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Influence of various operational parameters on the photocatalytic degradation of ciprofloxacin in aqueous media: a short review 不同操作参数对水介质中环丙沙星光催化降解的影响
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-05-19 DOI: 10.1080/15569543.2023.2213319
S. Imam, R. Adnan, Noor Haida Mohd Kaus, Najm Us Saqib
Abstract Ciprofloxacin (CIP) is a frequently prescribed antibiotic for various medicinal purposes that have been detected in surface water, wastewater, and wastewater treatment plants. It is a persistent organic pollutant due to its halogenated heterocyclic structure and high chemical stability at a wide range of pH. The presence of CIP in wastewater treatment plants is an indication that the antibiotic could not be removed via conventional methods. Recently, various researchers have reported the successful elimination of CIP from polluted water via photocatalytic degradation. The degradation efficacy of a photocatalyst is in direct relation to the choice of the photocatalyst and the experimental conditions employed. This review elaborates on the available literature on the photocatalytic degradation of CIP and the role of various operational parameters including photocatalyst type, modification and dosage, initial substrate concentration, pH of the reaction medium, and ionic components on the photocatalytic degradation of CIP in aqueous media. The obtained results revealed that better degradation results are recorded using various catalysts at acidic pH values, and up to 100% degradation efficiency can be achieved with catalyst modification.
摘要环丙沙星(Ciprofloxacin, CIP)是一种常用的抗生素,在地表水、废水和污水处理厂中均有检出。由于其卤化杂环结构和在大ph范围内的高化学稳定性,它是一种持久性有机污染物。污水处理厂中CIP的存在表明通过常规方法无法去除抗生素。近年来,许多研究人员报道了通过光催化降解技术成功地消除了污染水中的CIP。光催化剂的降解效果与光催化剂的选择和实验条件直接相关。本文综述了国内外关于光催化降解CIP的文献,以及各种操作参数(光催化剂类型、改性及用量、初始底物浓度、反应介质pH、离子组分等)对水介质中CIP光催化降解的影响。结果表明,在酸性pH值下,不同催化剂的降解效果较好,催化剂改性后的降解效率可达100%。
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引用次数: 38
Application of crosslinked chitosan-nanoclay composite beads for efficient removal of Ponceau S azo dye from aqueous medium 交联壳聚糖-纳米粘土复合微球在高效去除水中偶氮染料中的应用
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-05-11 DOI: 10.1080/15569543.2023.2204367
S. Çınar, Ayşe Dinçer, A. Eser, T. Aydemir
Abstract In this study, chitosan-nanoclay composite beads (CS/NC composite beads) were used to remove Ponceau S from aqueous solutions. CS/NC composites characterization was performed with FTIR, SEM-EDX, TGA, BET and XRD analyzes. The adsorption procedure was optimized by changing various parameters in batch experiments such as pH, dye concentration, contact time and temperature. Ponceau S adsorption took place at a higher rate in the acidic region, and the highest adsorption was observed at pH 2.0. The amount of adsorbed dye increased as the temperature increased at low dye concentrations and the time required to reach equilibrium was shorter than at higher dye concentrations. Linear and non-linear forms of Langmuir, Freundlich and Temkin adsorption models were applied. The adsorption behavior of Ponceau S is compatible with the linear Langmuir model, and the maximum adsorption capacity was found to be 140.85 mg g-1. Linear and nonlinear forms of adsorption kinetics and thermodynamic parameters were investigated for dye concentrations of 150-400 mg/L. The adsorption kinetics fit the linear pseudo-second-order kinetic model and the Ponceau S adsorption on CS/NC composites was spontaneous and endothermic. The results show that the CS/NC composites can be used as an effective adsorbent in industrial wastewater treatment.
摘要本研究采用壳聚糖-纳米粘土复合微珠(CS/NC复合微珠)去除水溶液中的胭脂红S。采用FTIR、SEM-EDX、TGA、BET和XRD对CS/NC复合材料进行了表征。通过改变pH、染料浓度、接触时间和温度等参数,对吸附过程进行了优化。胭脂红S在酸性区域的吸附速率较高,在pH 2.0时吸附率最高。在低染料浓度下,吸附的染料量随着温度的升高而增加,并且达到平衡所需的时间比在高染料浓度下更短。采用Langmuir、Freundlich和Temkin吸附模型的线性和非线性形式。胭脂红S的吸附行为符合线性Langmuir模型,最大吸附量为140.85 mg g-1。研究了染料浓度为150~400时吸附动力学和热力学参数的线性和非线性形式 mg/L。吸附动力学符合线性拟二阶动力学模型,CS/NC复合材料对胭脂红S的吸附是自发吸热的。结果表明,CS/NC复合材料可作为一种有效的工业废水吸附剂。
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引用次数: 0
Inhibition of phospholipase A2 from Naja haje and Naja nigricollis venoms by active fraction of Moringa oleifera leaves: in vitro and in silico methods 辣木叶活性组分对黑醋和黑醋毒磷脂酶A2的抑制作用:体外和电子方法
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-05-03 DOI: 10.1080/15569543.2023.2205538
A. Adeyi, Abideen Omobayo Jimoh, B. S. Ajisebiola, O. Adeyi, D. Metibemu, R. Okonji
Abstract Phospholipases are one of the principal toxic enzymes in snake venoms inducing a wide variety of pharmacological effects after envenomation. Natural inhibitors from plants are known to inhibit the toxic enzyme activities of snake venoms. In this study, ethanol crude extract of M. oleifera leaves was partitioned using n-hexane and ethyl acetate after which fractionation was done using column and thin layer chromatography. Subsequently, the inhibitory activities of the crude extract and sub-fractions of M. oleifera were investigated against phospholipases A2 isolated from Naja haje and Naja nigricollis venoms using in vitro and in-silico approaches while EchiTab-PLUS polyvalent antivenom was used as the standard drug. The molecular weight of isolated N. haje phospholipase A2 (NH-PL) and N. nigricollis phospholipase A2 (NN-PL) were 24.11 and 35.22 kDa respectively. NH-PL enzyme had a specific activity of 2.70 μM/min/mg substrate while NN-PL activity was 2.10 μM/min/mg substrate. The Km of NH-PL was 0.330 μM with Vmax of 0.085 μM/mL min while NN-PL had Vmax of 0.198 μM/mL.min and Km of 0.670 μM. M. oleifera n-hexane sub-fraction 5 (MOLH5) exhibited a total inhibition of NN-PL and NH-PL enzyme activities at all concentrations used. Molecular docking of the phytoconstituents of MOLH5 against the catalytic site of phospholipase A2 revealed 2-Hydrazino-8-hydroxy-4-phenylquinoline as the lead compound and a potential drug candidate with a docking score of −6.789 kcal/mol. Findings indicated that MOLH5 possesses phospholipase A2 natural inhibitors that could be explored as a therapy for snake envenoming.
磷脂酶是蛇毒中主要的毒性酶之一,在蛇毒中毒后可诱导多种药理作用。已知来自植物的天然抑制剂可以抑制蛇毒的毒性酶活性。本研究采用正己烷和乙酸乙酯对油橄榄叶乙醇粗提物进行分离,然后采用柱层析和薄层析进行分离。随后,以EchiTab-PLUS多价抗蛇毒血清为标准药,采用体外和芯片法研究了油橄榄粗提物和亚组分对日本Naja haje和Naja nigricollis毒液中磷脂酶A2的抑制活性。分离得到的哈氏黑僵菌磷脂酶A2 (NH-PL)和黑僵菌磷脂酶A2 (NN-PL)分子量分别为24.11和35.22 kDa。NH-PL酶的比活性为2.70 μM/min/mg底物,而NN-PL酶的比活性为2.10 μM/min/mg底物。NH-PL的Km为0.330 μM, Vmax为0.085 μM/mL min,而NN-PL的Vmax为0.198 μM/mL。min和Km为0.670 μM。油橄榄正己烷亚组分5 (MOLH5)在所有浓度下均表现出对NN-PL和NH-PL酶活性的完全抑制作用。将MOLH5的植物成分与磷脂酶A2的催化位点进行分子对接,发现2-肼基-8-羟基-4-苯基喹啉为先导化合物,对接得分为−6.789 kcal/mol。结果表明,MOLH5具有磷脂酶A2天然抑制剂,可作为蛇毒的治疗手段。
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引用次数: 0
A systematic review of the bioprospecting potential of Lonomia spp. (Lepidoptera: Saturniidae) 蝇蝇属生物勘探潜力的系统综述(鳞翅目:蝇科)
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-05-02 DOI: 10.1080/15569543.2023.2204348
Henrique G. Riva, A. R. Amarillo‐S
Abstract Toxins from venomous animals are proteins used for their defense or to hunt. Lonomia (Lepidoptera: Saturniidae) caterpillars can be lethal, and accidental inoculation of the venom from its bristles into human skin causes systemic blood coagulation disorders. Several reviews have investigated the pathophysiology of lonomic poisoning; however, considering the potential of venoms for bioprospecting, this review focuses on the different applications of substances derived from Lonomia spp. Following PRISMA guidelines, 39 articles were selected from 1032 papers published from 1996 to 2019. Nine different applications of substances derived from Lonomia spp. were identified: lonomic antivenom, use in cell culture, thrombosis treatment, wound healing, antiviral and antibiotic treatment, Lonomia population control, platelet adhesion research and cancer treatment. The most-reported application (38%) involved using lonomic components as cell survival promoters in cell culture. This review also notes the current knowledge gaps that block the practical use of these molecules. Several additional applications, including thrombosis treatment, wound healing, antiviral and antibiotic treatment, Lonomia population control, platelet adhesion research and cancer treatment, are limited by similar knowledge gaps related to the shortage or absence of in vivo studies. Finally, antiviral treatment and thrombosis treatment are two applications that require recombinant production of the molecule studied.
来自有毒动物的毒素是用于防御或狩猎的蛋白质。Lonomia(鳞翅目:Saturniidae)毛虫可能是致命的,并且意外地将其鬃毛中的毒液接种到人体皮肤上会导致全身血液凝固障碍。一些综述研究了慢性中毒的病理生理;但考虑到毒液的生物开发潜力,本文重点介绍了Lonomia spp衍生物质的不同应用。按照PRISMA指南,从1996年至2019年发表的1032篇论文中选择了39篇。鉴定了九种不同用途:抗蛇毒、细胞培养、血栓治疗、伤口愈合、抗病毒和抗生素治疗、洛诺米亚种群控制、血小板粘附研究和癌症治疗。报道最多的应用(38%)涉及在细胞培养中使用lonomic组分作为细胞存活促进剂。这篇综述还指出,目前的知识差距阻碍了这些分子的实际应用。其他一些应用,包括血栓治疗、伤口愈合、抗病毒和抗生素治疗、Lonomia种群控制、血小板粘附研究和癌症治疗,由于缺乏或缺乏体内研究而受到类似知识空白的限制。最后,抗病毒治疗和血栓治疗是需要重组生产所研究的分子的两个应用。
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引用次数: 0
Dose- and dosage-dependent spectrum of respiratory toxicity of cypermethrin in rabbits 氯氰菊酯对家兔呼吸毒性的剂量依赖性谱
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-04-27 DOI: 10.1080/15569543.2023.2204334
L. Ahmad, S. T. Gul, Xiaoxia Du, Riaz Hussain, M. R. Khanani, Shajeela Iram, A. U. Rehman, Ahrar Khan
Abstract Pyrethroids are popular insecticides. Shortness of breath and dyspnea are key signs of exposure; however, their respiratory effects are rarely studied. This study investigated the combination and ratios of specific blood tests and lung lesions as respiratory effects of cypermethrin (CY) in rabbits. The effects of CY at various doses and times are the novelty of this study. Doses (50, 100, and 150 mg.kg-1 body weight) of CY were injected intraperitoneally every week for up to 9 weeks in rabbits assigned into four equal groups. Data analysis revealed various respiratory signs, significantly (p ≤ 0.05) lower fibrinogen, higher neutrophils-lymphocytes (NL), LDH-lymphocytes (LL), and De-Ritis ratios (DR), and lesions in the lungs. The frequency and incidence of these effects were dose and dosage dependent. The CY leads to pulmonary signs and allergic effects. Lung injury increases cell-free heme in plasma, causing pulmonary edema with hemolysis. Emphysema and fibrosis followed the migration of basophils and mononuclear cells to the lungs. This study inferred that CY exposure caused lower fibrinogen, higher NL, LL, and DR ratios, and pulmonary lesions, which forecast poor immunity, especially increased risk for cardiac and lung diseases.
拟除虫菊酯是常用的杀虫剂。呼吸短促和呼吸困难是暴露的主要迹象;然而,它们对呼吸系统的影响很少被研究。本研究探讨了氯氰菊酯(CY)对家兔呼吸系统的影响。不同剂量和时间的CY的作用是本研究的新奇之处。剂量(50,100和150mg)。随机分为4组,连续9周,每周腹腔注射CY (kg-1体重)。数据分析显示呼吸体征不同,纤维蛋白原显著(p≤0.05)降低,中性粒细胞-淋巴细胞(NL)、ldl -淋巴细胞(LL)、De-Ritis比值(DR)升高,肺部病变明显(p≤0.05)。这些效应的发生频率和发生率是剂量依赖性的。CY会导致肺部症状和过敏反应。肺损伤使血浆中游离血红素增加,引起肺水肿伴溶血。肺气肿和纤维化随嗜碱性细胞和单核细胞向肺的迁移而发生。本研究推断CY暴露导致纤维蛋白原降低,NL、LL和DR比值升高,肺部病变,预示免疫力低下,尤其是心肺疾病的风险增加。
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引用次数: 1
Modulating insulin secretion and inflammation against sodium arsenite toxicity by levosimendan as a novel pancreatic islets’ protector 新型胰岛保护剂左西孟旦对亚砷酸钠毒性胰岛素分泌和炎症的调节作用
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-04-27 DOI: 10.1080/15569543.2023.2205515
M. Daniali, M. Navaei-Nigjeh, M. Baeeri, Soheyl Mirzababaei, M. Gholami, M. Rahimifard, M. Abdollahi
Abstract Levosimendan (LEVO) is a calcium sensitizer with established inotropic and vasodilator impacts associated with ATP-sensitive potassium channels (KATP). Although LEVO’s role in modulating oxidative stress of cardiac cells has been studied, in the current study, LEVO was used, for the first time, to investigate its preventive and therapeutic roles in pancreatic islets through viability, functionality, and inflammation pathways as well as oxidative stress against the toxicity induced by sodium arsenite (NaAsO2). Following the optimization studies to select the proper concentrations of LEVO and NaAsO2, isolated pancreatic islets were exposed to different combinations of NaAsO2 and LEVO. MTT assay, glucose-dependent insulin secretion test, investigation of oxidative stress and inflammation biomarkers in addition to qualification of the expressions of P16, P38, and NF-κB genes were performed to assess different underlying mechanisms to investigate the protective role of LEVO against NaAsO2-induced toxicity. This study demonstrated that NaAsO2-treated pancreatic islets’ exposure to LEVO improved their viability and functionality while modulating the generation of oxidative stress and inflammatory biomarkers. Therefore LEVO caused significant recoveries in the characteristics of the islets. The main conclusion is that LEVO showed protective impacts in pancreatic islets against exposure to NaAsO2. However, therapeutic uses of LEVO in the field of diabetes need further investigations. HIGHLIGHTS Sodium arsenite is responsible for activating the oxidative stress and inflammation pathways in pancreatic islet cells and consequently decreasing their viability and function. Treatment of pancreatic islets with sodium arsenite results in the loss of glucose-dependent insulin secretion (GDIS) which can be alleviated by levosimendan. Levosimendan modulates the decreased level of secreted insulin by preventing formation of reactive oxygen species (ROS) and inactivating the inflammatory biomarkers. Levosimendan improves the viability and function of sodium arsenite-treated pancreatic islets by modulating insulin secretion and glucose control. Levosimendan acts as a protective agent against the toxicity induced by sodium arsenite in pancreatic islets through modulating the viability, oxidative stress, inflammation, and function pathways. Graphical Abstract
摘要Levosimendan(LEVO)是一种钙增敏剂,具有与ATP敏感性钾通道(KATP)相关的变力和舒张作用。尽管LEVO在调节心脏细胞氧化应激中的作用已被研究,但在当前的研究中,LEVO首次被用于通过生存能力、功能和炎症途径以及氧化应激对抗亚砷酸钠(NaAsO2)诱导的毒性来研究其在胰岛中的预防和治疗作用。在选择适当浓度的LEVO和NaAsO2的优化研究之后,将分离的胰岛暴露于NaAsO2和LEVO的不同组合。MTT法、葡萄糖依赖性胰岛素分泌试验、氧化应激和炎症生物标志物的研究以及P16、P38和NF-κB基因的表达鉴定,以评估不同的潜在机制,从而研究LEVO对NaAsO2诱导的毒性的保护作用。这项研究表明,NaAsO2处理的胰岛暴露于LEVO提高了其生存能力和功能,同时调节了氧化应激和炎症生物标志物的产生。因此,LEVO使小岛的特性显著恢复。主要结论是,LEVO对暴露于NaAsO2的胰岛具有保护作用。然而,LEVO在糖尿病领域的治疗用途需要进一步研究。亮点亚砷酸钠负责激活胰岛细胞的氧化应激和炎症途径,从而降低其生存能力和功能。用亚砷酸钠治疗胰岛会导致葡萄糖依赖性胰岛素分泌(GDIS)的损失,左西孟旦可以减轻这种损失。左西孟丹通过防止活性氧(ROS)的形成和灭活炎症生物标志物来调节分泌胰岛素水平的降低。左西孟丹通过调节胰岛素分泌和葡萄糖控制,改善亚砷酸钠治疗的胰岛的生存能力和功能。左西孟丹通过调节胰岛的活力、氧化应激、炎症和功能途径,对亚砷酸钠诱导的胰岛毒性起到保护作用。图形摘要
{"title":"Modulating insulin secretion and inflammation against sodium arsenite toxicity by levosimendan as a novel pancreatic islets’ protector","authors":"M. Daniali, M. Navaei-Nigjeh, M. Baeeri, Soheyl Mirzababaei, M. Gholami, M. Rahimifard, M. Abdollahi","doi":"10.1080/15569543.2023.2205515","DOIUrl":"https://doi.org/10.1080/15569543.2023.2205515","url":null,"abstract":"Abstract Levosimendan (LEVO) is a calcium sensitizer with established inotropic and vasodilator impacts associated with ATP-sensitive potassium channels (KATP). Although LEVO’s role in modulating oxidative stress of cardiac cells has been studied, in the current study, LEVO was used, for the first time, to investigate its preventive and therapeutic roles in pancreatic islets through viability, functionality, and inflammation pathways as well as oxidative stress against the toxicity induced by sodium arsenite (NaAsO2). Following the optimization studies to select the proper concentrations of LEVO and NaAsO2, isolated pancreatic islets were exposed to different combinations of NaAsO2 and LEVO. MTT assay, glucose-dependent insulin secretion test, investigation of oxidative stress and inflammation biomarkers in addition to qualification of the expressions of P16, P38, and NF-κB genes were performed to assess different underlying mechanisms to investigate the protective role of LEVO against NaAsO2-induced toxicity. This study demonstrated that NaAsO2-treated pancreatic islets’ exposure to LEVO improved their viability and functionality while modulating the generation of oxidative stress and inflammatory biomarkers. Therefore LEVO caused significant recoveries in the characteristics of the islets. The main conclusion is that LEVO showed protective impacts in pancreatic islets against exposure to NaAsO2. However, therapeutic uses of LEVO in the field of diabetes need further investigations. HIGHLIGHTS Sodium arsenite is responsible for activating the oxidative stress and inflammation pathways in pancreatic islet cells and consequently decreasing their viability and function. Treatment of pancreatic islets with sodium arsenite results in the loss of glucose-dependent insulin secretion (GDIS) which can be alleviated by levosimendan. Levosimendan modulates the decreased level of secreted insulin by preventing formation of reactive oxygen species (ROS) and inactivating the inflammatory biomarkers. Levosimendan improves the viability and function of sodium arsenite-treated pancreatic islets by modulating insulin secretion and glucose control. Levosimendan acts as a protective agent against the toxicity induced by sodium arsenite in pancreatic islets through modulating the viability, oxidative stress, inflammation, and function pathways. Graphical Abstract","PeriodicalId":23211,"journal":{"name":"Toxin Reviews","volume":null,"pages":null},"PeriodicalIF":3.1,"publicationDate":"2023-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42391437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Phytochemical composition, toxicity, and repellent effects of medicinal plants Peganum harmala, Pterocarya fraxinifolia, and Tanacetum parthenium extracts against Sitophilus oryzae L. 药用植物苦参、黄叶翼木和白荆提取物对米象虫的植物化学成分、毒性和驱避作用。
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-02-16 DOI: 10.1080/15569543.2023.2178013
Mahmoud Fazeli-Dinan, Seyed Hanif Osia-Laghab, Mina Amini, A. Davoodi, S. H. Nikookar, Jamshid Yazdani Charati, M. Azadbakht, A. Enayati
Abstract Sitophilus oryzae is an important pest of stored rice and is usually controlled by the use of aluminum phosphide, which is dangerous to humans. Botanical insecticides deemed promising alternatives in controlling this pest. In this study, extracts of Peganum harmala seeds, Pterocarya fraxinifolia leaves, and Tanacetum parthenium flowers were evaluated against S. oryzae adults. Phytochemical analyses showed that steroid, terpenoid, tannin, alkaloid, and flavonoid are present in the extracts. Bioassays revealed repellency effects of all extracts, besides, P. harmala extract exerted significant mortality (93.33 ± 6.6%, LC50: 521.06 mg/ml) hence it may have applications in preventing infestation of stored rice by S. oryzae. Highlights Plant extracts studied in this research efficiently repel rice weevil. These plant extracts show significant toxicity against rice weevil. Alkaloid, steroid, terpenoid, tannin, and flavonoid are present in extracts of these plants.
摘要米螟是储藏水稻的一种重要害虫,通常使用对人类有危害的磷化铝进行防治。植物杀虫剂被认为是控制这种害虫的有前景的替代品。在本研究中,对骆驼蓬种子、五叶Pterocarya fraxinifolia叶和白头翁花的提取物进行了抗米曲霉成虫的评价。植物化学分析表明,提取物中含有甾体、萜类、单宁、生物碱和类黄酮。生物测定显示,所有提取物都具有排斥作用,此外,骆驼蓬提取物具有显著的死亡率(93.33 ± 6.6%,LC50:521.06 mg/ml),因此它可用于防止米曲霉对储藏的水稻的侵扰。亮点本研究所研究的植物提取物能有效抵御水稻象甲。这些植物提取物对稻象甲具有显著的毒性。生物碱、类固醇、萜类、单宁和类黄酮存在于这些植物的提取物中。
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引用次数: 0
Medicago sativa ameliorated cyclophosphamide-induced thrombocytopenia and oxidative stress in rats 苜蓿改善环磷酰胺诱导的大鼠血小板减少和氧化应激
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-02-14 DOI: 10.1080/15569543.2023.2175870
Z. Gholamnezhad, V. Rouki, R. Rezaee, M. Boskabady
Abstract Effect of Medicago sativa (MS) hydro-ethanolic extract against the cyclophosphamide (CP)-induced toxicity was evaluated in rats grouped as: Control; CP (100 mg/kg subcutaneous, day 1–3); and CP+ MS100, 200, and 400 mg/kg/day, orally for 14 days. Hematologic, lipid, hepatic and oxidative stress markers were analyzed. Platelet, WBC, RBC, Hb and Hct in the CP group were lower than the control. The MS200 and MS400 groups had lower lipids, liver enzymes, nitrite and malondialdehyde levels but higher platelet, WBC, thiol, superoxide dismutase and catalase levels than the CP group. MS ameliorated CP-induced thrombocytopenia, oxidative stress, and increases in serum lipids and hepatic enzymes.
摘要在以下大鼠中评价了紫花苜蓿(MS)水乙醇提取物对环磷酰胺(CP)诱导的毒性的影响:对照;CP(100 mg/kg皮下注射,第1-3天);和CP+MS100、200和400 mg/kg/天,口服14 天。分析血液学、脂质、肝脏和氧化应激标志物。CP组血小板、白细胞、红细胞、Hb、Hct均低于对照组。MS200和MS400组的脂质、肝酶、亚硝酸盐和丙二醛水平低于CP组,但血小板、WBC、硫醇、超氧化物歧化酶和过氧化氢酶水平高于CP组。MS改善了CP诱导的血小板减少、氧化应激以及血脂和肝酶的增加。
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引用次数: 1
Epidemiologic and spatiotemporal study on access to snakebite care in Northern Nigeria 尼日利亚北部获得蛇咬伤护理的流行病学和时空研究
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-02-11 DOI: 10.1080/15569543.2023.2177873
Naziru Halliru, M. M. Badamasi, I. Y. Tudunwada, Titus B Dajel, S. Abubakar, Auwalu S. Hamza, Sandra B. Oluwashola, Nasiru K. Nalado, M. Dahiru, Ibrahim Na’abdu, Umar N. Saleh, A. M. Daiyab, S. Mohammed, G. Iliyasu, H. Muhammad, A. Habib
Abstract The role of epidemiologic and spatiotemporal factors affecting access to care among snakebite patients in Nigeria are determined. In 2021 a total of 2,942 snakebite patients were prospectively studied at four designated Health Facilities for Managing Snakebites (HFMS). The patients came from 94 Local Government Areas (LGAs) in 12 states in northern Nigeria. It was found that 435 (14.8%) patients actually accessed care within ≤2 hours of bite although 38.0% could have reached the HFMS within the time by car. In certain areas 92% of patients would have been able to reach a secondary or tertiary facility within ≤2 hours. Similarly, 437 (14.9%) patients traveled distances of ≤20 Km to reach a designated HFMS although 86% of patients resided within 5 Km of a road network. There was longer median delay to access care (15 hours), more patients (365) and higher proportion not treated with antivenom (22%) in August the wettest month of the year. Furthermore the patients who died (47) took a median time of 48 hours compared to 11 hours among known survivors (2,649) to access care. Expanding antivenom access to other secondary and tertiary HF in high burden areas especially during peak seasons will potentially improve the outcome among patients.
摘要确定了影响尼日利亚蛇咬伤患者获得护理的流行病学和时空因素的作用。2021年,在四个指定的蛇咬伤管理卫生机构(HFMS)对2942名蛇咬伤患者进行了前瞻性研究。患者来自尼日利亚北部12个州的94个地方政府区。研究发现,435名(14.8%)患者在≤2 尽管38.0%的人可能在乘车时间内达到HFMS。在某些地区,92%的患者能够在≤2内到达二级或三级机构 小时。同样,437名(14.9%)患者的旅行距离≤20 Km达到指定的HFMS,尽管86%的患者居住在5 公路网的公里数。获得护理的中位延迟时间更长(15 小时),在一年中最潮湿的八月,更多的患者(365人)和更高比例的未接受抗蛇毒血清治疗(22%)。此外,死亡患者(47人)的中位时间为48 小时,相比之下为11 已知幸存者(2649人)获得护理的时间。在高负荷地区,特别是在高峰季节,扩大抗蛇毒血清对其他二级和三级HF的使用范围,可能会改善患者的预后。
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引用次数: 0
Gallic acid and sesame oil exert cardioprotection via mitochondrial protection and antioxidant properties on Ketamine-Induced cardiotoxicity model in rats 没食子酸和香油通过线粒体保护和抗氧化作用对氯胺酮致大鼠心脏毒性模型发挥心脏保护作用
IF 3.1 4区 医学 Q2 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-01-13 DOI: 10.1080/15569543.2023.2165503
A. Salimi, M. Shabani, Deniz Bayrami, Armin Saray, Nastaran Farshbaf Moghimi
Abstract Ketamine is a cardiotoxic agent and can deplete ATP in cardiomyocytes through mitochondrial dysfunction. We investigated the effects of gallic acid and sesame oil in ketamine-induced cardiotoxicity in rats. Male Wistar rats were randomly divided into six groups including control; ketamine; ketamine + gallic acid; ketamine + sesame oil; gallic acid and sesame oil. Serum cardiac marker, cardiac tissue oxidative stress markers, histopathological analysis and mitochondrial toxicity parameters (succinate dehydrogenase activity, mitochondrial swelling, reactive oxygen species (ROS) production and collapse of mitochondria membrane potential) were measured on the fifteen days of the study. The results showed that ketamine administration increased serum cardiac markers, oxidative stress parameters, histopathological alterations and mitochondrial dysfunction in cardiac tissue. Gallic acid and sesame oil administration in presence of ketamine was observed to decrease serum cardiac markers, oxidative stress parameters, histopathological alterations and mitochondrial dysfunction in cardiac tissue. The results suggest that gallic acid and sesame oil exert cardioprotection via mitochondrial protection, antioxidant properties and ultimately improving mitochondrial function and cardiac function.
氯胺酮是一种心脏毒性药物,可通过线粒体功能障碍消耗心肌细胞中的ATP。研究没食子酸和香油对氯胺酮致大鼠心脏毒性的影响。雄性Wistar大鼠随机分为6组:对照组;氯胺酮;氯胺酮+没食子酸;氯胺酮+香油;没食子酸和香油。在研究的第15天,测定血清心脏标志物、心脏组织氧化应激标志物、组织病理学分析和线粒体毒性参数(琥珀酸脱氢酶活性、线粒体肿胀、活性氧(ROS)产生和线粒体膜电位崩溃)。结果表明,氯胺酮增加了血清心脏标志物、氧化应激参数、组织病理学改变和心脏组织线粒体功能障碍。在氯胺酮存在的情况下,观察到没食子酸和芝麻油可降低血清心脏标志物、氧化应激参数、组织病理学改变和心脏组织线粒体功能障碍。结果表明,没食子酸和芝麻油通过线粒体保护、抗氧化作用发挥心脏保护作用,最终改善线粒体功能和心脏功能。
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引用次数: 0
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