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Improvement in the downstream processing of rhGH production in Pichia pastoris 毕赤酵母生产rhGH下游工艺的改进
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-07-01 DOI: 10.22034/IJPS.2018.35929
S. Azadi, S. Sadjady, S. Mortazavi, N. Naghdi, Roya Solaimanian, A. Mahboubi
Production of human proteins in Pichia pastoris has significant advantages. However, there is still need for improvement in various stages of its downstream processing like clarification and purification. In fact downstream processes are usually the most critical part of production of biotech products. This work aimed to evaluate the effect of two steps added to the downstream processes of human growth hormone (hGH) production in Pichia pastoris. Firstly the effect of clarification, with activated carbon, on capture of hGH by ion exchange chromatography (IEC) was investigated. For this purpose, a clarification process using activated carbon was used to remove process contaminants like pigments. The clarified sample was applied to the IEC column and the recovery of hGH, following IEC, was assessed using SDS-PAGE, Bradford protein assay and area under the curve (AUC). The obtained results showed that the AUC values were 2.81 and 5.61 for the with- and without-treatment samples, respectively. Protein recovery of clarified sample with activated carbon was 541 mg in comparison with 328 mg for the sample without treatment. The yield of IEC was also improved from 50.46% to 83.23% following treatment with activated carbon. Secondly, the effect of three concentrations of ammonium sulfate in the binding buffer on resolution of hGH upon elution on hydrophobic interaction chromatography (HIC) was investigated. Biological activity was used as the main criterion for evaluation of purified hGH using HIC. The obtained results indicated that by increasing the concentration of ammonium sulfate form 1 to 3 mol/L, resolution of hGH was improved, as the purified fraction using 3 mol/L of ammonium sulfate showed a specific activity of 3.1IU/mg. So the results of the present study demonstrated that activated carbon is a promising candidate for efficient clarification of recombinant hGH and improving the efficiency of the capture step. Therefore, it can be considered by biotech companies as a cost-effective and sustainable clarification procedure of recombinant proteins from high cell density cultures. This study also revealed that 3% ammonium sulfate has a positive effect on the separation of hGH variants with the desired biological activity.
在毕赤酵母中生产人蛋白具有显著的优势。然而,在其下游处理的各个阶段,如澄清和纯化,仍需要改进。事实上,下游工艺通常是生物技术产品生产中最关键的部分。这项工作旨在评估在毕赤酵母中人类生长激素(hGH)生产的下游过程中添加两个步骤的效果。首先研究了活性炭澄清对离子交换色谱法(IEC)捕获hGH的影响。为此,使用活性炭的澄清工艺用于去除工艺污染物,如颜料。将澄清的样品应用于IEC柱,并使用SDS-PAGE、Bradford蛋白测定和曲线下面积(AUC)评估IEC后hGH的回收率。所获得的结果显示,有治疗和无治疗样本的AUC值分别为2.81和5.61。与未经处理的样品的328mg相比,用活性炭澄清的样品的蛋白质回收率为541mg。用活性炭处理后,IEC的产率也从50.46%提高到83.23%。其次,研究了结合缓冲液中三种浓度的硫酸铵对疏水相互作用色谱(HIC)洗脱hGH的影响。以生物活性作为HIC评价纯化hGH的主要标准。结果表明:硫酸铵浓度增加1~3mol/L可提高hGH的分离度,由于用3mol/L硫酸铵纯化的部分显示出3.1IU/mg的比活性。因此本研究的结果表明,活性炭是有效澄清重组hGH和提高捕获步骤效率的有前途的候选者。因此,生物技术公司可以认为这是一种高细胞密度培养物中重组蛋白的成本效益和可持续的澄清程序。该研究还表明,3%硫酸铵对具有所需生物活性的hGH变体的分离具有积极作用。
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引用次数: 0
Neuroprotective and nootropic activity of Carica papaya seeds on Diabetes induced cognitive decline in rats 番木瓜籽对糖尿病诱导的大鼠认知能力下降的神经保护和促神经活性
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-07-01 DOI: 10.22034/IJPS.2019.35934
V. Eggadi, srilatha keshaveni, S. Bandaru, U. Kulandaivelu
The aim of present study is to investigate neuroprotective and nootropic activity of Petroleum Ether Extract of Carica papaya seeds (PEECPS) on diabetic induced cognitive decline rats. Rectangular maze and morris water maze models were used to evaluate nootropic activity and neuroprotective effects were studied by estimating acetyl cholinesterase (AchE), malondialdehyde (MDA), superoxide dismutase (SOD), nitric oxide (NO), catalase (CAT) and glutathione (GSH) levels in the brains of diabetic rats. In rectangular maze and morris water maze models, 400 mg/kg of PECPS were shown the significant effect when compared with diabetic control on day 75. Significant decrease in AchE (P<0.001), MDA (P<0.01), NO (P<0.05) and significantly (P<0.01) increased levels of SOD, CAT and GSH with PECPS (200 and 400 mg/kg) when compared with diabetic control. There is a need of further studies on Carica papaya seeds as it showed protection against diabetes induced cognitive decline to reveal its mode of action.
本研究的目的是研究番木瓜籽石油醚提取物(PEECPS)对糖尿病诱导的认知能力下降大鼠的神经保护和促神经活性。采用矩形迷宫和morris水迷宫模型,通过测定糖尿病大鼠脑内乙酰胆碱酯酶(AchE)、丙二醛(MDA)、超氧化物歧化酶(SOD)、一氧化氮(NO)、过氧化氢酶(CAT)和谷胱甘肽(GSH)水平,研究其促神经活动和神经保护作用。在矩形迷宫和morris水迷宫模型中,在第75天,与糖尿病对照组相比,400mg/kg的PECPS显示出显著效果。与糖尿病对照组相比,PECPS(200和400mg/kg)可显著降低AchE(P<0.001)、MDA(P<0.01)、NO(P<0.05),并显著提高SOD、CAT和GSH水平(P<0.01)。有必要对番木瓜种子进行进一步的研究,因为它可以预防糖尿病引起的认知能力下降,以揭示其作用模式。
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引用次数: 4
Macroscopic and Microscopic Diagnostic Features of the potential Herbal Drug Crataegus Almaatensis Pojark Endemic in Kazakhstan 哈萨克斯坦潜在中草药山楂Pojark地方病的宏观和显微诊断特征
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33737
E. Bekbolatova, N. V. Kurbatova, Z. Sakipova, L. Ibragimova, Saltanat I. Alpysbayeva, A. Kabdenova, W. Kukuła-Koch, F. Boylan
This study presents the results of anatomic-morphological examination of vegetative (leaves) and generative (flowers, fruits) organs of the endemic plant Crataegus almaatensis Pojark – family Rosaceae, growing in the foothills of Ile Alatau mountains, Almaty region of the Republic of Kazakhstan. The plant Crataegus almaatensis Pojark was examined during the phenological phase of flowering and fruit ripening periods. The macroscopic and microscopic diagnostic features were established, which will allow for the standardization of this herbal plant in order to ensure its quality, safety, and efficacy and to avoid adulteration, misuse in the process of medicines’ preparation on its basis. For the first time significant diagnostic macroscopic and microscopic features of the dried vegetative and generative organs of Crataegus almaatensis Pojark were described in detail. Currently not much is known about this species and this manuscript brings the information which are studied for the first time, according to the authors’ knowledge.
本研究介绍了生长在哈萨克斯坦共和国阿拉木图地区Ile Alatau山麓的特有植物Crataegus almatensis Pojark——蔷薇科植物的营养(叶)和生殖(花、果)器官的解剖形态学检查结果。在开花期和果实成熟期的酚期对植物山楂进行了研究。建立了宏观和微观诊断特征,这将有助于该草药的标准化,以确保其质量、安全性和有效性,并在此基础上避免在药物制备过程中掺假和滥用。首次详细描述了薄叶山楂干燥营养器官和生殖器官的重要诊断宏观和微观特征。据作者所知,目前对该物种的了解并不多,这份手稿带来了首次研究的信息。
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引用次数: 5
The Essential oil Composition of Arctium lappa Root and Leaf 牛蒡根、叶挥发油成分研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.88539.1447
Fariba Golbaz, S. Zarei, F. Garakani, F. Mojab
Using plants and natural products as medicine is increasing every day. The reason might be a tendency that the societies mostly have toward natural and original products especially natural drugs. Essential oilsare referred to aromatic composition which is found in different parts of a plant and can be used for different remedial and hygienic purposes. One of the plants which have been used a lot in folk medicine is Arctium lappa. This study is aimed at identifying the composition of its root and leaf essential oils. The essential oils from the roots and leaves of A. lappa (Asteraceae), which was collected from Mashhad (Farms of Agriculture School, Ferdowsi University), was extracted by hydrodistillation and then the composition was determined by GC/MS. Totally, 31 and 57 components (92.4 and 93.2% of essential oils of root and leaf) were identified, respectively. The root oil contains mainly 1, 3cyclo-octadiene (33.2%), E-caryophllene (6.8%), β-selinene (5.6%) and 9, 10-dehydro-isolongifolene (5.5%), whilst β-Thujone (11.6%), Caryophyllene oxide (8.3%), Cuminaldehyde (7.7%), Comphor (5.3%), DihydroEdulan II (5.3%), β -ionone (4.7%) and α- Thujone (3.4%) were major components in the leaf oil. Identification of the components was based on comparison of their mass spectra with standards. The chemical composition of essential oils from the herbs is being reported for the first time in Iran.
使用植物和天然产品作为药物的人数每天都在增加。原因可能是社会大多倾向于天然和原创产品,尤其是天然药物。精油是指存在于植物不同部位的芳香成分,可用于不同的治疗和卫生目的。牛蒡是民间常用的植物之一。本研究旨在鉴定其根和叶精油的成分。从马什哈德(Ferdowsi大学农业学院农场)采集的A.lappa(Asteraceae)的根和叶中提取精油,并通过GC/MS测定其组成。共鉴定出31种和57种成分,分别占根和叶精油的92.4%和93.2%。根油主要含有1,3环辛二烯(33.2%)、E-石竹烯(6.8%)、β-selinene(5.6%)和9/10脱氢异长形烯(5.5%),而β-Thujone(11.6%)、石竹烯氧化物(8.3%)、Cuminalde(7.7%)、Comphor(5.3%)、二氢EdulanII(5.3%。成分的鉴定是基于其质谱与标准品的比较。伊朗首次报道了这些草药精油的化学成分。
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引用次数: 4
The Anti-angiogenic Activity of Phoenix dactylifera seeds Methanol Extract in vivo study 凤尾草种子甲醇提取物体内抗血管生成活性研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33741
Zeena Husseina, A. Al-zubaidy, H. Sahib
The Anti-angiogenic Activity of Phoenix dactylifera seeds methanol extract in vivo study Abstract: The aim of the study was to identify the antiangiogenic activity of Phoenix dactylifera seeds methanolic extract in vivo and the probable anti-angiogenic mechanism of action. The date seeds were extracted with methanol using cold method, the crude extract was tested on chick chorioallantoic membrane (CAM) as an in vivo anti-angiogenic assay. The phytochemical analysis was carried out using Fourier transform infrared spectroscopy FT-IR and Gas chromatography mass spectrometry GC-MS analysis. The results showed significant inhibition of blood vessels growth, while the phytochemical analysis showed the presence of different chemicals including phenolic compounds, terpene, fatty acids, aliphatic alcohols and others. From the data above the mechanism of action may relate to the presence of the above named compounds, as they have direct perturbing action on blood vessels and prevent cell proliferation of endothelial cells growth via their potent antioxidant and anti-inflammatory effects.
凤凰籽甲醇提取物抗血管生成活性的体内研究摘要:本研究旨在确定凤凰籽甲醇提取液的体内抗血管生成作用及其可能的抗血管生成机制。用甲醇冷法提取椰枣种子,在鸡胚绒毛尿囊膜(CAM)上进行粗提物的体内抗血管生成试验。采用傅立叶变换红外光谱-傅立叶变换红外和气相色谱-质谱-质谱联用技术进行了植物化学分析。结果显示,血管生长受到显著抑制,而植物化学分析显示,存在不同的化学物质,包括酚类化合物、萜烯、脂肪酸、脂肪醇等。根据上述数据,作用机制可能与上述化合物的存在有关,因为它们对血管具有直接干扰作用,并通过其强大的抗氧化和抗炎作用阻止内皮细胞生长的细胞增殖。
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引用次数: 2
Evaluation of affordability and impoverishment effect of cardiovascular medicines in Iran 评价伊朗心血管药物的可负担性和贫困化效果
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33739
A. Farahani, H. Rasekh, S. Najafi, Farimah Rahimi, M. Akbari, Faegheh Salehnia, Homan Hemati, Fatemeh Jajali
Cardiovascular disease is one of the most important causes of death in the world. There are variety of plans and strategies to treatment and prevention of CVD. Medicines have significant role to reach the goals. Ensuring Affordability of medicines is very crucial to success in these programs. The impoverishment method which focuses on the impoverishing effect of the purchasing of medicines is one the most popular methods to quantifying affordability of medicines. We applied this method to measure affordability of cardiovascular medicines in Iran. We used two poverty lines 1.25 USD and 2 USD per day which are recommended by World Bank to access the affordability of medicines. Mono therapy with one anti platelet, beta blocker, ACE inhibitor and statin as well as combination therapy have been determined. Our study highlighted that the poorest households in Iran would be at risk of pushing under poverty line because of price of the medicines.
心血管疾病是世界上最重要的死亡原因之一。治疗和预防心血管疾病的计划和策略多种多样。药物在实现这些目标方面发挥着重要作用。确保药品的可负担性对这些规划的成功至关重要。贫困化法侧重于药品购买的贫困化效果,是量化药品可负担性的最常用方法之一。我们应用这种方法来衡量伊朗心血管药物的可负担性。我们使用了世界银行推荐的每日1.25美元和2美元两条贫困线,以实现药品的可负担性。抗血小板,受体阻滞剂,ACE抑制剂和他汀类药物的单一治疗以及联合治疗已经确定。我们的研究强调,由于药品的价格,伊朗最贫穷的家庭将面临推至贫困线以下的风险。
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引用次数: 3
Synthesis and characterization of mPEG-PCL copolymers as a polymersomes for delivery of enalapril as a model hydrophilic drug mPEG-PCL共聚物作为依那普利模型亲水药物递送聚合物的合成与表征
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33691
H. Danafar
Purpose: Enalapril maleate (EPM), was used for hypertension and congestive heart failure. In this way, an innovative delivery system with mPEG–PCL was synthesized and the release profile of the EPM from the drug-loaded polymersomes was evaluated. Methods: Di-block methoxy)-poly (ethylene glycol) - Poly (caprolactone) (mPEG-PCL) copolymers were synthesized and used to prepare of polymersomes for controlled release of EPM as hydrophilic model drug. MPEG-PCL copolymer was characterized in vitro by HNMR, FTIR, DSC and GPC techniques. The resulting polymersomes were characterized further by various techniques such as dynamic light scattering (DLS) and transmission electron microscopy (TEM). Results: The results of TEM shows the polymersomes formed had spherical structure and the size of nanoparticles is 80 nm. The loading and encapsulation efficiency of EPM were determinate by HPLC at 215 nm with loading and encapsulation efficiency 19.8% ± 2.12% and 85.6% ± 1.26%, respectively. Study on DSC results exposed strong interaction between EPM and copolymer. In vitro release of EPM from polymersomes was clearly sustained in all the time tested for this purpose. The sustained release of drug was hypothetically due to the entrapment of EPM in core of polymersomes. Polymersomes also showed acceptable stability for long periods of time. Conclusion: The results indicate the successful formulation of EPM loaded m-PEG/PCL polymersomes. Overall, the results was showed that m-PEG-PCL polymersomes can be considered as a promising carrier for hydrophilic drugs such as EPM.
目的:马来酸依那普利(EPM)用于治疗高血压和充血性心力衰竭。通过这种方式,合成了一种具有mPEG–PCL的创新递送系统,并评估了EPM从药物负载的多聚体中的释放特性。方法:合成二嵌段甲氧基-聚乙二醇-聚己内酯(mPEG-PCL)共聚物,并将其用于制备EPM作为亲水性模型药物的控释聚合物。采用HNMR、FTIR、DSC和GPC等技术对MPEG-PCL共聚物进行了体外表征。通过诸如动态光散射(DLS)和透射电子显微镜(TEM)的各种技术进一步表征所得到的多聚体。结果:TEM结果表明,所形成的多聚体具有球形结构,纳米颗粒的尺寸为80nm。用高效液相色谱法在215nm处测定了EPM的负载量和包封率,负载量和包封率分别为19.8%±2.12%和85.6%±1.26%。DSC结果表明,EPM和共聚物之间存在强烈的相互作用。EPM从多聚体的体外释放在为此目的测试的所有时间内都明显持续。假设药物的持续释放是由于EPM包埋在多聚体的核心中。多聚体在长时间内也显示出可接受的稳定性。结论:实验结果表明,制备的间-PEG/PCL多聚体是成功的。总之,结果表明,m-PEG-PCL多聚体可以被认为是一种很有前途的亲水性药物载体,如EPM。
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引用次数: 2
Evaluation of Anti biofilm and Antibiotic Potentiation Activities of Silver Nanoparticles Against some Nosocomial Pathogens 纳米银抗生物膜及增强抗菌活性的研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33684
A. Ebrahimi, Hosein Jafferi, S. Habibian, S. Lotfalian
Nowadays silver nanoparticles (AgNPs) are used as antimicrobial due to its well known physical, chemical, and biological properties. A large collection of bacterial cells adhering to a surface is called bacterial biofilm. Exposure to silver nano particles (AgNPs) may prevent colonization of new bacteria onto the biofilm. In the present work, we have investigated whether the biofilm formation of some hospital isolates of pathogenic bacteria can be influenced by AgNPs. Also we examined the susceptibility of the isolates to some antibiotics in combination with AgNPs. Standard strains of Pseudomonas aeruginosa, Acinetobacter baumannii, Enterococcus faecalis and Staphylococcus aureus, in addition to nine hospital isolates for each species were used. Tube double serial dilution method for determination of MIC of AgNPs against isolates was performed. Biofilm formation was evaluated by end smooth 96 cells micro titer plates. A disc diffusion method was used to assay the various antibiotics and combinations for bactericidal activity against the isolates. Mean MICs of AgNPs for Ps. aeruginosa, A. baumannii, E. faecalis and S. aureus were 3.125, 6.25, 6.25 and 12.5 ug/mL. respectively. AgNPs exhibited more than % 90 inhibitory effect on biofilm formation of the examined species. The results showed that AgNPs have strong anti bacterial and anti biofilm activity against the examined pathogens. Synergistic effects of AgNPs in combination with gentamicin, kanamycine, cephalosporin and penicillin were observed in different cases. Ps. aeruginosa and S. aureus showed more sensitivity (increase in fold) to examined antibiotics plus AgNPs compared to A. baumannii and E. faecalis. Our results demonstrated that AgNPs showing promising anti biofilm activity on hospital isolates of Ps. aeruginosa, A. baumannii, E. faecalis and S. aureus. The study also showed a possible combination of examined antibiotics with AgNPs which concluded as synergism.
银纳米粒子由于其众所周知的物理、化学和生物特性而被用作抗菌剂。附着在表面的大量细菌细胞被称为细菌生物膜。暴露于银纳米粒子(AgNPs)可能会阻止新细菌在生物膜上的定植。在目前的工作中,我们已经调查了一些医院分离的病原菌的生物膜形成是否会受到AgNPs的影响。此外,我们还检测了分离株对一些抗生素和AgNPs的易感性。使用了铜绿假单胞菌、鲍曼不动杆菌、粪肠球菌和金黄色葡萄球菌的标准菌株,以及每个物种的9个医院分离株。采用试管双串联稀释法测定AgNPs对分离株的MIC。通过末端光滑的96细胞微量滴定板评估生物膜的形成。采用圆盘扩散法测定各种抗生素及其组合对分离株的杀菌活性。铜绿假单胞菌、鲍曼氏杆菌、粪大肠杆菌和金黄色葡萄球菌的AgNPs平均MIC分别为3.125、6.25、6.25%和12.5ug/mL。分别地AgNPs对被检测物种的生物膜形成表现出超过90%的抑制作用。结果表明,AgNPs对所检测的病原体具有较强的抗菌和抗生物膜活性。在不同情况下观察了AgNPs与庆大霉素、卡那霉素、头孢菌素和青霉素的协同作用。铜绿假单胞菌和金黄色葡萄球菌对所检测的抗生素加AgNPs的敏感性(增加了倍)高于鲍曼菌和粪大肠杆菌。我们的研究结果表明,AgNPs对医院分离的铜绿假单胞菌、鲍曼菌、粪大肠杆菌和金黄色葡萄球菌显示出良好的抗生物膜活性。这项研究还表明,经检查的抗生素与AgNPs可能存在协同作用。
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引用次数: 8
Effect of Purple Variety Sweet Potato (Ipomoea batatas L.) Anthocyanin on Expression of Estrogen Receptor-Α and Endometrium Thickness on Uterus of Female White Rats (Rattus norvegicus) Exposed to Cigarette Smoke 紫甘薯花青素对吸烟雌性大鼠子宫雌激素受体-α表达和子宫内膜厚度的影响
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33738
S. Utami, R. Ratnawati, I. Wiyasa
Cigarette smoke contains around 4000 chemical substances including free radicals and carcinogens, which are xenobiotic agents in the body, affecting the reproductive system. Purple sweet potatoes contain the color pigment anthocyanin. The purple color pigment (anthocyanin) in purple sweet potatoes is a beneficial antioxidant because it can react with free radicals that can cause damage in the body. The goal of the research was to understand the effects of purple variety sweet potato (Ipomoea Batatas L) anthocyanin on the expression of estrogen receptor-α in the endometrium and endometrium thickness on white rats (Rattus norvegicus) exposed to cigarette smoke. The White rats used for the 5 groups were 30 white rats. Exposure to cigarette smoke was given at a rate of 2 sticks/day (each cigarette ± 4 minutes), for 8 weeks after the rats were found to be in the proestrus phase. Endometrium thickness was examined and measured using a Dot slide Olympus XC 10 light microscope and the Olyvia software. Expression of ER-α in the endometrium was measured by using the antibody ER-α (C-311) SC-787 and the immunohistochemistry and calculated by the Immunoratio software. Data were analyzed with the Shapiro-Wilk’s test, t-test and one-way ANOVA (F test). It was found that the average value of ER-α expression in the endometrium for the treatment group given purple variety sweet potato anthocyanin of a dose of 40 mg/Kg BW (15.51 ± 2.65) could increase ER-α expression in the endometrium of female white rats exposed to cigarette smoke. The average value of endometrium thickness for the treatment group given purple variety sweet potato anthocyanin at a dose of 40 mg/Kg BW (152.51±9.59 µm) showed an increase in the endometrium thickness of female white rats exposed to cigarette smoke. The dose of purple variety sweet potato anthocyanin that could increase ER-α expression in the endometrium and endometrium thickness of rats exposed to cigarette smoke was a dose of 40 mg/Kg BW. The higher the dose of purple variety sweet potato anthocyanin, the greater the effect on the prevention of the reduction of estrogen receptor-α expression and the prevention of the reduction of endometrium thickness on female white rats exposed to cigarette smoke.
香烟烟雾中含有约4000种化学物质,包括自由基和致癌物,这些物质是体内的异生物质,影响生殖系统。紫甘薯含有花青素。紫甘薯中的紫色色素(花青素)是一种有益的抗氧化剂,因为它可以与自由基反应,从而对身体造成损伤。本研究旨在了解紫甘薯花青素对吸烟大鼠(褐家鼠)子宫内膜雌激素受体-α表达和子宫内膜厚度的影响。用于5组的白色大鼠为30只白色大鼠。在发现大鼠处于发情前期后,以每天2支(每支香烟±4分钟)的速度暴露于香烟烟雾中,持续8周。使用点载玻片Olympus XC 10光学显微镜和Olyvia软件检查和测量子宫内膜厚度。应用抗体ER-α(C-311)SC-787和免疫组织化学方法检测子宫内膜中ER-α的表达,并用免疫组化软件计算。数据采用Shapiro-Wilk检验、t检验和单因素方差分析(F检验)进行分析。研究发现,紫甘薯花青素40mg/Kg体重处理组子宫内膜ER-α表达的平均值(15.51±2.65)可增加吸烟雌性大鼠子宫内膜ER-1α的表达。给予紫甘薯花青素40 mg/Kg BW剂量(152.51±9.59µm)的治疗组的子宫内膜厚度平均值显示,暴露于香烟烟雾中的雌性大鼠的子宫内膜厚增加。可增加吸烟大鼠子宫内膜ER-α表达和子宫内膜厚度的紫甘薯花青素剂量为40mg/Kg BW,吸烟对雌性大鼠雌激素受体-α表达减少和子宫内膜厚度减少的预防作用越大。
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引用次数: 1
Puzzling situation of acetaminophen toxicity in a referral hospital, Tehran, Iran 伊朗德黑兰一家转诊医院对乙酰氨基酚毒性的困惑状况
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-04-01 DOI: 10.22034/IJPS.2018.33742
A. Pajoumand, T. Alinia, Arezou Mahdavinejad, H. Talaie
Puzzling situation of acetaminophen toxicity in a referral hospital, Tehran, Iran Acetaminophen carries a higher risk of overdose. A puzzling situation of acetaminophen toxicity was encouraging enough to explore the epidemiologic situation of acetaminophen toxicity and its outcomes among patients acquired poisoning. This cross-sectional study retrospectively reviewed the medical records of 185 patients with acetaminophen poisoning referred to Loghman Hakim Hospital. Toxicity determined by acetaminophen serum concentration and time elapsed after drug ingestion. Demographics, laboratory markers, toxic hepatitis, renal failures and liver enzyme elevations were compared between toxic and non-toxic patients. Twelve cases belonged to the former group and 173 patients fitted with the latter one. Having a mean age of 24.27±7.19 and 21.58±3.47 years, respectively; females were predominant. The average serum acetaminophen level was 70.37±61.92 and 24.90±26.36 within toxic and nontoxic patients respectively. Median of consumed tablets were estimated as 40 for non-toxic and 18 for toxic patients (p=0.017). Mean hospital stay was 1.75±1.05 days for toxic patients and 1.35±3.25 days for the non-toxic group (p-value<0.001), and of whom 92.4 % discharged within the first day. The laboratory assessments revealed no significant difference between groups. No death was recorded. Whereas hepatotoxicity was present in three toxic patients, renal failure was predominant in non-toxic patients. Rarely, a rise in liver enzyme noticed, however, 33.33 % of toxic and 2.31 % of the non-toxic group had elevated AST; and 33.33 % of toxic versus 1.73 % percent of non-toxic patients had increased ALT. Acetaminophen toxicity is a worldwide noteworthy cause of poisoning which has distinct mortality and morbidity rates and showed an amazing and undebatable poisoning effect in the present study. A comprehensive study is required to examine the possible reasons for the difference between Iranian acetaminophen products with other non-Iranian company products. Keywords: Acetaminophen; Hepatotoxicity; Poisoning; Renal failure; Toxicity; Iranian
在伊朗德黑兰的一家转诊医院,对乙酰氨基酚的毒性令人困惑。对乙酰氨基苯酚服用过量的风险更高。令人困惑的对乙酰氨基酚毒性情况足以令人鼓舞,以探索对乙酰氨基苯酚毒性的流行病学情况及其在获得性中毒患者中的结果。这项横断面研究回顾性回顾了185名转诊至Loghman Hakim医院的对乙酰氨基酚中毒患者的医疗记录。通过对乙酰氨基酚血清浓度和药物摄入后经过的时间确定毒性。比较了毒性和无毒患者的人口学、实验室标志物、毒性肝炎、肾功能衰竭和肝酶升高。前一组12例,后一组173例。平均年龄分别为24.27±7.19岁和21.58±3.47岁;女性占主导地位。中毒和无毒患者的平均血清对乙酰氨基酚水平分别为70.37±61.92和24.90±26.36。无毒组服用片剂的中位数估计为40,有毒组为18(p=0.017)。有毒组的平均住院时间为1.75±1.05天,无毒组为1.35±3.25天(p值<0.001),其中92.4%在第一天内出院。实验室评估显示各组之间没有显著差异。没有死亡记录。尽管三名毒性患者存在肝毒性,但无毒患者的肾功能衰竭占主导地位。肝酶的升高很少被注意到,然而,33.33%的毒性组和2.31%的无毒组AST升高;对乙酰氨基酚中毒是世界范围内值得注意的中毒原因,其死亡率和发病率不同,在本研究中显示出惊人且不可预测的中毒效果。需要进行一项全面的研究,以检查伊朗对乙酰氨基酚产品与其他非伊朗公司产品之间差异的可能原因。关键词:对乙酰氨基酚;肝毒性;中毒;肾功能衰竭;毒性;伊朗
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Iranian Journal of Pharmaceutical Sciences
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