因子(BDNF)、核因子κB (NF-κB)、环磷酸腺苷(cAMP)反应因子结合蛋白(CREB)、核因子红细胞2相关因子2 (Nrf2)。测定大鼠脑区乙酰胆碱酯酶(AChE)和谷氨酸脱羧酶(GAD)活性及组织形态学变化。结果saehs可有效调节ucms诱导的神经行为障碍,并可提高血糖和血浆皮质酮水平。该提取物减轻了ucms诱导的丙二醛(MDA)、亚硝酸盐、促炎细胞因子、NF-κB和AChE的升高。此外,AEHS恢复了大脑区域内谷胱甘肽、过氧化氢酶、超氧化物歧化酶、CREB、BDNF、Nrf2、血清素和广泛性焦虑症活性的降低水平。此外,AEHS改善了ucms诱导的脑组织形态学改变。讨论/结论本研究表明,AEHS通过增强抗氧化防御和调节BDNF、CREB、Nrf2和NF-κB等关键信号通路,对慢性应激性神经行为障碍、生化和组织形态学改变具有神经保护作用。这些发现强调了AEHS在中医框架内缓解慢性应激相关精神障碍方面的潜在治疗应用。
{"title":"Aqueous extract of Hibiscus sabdariffa calyces offers neuroprotection against unpredictable chronic mild stress-induced neurobehavioral disorders and biochemical perturbations in male Swiss mice","authors":"Valiant Orodeh Adeoye ,&nbsp;Abayomi Mayowa Ajayi ,&nbsp;Peter Oghenebrorhie Orodeh ,&nbsp;Joseph Chimezie ,&nbsp;Love Enebeli ,&nbsp;Paul Ademola Adeleke ,&nbsp;Olatunde Owoeye ,&nbsp;Solomon Umukoro","doi":"10.1016/j.prmcm.2025.100665","DOIUrl":"10.1016/j.prmcm.2025.100665","url":null,"abstract":"<div><h3>Introduction</h3><div><em>Hibiscus sabdariffa</em> (commonly known as roselle or Chinese rose tea) is widely known for its soothing effects, particularly during prolonged stress. In Traditional Chinese Medicine (TCM), it is valued for its therapeutic benefits, including antihypertensive, anti-inflammatory, and hepatoprotective effects. This study explores the neuroprotective potential of the aqueous extract of <em>H. sabdariffa</em> calyces (AEHS) in mitigating stress-induced neurobehavioral and biochemical changes in mice subjected to unpredictable chronic mild stress (UCMS).</div></div><div><h3>Methods</h3><div>Thirty male Swiss mice were randomly assigned to five groups (<em>n</em> = 6) and treated orally. Groups 1 (control) and 2 (UCMS-control) received distilled water, whereas group 3–5 received AEHS at doses of 50, 100, and 200 mg/kg, respectively. Group 2–5 were subjected to unpredictable chronic mild stress (UCMS) daily for 21 days. The neurobehavioral assessments including locomotor activity, memory, anxiety and depressive-like behaviors conducted on days 20 and 21. On day 22, blood glucose and serum corticosterone levels were analyzed alongside oxidative stress biomarkers, nitrites, pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6), and serotonin levels in the prefrontal cortex, amygdala, and hippocampus. The brain-derived neurotrophic factor (BDNF), nuclear factor kappa B (NF-κB), cyclic adenosine monophosphate (cAMP)-response element binding protein (CREB), and nuclear factor erythroid 2-related factor 2 (Nrf2) were evaluated. The enzymatic activities of acetylcholinesterase (AChE) and glutamic acid decarboxylase (GAD) as well as the histomorphological changes in the brain regions were also assessed.</div></div><div><h3>Results</h3><div>AEHS effectively modulated UCMS-induced neurobehavioral disorders, along with elevated blood glucose and plasma corticosterone levels. The extract mitigated UCMS-induced increases in malondialdehyde (MDA), nitrites, pro-inflammatory cytokines, NF-κB, and AChE. Additionally, AEHS restored the diminished levels of glutathione, catalase, superoxide dismutase, CREB, BDNF, Nrf2, serotonin, and GAD activity within the brain regions. Furthermore, AEHS ameliorated UCMS-induced histomorphological alterations in the brain.</div></div><div><h3>Discussion/Conclusion</h3><div>This study demonstrated that AEHS confers neuroprotection against chronic stress-induced neurobehavioral disorders, biochemical and histomorphological alterations by enhancing antioxidant defenses and modulating key signaling pathways, including BDNF, CREB, Nrf2 and NF-κB. These findings underscore the potential therapeutic applications of AEHS in mitigating chronic stress-related psychiatric disturbances within the framework of TCM.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100665"},"PeriodicalIF":0.0,"publicationDate":"2025-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144756939","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
Harnessing traditional chinese medicine for wound healing and modern wound models: An overview 中医药治疗创面愈合与现代创面模型:综述
Pub Date : 2025-07-23 DOI: 10.1016/j.prmcm.2025.100664
Vishwjeet Singh , Singh Khushbu Ravindranath , Harishchandra Verma , Shivang Shukla , Anjali Rai , Tejas Patani , Triveni Mishra , Anuradha Mishra , Ramesh Kumar Gupta

Introduction

This study delves into the intricate dynamics of wound healing, emphasizing the critical role of various wound healing models in advancing therapeutic interventions and the use of various Chinese medicines used in wound treatment. These models, ranging from abrasions to incision and dead space wound models, provide invaluable insights into chronic wounds like venous leg ulcers and diabetic foot ulcers.

Methods

A systematic literature search was conducted using PubMed, Scopus, Web of Science, and Google Scholar to identify studies published between 1994 and 2023 on the use of Traditional Chinese Medicines (TCMs) in wound healing. A total of 196 articles were retrieved, of which 161 were selected based on relevance, experimental evidence, and mechanistic insights. The review emphasizes TCM-based formulations evaluated in in vivo, in vitro, and preclinical models, with a focus on their therapeutic roles and underlying molecular pathways in skin repair and regeneration.

Results

Animal models, despite not perfectly replicating human chronic wounds, have been instrumental in studying wound healing mechanisms, particularly the inflammatory phase and factors like bacterial biofilms. The exploration of apoptosis and extracellular matrix alterations within these models sheds light on crucial cellular and molecular events essential for wound closure. Additionally, the article discusses models for burn wounds, skin aging, blister wounds, and back punch wounds, highlighting their significance in understanding wound pathophysiology and testing treatment efficacy. Furthermore, traditional remedies like Shiunko and Wuwei Xiaodu Yin are explored for their therapeutic properties in promoting granulation tissue formation, wound healing, and anti-inflammatory effects.

Conclusion

Overall, the study underscores the importance of these diverse wound healing models in unraveling the complexities of tissue repair and guiding the development of effective treatments for various types of wounds using Chinese medicine.

Significance statement

This article highlights the critical role of diverse wound healing models in advancing therapeutic interventions, particularly in studying chronic wounds and evaluating the efficacy of Chinese medicinal plant-based treatments. This study provides insights into wound pathophysiology, inflammation, and tissue repair mechanisms by analyzing various models, including burns, abrasions, and incisions, emphasizing the potential of traditional remedies like Shiunko and Wuwei Xiaodu Yin in promoting wound healing.
本研究深入探讨了伤口愈合的复杂动力学,强调了各种伤口愈合模型在推进治疗干预和各种中药在伤口治疗中的应用中的关键作用。这些模型,从擦伤到切口和死腔伤口模型,为静脉性腿部溃疡和糖尿病足溃疡等慢性伤口提供了宝贵的见解。方法采用PubMed、Scopus、Web of Science、b谷歌Scholar等数据库系统检索1994 ~ 2023年发表的有关中药在创面愈合中的应用的文献。共检索了196篇文章,其中161篇是根据相关性、实验证据和机制见解选择的。这篇综述强调了基于中药的制剂在体内、体外和临床前模型中的评估,重点是它们在皮肤修复和再生中的治疗作用和潜在的分子途径。结果尽管动物模型不能完美地复制人类慢性伤口,但在研究伤口愈合机制,特别是炎症期和细菌生物膜等因素方面具有重要意义。在这些模型中对细胞凋亡和细胞外基质改变的探索揭示了伤口愈合所必需的关键细胞和分子事件。此外,本文还讨论了烧伤创面、皮肤老化创面、水疱创面和背击创面的模型,强调了它们对了解创面病理生理和检验治疗效果的意义。此外,传统的药物如熏子和五味消毒饮在促进肉芽组织形成、伤口愈合和抗炎作用方面的治疗特性也被探索出来。总之,本研究强调了这些不同的伤口愈合模型在揭示组织修复的复杂性和指导开发有效的中药治疗各种类型伤口方面的重要性。本文强调了不同的伤口愈合模式在推进治疗干预方面的关键作用,特别是在研究慢性伤口和评估中药植物治疗的疗效方面。本研究通过对烧伤、擦伤、切口等多种模型的分析,对创面病理生理、炎症及组织修复机制进行了深入的研究,并强调了熏子、五味消毒饮等传统疗法在促进创面愈合方面的潜力。
{"title":"Harnessing traditional chinese medicine for wound healing and modern wound models: An overview","authors":"Vishwjeet Singh ,&nbsp;Singh Khushbu Ravindranath ,&nbsp;Harishchandra Verma ,&nbsp;Shivang Shukla ,&nbsp;Anjali Rai ,&nbsp;Tejas Patani ,&nbsp;Triveni Mishra ,&nbsp;Anuradha Mishra ,&nbsp;Ramesh Kumar Gupta","doi":"10.1016/j.prmcm.2025.100664","DOIUrl":"10.1016/j.prmcm.2025.100664","url":null,"abstract":"<div><h3>Introduction</h3><div>This study delves into the intricate dynamics of wound healing, emphasizing the critical role of various wound healing models in advancing therapeutic interventions and the use of various Chinese medicines used in wound treatment. These models, ranging from abrasions to incision and dead space wound models, provide invaluable insights into chronic wounds like venous leg ulcers and diabetic foot ulcers.</div></div><div><h3>Methods</h3><div>A systematic literature search was conducted using PubMed, Scopus, Web of Science, and Google Scholar to identify studies published between 1994 and 2023 on the use of Traditional Chinese Medicines (TCMs) in wound healing. A total of 196 articles were retrieved, of which 161 were selected based on relevance, experimental evidence, and mechanistic insights. The review emphasizes TCM-based formulations evaluated in <em>in vivo, in vitro</em>, and preclinical models, with a focus on their therapeutic roles and underlying molecular pathways in skin repair and regeneration.</div></div><div><h3>Results</h3><div>Animal models, despite not perfectly replicating human chronic wounds, have been instrumental in studying wound healing mechanisms, particularly the inflammatory phase and factors like bacterial biofilms. The exploration of apoptosis and extracellular matrix alterations within these models sheds light on crucial cellular and molecular events essential for wound closure. Additionally, the article discusses models for burn wounds, skin aging, blister wounds, and back punch wounds, highlighting their significance in understanding wound pathophysiology and testing treatment efficacy. Furthermore, traditional remedies like Shiunko and Wuwei Xiaodu Yin are explored for their therapeutic properties in promoting granulation tissue formation, wound healing, and anti-inflammatory effects.</div></div><div><h3>Conclusion</h3><div>Overall, the study underscores the importance of these diverse wound healing models in unraveling the complexities of tissue repair and guiding the development of effective treatments for various types of wounds using Chinese medicine.</div></div><div><h3>Significance statement</h3><div>This article highlights the critical role of diverse wound healing models in advancing therapeutic interventions, particularly in studying chronic wounds and evaluating the efficacy of Chinese medicinal plant-based treatments. This study provides insights into wound pathophysiology, inflammation, and tissue repair mechanisms by analyzing various models, including burns, abrasions, and incisions, emphasizing the potential of traditional remedies like Shiunko and Wuwei Xiaodu Yin in promoting wound healing.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100664"},"PeriodicalIF":0.0,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144763936","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
Machine learning-driven discovery of STAT3 as a pivotal target for Wen-Wei-San-Ji formula in chronic atrophic gastritis therapy 机器学习驱动下发现STAT3作为温胃散胃方治疗慢性萎缩性胃炎的关键靶点
Pub Date : 2025-07-20 DOI: 10.1016/j.prmcm.2025.100663
Tingting Huang , Lu Wang , Mengru Dou , Jia Guo , Kaihua Long , Yuan Wang , Yang Liu , Bo Wang , Weijian Zhao , Shanrong Han , Jingyi Bai , Xinli Wen , Ye Li , Yuxi Liu , Hong Zhang

Background

Wen-Wei-San-Ji Formula (WWSJ) is a Traditional Chinese medicine (TCM) formula used in treatment of chronic atrophic gastritis (CAG), demonstrating significant clinical efficacy. However, its specific mechanism of action remains unclear. This study investigates the molecular mechanisms and active components of WWSJ for CAG by employing network pharmacology, machine learning, and molecular docking, complemented by experimental validation.

Methods

Active compounds and targets of WWSJ were screened using TCMSP and Uniprot databases, while targets for CAG were collected from GeneCards and OMIM databases. Protein-protein-interaction and herb-compound-target networks were constructed using by STRING and Cytoscape. Functional enrichment was performed with DAVID. Machine learning (PCA/LASSO/RF) identified core targets from GEO data. In molecular docking studies, AutoDock Vina was used to evaluate binding activity. In vitro and in vivo experiments were conducted to validate the results.

Results

A total of 53 active ingredients with (OB)≥30% and (DL)≥0.1 from WWSJ were selected. Targets of the formula (1657) and CAG disease (923) were screened, resulting in the identification of 207 common targets. Functional analysis of WWSJ by GO and KEGG revealed 742 Biological Processes (BP), 85 Cellular Components (CC), 116 Molecular Functions (MF), and 149 signaling pathways associated with CAG. Additionally, 5 core genes were identified through machine learning and molecular docking. The compounds demonstrated strong binding affinity with the target proteins, especially STAT3. Therefore, we hypothesized that WWSJ can treat CAG through inhibiting STAT3 signaling. Results of cell and animal experiments indicated that WWSJ is effective in the treatment of CAG through the inhibition of STAT3.

Conclusion

Integrated network pharmacology predictions and machine learning optimization identified STAT3 as the primary therapeutic target of WWSJ. Experimental studies confirmed that WWSJ alleviates CAG by suppressing STAT3 phosphorylation.
温胃散积方(WWSJ)是治疗慢性萎缩性胃炎(CAG)的中药方剂,临床疗效显著。然而,其具体作用机制尚不清楚。本研究采用网络药理学、机器学习、分子对接等方法,结合实验验证,探讨了WWSJ对CAG的分子机制和活性成分。方法利用TCMSP和Uniprot数据库筛选WWSJ的活性化合物和靶点,从GeneCards和OMIM数据库筛选CAG的靶点。利用STRING和Cytoscape构建蛋白-蛋白相互作用网络和中草药-化合物-靶点网络。用DAVID进行功能富集。机器学习(PCA/LASSO/RF)从GEO数据中识别核心目标。在分子对接研究中,AutoDock Vina用于评价结合活性。通过体外和体内实验对结果进行验证。结果共筛选出53种有效成分,其中(OB)≥30%,(DL)≥0.1。对公式靶点(1657)和CAG病靶点(923)进行筛选,共鉴定出207个共同靶点。通过GO和KEGG对WWSJ进行功能分析,发现742个生物过程(BP)、85个细胞成分(CC)、116个分子功能(MF)和149个信号通路与CAG相关。此外,通过机器学习和分子对接鉴定出5个核心基因。这些化合物与靶蛋白具有较强的结合亲和力,尤其是与STAT3。因此,我们假设WWSJ可以通过抑制STAT3信号传导来治疗CAG。细胞和动物实验结果表明,WWSJ通过抑制STAT3对CAG有治疗作用。结论综合网络药理学预测和机器学习优化确定STAT3为WWSJ的主要治疗靶点。实验研究证实,WWSJ通过抑制STAT3磷酸化来缓解CAG。
{"title":"Machine learning-driven discovery of STAT3 as a pivotal target for Wen-Wei-San-Ji formula in chronic atrophic gastritis therapy","authors":"Tingting Huang ,&nbsp;Lu Wang ,&nbsp;Mengru Dou ,&nbsp;Jia Guo ,&nbsp;Kaihua Long ,&nbsp;Yuan Wang ,&nbsp;Yang Liu ,&nbsp;Bo Wang ,&nbsp;Weijian Zhao ,&nbsp;Shanrong Han ,&nbsp;Jingyi Bai ,&nbsp;Xinli Wen ,&nbsp;Ye Li ,&nbsp;Yuxi Liu ,&nbsp;Hong Zhang","doi":"10.1016/j.prmcm.2025.100663","DOIUrl":"10.1016/j.prmcm.2025.100663","url":null,"abstract":"<div><h3>Background</h3><div>Wen-Wei-San-Ji Formula (WWSJ) is a Traditional Chinese medicine (TCM) formula used in treatment of chronic atrophic gastritis (CAG), demonstrating significant clinical efficacy. However, its specific mechanism of action remains unclear. This study investigates the molecular mechanisms and active components of WWSJ for CAG by employing network pharmacology, machine learning, and molecular docking, complemented by experimental validation.</div></div><div><h3>Methods</h3><div>Active compounds and targets of WWSJ were screened using TCMSP and Uniprot databases, while targets for CAG were collected from GeneCards and OMIM databases. Protein-protein-interaction and herb-compound-target networks were constructed using by STRING and Cytoscape. Functional enrichment was performed with DAVID. Machine learning (PCA/LASSO/RF) identified core targets from GEO data. In molecular docking studies, AutoDock Vina was used to evaluate binding activity. <em>In vitro</em> and <em>in vivo</em> experiments were conducted to validate the results.</div></div><div><h3>Results</h3><div>A total of 53 active ingredients with (OB)≥30% and (DL)≥0.1 from WWSJ were selected. Targets of the formula (1657) and CAG disease (923) were screened, resulting in the identification of 207 common targets. Functional analysis of WWSJ by GO and KEGG revealed 742 Biological Processes (BP), 85 Cellular Components (CC), 116 Molecular Functions (MF), and 149 signaling pathways associated with CAG. Additionally, 5 core genes were identified through machine learning and molecular docking. The compounds demonstrated strong binding affinity with the target proteins, especially STAT3. Therefore, we hypothesized that WWSJ can treat CAG through inhibiting STAT3 signaling. Results of cell and animal experiments indicated that WWSJ is effective in the treatment of CAG through the inhibition of STAT3.</div></div><div><h3>Conclusion</h3><div>Integrated network pharmacology predictions and machine learning optimization identified STAT3 as the primary therapeutic target of WWSJ. Experimental studies confirmed that WWSJ alleviates CAG by suppressing STAT3 phosphorylation.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100663"},"PeriodicalIF":0.0,"publicationDate":"2025-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144722860","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
Imperatorin suppresses NSCLC via interaction with PI3K/AKT pathway and PD-L1: Computational and experimental evidence Imperatorin通过与PI3K/AKT通路和PD-L1相互作用抑制NSCLC:计算和实验证据
Pub Date : 2025-07-13 DOI: 10.1016/j.prmcm.2025.100661
Yifei Xu , Shunjiang Jia , Zhijian Liang , Shuxian Gong , Zhongyuan Long , Yuwei Wang , Huanling Lai

Background

Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality globally, underscoring the critical need for novel therapeutic agents. Imperatorin (IMP), a natural furanocoumarin compound derived from various traditional Chinese medicine plants including Angelica dahurica (Baizhi) and Peucedanum praeruptorum (Qianhu), has shown promising anti-cancer properties. This study aimed to elucidate the therapeutic mechanisms of IMP against NSCLC.

Methods

The anti-NSCLC activity of IMP was evaluated through in vitro cytotoxicity and colony formation assays. Network pharmacology analysis was employed to identify potential targets of IMP in NSCLC. Molecular docking simulations predicted binding affinities and interactions between IMP and its targets. The antitumor efficacy and molecular mechanisms of IMP were further validated using in vivo xenograft models.

Results

IMP exhibited time-dependent growth inhibition in NSCLC cell lines H1975 and A549, with 48-hour IC50 values of 5.28 ± 0.50 µM and 14.17 ± 3.02 µM, respectively, while showing minimal cytotoxicity toward normal lung CCD19-Lu cells. In vivo, IMP significantly suppressed tumor growth in a nude mouse xenograft model. Network pharmacology identified 379 common targets between IMP and NSCLC, predominantly associated with the PI3K-AKT signaling pathway, with the PD-L1 signaling pathway emerging as an additional relevant target. Molecular docking analysis revealed strong interactions between IMP and key PI3K/AKT pathway proteins. Subsequent in vivo experiments confirmed that IMP treatment inhibited PI3K and AKT activation while downregulating PD-L1 expression.

Conclusions

Our findings demonstrate that IMP exerts multi-target effects against NSCLC, particularly through modulation of the PI3K/AKT and PD-L1 pathways, suggesting its potential as both a therapeutic agent and an immunomodulator in NSCLC treatment.
非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因,强调了对新型治疗药物的迫切需求。欧前胡素(IMP)是一种天然呋喃香豆素类化合物,从白芷、前胡等多种中药植物中提取,具有良好的抗癌作用。本研究旨在阐明IMP对非小细胞肺癌的治疗机制。方法通过体外细胞毒性和集落形成试验评价IMP的抗nsclc活性。采用网络药理学分析方法确定IMP在NSCLC中的潜在靶点。分子对接模拟预测了IMP与其靶标之间的结合亲和力和相互作用。通过体内异种移植模型进一步验证IMP的抗肿瘤功效和分子机制。结果simp对非小细胞肺癌细胞株H1975和A549具有时间依赖性的生长抑制作用,48小时IC50值分别为5.28±0.50µM和14.17±3.02µM,而对正常肺CCD19-Lu细胞的细胞毒性很小。在体内,IMP显著抑制裸鼠异种移植瘤模型的肿瘤生长。网络药理学鉴定出IMP和NSCLC之间的379个共同靶点,主要与PI3K-AKT信号通路相关,PD-L1信号通路是一个额外的相关靶点。分子对接分析显示IMP与PI3K/AKT关键通路蛋白之间存在强相互作用。随后的体内实验证实,IMP处理抑制了PI3K和AKT的激活,同时下调了PD-L1的表达。结论研究结果表明,IMP对非小细胞肺癌具有多靶点作用,特别是通过调节PI3K/AKT和PD-L1通路,提示其作为非小细胞肺癌治疗药物和免疫调节剂的潜力。
{"title":"Imperatorin suppresses NSCLC via interaction with PI3K/AKT pathway and PD-L1: Computational and experimental evidence","authors":"Yifei Xu ,&nbsp;Shunjiang Jia ,&nbsp;Zhijian Liang ,&nbsp;Shuxian Gong ,&nbsp;Zhongyuan Long ,&nbsp;Yuwei Wang ,&nbsp;Huanling Lai","doi":"10.1016/j.prmcm.2025.100661","DOIUrl":"10.1016/j.prmcm.2025.100661","url":null,"abstract":"<div><h3>Background</h3><div>Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality globally, underscoring the critical need for novel therapeutic agents. Imperatorin (IMP), a natural furanocoumarin compound derived from various traditional Chinese medicine plants including <em>Angelica dahurica</em> (Baizhi) and <em>Peucedanum praeruptorum</em> (Qianhu), has shown promising anti-cancer properties. This study aimed to elucidate the therapeutic mechanisms of IMP against NSCLC.</div></div><div><h3>Methods</h3><div>The anti-NSCLC activity of IMP was evaluated through in vitro cytotoxicity and colony formation assays. Network pharmacology analysis was employed to identify potential targets of IMP in NSCLC. Molecular docking simulations predicted binding affinities and interactions between IMP and its targets. The antitumor efficacy and molecular mechanisms of IMP were further validated using in vivo xenograft models.</div></div><div><h3>Results</h3><div>IMP exhibited time-dependent growth inhibition in NSCLC cell lines H1975 and A549, with 48-hour IC50 values of 5.28 ± 0.50 µM and 14.17 ± 3.02 µM, respectively, while showing minimal cytotoxicity toward normal lung CCD19-Lu cells. In vivo, IMP significantly suppressed tumor growth in a nude mouse xenograft model. Network pharmacology identified 379 common targets between IMP and NSCLC, predominantly associated with the PI3K-AKT signaling pathway, with the PD-L1 signaling pathway emerging as an additional relevant target. Molecular docking analysis revealed strong interactions between IMP and key PI3K/AKT pathway proteins. Subsequent in vivo experiments confirmed that IMP treatment inhibited PI3K and AKT activation while downregulating PD-L1 expression.</div></div><div><h3>Conclusions</h3><div>Our findings demonstrate that IMP exerts multi-target effects against NSCLC, particularly through modulation of the PI3K/AKT and PD-L1 pathways, suggesting its potential as both a therapeutic agent and an immunomodulator in NSCLC treatment.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100661"},"PeriodicalIF":0.0,"publicationDate":"2025-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144662619","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
Phytochemical constituents, therapeutic potential and toxicity of Gardenia jasminoides Ellis: An in-depth review 栀子的植物化学成分、治疗潜力和毒性研究进展
Pub Date : 2025-07-12 DOI: 10.1016/j.prmcm.2025.100662
Mahima Tiwari, Suruchi, Ajay Kumar Gupta, Dipti Pal, Sanmati Kumar Jain

Introduction

Gardenia jasminoides Ellis (GJE), also known as "Cape Jasmine," is an East Asian blooming species indigenous to East Asia. This plant has extensive utility in the history of Traditional Chinese Medicine and is acknowledged for its ability to combat inflammation, safeguard liver health and possess antioxidant capabilities.

Objective

This review seeks to examine the ethnopharmacological importance of GJE, emphasizing its historical applications, bioactive constituents, and possible therapeutic benefits as well as toxicity.

Methods

An investigation into the phytoconstituents, extraction techniques, and pharmacological effects of the GJE was conducted using a variety of academic databases and search engines. These included Google Scholar, PubMed, China National Knowledge Infrastructure (CNKI), Flora of China, Wanfang Database, Plant of the World Online, ChemSpider, European and Mediterranean Plant Protection Organization (EPPO) Global Database, Springer Link, and Science Direct.

Outcomes

An examination uncovers a variety of bioactive phytoconstituents, such as flavonoids, iridoid glycosides, gardenia’s yellow pigment, monoterpenoids, sesquiterpenoids, triterpenoids, organic acids and their derivatives, along with other compounds. These components are crucial to the wide-ranging pharmacological applications, which encompass antioxidant, anti-inflammatory, anti-diabetic, cardiovascular disorders, neurodisorders, anti-tumor, treatment of liver injury, anti-hepatic injury, gastrocellular activity, improvement of gut microbiota, atopic dermatitis, anti-viral, improvement of the quality of sleep, protection from blue light and ultraviolet rays, vitiligo, inhibition of retinal damage, antibacterial activity, anti-senescence activity, anti-thrombosis, osteoporosis protection and postmenopausal syndrome treatment.

Conclusion

GJE is an important medicinal plant recognized for its diverse pharmacological advantages, which are underpinned by its extensive phytochemical composition. Despite its considerable therapeutic promise, it is essential to take its toxicity into account, especially at elevated doses. Additional research is necessary to evaluate its safety profile and enhance its medicinal uses.
栀子花(ardenia jasminoides Ellis, GJE),又名“海角茉莉花”,是一种原产于东亚的东亚开花植物。这种植物在中国传统医学史上有着广泛的用途,被认为具有抗炎症、保护肝脏健康和抗氧化能力的能力。目的本文综述了GJE的民族药理学意义,重点介绍了GJE的历史应用、生物活性成分、可能的治疗效益和毒性。方法利用各种学术数据库和搜索引擎,对其植物成分、提取工艺和药理作用进行研究。其中包括谷歌Scholar、PubMed、中国知网、中国植物志、万方数据库、世界植物网、ChemSpider、欧洲和地中海植物保护组织(EPPO)全球数据库、施普林格Link和Science Direct。结果发现了多种生物活性植物成分,如黄酮类化合物、环烯醚萜苷、栀子黄色素、单萜类、倍半萜类、三萜类、有机酸及其衍生物,以及其他化合物。这些成分对广泛的药理学应用至关重要,包括抗氧化、抗炎、抗糖尿病、心血管疾病、神经疾病、抗肿瘤、治疗肝损伤、抗肝损伤、胃细胞活性、改善肠道微生物群、特应性皮炎、抗病毒、改善睡眠质量、防止蓝光和紫外线、白癜风、抑制视网膜损伤、抗菌活性、抗衰老活性,抗血栓形成,骨质疏松保护和绝经后综合征治疗。结论乙脑是一种重要的药用植物,其丰富的化学成分为其丰富的药理作用奠定了基础。尽管它具有相当大的治疗前景,但必须考虑到它的毒性,特别是在高剂量时。需要进一步的研究来评估其安全性并提高其药用价值。
{"title":"Phytochemical constituents, therapeutic potential and toxicity of Gardenia jasminoides Ellis: An in-depth review","authors":"Mahima Tiwari,&nbsp;Suruchi,&nbsp;Ajay Kumar Gupta,&nbsp;Dipti Pal,&nbsp;Sanmati Kumar Jain","doi":"10.1016/j.prmcm.2025.100662","DOIUrl":"10.1016/j.prmcm.2025.100662","url":null,"abstract":"<div><h3>Introduction</h3><div><em>Gardenia jasminoides Ellis</em> (GJE), also known as \"Cape Jasmine,\" is an East Asian blooming species indigenous to East Asia. This plant has extensive utility in the history of Traditional Chinese Medicine and is acknowledged for its ability to combat inflammation, safeguard liver health and possess antioxidant capabilities.</div></div><div><h3>Objective</h3><div>This review seeks to examine the ethnopharmacological importance of GJE<em>,</em> emphasizing its historical applications, bioactive constituents, and possible therapeutic benefits as well as toxicity.</div></div><div><h3>Methods</h3><div>An investigation into the phytoconstituents, extraction techniques, and pharmacological effects of the GJE was conducted using a variety of academic databases and search engines. These included Google Scholar, PubMed, China National Knowledge Infrastructure (CNKI), Flora of China, Wanfang Database, Plant of the World Online, ChemSpider, European and Mediterranean Plant Protection Organization (EPPO) Global Database, Springer Link, and Science Direct.</div></div><div><h3>Outcomes</h3><div>An examination uncovers a variety of bioactive phytoconstituents, such as flavonoids, iridoid glycosides, gardenia’s yellow pigment, monoterpenoids, sesquiterpenoids, triterpenoids, organic acids and their derivatives, along with other compounds. These components are crucial to the wide-ranging pharmacological applications, which encompass antioxidant, anti-inflammatory, anti-diabetic, cardiovascular disorders, neurodisorders, anti-tumor, treatment of liver injury, anti-hepatic injury, gastrocellular activity, improvement of gut microbiota, atopic dermatitis, anti-viral, improvement of the quality of sleep, protection from blue light and ultraviolet rays, vitiligo, inhibition of retinal damage, antibacterial activity, anti-senescence activity, anti-thrombosis, osteoporosis protection and postmenopausal syndrome treatment.</div></div><div><h3>Conclusion</h3><div>GJE is an important medicinal plant recognized for its diverse pharmacological advantages, which are underpinned by its extensive phytochemical composition. Despite its considerable therapeutic promise, it is essential to take its toxicity into account, especially at elevated doses. Additional research is necessary to evaluate its safety profile and enhance its medicinal uses.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100662"},"PeriodicalIF":0.0,"publicationDate":"2025-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144687239","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
Interactions between traditional chinese medicine and gut microbiota in chronic diseases 慢性疾病中中药与肠道菌群的相互作用
Pub Date : 2025-07-10 DOI: 10.1016/j.prmcm.2025.100659
Lei Chen , Meijun Liu , Xiaoli Chen , Aiping Lyu , Kenneth Cheung , Yongai Xiong

Introduction

The gut microbiota (GM) is a vast and dynamic community of microorganisms residing in the mammalian gastrointestinal tract. It plays a vital role in the absorption, digestion, metabolism, and distribution of food and drugs. Dysbiosis of GM is increasingly recognized as a key contributor to the development of intestinal disorders such as irritable bowel syndrome (IBS), Crohn's disease, and colorectal cancer. Moreover, GM communicates with distant organs through various axes, including the brain-gut, liver-gut, and lung-gut axes, thereby participating in the pathogenesis of systemic diseases such as Alzheimer's disease, non-alcoholic fatty liver disease, liver cancer, and lung cancer.

Methods

This review systematically examines the recent literature on the bidirectional interaction between traditional Chinese medicine (TCM) and GM, focusing on preclinical and clinical studies. Emphasis is placed on the mechanisms through which GM influences the pharmacokinetics and pharmacodynamics of TCM, including microbial enzymatic activities such as hydrolysis, redox reactions, and deacetylation.

Results

GM can significantly impact both the efficacy and toxicity of TCM by transforming its active ingredients. Conversely, TCM and its active compounds also modulate the composition and function of GM, contributing to the prevention and treatment of chronic diseases. Key chronic conditions covered in this review include gastrointestinal, neurological, hepatic, and pulmonary diseases.

Discussion

The interaction between TCM and GM represents a promising avenue for personalized medicine and targeted interventions for GM-related diseases. Understanding these complex interactions provides a theoretical basis for developing novel TCM-based strategies to prevent and treat chronic conditions through modulation of the gut microbiota.
肠道微生物群(GM)是一个巨大的和动态的微生物群落居住在哺乳动物胃肠道。它在食物和药物的吸收、消化、代谢和分布中起着至关重要的作用。转基因生物的生态失调越来越被认为是肠易激综合征(IBS)、克罗恩病和结直肠癌等肠道疾病发展的关键因素。此外,基因还通过脑-肠、肝-肠、肺-肠等多种轴向远端器官传递信息,从而参与阿尔茨海默病、非酒精性脂肪性肝病、肝癌、肺癌等全身性疾病的发病机制。方法系统回顾了近年来有关中药与转基因双向相互作用的文献,重点介绍了临床前和临床研究。重点放在转基因影响中药药代动力学和药效学的机制上,包括微生物酶活性,如水解、氧化还原反应和去乙酰化。结果转基因通过改变中药的有效成分,对中药的疗效和毒性均有显著影响。相反,中药及其活性化合物也调节转基因的组成和功能,有助于预防和治疗慢性疾病。本综述中涉及的主要慢性疾病包括胃肠道、神经系统、肝脏和肺部疾病。中医药与转基因之间的相互作用为转基因相关疾病的个性化医疗和针对性干预提供了一条有希望的途径。了解这些复杂的相互作用为开发新的基于tcm的策略提供了理论基础,通过调节肠道微生物群来预防和治疗慢性疾病。
{"title":"Interactions between traditional chinese medicine and gut microbiota in chronic diseases","authors":"Lei Chen ,&nbsp;Meijun Liu ,&nbsp;Xiaoli Chen ,&nbsp;Aiping Lyu ,&nbsp;Kenneth Cheung ,&nbsp;Yongai Xiong","doi":"10.1016/j.prmcm.2025.100659","DOIUrl":"10.1016/j.prmcm.2025.100659","url":null,"abstract":"<div><h3>Introduction</h3><div>The gut microbiota (GM) is a vast and dynamic community of microorganisms residing in the mammalian gastrointestinal tract. It plays a vital role in the absorption, digestion, metabolism, and distribution of food and drugs. Dysbiosis of GM is increasingly recognized as a key contributor to the development of intestinal disorders such as irritable bowel syndrome (IBS), Crohn's disease, and colorectal cancer. Moreover, GM communicates with distant organs through various axes, including the brain-gut, liver-gut, and lung-gut axes, thereby participating in the pathogenesis of systemic diseases such as Alzheimer's disease, non-alcoholic fatty liver disease, liver cancer, and lung cancer.</div></div><div><h3>Methods</h3><div>This review systematically examines the recent literature on the bidirectional interaction between traditional Chinese medicine (TCM) and GM, focusing on preclinical and clinical studies. Emphasis is placed on the mechanisms through which GM influences the pharmacokinetics and pharmacodynamics of TCM, including microbial enzymatic activities such as hydrolysis, redox reactions, and deacetylation.</div></div><div><h3>Results</h3><div>GM can significantly impact both the efficacy and toxicity of TCM by transforming its active ingredients. Conversely, TCM and its active compounds also modulate the composition and function of GM, contributing to the prevention and treatment of chronic diseases. Key chronic conditions covered in this review include gastrointestinal, neurological, hepatic, and pulmonary diseases.</div></div><div><h3>Discussion</h3><div>The interaction between TCM and GM represents a promising avenue for personalized medicine and targeted interventions for GM-related diseases. Understanding these complex interactions provides a theoretical basis for developing novel TCM-based strategies to prevent and treat chronic conditions through modulation of the gut microbiota.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100659"},"PeriodicalIF":0.0,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144657014","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
Transcriptomics revealed potential anti-inflammatory mechanisms of ethanol extracts of propolis and tree gum in lipoteichoic acid and interferon-γ-stimulated RAW264.7 macrophages 转录组学揭示了蜂胶和树胶乙醇提取物对脂壁酸和干扰素γ刺激的RAW264.7巨噬细胞的潜在抗炎机制
Pub Date : 2025-07-07 DOI: 10.1016/j.prmcm.2025.100660
Zongze Li, Zhengxin Liu, Yuyang Guo, Yujing Tang, Ting Li, Shuangshuang Gao, Hongzhuan Xuan

Introduction

Poplar propolis, a traditional Chinese medicine abundant in phenolic acids and flavonoid compounds, demonstrates remarkable anti-inflammatory activity. It is currently widely applied in the pharmaceutical and health product industries for the prevention and adjuvant treatment of various diseases. However, due to the limited availability of natural propolis, its primary plant source—tree gum—is often used as an adulterant, posing significant challenges for the authenticity and quality control of propolis products. Therefore, this study aimed to compare the anti-inflammatory effects of ethanol extracts of poplar propolis (EEP) and tree gum (EEG) on RAW264.7 macrophages co-stimulated with lipoteichoic acid (LTA) and interferon-gamma (IFN-γ) using in vitro cellular assays. Furthermore, transcriptomic analysis was employed to elucidate the molecular mechanisms underlying the anti-inflammatory activities of EEP and EEG.

Methods

Widely targeted metabolomics was used to analyze metabolites of EEP and EEG. A RAW264.7 macrophage inflammation model was established using LTA and IFN-γ co-stimulation, and optimal concentrations of EEP and EEG were determined. ELISA and RT-qPCR were used to assess inflammatory cytokines, inflammation-related genes, and antioxidant genes. Reactive oxygen species (ROS) levels were measured with a DCFH-DA probe. Transcriptomics, RT-qPCR, and Western blotting were employed to evaluate signaling pathway-related markers.

Results

The results showed that 1635 metabolites were identified in EEP and 1545 metabolites were identified in EEG by widely targeted metabolomics. Compared to EEG, EEP more effectively inhibited the release of inflammatory factors, regulated inflammatory gene expression, reduced ROS production, and elevated antioxidant gene expression. RT-qPCR and Western blot analyses revealed that EEP and EEG suppressed the inflammatory response in LTA/IFN-γ-stimulated RAW264.7 macrophages by downregulating cell adhesion molecule expression, inhibiting the MAPK signaling pathway, and activating the autophagy pathway.

Discussion

Propolis exhibited superior efficacy over tree gum in suppressing inflammatory responses and enhancing antioxidant defenses. These findings offer a theoretical foundation for the quality control and further development of propolis as a potential anti-inflammatory agent.
杨树蜂胶是一种富含酚酸和黄酮类化合物的中药,具有显著的抗炎活性。目前广泛应用于医药和保健品行业,用于各种疾病的预防和辅助治疗。然而,由于天然蜂胶的可用性有限,其主要植物来源树胶经常被用作掺假剂,这对蜂胶产品的真实性和质量控制提出了重大挑战。因此,本研究旨在通过体外细胞实验比较杨树蜂胶乙醇提取物(EEP)和树胶乙醇提取物(EEG)对脂质胆酸(LTA)和干扰素γ (IFN-γ)共刺激RAW264.7巨噬细胞的抗炎作用。此外,转录组学分析被用于阐明脑电图和脑电图抗炎活性的分子机制。方法采用广泛靶向代谢组学方法分析脑电图和脑电图代谢物。采用LTA和IFN-γ共刺激建立RAW264.7巨噬细胞炎症模型,并确定最佳脑电图和脑电图浓度。采用ELISA和RT-qPCR检测炎症因子、炎症相关基因和抗氧化基因。用DCFH-DA探针检测活性氧(ROS)水平。转录组学、RT-qPCR和Western blotting用于评估信号通路相关标记物。结果应用广泛靶向的代谢组学方法,在脑电图中鉴定出1635种代谢物,在脑电图中鉴定出1545种代谢物。与脑电图相比,脑电图更有效地抑制炎症因子的释放,调节炎症基因的表达,减少ROS的产生,提高抗氧化基因的表达。RT-qPCR和Western blot分析显示,脑电图和脑电图通过下调细胞粘附分子表达,抑制MAPK信号通路,激活自噬通路,抑制LTA/IFN-γ刺激的RAW264.7巨噬细胞的炎症反应。蜂胶在抑制炎症反应和增强抗氧化防御方面表现出优于树胶的功效。这些发现为蜂胶作为一种潜在的抗炎剂的质量控制和进一步开发提供了理论基础。
{"title":"Transcriptomics revealed potential anti-inflammatory mechanisms of ethanol extracts of propolis and tree gum in lipoteichoic acid and interferon-γ-stimulated RAW264.7 macrophages","authors":"Zongze Li,&nbsp;Zhengxin Liu,&nbsp;Yuyang Guo,&nbsp;Yujing Tang,&nbsp;Ting Li,&nbsp;Shuangshuang Gao,&nbsp;Hongzhuan Xuan","doi":"10.1016/j.prmcm.2025.100660","DOIUrl":"10.1016/j.prmcm.2025.100660","url":null,"abstract":"<div><h3>Introduction</h3><div>Poplar propolis, a traditional Chinese medicine abundant in phenolic acids and flavonoid compounds, demonstrates remarkable anti-inflammatory activity. It is currently widely applied in the pharmaceutical and health product industries for the prevention and adjuvant treatment of various diseases. However, due to the limited availability of natural propolis, its primary plant source—tree gum—is often used as an adulterant, posing significant challenges for the authenticity and quality control of propolis products. Therefore, this study aimed to compare the anti-inflammatory effects of ethanol extracts of poplar propolis (EEP) and tree gum (EEG) on RAW264.7 macrophages co-stimulated with lipoteichoic acid (LTA) and interferon-gamma (IFN-γ) using in vitro cellular assays. Furthermore, transcriptomic analysis was employed to elucidate the molecular mechanisms underlying the anti-inflammatory activities of EEP and EEG.</div></div><div><h3>Methods</h3><div>Widely targeted metabolomics was used to analyze metabolites of EEP and EEG. A RAW264.7 macrophage inflammation model was established using LTA and IFN-γ co-stimulation, and optimal concentrations of EEP and EEG were determined. ELISA and RT-qPCR were used to assess inflammatory cytokines, inflammation-related genes, and antioxidant genes. Reactive oxygen species (ROS) levels were measured with a DCFH-DA probe. Transcriptomics, RT-qPCR, and Western blotting were employed to evaluate signaling pathway-related markers.</div></div><div><h3>Results</h3><div>The results showed that 1635 metabolites were identified in EEP and 1545 metabolites were identified in EEG by widely targeted metabolomics. Compared to EEG, EEP more effectively inhibited the release of inflammatory factors, regulated inflammatory gene expression, reduced ROS production, and elevated antioxidant gene expression. RT-qPCR and Western blot analyses revealed that EEP and EEG suppressed the inflammatory response in LTA/IFN-γ-stimulated RAW264.7 macrophages by downregulating cell adhesion molecule expression, inhibiting the MAPK signaling pathway, and activating the autophagy pathway.</div></div><div><h3>Discussion</h3><div>Propolis exhibited superior efficacy over tree gum in suppressing inflammatory responses and enhancing antioxidant defenses. These findings offer a theoretical foundation for the quality control and further development of propolis as a potential anti-inflammatory agent.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"16 ","pages":"Article 100660"},"PeriodicalIF":0.0,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144604675","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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