antiinflammatory

抗炎
  • 文章类型: Journal Article
    黄酮类化合物是各种水果中的生物活性化学物质,植物,蔬菜,和叶子,在医学科学中有很好的用途。这些天然化学物质的健康特性被广泛接受,并且正在努力提取被称为类黄酮的特定成分。黄酮类化合物表现出多种生物活性,抗癌,抗氧化活性,抗胆碱酯酶活性,抗炎活性,抗疟疾活性,抗糖尿病活性,神经退行性疾病,心血管效应,保肝作用,和抗病毒和抗菌活性。本研究旨在考察类黄酮调查研究的流行趋势,阐明类黄酮的活性,检查它们的各种功能和用途,评估类黄酮作为慢性疾病预防药物的潜力,并概述该领域未来的研究机会。本文探讨了黄酮类化合物在预防和管理各种疾病中的多种功能。
    Flavonoids are biologically active chemicals in various fruits, plants, vegetables, and leaves, which have promising uses in medicinal science. The health properties of these natural chemicals are widely accepted, and efforts are underway to extract the specific components referred to as flavonoids. Flavonoids demonstrate a diverse range of bio-activities, anticancer, antioxidant activity, anti-cholinesterase activity, antiinflammatory activity, antimalarial activity, antidiabetic activity, neurodegenerative disease, cardiovascular effect, hepatoprotective effects, and antiviral and antimicrobial activity. This study aims to examine the prevailing trends in flavonoid investigation studies, elucidate the activity of flavonoids, examine their various func-tions and uses, assess the potential of flavonoids as preventive medications for chronic diseases, and outline future research opportunities in this field. This review explores the diverse functions of flavonoids in preventing and managing various diseases.
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  • 文章类型: Journal Article
    目的:糖尿病(DM)是一组代谢性疾病,其特征是由于胰岛素的产生或功能异常而导致血液中葡萄糖水平升高。医学营养治疗(MNT)是糖尿病管理的重要组成部分。膳食脂肪在慢性疾病的预防和进展中都是必不可少的。ω-3多不饱和脂肪酸因其对健康的有利影响而被认识到。它们有助于控制所有类型糖尿病患者的血糖水平和血脂状况。此外,它们减少了与DM相关的心血管事件和死亡的发生.
    结果:在评估抗氧化剂后,抗炎,抗血脂,和omega-3脂肪酸补充剂的抗糖尿病机制,以及随机对照研究的结果,很明显,这些补充剂在预防和治疗糖尿病方面都有积极的作用,以及预防和治疗与糖尿病有关的并发症,特别是心血管疾病。然而,目前的证据不支持在糖尿病患者中使用omega-3补充剂来预防或治疗心血管事件.建议所有类型的糖尿病患者每周两次在饮食中加入富含脂肪的鱼类和富含omega-3脂肪酸的食物,这是为普通人群规定的。
    OBJECTIVE: Diabetes mellitus (DM) is a group of metabolic illnesses characterized by elevated levels of glucose in the bloodstream as a result of abnormalities in the generation or function of insulin. Medical Nutrition Therapy (MNT) is an essential component of diabetes management. Dietary fats are essential in both the prevention and progression of chronic diseases. Omega-3 polyunsaturated fatty acids are recognized for their advantageous impact on health. They assist in controlling blood sugar levels and lipid profile in patients with all types of diabetes. Furthermore, they reduce the occurrence of cardiovascular events and death linked to DM.
    RESULTS: After evaluating the antioxidant, anti-inflammatory, antilipidemic, and antidiabetic mechanisms of omega-3 fatty acid supplements, as well as the results from randomized controlled studies, it is clear that these supplements have positive effects in both preventing and treating diabetes, as well as preventing and treating complications related to diabetes, specifically cardiovascular diseases. However, current evidence does not support the use of omega-3 supplementation in people with diabetes for the purpose of preventing or treating cardiovascular events. People with all types of diabetes are suggested to include fatty fish and foods high in omega-3 fatty acids in their diet twice a week, as is prescribed for the general population.
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  • 文章类型: Journal Article
    虽然肝素在近一个世纪以来一直是临床实践中的关键抗凝剂,近年来,人们对其作为有效的抗炎和抗病毒剂的作用越来越感兴趣,以及抗癌剂。为了应对基于注射的输送的挑战,探索患者友好的途径,如口服和肺部分娩至关重要.这篇综述特别强调了吸入肝素的多种治疗益处。总之,这篇评论是一个有价值的信息来源,深入了解吸入肝素的各种治疗优势及其在临床环境中的潜在应用。
    While heparin has traditionally served as a key anticoagulant in clinical practice for nearly a century, recent years have witnessed a growing interest in its role as a potent antiinflammatory and antiviral agent, as well as an anticancer agent. To address challenges with injection-based delivery, exploring patient-friendly routes such as oral and pulmonary delivery is crucial. This review specifically highlights the multiple therapeutic benefits of inhaled heparin. In summary, this review serves as a valuable source of information, providing deep insights into the diverse therapeutic advantages of inhaled heparin and its potential applications within clinical contexts.
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  • 文章类型: Journal Article
    近年来,已经采取了各种举措来控制COVID-19大流行,从限制社会活动的措施到分析药物和疫苗。关于草药的研究在各个国家也越来越多地作为辅助疗法或补充剂进行。因此,本系统综述旨在通过随机对照试验方法,通过临床试验,对各国草药的疗效进行分析。住院时间(LOS)的结果,负转换时间(NCT),负转化率(NCR)是主要焦点。
    使用包括PubMed在内的知名数据库对2019年至2023年的文献进行了广泛的回顾,Scopus,还有Cochrane.搜索包括相关关键词,如“随机对照试验,\"\"COVID-19,\"和\"草药。\"
    共有8篇文章是纳入标准的一部分,结果为LOS,NCT,NCR就LOS结果而言,所有类型的草药都显示出显著的效果,如波斯医学草药(PM草药),波斯大麦水(PBW),金银颗粒(JY颗粒),热毒宁注射液,和余甘菊(Amla)。然而,只有JY颗粒在NCR结局中显示出显著结果,而JY颗粒和热毒宁注射液对降低NCT有明显效果。
    这些发现丰富了我们对草药在影响LOS方面的潜在益处的理解。COVID-19患者的NCR和NCT参数。草药通过抗病毒治疗COVID-19,抗炎,和免疫调节机制。
    UNASSIGNED: In recent years, diverse initiatives have been carried out to control the COVID-19 pandemic, ranging from measures restricting social activities to analyzing drugs and vaccines. Studies on herbal medicines are also increasingly conducted in various countries as an adjuvant therapy or supplement. Therefore, this systematic review aimed to investigate the efficacy of herbal medicines analyzed from various countries through clinical trials with the randomized controlled trial method. The outcomes of Length of Stay (LOS), Negative Conversion Time (NCT), and Negative Conversion Rate (NCR) were the main focus.
    UNASSIGNED: An extensive review of literature spanning from 2019 to 2023 was carried out using well-known databases including PubMed, Scopus, and Cochrane. The search included relevant keywords such as \"randomized controlled trial,\" \"COVID-19,\" and \"herbal medicine.\"
    UNASSIGNED: A total of 8 articles were part of the inclusion criteria with outcomes of LOS, NCT, and NCR. In terms of LOS outcomes, all types of herbal medicines showed significant results, such as Persian Medicine Herbal (PM Herbal), Persian Barley Water (PBW), Jingyin Granules (JY granules), Reduning Injection, and Phyllanthus emblica (Amla). However, only JY granules showed significant results in NCR outcome, while JY granules and Reduning Injection showed significant results in reducing NCT.
    UNASSIGNED: These findings enrich our understanding of the potential benefits of herbal medicines in influencing LOS, NCR and NCT parameters in COVID-19 patients. Herbal medicines worked to treat COVID-19 through antiviral, anti-inflammatory, and immunomodulatory mechanisms.
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  • 文章类型: Journal Article
    新生儿时代死亡和发病的一个重要原因是缺氧缺血性脑病(HIE)。这项研究检查了实验性HIE大鼠模型中的组织病理学分析和丁香素(SYR)的神经保护作用。
    在产后第七天,在气体麻醉下使用HIE模型将24只Wistar白化病大鼠分为3组进行评估。在实验中,A组接受10mg/kgSYR加二甲基亚砜(DMSO),B组仅接受DMSO,C组为假手术组。免疫组织化学技术用于评估凋亡细胞测量和促炎细胞因子(TNF-α和IL-1β一级抗体)。
    评估患有缺氧缺血性脑损伤的大鼠的细胞凋亡。SYR和假手术组具有统计学上较少的经历凋亡的细胞(p<0.001)。在免疫组织化学染色过程中,两组之间在IL-1β和TNF-α方面没有差异。SYR组海马的组织学评价中神经元变性显著降低(p=0.01)。在SYR组和对照组之间观察到关于细胞周和血管周水肿的统计学显著差异(p=0.01)。
    SYR减少细胞凋亡,血管周围和细胞周围水肿,和大鼠脑组织中的神经元变性。这些结果增加了SYR可能对HIE带来的损害具有神经保护作用的可能性。这是在HIE范式中对SYR\的功能的首次研究。
    UNASSIGNED: A significant cause of mortality and morbidity in the neonatal era is hypoxic-ischemic encephalopathy (HIE). This study examined the histopathological analysis and neuroprotective impact of syringin (SYR) in an experimental HIE rat model.
    UNASSIGNED: On the 7th postnatal day, 24 Wistar albino rats were evaluated in 3 groups using the HIE model under gas anesthesia. In the experiment, Group A received 10 mg/kg SYR plus dimethyl sulfoxide (DMSO), Group B received DMSO only, and Group C served as a sham group. Immunohistochemical techniques were used to assess apoptotic cell measurement and proinflammatory cytokines (TNF-α and IL-1β primary antibodies).
    UNASSIGNED: Rats suffering from hypoxic-ischemic brain damage had their apoptosis assessed. The SYR and sham groups had statistically fewer cells undergoing apoptosis (p < 0.001). There was no difference between the groups in terms of IL-1β and TNF-α during immunohistochemical staining. Neuronal degeneration was significantly lower in the histological evaluation of the hippocampus in the SYR group (p = 0.01). A statistically significant difference (p = 0.01) was observed between the SYR and the control groups regarding pericellular and perivascular edema.
    UNASSIGNED: SYR reduced apoptosis, perivascular and pericellular edema, and neuronal degeneration in rat cerebral tissue. These results raise the possibility that SYR may have a neuroprotective effect on the harm brought on by HIE. This is the first investigation of SYR\'s function within the HIE paradigm.
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  • 文章类型: Journal Article
    扰乱或破坏皮肤伤口的正常愈合过程可能导致其进展为慢性状态。慢性伤口通常会导致感染增加,因为它们的愈合时间长,营养不良,氧气流量不足,随后影响伤口进展。明胶是天然胶原蛋白的主要结构,因其价格低廉,被广泛应用于生物医学领域,广泛的可用性,生物相容性,和降解性。然而,明胶可以表现出不同的定制的物理性质和差的抗菌活性。明胶基生物材料的研究发现了改善明胶抗菌性能差和机械性能低的挑战。在慢性伤口中,明胶基生物材料可以促进伤口止血,增强伤口周围的抗菌和抗炎特性,促进血管和上皮细胞再生。在这篇文章中,我们首先介绍伤口愈合的自然过程。第二,我们介绍了明胶基生物材料和明胶作为添加剂在伤口愈合中的作用。最后,我们提出了明胶基生物材料的未来意义。
    Disturbing or disrupting the regular healing process of a skin wound may result in its progression to a chronic state. Chronic wounds often lead to increased infection because of their long healing time, malnutrition, and insufficient oxygen flow, subsequently affecting wound progression. Gelatin-the main structure of natural collagen-is widely used in biomedical fields because of its low cost, wide availability, biocompatibility, and degradability. However, gelatin may exhibit diverse tailored physical properties and poor antibacterial activity. Research on gelatin-based biomaterials has identified the challenges of improving gelatin\'s poor antibacterial properties and low mechanical properties. In chronic wounds, gelatin-based biomaterials can promote wound hemostasis, enhance peri-wound antibacterial and anti-inflammatory properties, and promote vascular and epithelial cell regeneration. In this article, we first introduce the natural process of wound healing. Second, we present the role of gelatin-based biomaterials and gelatin as an additive in wound healing. Finally, we present the future implications of gelatin-based biomaterials.
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  • 文章类型: Journal Article
    植物化学研究防风菜的根(Turcz。)Schischk分离了十二种香豆素衍生物,包括一种新的3,4-二氢异香豆素(1)和十一种已知的3,4-未取代的香豆素(2-12)。化合物1-12的结构阐明通过参考文献的1D和2DNMR光谱建立,与高分辨率质谱分析。使用LPS诱导的RAW264.7炎症细胞模型来确定所有分离的化合物在体外的潜在抗炎活性。结果显示,化合物3显著抑制脂多糖(LPS)诱导的巨噬细胞NO的产生(IC50=4.54±1.71μM),比阳性对照(L-NMMA)更活跃。
    Phytochemical investigation of the roots of Saposhnikovia divaricata (Turcz.) Schischk resulted in the isolation of twelve coumarin derivatives including one new 3,4-dihydroisocoumarin (1) and eleven known 3,4-unsubstituted coumarins (2-12). Structural elucidation of compounds 1-12 was established by 1D and 2D NMR spectra referring to the literature, together with high-resolution mass spectrometric analysis. LPS-induced RAW264.7 inflammatory cell model was used to determine the potential antiinflammation activity of all the isolated compounds in vitro. The results showed that compound 3 significantly inhibited the production of lipopolysaccharide (LPS)-induced NO in macrophages (IC50 = 4.54 ± 1.71 μM), more active than the positive control (L-NMMA).
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  • 文章类型: Journal Article
    简介:癌症,一个重大的全球健康问题,需要创新的治疗方法。慢性炎症在癌症发展中的关键作用强调了新治疗策略的紧迫性。苯并噻唑衍生物由于其独特的结构和广谱的生物效应而显示出希望。本研究旨在基于苯并噻唑骨架的优势,探索同时具有抗炎和抗癌作用的新型抗肿瘤小分子药物。方法:采用核磁共振(NMR)对化合物进行表征,液相色谱-质谱(LC-MS)和高效液相色谱(HPLC)的结构以及纯度和其他相关的理化性质。采用MTT法评价化合物对人表皮样癌细胞系(A431)和人非小细胞肺癌细胞株(A549、H1299)增殖的影响。使用酶联免疫吸附测定(ELISA)评估化合物对小鼠单核细胞巨噬细胞(RAW264.7)中炎性因子IL-6和TNF-α表达水平的影响。流式细胞术评价化合物对A431和A549细胞凋亡和细胞周期的影响。化合物对A431和A549细胞迁移的影响通过划痕伤口愈合试验来评价。化合物对A431和A549细胞中蛋白质表达水平的影响通过蛋白质印迹分析来评估。物理化学参数,药代动力学特性,使用瑞士ADME和admetSAR网络服务器预测活性化合物的毒性和药物相似性。结果:设计合成了25个新型苯并噻唑类化合物,通过频谱图验证确认了它们的结构。通过一系列生物活性评估筛选活性化合物6-氯-N-(4-硝基苄基)苯并[d]噻唑-2-胺(化合物B7),显著抑制A431、A549和H1299癌细胞的增殖,降低IL-6和TNF-α的活性,阻碍细胞迁移。此外,浓度为1、2和4μM,B7表现出与先导化合物7-氯-N-(2,6-二氯苯基)苯并[d]噻唑-2-胺(化合物4i)相似的促凋亡和细胞周期阻滞作用。Western印迹分析证实B7抑制A431和A549细胞中的AKT和ERK信号通路。ADMET的预测结果表明B7具有良好的药物性质。讨论:本研究创新性地开发了一系列苯并噻唑衍生物,由于其显着的双重抗癌和抗炎活性,因此重点关注化合物B7。B7以其显着降低A431,A549和H1299细胞系中癌细胞增殖并降低炎性细胞因子IL-6和TNF-α水平的能力而脱颖而出。这些结果将B7B7定位为双重作用癌症治疗的有希望的候选者。这项研究的机理探索,强调B7同时抑制AKT和ERK途径,为解决肿瘤细胞的存活机制和促进癌症进展的炎症环境提供了一种新的策略。
    Introduction: Cancer, a significant global health concern, necessitates innovative treatments. The pivotal role of chronic inflammation in cancer development underscores the urgency for novel therapeutic strategies. Benzothiazole derivatives exhibit promise due to their distinctive structures and broad spectrum of biological effects. This study aims to explore new anti-tumor small molecule drugs that simultaneously anti-inflammatory and anticancer based on the advantages of benzothiazole frameworks. Methods: The compounds were characterized by nuclear magnetic resonance (NMR), liquid chromatograph-mass spectrometer (LC-MS) and high performance liquid chromatography (HPLC) for structure as well as purity and other related physicochemical properties. The effects of the compounds on the proliferation of human epidermoid carcinoma cell line (A431) and human non-small cell lung cancer cell lines (A549, H1299) were evaluated by MTT method. The effect of compounds on the expression levels of inflammatory factors IL-6 and TNF-α in mouse monocyte macrophages (RAW264.7) was assessed using enzyme-linked immunosorbent assay (ELISA). The effect of compounds on apoptosis and cell cycle of A431 and A549 cells was evaluated by flow cytometry. The effect of compounds on A431 and A549 cell migration was evaluated by scratch wound healing assay. The effect of compounds on protein expression levels in A431 and A549 cells was assessed by Western Blot assay. The physicochemical parameters, pharmacokinetic properties, toxicity and drug similarity of the active compound were predicted using Swiss ADME and admetSAR web servers. Results: Twenty-five novel benzothiazole compounds were designed and synthesized, with their structures confirmed through spectrogram verification. The active compound 6-chloro-N-(4-nitrobenzyl) benzo[d] thiazol-2-amine (compound B7) was screened through a series of bioactivity assessments, which significantly inhibited the proliferation of A431, A549 and H1299 cancer cells, decreased the activity of IL-6 and TNF-α, and hindered cell migration. In addition, at concentrations of 1, 2, and 4 μM, B7 exhibited apoptosis-promoting and cell cycle-arresting effects similar to those of the lead compound 7-chloro-N-(2, 6-dichlorophenyl) benzo[d] thiazole-2-amine (compound 4i). Western blot analysis confirmed that B7 inhibited both AKT and ERK signaling pathways in A431 and A549 cells. The prediction results of ADMET indicated that B7 had good drug properties. Discussion: This study has innovatively developed a series of benzothiazole derivatives, with a focus on compound B7 due to its notable dual anticancer and anti-inflammatory activities. B7 stands out for its ability to significantly reduce cancer cell proliferation in A431, A549, and H1299 cell lines and lower the levels of inflammatory cytokines IL-6 and TNF-α. These results position B7B7 as a promising candidate for dual-action cancer therapy. The study\'s mechanistic exploration, highlighting B7\'s simultaneous inhibition of the AKT and ERK pathways, offers a novel strategy for addressing both the survival mechanisms of tumor cells and the inflammatory milieu facilitating cancer progression.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    背景:源自天然来源的植物产品已在药物中用作原料,并在药物和其他相关卫生部门中用作新型药物分子。植物化学品具有许多药用潜力,包括抗衰老,抗癌,抗微生物,抗氧化剂,和药物中的抗炎活性。草药产品在现代医学中的开发和生物应用标志着传统药用植物在医疗保健系统中的价值。
    方法:本研究的目的是探索蒿甲醚在医学中的药用价值和治疗潜力的科学知识。然而,通过对PubMed收集的不同科学研究工作的科学数据分析,对其在医学中的药理活性进行了科学研究,Google,ScienceDirect和GoogleScholar旨在了解蒿甲醚在医学中的生物学重要性。此外,本工作还讨论了artemetin的分析数据。
    结果:目前的工作和科学数据表明了artemetin在医学中的生物学潜力。Artemetin来自许多药用植物和膳食草药,包括艾蒿,Artemisiaargyi,Achilleamillefolium,和三叶草。蒿甲醚具有抗疟疾作用,抗氧化剂,抗凋亡,抗微生物,抗肿瘤,抗动脉粥样硬化,抗炎,降压和保肝作用。Further,蒿甲醚对脂质氧化的生物学作用,细胞因子产生,脂氧合酶,在目前的工作中也研究了雌激素样作用。本文对蒿甲醚的分析数据表明了它们在分离中的重要作用,分离,并鉴定不同类别的纯植物化学物质,包括医药上的蒿甲醚。
    结论:对青蒿素的科学数据分析表明其在医学上的治疗潜力,可用于开发针对不同人类疾病的新科学方法。
    BACKGROUND: Plant products derived from natural sources have been used in medicine as a raw material and newer kinds of drug molecules in pharmaceuticals and other allied health sectors. Phytochemicals have numerous medicinal potentials, including anti- ageing, anti-carcinogenic, anti-microbial, anti-oxidant, and anti-inflammatory activity in medicine. Development and biological application of herbal products in modern medicine signified the value of traditional medicinal plants in health care systems.
    METHODS: The objective of the present study was to explore the scientific knowledge of the medicinal importance and therapeutic potential of artemetin in medicine. However, scientific investigations for their pharmacological activities in medicine have been done through scientific data analysis of different scientific research work collected from PubMed, Google, Science Direct and Google Scholar in order to know the biological importance of artemetin in medicine. Moreover, analytical data of artemetin have also been discussed in the present work.
    RESULTS: The present work scientific data signified the biological potential of artemetin in medicine. Artemetin has been derived from numerous medicinal plants and dietary herbs, including Artemisia absinthium, Artemisia argyi, Achillea millefolium, and Vitex trifolia. Artemetin has anti-malarial, anti-oxidant, anti-apoptotic, anti-microbial, anti-tumoral, antiatherosclerotic, anti-inflammatory, hypotensive and hepatoprotective effects. Further, the biological role of artemetin on lipid oxidation, cytokine production, lipoxygenase, and estrogen- like effects was also investigated in the present work. Analytical data on artemetin in the present paper signified their important role in the isolation, separation, and identification of different classes of pure phytochemicals, including artemetin in medicine.
    CONCLUSIONS: Scientific data analysis of artemetin signified its therapeutic potential in medicine for the development of newer scientific approaches for different human disorders.
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