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SFI Reduces the Nucleocytoplasmic Transportation of HMGB1 by Upregulating HDAC3 in LPS-induced RAW264.7 Cells SFI通过上调HDAC3在lps诱导的RAW264.7细胞中减少HMGB1的核质转运
Pub Date : 2023-10-10 DOI: 10.53043/2347-3894.acam11010
Xiaoteng Huang, Wenting Shan, Fei Ai, Xin Wei, Xia Liu
Shenfu injection (SFI) is widely used for treating endotoxin shock in China. In the present study, to investigate the anti-inflammatory effects of SFI and further explored the potential mechanism of HMGB1 nuclear translocation, we established a vitro cell model provoked by lipopolysaccharide (LPS), observed nucleocytoplasmic translocation of high mobility group box 1 (HMGB1) and the relationship between histone deacetylase 3 (HDAC3) and HMGB1 under SFI intervention. The results showed that SFI upregulated the transcription and expression of HDAC3 in RAW264.7 cells, inhibited the nuclear to cytoplasmic translocation of HMGB1 and its subsequent extracellular release, and depressed the secretion of HMGB1, interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α). However, targeted knockdown of HDAC3 induced an increase in HMGB1 translocation to the cytoplasm, and HMGB1 localization was not altered significantly following LPS stimulation. SFI failed to reverse the abnormal localization of HMGB1. These results suggested that SFI may inhibit LPS-induced HMGB1 nuclear translocation in RAW264.7 cells through upregulating HDAC3 expression, thereby inhibiting its downstream pathway and suppressing inflammatory response.
参附注射液(SFI)在国内广泛用于治疗内毒素休克。本研究为研究SFI的抗炎作用,进一步探讨HMGB1核易位的潜在机制,我们建立脂多糖(LPS)诱导的体外细胞模型,观察SFI干预下高迁移率组盒1 (HMGB1)核质易位及组蛋白去乙酰化酶3 (HDAC3)与HMGB1的关系。结果表明,SFI上调了RAW264.7细胞中HDAC3的转录和表达,抑制了HMGB1的核质易位及其随后的细胞外释放,抑制了HMGB1、白细胞介素-1β (IL-1β)和肿瘤坏死因子-α (TNF-α)的分泌。然而,靶向敲低HDAC3诱导HMGB1向细胞质的易位增加,并且在LPS刺激下HMGB1的定位没有明显改变。SFI未能逆转HMGB1的异常定位。这些结果表明,SFI可能通过上调HDAC3的表达,抑制lps诱导的RAW264.7细胞HMGB1核易位,从而抑制其下游通路,抑制炎症反应。
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引用次数: 0
The Controversy: Whether Sucralose Could Increase Blood Glucose in The Body? 争议:三氯蔗糖是否会增加体内血糖?
Pub Date : 2023-06-24 DOI: 10.53043/2347-3894.acam11008
Mengqiu Li, Ziyang Lin, Minyi Li, Yongjin Zhu, Ting-ting Duan, Lanqing Meng, Xianlong Zhang, T. Xia, G. Lin, Xiuqing Lu, Zhenghai Li, Junzheng Yang
Sucralose is the most used artificial sweetener around the world, accounted for 30% of the global low-calorie sweetener market in 2016. According to the inspection of 19915 pre-packaged foods in Hong Kong, sucralose is the most used non-nutritive sweetener, followed by acesulfame. In addition to the food industry, sucralose can also be used as one kind of subsidiary materials for correcting taste in suspension agent, oral liquid, tablets, and granules, which could cover up the bitter taste of medicines such as aspirin or traditional Chinese medicine compound. The Food and Drug Administration (FDA) had approved the use of sucralose, but whether sucralose intake has effect on blood glucose is not clarified clearly. For this purpose, we collected and summarized the clinical studies to evaluate the effect of sucralose intake on blood glucose since 1996 from PubMed database, hope it may provide some evidence for sucralose applications in food excipient or drug sweet excipient.
三氯蔗糖是世界上使用最多的人造甜味剂,2016年占全球低热量甜味剂市场的30%。根据对香港19915种预包装食品的检查,三氯蔗糖是使用最多的非营养性甜味剂,其次是安赛美。除了在食品工业中,三氯蔗糖还可以作为一种辅料,在悬浮剂、口服液、片剂和颗粒剂中纠正味道,从而掩盖阿司匹林或中药复方等药物的苦味。美国食品药品监督管理局(FDA)已经批准使用三氯蔗糖,但三氯蔗糖的摄入是否对血糖有影响尚不清楚。为此,我们从PubMed数据库中收集并总结了自1996年以来评估三氯蔗糖摄入对血糖影响的临床研究,希望为三氯蔗糖在食品辅料或药物甜味辅料中的应用提供一些证据。
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引用次数: 0
Magnesium – The Metabolic Blockbuster 镁——代谢大片
Pub Date : 2023-06-24 DOI: 10.53043/2347-3894.acam11009
Uwe Gröber
Magnesium is primarily found within the cell where it acts as a counter ion for the energy-rich ATP and nuclear acids. Magnesium is a cofactor in more than 600 pacemaker enzyme systems, encompassing approximately 80% of all known metabolic functions, that regulate elementary biochemical reactions in the body, including protein synthesis, muscle and nerve transmission, neuromuscular conduction, blood glucose control, and blood pressure regulation. Some magnesium-dependent enzymes are Na+/ K+-ATPase, hexokinase, creatine kinase, protein kinase, and cyclases. Magnesium is also necessary for structural function of proteins, nucleic acids, or mitochondria. It is required for DNA and RNA synthesis, reproduction, and for both aerobic and anaerobic energy production—oxidative phosphorylation and glycolysis either indirectly as a part of magnesium-ATP complex, or directly as an enzyme activator [1-3].
镁主要存在于细胞内,作为富含能量的ATP和核酸的反离子。镁是600多个起搏器酶系统中的辅因子,约占所有已知代谢功能的80%,调节身体的基本生化反应,包括蛋白质合成、肌肉和神经传递、神经肌肉传导、血糖控制和血压调节。一些镁依赖性酶是Na+/K+-ATP酶、己糖激酶、肌酸激酶、蛋白激酶和环化酶。镁也是蛋白质、核酸或线粒体结构功能所必需的。它是DNA和RNA合成、繁殖以及有氧和无氧能量生产所必需的——氧化磷酸化和糖酵解,间接作为镁ATP复合物的一部分,或直接作为酶激活剂[1-3]。
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引用次数: 0
Physical, Chemical and Biological Characteristics of Sri Lankan Bee Honey Varieties 斯里兰卡蜂蜜品种的物理、化学和生物学特性
Pub Date : 2023-03-05 DOI: 10.53043/2347-3894.acam11004
T. Tennakoon, L.P.S. Vinodani, W. Warnasooriya, N. R. Amarasinghe, J. Madushani
Objectives: Honey has abundant medicinal properties. It is formed by floral nectar, swaps of plants, and the secretions of bees. The current study determined the physical, chemical, and biological characteristics of Sri Lankan raw bee honey varieties. Methods: A honey stock/library was created using local honey produced by Apis cerana, and Apis dorsata. Colour, conductivity, cell constant and pH were determined under physical tests while free acidity, water content and hydroxymethylfurfural content were determined under chemical tests. Evaluation of biological activities includes checking for antimicrobial activity, antioxidant activity and enzymatic activity. Results: The pH values recorded for A. dorsata and A. cerana honey ranged from 4.14–5.55 and 4.54–6.33, respectively. The electrical conductivity of all the samples ranged from 0.39-2.59 mS cm-1. The free acidity of honey samples of A. dorsata was between 25-81.7 meq/kg and that for A. cerana was between 40- 82.7 meq/kg. The hydroxymethylfurfural content of honey samples of A. dorsata and A. cerana were 9.38-49.50 mg/kg and 7.49-53.94 mg/kg, respectively. The two honey varieties were similar in chemical and physical characteristics tested except for water content where the water content of honey from A. dorsata was significantly higher than that of A. cerana. All honey samples investigated had antibacterial activity against gram-negative bacteria E. coli and gram-positive bacteria S. aureus. A. cerana honey had higher antioxidant activity than A. dorsata honey while A. dorsata honey had higher enzymatic activity than A. cerana honey. Conclusions: The present study reveals that the physiochemical properties of two honey varieties were similar except for water content while biological properties were significantly different. This study indicates that honey from both A. dorsata and A. cerana of Sri Lanka has potential therapeutic activities that can be used to develop natural drug formulations.
目的:蜂蜜具有丰富的药用价值。它是由花蜜、植物交换物和蜜蜂的分泌物组成的。目前的研究确定了斯里兰卡原料蜂蜂蜜品种的物理、化学和生物学特性。方法:以中国原蜜和意大利原蜜为原料,建立蜂蜜库。通过物理测试测定颜色、电导率、细胞常数和pH值,通过化学测试测定游离酸度、含水量和羟甲基糠醛含量。生物活性评价包括抗菌活性、抗氧化活性和酶活性的检测。结果:蜜蜂和蜜蜂蜂蜜的pH值分别为4.14 ~ 5.55和4.54 ~ 6.33。所有样品的电导率范围为0.39 ~ 2.59 mS cm-1。蜜样的游离酸度在25 ~ 81.7 meq/kg之间,蜜蜂的游离酸度在40 ~ 82.7 meq/kg之间。蜜中羟基甲基糠醛含量分别为9.38 ~ 49.50 mg/kg和7.49 ~ 53.94 mg/kg。两种蜂蜜的化学和物理特性测试结果相似,但水分含量不同,其中蜜的含水量显著高于蜜蜂。所有蜂蜜样品均对革兰氏阴性菌大肠杆菌和革兰氏阳性菌金黄色葡萄球菌具有抗菌活性。蜜蜂蜂蜜的抗氧化活性高于蜜蜂蜂蜜,蜜蜂蜂蜜的酶活性高于蜜蜂蜂蜜。结论:两种蜂蜜的理化性质除水分含量外基本相同,但其生物学性质存在显著差异。该研究表明,来自斯里兰卡的A. dorsata和A. cerana的蜂蜜具有潜在的治疗活性,可用于开发天然药物配方。
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引用次数: 0
Bioinformatics-based Prediction of Character of Envelope Glycoprotein and Analysis of Epitopes of B- and T-cell of gp120 基于生物信息学的gp120包膜糖蛋白特征预测及B、t细胞表位分析
Pub Date : 2023-03-05 DOI: 10.53043/2347-3894.acam11006
Meijie Liang, W. Hong, Jiping Shao
1Objectives: To analyze the characteristics of gp120 gene sequence and protein structure of HIV-1 CRF01_AE and to predict B- and T-cell epitopes and to forecast binding sites between gp120 and mD1.22 by using bioinformatics in order to lay a foundation for the research and development of AIDS vaccines and peptide-based drugs. Methods: The gene sequences and the amino acid sequences of gp120 were obtained from NCBI GeneBank database. Physicochemical property, membrane-panning region, PTMs sites of gp120 and secondary structure were analyzed by Expasy ProtParam, TMpred, NetPhos and GlycoMine and SOPMA, respectively. Epitopes of B-cell were predicted by VaxiJen v2.0, AllerTOP v2.0 and IEDB while epitopes of T-cell were predicted by IEDB. Protein-protein docking were forecast by Z-dock, pymol and so on. Results: The calculation formula of gp120 is C1033H1633N299O319S9. The number of amino acids is 211, and the molecular weight is 23633.68. The theoretical isoelectric point (pI) is 7.76. It is estimated that 17 residues are phosphorylation sites, while gp120 has more than 5 glycosylation sites. The protein contains alpha helix (blue mark), beta turn (green mark), random coil (purple mark) and thin slice (red mark), which are 26.54%, 6.16%, 40.28% and 27.01% respectively. We selected the top 10 possible epitopes of B cells, but only the top 5 epitopes of MHC-I. The most possible binding site between gp120 and mD1.22 was showed. Conclusion: With the potential humoral immunity and cellular immunity, gp120 of HIV-1 is a promising target for HIV-1 treating. The interaction of gp120 with CD4 is the first step of HIV cycle which allows the entry of HIV into CD4+ T-cells. This study has analyzed and predicted the binding sites between gp120 and mD1.22 and the character and B-cell and T-cell epitopes of gp120, could be a foundation for subsequent study of developing vaccine and polypeptide drugs.
1目的:利用生物信息学方法分析HIV-1 CRF01_AE的gp120基因序列和蛋白结构特征,预测B细胞和t细胞表位,预测gp120与mD1.22的结合位点,为艾滋病疫苗和肽类药物的研发奠定基础。方法:从NCBI GeneBank数据库中获取gp120的基因序列和氨基酸序列。利用Expasy ProtParam、TMpred、NetPhos和GlycoMine和SOPMA分别分析gp120的理化性质、膜淘区、PTMs位点和二级结构。用VaxiJen v2.0、AllerTOP v2.0和IEDB预测b细胞的表位,用IEDB预测t细胞的表位。用Z-dock、pymol等预测蛋白对接。结果:gp120的计算公式为C1033H1633N299O319S9。氨基酸数为211个,分子量为23633.68。理论等电点(pI)为7.76。估计有17个残基是磷酸化位点,而gp120有5个以上的糖基化位点。该蛋白含有α螺旋(蓝色标记)、β转(绿色标记)、随机线圈(紫色标记)和薄片(红色标记),分别占26.54%、6.16%、40.28%和27.01%。我们选择了B细胞可能的前10个表位,但只选择了MHC-I的前5个表位。显示gp120与mD1.22最可能的结合位点。结论:gp120具有潜在的体液免疫和细胞免疫功能,是治疗HIV-1的理想靶点。gp120与CD4的相互作用是HIV周期的第一步,它允许HIV进入CD4+ t细胞。本研究分析并预测了gp120与mD1.22的结合位点、gp120的性质及b细胞和t细胞表位,为后续疫苗和多肽药物的研究奠定了基础。
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引用次数: 0
Efficacy and Safety of Chinese Medicine in the Treatment of Patients with Pulmonary Nodules-A Multicenter Open Label Randomized Controlled Study: A Study Protocol for a Randomized Controlled Trial 中药治疗肺结节的疗效和安全性——一项多中心开放标签随机对照研究:一项随机对照试验的研究方案
Pub Date : 2023-03-05 DOI: 10.53043/2347-3894.acam11007
Lixing Liu, Pei-xin Li, Qinglin Zhang, Rui Zhou, Lilian Feng
As the popularity of early screening of tumors, more and more people have detected pulmonary nodules, of which about 3.48% was lung cancer. However, false positive rates accounted for 1.4-23.3% according to trials reported. Therefore, pulmonary nodules may be over treated. In the clinical practice, we found that traditional Chinese medicine treatment makes some patients’ lung nodules shrink or even disappear but this effect needs to be approved. Therefore, we design this global network randomized controlled study (RCT) study to explore the efficacy and safety of traditional Chinese medicine in the treatment of pulmonary nodules. This study is a multicenter, open, prospective, randomized, controlled study. In this study, participants will be randomly assigned to traditional Chinese medicine or routine treatment observation group. About 166 patients with pulmonary nodules will be registered within 12 months and followed up for at least 2 years. The important feature of this clinical trial is to provide services to patients with pulmonary nodules worldwide by combining online and offline diagnosis and treatment, excluding interference factors such as region, climate, environment, eating habits etc. At the same time, it also will save costs and improves patient compliance. This trial design will also conduct subgroup analysis on the population of traditional Chinese medicine in the treatment of pulmonary nodules and establish a mathematical model to analyze the dominant population of traditional Chinese medicine in pulmonary nodules and the predictive factors of curative effect.
随着肿瘤早期筛查的普及,越来越多的人检出肺结节,其中约3.48%为肺癌。然而,根据报道的试验,假阳性率占1.4-23.3%。因此,肺结节可能被过度治疗。在临床实践中,我们发现中药治疗使部分患者的肺结节缩小甚至消失,但这种效果需要得到批准。因此,我们设计了这项全球网络随机对照研究(RCT)研究,探讨中药治疗肺结节的有效性和安全性。本研究是一项多中心、开放、前瞻性、随机、对照研究。本研究将受试者随机分为中药组和常规治疗组。约166例肺结节患者将在12个月内登记并随访至少2年。本临床试验的重要特点是通过线上线下结合诊疗,排除地域、气候、环境、饮食习惯等干扰因素,为全球肺结节患者提供服务。同时,它还将节省成本并提高患者的依从性。本试验设计还将对中药治疗肺结节的人群进行亚组分析,建立数学模型,分析中药治疗肺结节的优势人群及疗效预测因素。
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引用次数: 0
Rare Clinical Conditions Caused by Dry Eye 罕见的干眼症临床症状
Pub Date : 2023-03-05 DOI: 10.53043/2347-3894.acam11005
Du Fusheng, Du Yanping, Ping Jiejie
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引用次数: 0
Forensic Naturopathy in the Treatment of Self Harm, Suicide Attempts, and Violence 法医自然疗法在治疗自我伤害,自杀企图和暴力
Pub Date : 2023-02-10 DOI: 10.53043/2347-3894.acam11002
Marian x Marian Mulligan*
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引用次数: 0
The Molecular Mechanisms underlying the Therapeutic Effect of Berberine in Inflammatory Skin Diseases 黄连素治疗炎症性皮肤病的分子机制
Pub Date : 2023-02-10 DOI: 10.53043/2347-3894.acam11001
T. Andoh, T. Shimizu
Clinical therapy of chronic inflammatory skin diseases such as atopic dermatitis is extremely difficult. Recently, the use of a number of traditional herbal medicines has been attempted to treat these skin diseases. Orengedokuto is a traditional herbal medicine consisting of four crude natural medicines, and in the field of dermatology, it is used to treat skin diseases accompanied by inflammation and pruritus. Our recent animal study showed that berberine, a major component of Orengedokuto, improves skin inflammation and itching in mice with atopy-like dermatitis. Furthermore, we identified EIF3F and MALT1 as factors involved in the suppression of cytokine production by berberine. In addition, berberine also activates AMP-activated protein kinase, which is involved in the expression of inflammatory and anti-inflammatory cytokines. In addition, berberine also attenuates epidermal hyperplasia though the inhibition of CDC6 expression. Taken together, these findings indicate that berberine improves inflammatory skin diseases by controlling gene expression related to both inflammation, anti-inflammation and keratinocyte hyperproliferation.
特应性皮炎等慢性炎症性皮肤病的临床治疗极其困难。最近,人们尝试使用一些传统草药来治疗这些皮肤病。Orengedokuto是一种由四种天然药材组成的传统草药,在皮肤病学领域,它用于治疗伴有炎症和瘙痒的皮肤病。我们最近的动物研究表明,黄连素是Orengedokuto的主要成分,可以改善特应性皮炎小鼠的皮肤炎症和瘙痒。此外,我们确定EIF3F和MALT1是参与抑制黄连素产生细胞因子的因素。此外,黄连素还激活AMP活化蛋白激酶,该激酶参与炎症和抗炎细胞因子的表达。此外,黄连素还通过抑制CDC6的表达来减轻表皮增生。总之,这些发现表明,黄连素通过控制与炎症、抗炎和角质形成细胞过度增殖相关的基因表达来改善炎症性皮肤病。
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引用次数: 0
Reward Deficiency Syndrome Solution System (RDSSS) A Genetically Driven Putative Inducer of "Dopamine Homeostasis" as a Futuristic Alternative to Enhance Rehabilitation Instead of Incarceration. 奖赏缺失综合症解决方案系统(RDSSS)--一种基因驱动的 "多巴胺平衡 "推定诱导剂,可替代监禁,促进康复。
Pub Date : 2023-01-01 Epub Date: 2023-01-11 DOI: 10.53043/2347-3894.acam11003
Kenneth Blum, Richard Green, Paul Mullen, David Han, Abdalla Bowirrat, Igor Elman, John B Floyd, Panayotis K Thanos, David Baron, Mark S Gold, Rajendra D Badgaiyan
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引用次数: 0
期刊
Asian journal of complementary and alternative medicine : A-CAM
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