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Unveiling the potential of Chinese herbs in combating cervical cancer: Understanding their mechanisms of action and herbal formulations 揭示中草药抗击宫颈癌的潜力:了解中草药的作用机制和配方
Pub Date : 2024-08-13 DOI: 10.1016/j.prmcm.2024.100497
Priyanka Ray, Diptayan Paul

Introduction

Within the framework of Traditional Chinese Medicine (TCM), this study investigates the vast field of Chinese herbal medicine's potential as a powerful weapon in the fight against cervical cancer.

Methods

A thorough search was made through Scopus, PubMed, ResearchGate, and Elsevier Journals for future studies on the healing and cervical cancer-fighting properties of Chinese plants and herbal formulations.

Result

Scutellaria baicalensis, Curcuma longa, Ganoderma lucidum, Camptotheca acuminata, Antrodia cinnamomea, Terminalia catappa, Chelidonium majus, Lycopodium clavatum, and Myrica cerifera possess cancer-fighting bioactive compounds. Baicalein in Scutellaria baicalensis suppresses cervical cancer growth and alters Notch signaling, while curcumin in Curcuma longa inhibits cell migration, invasion, and HPV oncogenes, also reducing inflammation and protecting cells. Ganoderma lucidum lowers inflammation, boosts the immune system, and blocks JAK/STAT5 signaling, preventing EMT in cervical cancer cells. Camptothecin in Camptotheca acuminata inhibits DNA topoisomerase I, reducing cancer cell growth, with Antrodia cinnamomea controlling apoptosis. Terminalia catappa uses MMP-9 and MAPK to inhibit spread, while Chelidonium majus, Lycopodium clavatum, and Myrica cerifera induce apoptosis and cell cycle arrest. Zhidai Decoction and Guizhi-Fuling-decoction suggest traditional Chinese medicine can treat HPV and cervical cancer.

Discussion

Scutellaria baicalensis, Curcuma longa, Ganoderma lucidum, Camptotheca acuminata, Antrodia cinnamomea, Terminalia catappa, Chelidonium majus, Lycopodium clavatum, and Myrica cerifera possess bioactive substances effective against cancer. They work through mechanisms like inhibiting cell growth, altering signaling pathways, and inducing apoptosis. Traditional Chinese medicine formulations like Zhidai Decoction and Guizhi-Fuling-decoction show potential in treating HPV and cervical cancer.

方法 通过 Scopus、PubMed、ResearchGate 和 Elsevier 期刊进行了全面搜索,以了解未来有关中国植物和中草药配方的治疗和宫颈癌抗癌特性的研究。结果黄芩、莪术、灵芝、淫羊藿、肉桂、鸡血藤、车前子、枸杞子和制何首乌具有抗癌生物活性化合物。黄芩中的黄芩素能抑制宫颈癌的生长,改变 Notch 信号传导,而姜黄中的姜黄素能抑制细胞迁移、侵袭和人乳头瘤病毒的致癌基因,还能减轻炎症,保护细胞。灵芝能减轻炎症,增强免疫系统,阻断 JAK/STAT5 信号传导,防止宫颈癌细胞发生 EMT。喜树中的喜树碱能抑制 DNA 拓扑异构酶 I,减少癌细胞的生长,而肉桂中的杏仁则能控制细胞凋亡。鸡血藤利用 MMP-9 和 MAPK 抑制扩散,而车前子、狼毒和肉豆蔻则诱导细胞凋亡和细胞周期停滞。讨论黄芩、莪术、灵芝、淫羊藿、肉桂、鸡血藤、诃子、枸杞子、枸杞子、枸杞子、肉豆蔻、肉豆蔻、肉豆蔻、肉豆蔻、肉豆蔻、肉豆蔻、肉豆蔻、肉豆蔻、肉豆蔻等具有抗癌生物活性物质。它们通过抑制细胞生长、改变信号通路和诱导细胞凋亡等机制发挥作用。传统中药配方,如枳壳煎剂和桂枝茯苓煎剂,在治疗人乳头瘤病毒和宫颈癌方面显示出潜力。
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引用次数: 0
In vivo components analysis of Shenhua tablets active in IgA nephropathy 对 IgA 肾病有活性的神华片的体内成分分析
Pub Date : 2024-08-11 DOI: 10.1016/j.prmcm.2024.100493
Huiqiang Liu , Ping Li , Fengting Yin , Hui Sun , Ying Zheng , Chang Liu , Xiangmei Chen , Xiaotong Yan , Xijun Wang

Introduction

Shenhua Tablet (SH), a traditional Chinese medicine (TCM) formulation with seven herbs, is widely used in the clinical treatment of Immunoglobulin A (IgA) nephropathy. Despite its effectiveness, the specific active components of SH in vivo remain unidentified, presenting a challenge for further research on its pharmacodynamic material basis.

Methods

A rat model of IgA nephropathy was treated with Shenhua Tablet (SH) to evaluate its potential in protecting kidney function. UHPLC-Q/Orbitrap/LTQ MS was utilized to identify active components of SH in vivo under the active condition for intervening IgA.

Results

SH significantly ameliorated Thy-1 antibody-induced IgA nephropathy by decreasing glomerular injury, suppressing pro-inflammatory factor secretion, and inhibiting mesangial cell proliferation. 83 kinds of prototypal compounds absorbed into the blood were comprehensively characterized, along with 145 metabolites arising from Phase I and Phase II metabolic reactions. and the metabolic pathways of these metabolites were elucidated for the first time. 10 active components were found to be correlated with the effectiveness of SH, including Atractylenolide I, chlorogenic acid, ferulic acid, salidroside+SO3, calycosin+O, furanodiene, paeoniflorin-H2, germacron+O, formononetin+C6H8O6, and calycosin.

Discussion

The results fill the current research gap on the active components of SH and examine its potential renoprotective effects on IgA nephropathy. This study provides valuable references and insights for elucidating the active components and mechanisms of action of SH in treating IgA nephropathy.

简介:神化七味片(Shenhua Tablet,SH)是一种七味中药制剂,广泛应用于免疫球蛋白A(IgA)肾病的临床治疗。方法用神华片治疗大鼠 IgA 肾病模型,评估其保护肾功能的潜力。结果神华片通过减少肾小球损伤、抑制促炎因子分泌和抑制系膜细胞增殖,显著改善了Thy-1抗体诱导的IgA肾病。对吸收入血的 83 种原型化合物以及 145 种 I 期和 II 期代谢反应产生的代谢物进行了全面鉴定,并首次阐明了这些代谢物的代谢途径。研究发现,白术内酯Ⅰ、绿原酸、阿魏酸、水杨甙+SO3、钙苷+O、呋喃二烯、芍药苷-H2、胚芽鞘氨醇+O、甲萘素+C6H8O6和钙苷等10种活性成分与SH的有效性相关。这项研究为阐明 SH 在治疗 IgA 肾病中的活性成分和作用机制提供了有价值的参考和见解。
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引用次数: 0
Application of bioactivity validation as quality control approach: Panax notoginseng dominated scientific-driven new TCM formulae-BPAid from laboratory to industrial scale 应用生物活性验证作为质量控制方法:以三七为主导的科学驱动型中药新配方--BPAid从实验室到工业规模的应用
Pub Date : 2024-08-09 DOI: 10.1016/j.prmcm.2024.100496
Wan Yin Tew , Yean Chun Loh , Chong Seng Yan , Hui Wei Loh , Chen Jingying , Chen Ying , Lee Suan Chua , Guo Longgang , Xu Wen , Xu Wei , Mun Fei Yam

Background

In the realm of Chinese medicine, quality control and pharmacodynamics are crucial to ensure the consistency in scaled-up process from the laboratory to commercial operations. This study aims to analyse bioactivity consistency between laboratory observations and commercial processes.

Method

The preparation of BPAid (5: 2: 9: 1 for Uncaria rhynchophylla (UR): Pueraria thomsonii (PT): Panax notoginseng (PN): Alisma orientale (AO) was divided into three methods: laboratory-scale maceration (BPAidM), industrial-scale flash extract method (BPAidFE), decoction method (BPAidD). The vasodilatory and antihypertensive effects of the extracts were examined through ex vivo and in vivo studies. The chemical fingerprint of each extract was analysed using tri-step FTIR spectroscopy, and UPLC-MS/MS was used for standard marker quantification.

Results

BPAidM exhibited the highest vasodilatory effect, followed by BPAidFE, and BPAidD with EC50 values of 11.25 ± 2.30 mg/mL, 39.23 ± 12.55 mg/mL, 24.33 ± 6.26 mg/mL, and 198.71 ± 127.21 mg/mL: RMAX values of 106.53 ± 7.95%, 82.92 ± 5.22%, 76.35 ± 4.51%, and 60.62 ± 5.7%, respectively. In in vivo antihypertensive studies, all extracts significantly reduced the blood pressure of Spontaneously Hypertensive rats (SHRs). The tri-step FTIR revealed the presence of phenolic compounds, esters, and saccharides in BPAid extracts. BPAidM contained the highest total standard marker in the UPLC-MS/MS quantification, followed by BPAidFE, and BPAidD.

Conclusion

Ultimately, the flash extract technique is recommended to produce BPAid to meet the global demand.

背景在中药领域,质量控制和药效学对于确保从实验室到商业运作的放大过程的一致性至关重要。本研究旨在分析实验室观察结果与商业工艺之间生物活性的一致性:葛根(Pueraria thomsonii,PT):三七(Panax notoginseng,PN):实验方法分为三种:实验室浸渍法(BPAidM)、工业规模闪蒸提取法(BPAidFE)和煎煮法(BPAidD)。通过体内外研究考察了提取物的血管扩张和降压作用。使用三步傅立叶变换红外光谱分析了每种提取物的化学指纹图谱,并使用 UPLC-MS/MS 进行标准标记物定量:RMAX 值分别为 106.53 ± 7.95%、82.92 ± 5.22%、76.35 ± 4.51% 和 60.62 ± 5.7%。在体内降压研究中,所有提取物都能显著降低自发性高血压大鼠(SHR)的血压。三步傅立叶变换红外光谱显示,双酚 Aid 提取物中含有酚类化合物、酯类和糖类。在 UPLC-MS/MS 定量分析中,BPAidM 的总标准标记物含量最高,其次是 BPAidFE 和 BPAidD。
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引用次数: 0
Unveiling the therapeutic potential and nanotechnological approaches for the delivery of tanshinone IIA 揭示丹参酮 IIA 的治疗潜力和纳米技术方法
Pub Date : 2024-08-09 DOI: 10.1016/j.prmcm.2024.100494
Diya Arora, Vanshita, Keshav Bansal

Introduction

Phytochemicals, as dietary ingredients, are being extensively studied for the treatment and prevention of many illnesses. Tanshinone IIA, a plant-derived diterpene quinone has demonstrated various therapeutic effects. However, limitations like low solubility, bioavailability and stability, weak targeting biodistribution, and short half-life make Tan IIA an unlikely candidate for effective therapy. Nanoformulations based on natural substances are gaining interest as a treatment approach for various human diseases, as they provide an effective alternative to conventional approaches, which are frequently linked with a number of adverse effects and complications.

Methods

The study comprises a thorough assessment of existing research findings from a variety of sources in order to collect data on Tan IIA therapeutic properties and innovative delivery systems. Literature was compiled from various databases, including Scopus, Embase, PubMed, and Google Scholar, using keywords such as "Tanshinone IIA" or "diterpenes" in combination with "Traditional Chinese medicine", "Therapeutic potential", "Neuroprotection", "Anti-cancer", "Cardioprotection", "Nanocarriers", or "Liposomes".

Results

The findings demonstrated that Tan IIA possesses a broad array of pharmacological effects including its antidiabetic, anticancer, antioxidant, and anti-inflammatory activities. Tan IIA nanoformulations have shown good encapsulation efficiency, sustained release, stability, extended circulation duration, increased accumulation at diseased sites, and improved therapeutic efficacy, leading to improved therapeutic effectiveness for a plethora of disorders.

Discussion

Nanostructured particles provide several benefits in addressing issues such as limited bioavailability and the stability of phytochemicals by overcoming biological barriers. Certainly, the use of nano-drug delivery carriers for plant products is the current trend. Furthermore, the therapeutic applications of these nanoformulations must be studied in humans. Such investigation, as well as thorough evaluation and dosage optimization, may pave the way for Tanshinone IIA's commercial feasibility.

引言 植物化学物质作为膳食成分,正被广泛研究用于治疗和预防多种疾病。丹参酮 IIA 是一种从植物中提取的二萜醌,具有多种治疗效果。然而,由于溶解度、生物利用度和稳定性低,靶向生物分布弱,半衰期短,丹参酮 IIA 不太可能成为有效治疗的候选药物。基于天然物质的纳米制剂作为一种治疗各种人类疾病的方法正受到越来越多的关注,因为它们为传统方法提供了一种有效的替代方法,而传统方法往往与一些不良反应和并发症联系在一起。使用 "丹参酮 IIA "或 "二萜 "等关键词,结合 "中药"、"治疗潜力"、"神经保护"、"抗癌"、"心脏保护"、"纳米载体 "或 "脂质体",从 Scopus、Embase、PubMed 和 Google Scholar 等各种数据库中汇编了相关文献。结果研究结果表明,Tan IIA 具有广泛的药理作用,包括抗糖尿病、抗癌、抗氧化和抗炎活性。Tan IIA 纳米制剂具有良好的封装效率、持续释放性、稳定性、延长循环时间、增加在病变部位的蓄积和提高疗效,从而提高了对多种疾病的治疗效果。 讨论纳米结构颗粒通过克服生物障碍,在解决植物化学物质的生物利用度有限和稳定性等问题方面具有多种优势。当然,将纳米药物输送载体用于植物产品是当前的趋势。此外,这些纳米制剂的治疗应用必须在人体中进行研究。此类研究以及全面评估和剂量优化可能会为丹参酮 IIA 的商业可行性铺平道路。
{"title":"Unveiling the therapeutic potential and nanotechnological approaches for the delivery of tanshinone IIA","authors":"Diya Arora,&nbsp;Vanshita,&nbsp;Keshav Bansal","doi":"10.1016/j.prmcm.2024.100494","DOIUrl":"10.1016/j.prmcm.2024.100494","url":null,"abstract":"<div><h3>Introduction</h3><p>Phytochemicals, as dietary ingredients, are being extensively studied for the treatment and prevention of many illnesses. Tanshinone IIA, a plant-derived diterpene quinone has demonstrated various therapeutic effects. However, limitations like low solubility, bioavailability and stability, weak targeting biodistribution, and short half-life make Tan IIA an unlikely candidate for effective therapy. Nanoformulations based on natural substances are gaining interest as a treatment approach for various human diseases, as they provide an effective alternative to conventional approaches, which are frequently linked with a number of adverse effects and complications.</p></div><div><h3>Methods</h3><p>The study comprises a thorough assessment of existing research findings from a variety of sources in order to collect data on Tan IIA therapeutic properties and innovative delivery systems. Literature was compiled from various databases, including Scopus, Embase, PubMed, and Google Scholar, using keywords such as \"Tanshinone IIA\" or \"diterpenes\" in combination with \"Traditional Chinese medicine\", \"Therapeutic potential\", \"Neuroprotection\", \"Anti-cancer\", \"Cardioprotection\", \"Nanocarriers\", or \"Liposomes\".</p></div><div><h3>Results</h3><p>The findings demonstrated that Tan IIA possesses a broad array of pharmacological effects including its antidiabetic, anticancer, antioxidant, and anti-inflammatory activities. Tan IIA nanoformulations have shown good encapsulation efficiency, sustained release, stability, extended circulation duration, increased accumulation at diseased sites, and improved therapeutic efficacy, leading to improved therapeutic effectiveness for a plethora of disorders.</p></div><div><h3>Discussion</h3><p>Nanostructured particles provide several benefits in addressing issues such as limited bioavailability and the stability of phytochemicals by overcoming biological barriers. Certainly, the use of nano-drug delivery carriers for plant products is the current trend. Furthermore, the therapeutic applications of these nanoformulations must be studied in humans. Such investigation, as well as thorough evaluation and dosage optimization, may pave the way for Tanshinone IIA's commercial feasibility.</p></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"12 ","pages":"Article 100494"},"PeriodicalIF":0.0,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667142524001362/pdfft?md5=ad2729d280ed1e0f3f6e3d617332dc7a&pid=1-s2.0-S2667142524001362-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141952341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dendrobium nobile alkaloids modulate calcium dysregulation and neuroinflammation in Alzheimer's disease: A bioinformatic analysis 金钗石斛生物碱可调节阿尔茨海默病的钙失调和神经炎症:生物信息学分析
Pub Date : 2024-08-05 DOI: 10.1016/j.prmcm.2024.100495
Iman Touati , Yassir Boulaamane , Mohammed Reda Britel , Amal Maurady

Introduction

Dendrobium nobile Lindl alkaloids, or DNLA for short, are the most active ingredients found in D.nobile, a top grade plant in Shen Nong Ben Cao Jing, with an extensive history of medicinal use in Chinese traditional medicine (TCM) as a multifunctional therapeutic agent. Recent evidence has emerged linking the neuroprotective and anti-aging effects of DNLA to their involvement in promoting autophagy of toxic amyloid-β (Aβ) plaques and modulation of key enzymes involved in the hyperphosphorylation of Tau proteins. Although amyloid buildup and the aggregation of Tau proteins are central to the onset of Alzheimer's disease (AD), evidence on how DNLA relate to other overlooked dysregulated AD-associated pathways is still lacking.

Methods

We intend on deciphering the underlying mechanisms driving the anti-AD effect of DNLA, using a combination of network analysis based on differentially expressed genes found in AD patients, target fishing, centrality analysis, enrichment analysis and hub genes identification.

Results

In total, 2069 genes were found differentially expressed in SRP181886 and a PPI network constructed with common targets between DNLA and AD. Five hub genes were identified having a discriminatory power greater than 0.7; HTR2A, GRIN2B, GABRA1, HTR2C, GRIN2A, with the former being the top bottleneck node in the network. Enrichment analysis found that DNLA exert an anti-AD effect through the regulation of the calcium signaling pathway and the serotonergic system, by modulating key receptors implicated in excitatory/inhibitory neurotransmission. Additionally, DNLA were found to modulate two subunits of NMDA receptor involved in the release of pro-inflammatory cytokines, underlying the possible involvement of DNLA in neuroinflammation.

Discussion

This further emphasizes the therapeutic value of D.nobile and the multi-target, multi-pathway potential of DNLA to counteract the deleterious effects of calcium dysregulation and excitatory toxicity in AD, while providing evidence-based rationale behind the traditional use of D. nobile in TCM.

导言金钗石斛(Dendrobium nobile Lindl alkaloids,简称DNLA)是《神农本草经》中最高级植物金钗石斛中发现的最有效成分,在中国传统医学(中医)中作为一种多功能治疗药物有着广泛的药用历史。最近有证据表明,DNLA 的神经保护和抗衰老作用与它们参与促进有毒淀粉样蛋白-β(Aβ)斑块的自噬和调节参与 Tau 蛋白过度磷酸化的关键酶有关。虽然淀粉样蛋白的堆积和Tau蛋白的聚集是阿尔茨海默病(AD)发病的核心原因,但目前仍缺乏证据证明DNLA与其他被忽视的AD相关途径失调之间的关系。结果在 SRP181886 中总共发现了 2069 个差异表达基因,并构建了 DNLA 和 AD 之间具有共同靶点的 PPI 网络。其中,HTR2A、GRIN2B、GABRA1、HTR2C、GRIN2A 是该网络中最重要的瓶颈节点。富集分析发现,DNLA 通过调节与兴奋/抑制性神经递质有关的关键受体,通过调节钙信号通路和血清素能系统发挥抗AD 作用。讨论这进一步强调了金钗的治疗价值以及 DNLA 多靶点、多途径的潜力,以对抗 AD 中钙调节失调和兴奋毒性的有害影响,同时为金钗在中医药中的传统应用提供了循证依据。
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引用次数: 0
A comprehensive review of cellular stress response pathway system of Rhizoma coptidis 黄连细胞应激反应途径系统综述
Pub Date : 2024-08-03 DOI: 10.1016/j.prmcm.2024.100491
Alok Batt , Kuldeep Singh , Jeetendra Kumar Gupta , Dilip Kumar Chanchal , Kamlesh Kumar , Anubhav Dubey , Shivendra Kumar , Divya Jain

Introduction

Cellular stress responses play a crucial role in maintaining cellular homeostasis and combating various pathological conditions. Understanding the stress response mechanisms triggered by R. coptidis is critical for harnessing its therapeutic potential. This herb is widely used, but the precise cellular mechanisms through which it exerts its therapeutic effects remain less explored. This review aims to elucidate how R. coptidis affects key cellular pathways and its potential as a therapeutic agent.

Method

This review examines existing evidence on the cellular mechanisms and stress response pathways influenced by R. coptidis. The analysis focuses on the regulation of NF-κB, MAPK, PI3K-Akt, AMPK, ERS, and oxidative stress pathways. Sources include peer-reviewed articles, clinical studies, and traditional Chinese medicine (TCM) literature.

Results

Evidence indicates that R. coptidis exerts beneficial effects on various diseases by modulating the NF-κB, MAPK, PI3K-Akt, AMPK, ERS, and oxidative stress pathways. By targeting these pivotal pathways, R. coptidis mitigates cellular damage and restores homeostasis under pathological conditions.

Conclusion

Understanding the cellular stress response and molecular mechanisms of R. coptidis highlights its multifaceted therapeutic potential. These findings underscore the importance of integrating TCM approaches into modern therapeutic strategies for combating complex diseases. Further investigations into the molecular targets and clinical efficacy of R. coptidis are needed to fully realize its therapeutic potential.

引言 细胞应激反应在维持细胞稳态和对抗各种病症方面发挥着至关重要的作用。了解 R. coptidis 引发的应激反应机制对于利用其治疗潜力至关重要。这种草药被广泛使用,但对其发挥治疗作用的确切细胞机制的探索仍然较少。本综述旨在阐明 R. coptidis 如何影响关键的细胞通路及其作为治疗剂的潜力。分析的重点是 NF-κB、MAPK、PI3K-Akt、AMPK、ERS 和氧化应激途径的调节。结果有证据表明,R. coptidis 可通过调节 NF-κB、MAPK、PI3K-Akt、AMPK、ERS 和氧化应激途径对各种疾病产生有益影响。通过靶向这些关键途径,R. coptidis 可减轻细胞损伤并恢复病理条件下的平衡。这些发现强调了将中医方法融入现代治疗策略以防治复杂疾病的重要性。要充分发挥 R. coptidis 的治疗潜力,还需要进一步研究其分子靶点和临床疗效。
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引用次数: 0
Erratum to “Exploring the potential mechanism of Dayuanyin in treating acute lung injury: A network pharmacology and experimental verification approach” [Pharmacological Research - Modern Chinese Medicine, Volume 12, September 2024, 100483] 对《大黄治疗急性肺损伤的潜在机制探讨》的勘误:网络药理学与实验验证方法"[《药理研究-现代中药》第12卷,2024年9月,100483] 更正
Pub Date : 2024-08-02 DOI: 10.1016/j.prmcm.2024.100489
Bei Huang , Wen Zhang , Rui Li , Yifei Xie , Haiguang Yang , Junke Song , Xiaobin Pang , Guanhua Du
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引用次数: 0
Neuroprotective effects of Hibiscus sabdariffa var. altissima on cerebral ischemia‒Reperfusion injury in rats 木槿花对大鼠脑缺血再灌注损伤的神经保护作用
Pub Date : 2024-08-02 DOI: 10.1016/j.prmcm.2024.100485
Adjia Hamadjida , Saida Nkuketgnigni Njemguie , Rigobert Espoir Ayissi Mbomo , Stephen Nkengbang Foudjih , Véronique France Prisca Amayapa , Jean Pierre Kilekoung Mingoas , Fidèle Ntchapda

Background

Hibiscus sabdariffa var. altissima, which is known for its high-quality fiber, is commonly used in Traditional Chinese Medicine (TCM) for its diuretic, choleretic, analgesic, antitussive, and hypotensive effects. Furthermore, the flowers have been used to treat diabetes, hypertension, atherosclerosis, and obesity. However, there are no studies assessing its neuroprotective effects on cerebral ischemia, unlike the sabdariffa variety known for its neuroprotective effects. Therefore, this study was aimed to investigate the potential efficacy of Hibiscus sabdariffa var. altissima extract (HAS) and its underlying mechanism on oxidative stress and neuroinflammation during cerebral ischemia-reperfusion (I/R) injury.

Methods

A model of cerebral ischemia was established in male Wistar rats through middle cerebral artery occlusion (MCAO) and reperfusion. Rats were randomly divided into the sham, IR, IR + HSA100, IR + HSA200, IR + HSA400 and IR + Eda groups and were treated for 14 consecutive days. The neurological deficit score and the cylinder test were performed to assess neurological impairment. Oxidative stress was determined by measuring the levels of malondialdehyde (MDA) and antioxidant markers such as reduced glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) were measured to evaluate antioxidant activities. In addition, the levels of inflammatory cytokines, including tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6), were also determined.

Results

Our results demonstrated that HSA significantly ameliorated neurological impairment and reduced the volume of brain infarct. HSA also decreased the levels of MDA and enhanced the antioxidant activities of GSH, SOD and CAT in brain tissues. Furthermore, HSA decreased the expression of the proinflammatory cytokines TNF-α, IL-1β and IL-6 in the serum.

Conclusion

These findings demonstrated that HSA exhibited a potential neuroprotective effect against cerebral I/R injury, possibly by improving oxidative stress and attenuating inflammatory responses. Therefore, HSA could be used as a potential therapeutic option for cerebral ischemic injuries.

背景木槿花(Hibiscus sabdariffa var. altissima)以其优质纤维而闻名,中医常用其利尿、利胆、镇痛、止咳和降压作用。此外,菊花还被用于治疗糖尿病、高血压、动脉粥样硬化和肥胖症。然而,目前还没有研究评估其对脑缺血的神经保护作用,这与以神经保护作用而闻名的沙巴叶品种不同。因此,本研究旨在探讨木槿提取物(HAS)对脑缺血再灌注(I/R)损伤过程中氧化应激和神经炎症的潜在疗效及其内在机制。方法通过大脑中动脉闭塞(MCAO)和再灌注建立雄性 Wistar 大鼠脑缺血模型。将大鼠随机分为假组、IR 组、IR + HSA100 组、IR + HSA200 组、IR + HSA400 组和 IR + Eda 组,连续治疗 14 天。进行神经功能缺损评分和量筒测试以评估神经功能损伤。通过测量丙二醛(MDA)水平确定氧化应激,并测量还原型谷胱甘肽(GSH)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)等抗氧化标志物以评估抗氧化活性。此外,还测定了肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)等炎症细胞因子的水平。HSA 还降低了脑组织中 MDA 的水平,提高了 GSH、SOD 和 CAT 的抗氧化活性。此外,HSA 还能降低血清中促炎细胞因子 TNF-α、IL-1β 和 IL-6 的表达。因此,HSA 可作为脑缺血损伤的一种潜在治疗选择。
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引用次数: 0
Neuroprotective action of hordenine against the Aluminium Chloride (AlCl3) induced Alzheimer's diseases & associated memory impairment in experimental rats 大麦芽碱对氯化铝(AlCl3)诱导的阿尔茨海默病及实验鼠相关记忆损伤的神经保护作用
Pub Date : 2024-08-02 DOI: 10.1016/j.prmcm.2024.100492
Mohit Agrawal , Manmohan Singhal , Bhupesh Chander Semwal , Swamita Arora , Bhoopendra Singh , Vandana Sikarwar , Pranshul Sethi , Hema Chaudhary , Wasim Akram , Samir Bhargva , Bhavna Kumar , Sunam Saha , Shivendra Kumar

Objective

To investigate the neuroprotective action of hordenine against the cognitive dysfunction induced by aluminium chloride (AlCl3) in Wistar rats

Methodology

Rats were given oral doses of hordenine (25 and 50 mg/kg), donepezil (5 mg/kg), and AlCl3 (175 mg/kg) for 28 days. During the study, neurobehavioral parameters included Morris water maze (MWM), open field test (OFT), and novel object recognition test (NORT) to assess the cognitive effect. On the 29th day rats were sacrificed and brain tissues removed for biochemical and histopathological analyses.

Results

AlCl3 rats exhibited altered neurobehavioral patterns and cognitive impairment in experimental rats. Although AlCl3 raised the levels of mid-brain acetylcholinesterase (AChE), lipid peroxidation (LPO), nitrite, tumour necrosis factor-α (TNF-α), interleukin-β (IL-β), nuclear factor-kappa B (NF-κB), brain-derived neurotrophic factor (BDNF), and it decreased the levels of antioxidants including glutathione (GSH), catalase, superoxide dismutase (SOD), and body weight. In cortical and hippocampal slices, AlCl3 also revealed anatomical alterations that resulted in a decrease in the density of microglia. But donepezil and hordenine reversed these alterations to normal while demonstrating a neuroprotective effect against AD which is caused by AlCl3.

Conclusion

Hordenine improved memory and other cognitive functions, demonstrating a neuroprotective effect against AlCl3-induced Alzheimer's disease. These findings imply that hordenine may be able to reverse the effects of oxidative stress and neuroinflammation, improve cognitive decline, and protect the brain's histological structure.

目的 研究大麦芽碱对氯化铝(AlCl3)诱导的 Wistar 大鼠认知功能障碍的神经保护作用方法 给大鼠口服大麦芽碱(25 和 50 mg/kg)、多奈哌齐(5 mg/kg)和 AlCl3(175 mg/kg),连续 28 天。研究期间,神经行为指标包括莫里斯水迷宫(MWM)、开阔地测试(OFT)和新物体识别测试(NORT),以评估认知效应。第 29 天,大鼠被处死,脑组织被取出进行生化和组织病理学分析。虽然 AlCl3 提高了中脑乙酰胆碱酯酶 (AChE)、脂质过氧化物 (LPO)、亚硝酸盐、肿瘤坏死因子-α (TNF-α)、白细胞介素-β (IL-β)、核因子-Kappa B (NF-κB)、脑源性神经营养因子 (NF-κB)脑源性神经营养因子(BDNF),并降低抗氧化剂的水平,包括谷胱甘肽(GSH)、过氧化氢酶、超氧化物歧化酶(SOD)和体重。在大脑皮层和海马切片中,AlCl3 还显示出解剖学改变,导致小胶质细胞密度下降。结论大麦芽碱能改善记忆力和其他认知功能,对 AlCl3 引起的阿尔茨海默病具有神经保护作用。这些研究结果表明,大麦芽碱可能能够逆转氧化应激和神经炎症的影响,改善认知功能的衰退,并保护大脑的组织结构。
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引用次数: 0
Erratum to “The efficacy of Panax ginseng in obesity and the related metabolic disorders” [Pharmacological Research - Modern Chinese Medicine, Volume 1, December 2021, 100013] 三七对肥胖症及相关代谢紊乱的疗效》(《药理研究-现代中药》第1卷,2021年12月,100013)的勘误
Pub Date : 2024-08-02 DOI: 10.1016/j.prmcm.2024.100490
Charalampia Amerikanou, Andriana C. Kaliora, Aristea Gioxari
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引用次数: 0
期刊
Pharmacological Research - Modern Chinese Medicine
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