Curcuma longa

姜黄
  • 文章类型: Journal Article
    这项研究开发了环境友好的封端技术,通过利用罗莎rubiginosa花的提取物作为还原剂和螯合剂,从异丙醇钛合成姜黄涂层二氧化钛(CR-TiO2)的纳米颗粒。生物合成的纳米粒子显示出优异的抗菌,电化学,和光催化性能由于多孔TiO2纳米结构的存在。XRD图谱显示了TiO2纳米颗粒的结晶度和相纯度。BET分析证明了材料的中孔性质,比表面积为134m2g-1。振动光谱表明,姜黄的类黄酮中的羟基可作为具有可见发光的TiO2纳米多孔结构的官能化试剂,这在荧光光谱中得到了证明,适用于光催化研究。抗菌研究表明,TiO2纳米颗粒对铜绿假单胞菌具有良好的推论,并证明它是一种具有氧化电位的优异的抗假单胞菌剂。在可见光条件下,在TiO2存在下观察到酚红染料的最大降解。使用生物TiO2三电极系统制造的超级电容器表现出128Fg-1(10mVs-1)的比电容,表明它是一种优秀的电极材料。在50mVs-1扫描速率下的LSV曲线表明,CR-TiO2电极的氧还原电位(ORR)为121mV。本研究是纳米粒子在环境可持续性考虑中的新应用,也是解决能源危机的局限性较少。良好区分的抗糖尿病和BSA变性潜力表明,这些多孔TiO2纳米结构可用于作为葡萄糖抑制剂和口服抗炎药的药物递送,并限制不良副作用。
    This study develops environmentally benign capping technique to synthesize nanoparticles of Curcuma longa-coated titanium dioxide (CR-TiO2) from titanium isopropoxide by utilizing the extract of Rosa rubiginosa flowers as reducing and chelating agent. The biogenically synthesized nanoparticles revealed excellent anti-bacterial, electrochemical, and photocatalytic properties due to the presence of porous TiO2 nanostructures. The sharp peaks by XRD pattern showed the crystallinity and phase purity of TiO2 nanoparticles. BET analysis proved mesoporous nature of the materials with specific surface area of 134 m2 g -1. The vibrational spectra suggest hydroxyl groups from flavonoids of Curcuma longa acting as functionalizing agent for TiO2 nanoporous structures with visible luminescence, which is proven in fluorescence spectra and is applicable for photocatalytic studies. The anti-bacterial studies showed good inference on TiO2 nanoparticles against Pseudomonas auruginosa and proved it to be an excellent antipseudomonal agent with the oxidative potential. The maximum degradation of phenol red dye in the presence of TiO2 under visible light conditions was observed. The supercapacitor fabricated using the biogenic TiO2 three-electrode system exhibited a specific capacitance of 128 Fg-1 (10 mV s-1), suggesting it as an excellent electrode material. The LSV curve at 50 mV s-1 scan rate showed that oxygen reduction potential (ORR) of CR-TiO2 electrodes was 121 mV. The present study is a new application of nanoparticles in sustainability consideration of the environment as well as a solution to the power crisis with fewer limitations. The well-distinguished antidiabetic and BSA denaturation potential suggests that these porous TiO2 nanostructures can be useful for drug delivery as glucose inhibitors and oral anti-inflammatory drugs with the restriction of adverse side effects.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    姜黄根茎(CLR),由于其有效的抗氧化植物化学成分,研究了其对双酚A(BPA)引起的心血管和肾脏损害的影响。
    随机选择60只大鼠,并分组为控制,BPA(100mg/kg),BPA和CLR100mg/kg,BPA和CLR200mg/kg,CLR100mg/kg,和CLR200mg/kg,持续21天。氧化应激指数,抗氧化状态,血压参数,遗传毒性,和免疫组化测定。
    暴露于BPA毒性作用的大鼠血压升高,微核多染红细胞的频率降低,与用CLR处理的大鼠相比,抗氧化酶的活性降低。此外,给予CLR显著(p<0.05)降低了丙二醛含量并降低了血清髓过氧化物酶活性。免疫组织化学评估显示,与CLR治疗组相比,BPA组的心肌肌钙蛋白和Caspase3的表达显着增加(p<0.05)。
    C.Longa通过减轻氧化应激改善了双酚A的心脏毒性和肾毒性作用,高血压,和遗传毒性。
    UNASSIGNED: Curcuma longa Rhizome (CLR), due to its potent antioxidant phytochemical constituents, was investigated for its effects on bisphenol A (BPA)-induced cardiovascular and renal damage.
    UNASSIGNED: Sixty rats were randomly selected, and grouped as control, BPA (100 mg/ kg), BPA and CLR 100 mg/kg, BPA and CLR 200 mg/kg, CLR 100 mg/kg, and CLR 200 mg/kg for 21 days. Oxidative stress indices, antioxidant status, blood pressure parameters, genotoxicity, and immunohistochemistry were determined.
    UNASSIGNED: Rats exposed to the toxic effects of BPA had heightened blood pressure, lowered frequency of micronucleated polychromatic erythrocytes, and decreased activities of antioxidant enzymes compared with rats treated with CLR. Moreover, administration of CLR significantly (p<0.05) lowered malondialdehyde content and reduced the serum myeloperoxidase activity. Immunohistochemical evaluation revealed significantly (p<0.05) increased expressions of cardiac troponin and Caspase 3 in the BPA group compared with the CLR-treated groups.
    UNASSIGNED: C. longa ameliorated cardiotoxic and nephrotoxic actions of bisphenol-A via mitigation of oxidative stress, hypertension, and genotoxicity.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    姜黄素,作为抗肿瘤剂,由于其代谢物在癌组织中缺乏有效水平,因此未广泛用于癌症治疗。解决载体的障碍和将药物递送到治疗作用的特定部位,同时减少副作用是优先事项。叶酸受体在恶性细胞中表达高,在正常细胞中表达低。叶酸作为靶向配体可以选择性地靶向癌细胞。因此,这篇叙述性综述旨在概述研究不同类型叶酸修饰的姜黄素作为载体和传递剂的研究及其增强治疗药物疗效的结构特性.使用PubMed进行文献检索,Scopus,WebofScience,和谷歌学者数据库。确定了针对该主题的38项临床前研究。目前的研究结果表明,叶酸修饰的纳米颗粒含有姜黄素作为一种有前途的治疗方法可以有效地改善不同类型的癌症。体外研究显示了更高的细胞摄取和细胞毒性效应,更高的细胞抑制,和抗增殖与较低剂量的姜黄素。体内研究表明,在施用叶酸修饰的含有姜黄素的纳米颗粒后,肿瘤抑制更多,肿瘤体积更小,没有毒性。未来的临床试验需要证实叶酸修饰的姜黄素作为癌症治疗新的药物递送平台的有益效果。
    Curcumin, as an anti-tumor agent, is not widely used in cancer treatment due to the lack of effective levels of its metabolites in cancerous tissue. Addressing the barriers to the carrier and delivery of drugs to the specific sites of therapeutic action while reducing side effects is a priority. Folate receptor expression is high in malignant and low in normal cells. Folate as a targeted ligand could selectively target cancer cells. Thus, this narrative review aimed to provide an overview of the studies that have investigated the different types of folate-modified curcumin as a carrier and deliverer and their structural properties that enhance therapeutic drug efficacy. A literature search was performed using PubMed, Scopus, Web of Science, and Google Scholar databases. Thirty-eight preclinical studies addressing this topic were identified. The findings of the current review have shown that folate-modified nanoparticles containing curcumin as a promising therapeutic approach can be effective in improving different types of cancers. In vitro studies have shown a higher cellular uptake and cytotoxicity effect, higher cell inhibition, and anti-proliferation with a lower dosage of curcumin. In vivo studies have shown more tumor suppression and smaller tumor volume without toxicity after the administration of folate-modified nanoparticles containing curcumin. Future clinical trials are needed to confirm the beneficial effect of folate-modified curcumin as a new drug delivery platform for cancer treatment.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    姜黄素,从姜黄根茎中提取的疏水性多酚,现在被认为是治疗神经系统疾病的候选药物,包括帕金森病(PD),阿尔茨海默病(AD),亨廷顿病(HD),多发性硬化(MS),肌萎缩侧索硬化(ALS),和朊病毒病,由于其有效的抗炎作用,抗氧化潜力,抗癌,免疫调节,神经保护,抗增殖,和抗菌活性。传统上,姜黄素已在亚洲用于医疗和饮食目的,印度,和中国。然而,低水溶性,血液稳定性差,高代谢率,有限的生物利用度,和通过血脑屏障(BBB)的能力很少限制了姜黄素的临床应用,尽管这种药物具有重要的药理活性。各种各样的纳米载体,包括脂质体,胶束,树枝状聚合物,立方体纳米粒子,聚合物纳米颗粒,和固体脂质纳米粒已经成功地开发了有效地将活性药物递送到脑细胞。脑特异性配体在纳米颗粒表面上的功能化使它们具有靶特异性,这应该显着提高生物利用度并减少有害影响。本文的目的是总结姜黄素和/或含姜黄素的纳米颗粒在最常见的神经退行性疾病中的研究。突出了这种营养食品的高神经保护潜力。
    Curcumin, a hydrophobic polyphenol extracted from the rhizome of Curcuma longa, is now considered a candidate drug for the treatment of neurological diseases, including Parkinson\'s Disease (PD), Alzheimer\'s Disease (AD), Huntington\'s Disease (HD), Multiple Sclerosis (MS), Amyotrophic Lateral Sclerosis (ALS), and prion disease, due to its potent anti-inflammatory, antioxidant potential, anticancerous, immunomodulatory, neuroprotective, antiproliferative, and antibacterial activities. Traditionally, curcumin has been used for medicinal and dietary purposes in Asia, India, and China. However, low water solubility, poor stability in the blood, high rate of metabolism, limited bioavailability, and little capability to cross the blood-brain barrier (BBB) have limited the clinical application of curcumin, despite the important pharmacological activities of this drug. A variety of nanocarriers, including liposomes, micelles, dendrimers, cubosome nanoparticles, polymer nanoparticles, and solid lipid nanoparticles have been developed with great success to effectively deliver the active drug to brain cells. Functionalization on the surface of nanoparticles with brain-specific ligands makes them target-specific, which should significantly improve bioavailability and reduce harmful effects. The aim of this review is to summarize the studies on curcumin and/or nanoparticles containing curcumin in the most common neurodegenerative diseases, highlighting the high neuroprotective potential of this nutraceutical.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    姜黄素(CUR)作为食品中发现的生物活性化合物的普遍性和多功能性,化妆品,药物需要从亲本植物中获得最纯净的形式,尤其是姜黄.要有有效的合成,提取,和CUR的纯化,环境可持续,绿色,成本实惠,和安全的方法是非常重要的。为此,我们考虑CUR提取的最新进展,净化,和生物合成。CUR提取中采用的常规和新颖的高通量技术,包括酶辅助,微波辅助,超声辅助,加压液体(亚临界),超临界流体,脉冲电场辅助,和基于离子液体的萃取技术进行了全面的讨论。考虑了CUR的化学/生物合成,并讨论了最近在代谢工程策略方面的进展,以提高CUR的产量。此外,与CUR纯化相关的新技术,如柱层析,半制备高效液相色谱法,高速逆流色谱,制备超临界流体色谱,和结晶进行了详细的讨论。最后,我们讨论了CUR的中试规模以及工业生产和食品应用。
    The ubiquity and versatility of curcumin (CUR) as a bioactive compound found in foods, cosmetics, and pharmaceuticals create the need for its obtainment in the purest forms from the parent plants, especially Curcuma longa. To have efficient synthesis, extraction, and purification of CUR, environmentally sustainable, green, cost-affordable, and safe methods are of immense significance. To this end, we consider recent advancements in CUR extraction, purification, and biosynthesis in this review. The conventional and novel high-throughput techniques employed in CUR extraction including enzyme-assisted, microwave-assisted, ultrasound-assisted, pressurized liquid (subcritical), supercritical fluid, pulsed electric fields-assisted, and ionic liquids-based extraction techniques were comprehensively discussed. The chemical/bio-syntheses of CUR were considered, and the recent advancements in metabolic engineering strategies to enhance the production of CUR were deliberated. Furthermore, novel technologies associated with CUR purification, such as column chromatography, semi-preparative high-performance liquid chromatography, high-speed counter-current chromatography, preparative supercritical fluid chromatography, and crystallization were discussed in detail. We concluded by discussing the pilot scale and industrial production and food applications of CUR.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    外阴阴道念珠菌病(VVC)是15至49岁育龄妇女中的一个真正的妇科问题。最近的一项分析表明,75%的女性每年至少会发生一次,虽然观察到5%的患者复发性阴道真菌病-这些患者每年可能会出现四次或更多次不适。这种病理在85-90%的病例中是由白色念珠菌物种的真菌引起的。由于疼痛和瘙痒,它代表了女性患者的棘手医学问题。由于观察到对标准制剂耐药的菌株数量增加,并且在使用局部或口服优先治疗时这种病理的复发增加,如氟康唑,进行了一项分析,以开发使用诸如dill之类的草药治疗VVC的替代方法,姜黄,还有小檗碱.对包含近年来科学文章的数据库进行了深入分析,从而有可能得出令人满意的结论,以支持草药疗法对有关病理的有效性。尽管植物疗法尚未获得食品和药物管理局的批准,对于对现有治疗有抗性的菌株,它似乎是一种有希望的治疗解决方案。目前正在进行的研究旨在比较经典药物疗法和草药疗法治疗阴道念珠菌病,以提高医疗能力和知识,以照顾妇科患者的健康和长期舒适。
    Vulvovaginal candidiasis (VVC) is a real gynecological problem among women of reproductive age from 15 to 49. A recent analysis showed that 75% of women will have an occurrence at least once per year, while 5% are observed to have recurrent vaginal mycosis-these patients may become unwell four or more times a year. This pathology is caused in 85-90% of cases by fungi of the Candida albicans species. It represents an intractable medical problem for female patients due to pain and pruritus. Due to the observation of an increasing number of strains resistant to standard preparations and an increase in the recurrence of this pathology when using local or oral preferential therapy, such as fluconazole, an analysis was launched to develop alternative methods of treating VVC using herbs such as dill, turmeric, and berberine. An in-depth analysis of databases that include scientific articles from recent years made it possible to draw satisfactory conclusions supporting the validity of herbal therapy for the pathology in question. Although phytotherapy has not yet been approved by the Food and Drug Administration, it appears to be a promising therapeutic solution for strains that are resistant to existing treatments. There is research currently undergoing aimed at comparing classical pharmacotherapy and herbal therapy in the treatment of vaginal candidiasis for the purpose of increasing medical competence and knowledge for the care of the health and long-term comfort of gynecological patients.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    目的:在本研究中,我们采用多维数据挖掘方法来检查徐智音教授治疗甲状腺结节的临床实例。我们的目标是了解症状的模式,根本原因,和甲状腺结节的治疗方法。通过这样做,目的是提炼基本方面,汇编徐智印教授的临床见解,调查他的学术观点。
    方法:将2009-2019年徐智银教授的临床诊断和治疗输入MicrosoftExcel。随后,收集的数据被导入MedcaseV5.2系统,以便于数据挖掘.各种技术,例如基于频率的方法,关联规则分析,和聚类,包括分散式系统集群方法,用于一组346例,涉及符合指定标准的甲状腺结节患者。主要重点是从医疗记录中提取有关症状和根本原因的见解。通过将这些发现与徐智音教授的临床专业知识相结合,我们检查并总结了数据挖掘过程的结果。
    结果:使用跨多维挖掘技术成功提取了基本处方。利用这些处方的分散分组,并参考频联系统的聚类分析,徐智银教授提出的解决甲状腺结节的基本处方包括以下成分:甘草,牡丹皮,赤芍,姜黄,姜黄,桃子种子,陈列柜,半夏,夏枯草,Ostreaeconcha,皂角脊椎,鹿茸和党参。
    结论:使用频率方法获得基本处方,关联规则技术,k均值聚类方法,和系统的聚类方法。研究结果相互印证,证明了徐智音教授对甲状腺结节的区分和治疗方法体现在针对特定疾病的独特处方中。
    OBJECTIVE: In this study, we employed a multi-dimensional data mining approach to examine the clinical instances where Professor Xu Zhiyin treated thyroid nodules. Our aim is to understand the patterns of symptoms, underlying causes, and treatment approaches used for thyroid nodules. By doing so, the intention is to distill the essential aspects, compile Professor Xu Zhiyin\'s clinical insights, and investigate his scholarly perspectives.
    METHODS: Professor Xu Zhiyin\'s clinical diagnoses and treatments spanning from 2009 to 2019 were entered into Microsoft Excel. Subsequently, the collected data was imported into the Medcase V5.2 system to facilitate data mining. Various techniques, such as frequency-based method, association rule analysis, and clustering, including a decentralized system clustering approach, were employed on a set of 346 cases involving patients with thyroid nodules that conformed to the specified criteria. The primary focus was on extracting insights regarding symptoms and the underlying causes from the medical records. By integrating these findings with Professor Xu Zhiyin\'s clinical expertise, we examined and summarized the outcomes of the data mining process.
    RESULTS: The fundamental prescriptions were successfully extracted using the techniques for mining across multiple dimensions. Utilizing the scattered grouping of these prescriptions and with reference to the cluster analysis of the frequency-linked system, the fundamental prescriptions proposed by Professor Xu Zhiyin for addressing thyroid nodules encompass the following ingredients: Glycyrrhiza uralensis Fisch, Cortex Moutan, Paeoniae radix rubra, Curcuma longa L., Radix Curcumae, persica seed, Citri Reticulatae Viride Pericarpium, Pinellia ternata, Spica Prunellae, Ostreae concha, Gleditsia sinensis spine, Tuckahoe and Radix Codonopsis.
    CONCLUSIONS: The fundamental prescriptions were acquired using the frequency approach, association rule technique, k-means clustering approach, and systematic clustering approach. The research findings corroborate one another, demonstrating that Professor Xu Zhiyin\'s approach to distinguishing and treating thyroid nodules is embodied in distinct prescriptions tailored to specific diseases.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    基于菠萝汁的饮料混合物(80-100%),开发了不同浓度的姜黄(0-20%)和生姜(0-20%)汁。单独的菠萝汁表现出15.90-16.03°白利糖度的总可溶性固体(TSS)含量。总多酚含量(TPC)在0.32至1.79mgGAE/mL之间变化,1,1-二苯基-2-吡啶酰肼(DPPH)的抑制作用在40.56%至86.19%之间,与TPC,姜黄素和其他姜黄素相关。具有高纸浆含量的制剂显示出比具有低纸浆含量的制剂显著更高的TPC和更大的DPPH抑制。果肉含量高的姜黄和生姜的挥发性化合物含量较高。小组成员在味道和口感属性上观察到显着差异,并且由于口感更好,低浆汁与适口性增加相关。更高的甜度,减少了苦味,辣味,纸浆,和辣味。感官小组成员最优选具有10%姜黄汁和10%或更少的姜汁的菠萝汁混合物。
    Beverage mixtures based on pineapple juice (80-100%), with varying concentrations of turmeric (0-20%) and ginger (0-20%) juice were developed. The pineapple juice alone exhibited a total soluble solid (TSS) content of 15.90-16.03 °Brix. The total polyphenols content (TPC) varied between 0.32 and 1.79 mg GAE/mL, and the 1,1-diphenyl-2-picrylhydrazyl (DPPH) inhibition was between 40.56% and 86.19% and correlated with the TPC and curcumin and other curcuminoids. The formulations with a high pulp content showed a significantly higher TPC and greater DPPH inhibition than those with a low pulp content. Turmeric and ginger with a high amount of pulp had a higher abundance of volatile compounds. Significant differences were observed by the panelists in the taste and mouthfeel attributes and the low-pulp juices were associated with increased palatability due to the better mouthfeel, higher sweetness, and decreased bitterness, pepperiness, pulpiness, and spiciness. The pineapple juice mixtures with 10% turmeric juice and 10% or less ginger juice were most preferred by sensory panelists.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    联合治疗和多靶点药物最近吸引了很多关注作为有前途的工具,以对抗许多具有挑战性的疾病,因此,代表了一个新的研究重点领域。当前项目的目的是筛选多靶标化合物,并研究它们对对乙酰氨基酚诱导的肝损伤的个体和联合作用。在这项研究中,通过使用分子对接,从姜黄和Cinnamomumzeylanicum中存在的40种主要化合物中选择了2种最佳的肝保护性多靶向化合物,ADMET分析,和辉瑞的第五条规则。选定的两种化合物,槲皮素和姜黄素,显示对CYP2E1酶的高结合亲和力,MAPK,和导致肝损伤的TLR4受体。候选物使癌细胞系(HepG2和Huh7)的活力降低,但对正常细胞系(Vero)没有影响。生化参数检查(ALT,AST,ALP,和胆红素)与对照组相比,显示了候选药物的肝保护作用,组织学发现证实了这一点。一起来看,槲皮素和姜黄素不仅满足药物样评估标准,并且被证明通过预防肝损伤而具有多靶向性,而且还具有抗癌活性。
    Combination therapy and multitarget drugs have recently attracted much attention as promising tools to fight against many challenging diseases and, thus, represent a new research focus area. The aim of the current project was to screen multitarget compounds and to study their individual and combined effects on acetaminophen-induced liver injury. In this study, 2 of the best hepatoprotective multitargeting compounds were selected from a pool of 40 major compounds present in Curcuma longa and Cinnamomum zeylanicum by using molecular docking, ADMET profiling, and Pfizer\'s rule of five. The two selected compounds, quercetin and curcumin, showed a high binding affinity for the CYP2E1 enzyme, MAPK, and TLR4 receptors that contribute to liver injury. The candidates caused the decreased viability of cancer cell lines (HepG2 and Huh7) but showed no effect on a normal cell line (Vero). Examination of biochemical parameters (ALT, AST, ALP, and bilirubin) showed the hepatoprotective effect of the candidate drugs in comparison with the control group, which was confirmed by histological findings. Taken together, quercetin and curcumin not only satisfied the drug-like assessment criterion and proved to be multitargeting by preventing liver damage but also showed anticancer activities.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:氧化应激是指细胞内活性氧(ROS)水平内的非稳态升高,并且与几种神经相关的病理状况有关。双氯芬酸是一种常用的非甾体抗炎药(NSAID),用于通过减少炎症来治疗疼痛和疼痛。双氯芬酸还通过改变线粒体内的稳态平衡而与凋亡细胞死亡的诱导相关。在本报告中,由Bacopamonnieri叶构成的BNC制剂的神经保护作用,对黑麦草和姜黄根茎种子进行了研究。
    方法:使用FT-IR和LC-MS以及感官评价表征合成的制剂。此后,随后在SH-SY5Y细胞中研究BNC制剂对双氯芬酸诱导的氧化应激的神经保护功效。用合成制剂预处理细胞,随后评估双氯芬酸诱导的细胞毒性的改善,和ROS增强。通过评估核形态的变化,进一步探索合成制剂的神经保护作用。和细胞凋亡的缓解,并伴随着对caspase-3和-9激活的调节作用。
    结果:发现双氯芬酸对人神经母细胞瘤SHSY5Y细胞具有相当大的细胞毒性。有趣的是,双氯芬酸介导的毒性在用BNC制剂预处理的SH-SY5Y细胞中显著降低。双氯芬酸处理的SHSY5Y细胞内的增加的ROS水平在BNC制剂预处理的SH-SY5Y细胞中也降低。此外,BNC制剂预处理的SH-SY5Y细胞也表现出减少的线粒体膜电位耗散。caspase-3和-9,以及双氯芬酸处理后的细胞凋亡。
    结论:这些发现表明,的确,双氯芬酸在SH-SY5Y细胞中诱导大量ROS介导的凋亡,这进一步有趣地改善了双氯芬酸钠介导的对SH-SY5Y细胞的细胞毒性作用。该手稿进一步收集了有关针对运动和非运动脑功能障碍的准备及其申请中已发布或授予的可用国家和国际专利的信息。
    Oxidative stress refers to non-homeostatic elevation within intracellular reactive oxygen species (ROS) levels and is associated with several neuro-related pathological conditions. Diclofenac is a commonly prescribed non-steroidal anti-inflammatory drug (NSAID) for treating aches and pain by reducing inflammation. Diclofenac is also associated with the induction of apoptotic cell death by altering the homeostatic balance within mitochondria. In the present report, the neuroprotective effects of BNC formulation constituted by Bacopa monnieri leaves, Nigella sativa and Curcuma longa rhizome seeds were investigated.
    The synthesized formulation was characterized using FT-IR and LC-MS along with organoleptic evaluation. Thereafter neuroprotective efficacy of BNC formulation was subsequently investigated against Diclofenac-induced oxidative stress in SH-SY5Y cells. The cells were pretreated with synthesized formulation and subsequently evaluated for amelioration in Diclofenac-induced cytotoxicity, and ROS augmentation. The neuroprotective effect of synthesized formulation was further explored by evaluating the changes in nuclear morphology, and apoptosis alleviation with concomitant regulatory effects on caspase-3 and -9 activation.
    Diclofenac was found to be considerably cytotoxic against human neuroblastoma SHSY5Y cells. Intriguingly, Diclofenac-mediated toxicity was reduced significantly in SH-SY5Y cells pretreated with BNC formulation. Augmented ROS levels within Diclofenac-treated SHSY5Y cells were also reduced in the BNC formulation pretreated SH-SY5Y cells. Furthermore, BNC formulation pretreated SH-SY5Y cells also exhibited reduced dissipation of mitochondrial membrane potential, caspase-3 and -9, along with apoptosis after Diclofenac treatment.
    These findings indicated that, indeed, Diclofenac induces considerable ROSmediated apoptosis in SH-SY5Y cells, which further intriguingly ameliorated Diclofenacmediated cytotoxic effects on SH-SY5Y cells. This manuscript further collected information about available National and International patents published or granted in preparation of and thereof applications against motor and non-motor brain dysfunctions.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

公众号