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Blood Glucose and Glycogen Levels as Indicators of Stress in the Freshwater Fish, Cirrihinus mrigal under Cyphenothrin Intoxication 氯氰菊酯中毒淡水鱼血糖和糖原水平作为应激指标的研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/30444
Sapna S. Anigol, Srinivas B Neglur, M. David
Pesticides are non-biodegradable substances used to control bugs, weeds, snails, and plant diseases. They are widely utilised in forestry, farming, and veterinary practices and are of incredible general well-being significance. Pesticides can be ordered by their utilisation into three significant sorts (in particular insect sprays, herbicides, and fungicides). Water defilement by these pesticides is known to prompt harmful effects on the creation, proliferation, and survivability of aquatic life forms, like green growth, amphibian plants, and fish (shellfish and finfish species). The information presented in this study is used to assess the negative effects of exposing fish species to pesticide concentrations. Pyrethroids are regularly utilised around the home and in agricultural production to control bugs. Human contact with at least one pyrethroid bug spray is reasonable. These synthetic substances cause serious harm to aquatic biological systems, particularly fish. The principle points and objective of the present investigation are to assess the effect of cyphenothrin on carbohydrate metabolism in the fish. Cirrihinus mrigal is a monetarily significant Indian major carp. A freshwater fish, Cirrihinus mrigal, was exposed to bug spray, i.e., cyphenothrin a manufactured pyrethroid. The LC50 for cyphenothrin at 96 hrs was 6 μg/L by probit analysis. One-fifth of LC50 (120 μg/L), was chosen as the sublethal focus. The fish were subjected to sub-lethal concentrations for 10, 20, 30 and 40 days, and the changes in starch digestion, for example, absolute glycogen, as well as the activities of catalysts Lactate Dehydrogenase (LDH) and Succinate Dehydrogenase (SDH) in critical organs, such as the gill, kidney, and liver, were studied.
农药是一种不可生物降解的物质,用于控制昆虫、杂草、蜗牛和植物病害。它们被广泛应用于林业、农业和兽医实践,具有令人难以置信的总体福祉意义。农药可按其用途分为三大类(特别是杀虫剂、除草剂和杀菌剂)。众所周知,这些农药对水的污染会对水生生物的产生、繁殖和生存能力产生有害影响,比如绿色植物、两栖植物和鱼类(贝类和鱼类)。本研究提供的信息用于评估将鱼类暴露于杀虫剂浓度的负面影响。拟除虫菊酯类杀虫剂经常在家庭周围和农业生产中使用,以控制虫子。人类至少接触一种拟除虫菊酯杀虫剂是合理的。这些合成物质对水生生物系统,特别是鱼类造成严重危害。本研究的主要目的是评价氯氰菊酯对鱼类碳水化合物代谢的影响。Cirrihinus mrigal是一种重要的印度鲤鱼。将一种淡水鱼(Cirrihinus mrigal)暴露于杀虫剂,即氯氰菊酯(一种人造拟除虫菊酯)。经probit分析,氯氰菊酯96 h的LC50为6 μg/L。取五分之一LC50 (120 μg/L)作为亚致死灶。分别在亚致死浓度下处理10、20、30和40天,研究鱼的淀粉消化(如绝对糖原)以及鳃、肾和肝等关键器官中乳酸脱氢酶(LDH)和琥珀酸脱氢酶(SDH)的活性变化。
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引用次数: 0
Validating the Antimicrobial Potentiality of Peptides from Pods of Acacia nilotica Willd.ex Delile: A Spotlight on Bacterial Fauna 尼罗Acacia nilotica Willd.ex Delile豆荚肽的抗菌潜力验证:细菌区系研究热点
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/31892
R. Shukla, Veena Sharma
Contagious infections cause over 17 million human deaths in a year among which diseases caused by bacteria are the most prominent ones. Additionally, in the last few years, the haphazard usage of antibiotics has provoked the condition of multifarious defiance in the bacterial strains against these chemical drugs thus contributing to an upsurge towards severe economic and communal welfare-related uncertainties. Thus, to annihilate such situations there is a compelling demand to explore novel substitutes to overcome these concerns. Hence, such problematic situations bring up the limelight towards plant-derived proteins/peptides possessing antimicrobial activity which prove to be excellent alternatives against bacterial pathogens causing serious maladies in humans. Therefore, in this context the current study investigated the antibacterial potential of the Ethanol, Methanol and Chloroform peptides/protein isolate obtained from pods of Acacia nilotica by Disc-Diffusion Assay and MIC (Minimum Inhibitory Concentration) against E. coli and B. subtilis bacterial strains. The antibacterial activity of all three solvent peptide isolates was found to be exhibiting antimicrobial activity at a concentration of 100μg/ml against B. subtilis with Disc-Diffusion as well as MIC with Chloroform isolate displaying the highest activity against gram-positive Bacillus species. Therefore, such plant-derived antibacterial proteins/peptides in the future can be used as a therapeutic drug to combat various severe bacterial maladies thus providing a better alternative than antibiotics both in terms of safety against unwanted secondary effects as well as will also help in bringing down the graphs of Antimicrobial Resistance (AMR) posing a serious threat to the human health. As a result, the study concludes that peptide isolates obtained from Acacia nilotica pods are effective against gram-positive Bacillus species, making them an important antibacterial compound.
传染性感染在一年内导致1700多万人死亡,其中细菌引起的疾病最为突出。此外,在过去几年中,抗生素的随意使用引发了菌株对这些化学药物的各种反抗,从而导致严重的经济和社区福利相关不确定性激增。因此,为了消除这种情况,迫切需要探索新的替代品来克服这些担忧。因此,这种有问题的情况引起了人们对具有抗菌活性的植物衍生蛋白质/肽的关注,这些蛋白质/肽被证明是对抗导致人类严重疾病的细菌病原体的极好替代品。因此,在这种情况下,本研究通过圆盘扩散法和MIC(最小抑制浓度)研究了从尼罗Acacia荚中获得的乙醇、甲醇和氯仿肽/蛋白质分离物对大肠杆菌和枯草芽孢杆菌菌株的抗菌潜力。所有三种溶剂肽分离物在浓度为100μg/ml时均表现出对枯草芽孢杆菌的盘扩散抗菌活性,氯仿分离物的MIC对革兰氏阳性芽孢杆菌表现出最高的抗菌活性。因此,这种植物来源的抗菌蛋白/肽在未来可以用作治疗药物,以对抗各种严重的细菌疾病,从而在对抗不必要的副作用的安全性方面提供了比抗生素更好的替代品,也将有助于降低对人类健康构成严重威胁的抗微生物耐药性(AMR)。因此,该研究得出结论,从尼罗金合欢荚中获得的肽分离物对革兰氏阳性芽孢杆菌有效,使其成为一种重要的抗菌化合物。
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引用次数: 1
Toxic Effects Associated With Neonicotinoid Exposure on Non-target Organisms: A Review 新烟碱类物质对非靶生物的毒性作用研究进展
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/30246
Leena Khurana, P. Chaturvedi, C. Sharma, P. Bhatnagar, Nidhi Gupta
The neonicotinoid class of insecticide is nicotine-like neuro-toxicants used to control the pests of agriculture crops and ornamental plants. They act as selective agonists of acetylcholine receptors in the central nervous system of insect pests and work by disrupting their nerve impulses. Some of the properties of this class of insecticides are a long half-life in soil, low volatility, and higher water solubility, leading to their accumulation in soil, underground water, and water bodies due to surface runoff. This, in turn, results in exposure to many beneficial non-target aquatic and soil fauna such as arthropods, fish, birds, mammals, etc. Although it has a selective mode of action for insects, some in vivo and in vitro investigations have also shown toxicity in non-target invertebrates and vertebrates. Initially, neonicotinoid toxicity was observed in honey bees, which are essential pollinators of crops. Later, studies reported the accumulation of neonicotinoid residues leading to the mortality of aquatic fauna, including salt marsh and freshwater mosquitoes, brine shrimp, fleas, and crayfish. Imidacloprid exposure led to disruption of larval development in the Mayfly larvae. Also, earthworms that play a crucial role in enhancing soil fertility were drastically affected by acetamiprid, clothianidin, imidacloprid, nitenpyram, and thiacloprid. Apart from these, toxicological impacts were also observed in vertebrates such as birds, where imidacloprid, clothianidin, acetamiprid, and thiacloprid caused reproductive, metabolic, and morphological alterations. Similarly, imidacloprid and acetamiprid caused gills, brain and liver dysfunction with embryo mortality. Even after the selective action of neonicotinoids, instances of mammalian toxicity were also reported in many in vivo studies. DNA damage and liver dysfunctions due to imidacloprid in rabbits were observed in various studies. In a recent study, imidacloprid exposure led to DNA damage and oxidative stress in bone marrow-derived mesenchymal cells of buffalo. Also, many instances of neurotoxicity, reproductive toxicity, immunotoxicity, genotoxicity and cytotoxicity in mouse and rat models were observed due to different neonicotinoids. Many in vitro studies using mammalian cell lines have also established potential risks of neonicotinoid exposure. This review, therefore, is a compilation of various toxicity studies of different types of neonicotinoid pesticides in both nontarget invertebrates and vertebrates, including several kinds of toxicities caused in mammals with neonicotinoid exposure.
新烟碱类杀虫剂是一种类似尼古丁的神经毒剂,用于控制农作物和观赏植物的害虫。它们在害虫的中枢神经系统中充当乙酰胆碱受体的选择性激动剂,通过破坏它们的神经冲动发挥作用。这类杀虫剂的一些特性是在土壤中半衰期长、挥发性低、水溶性高,导致它们因地表径流而在土壤、地下水和水体中积累。这反过来又导致接触许多有益的非目标水生和土壤动物,如节肢动物、鱼类、鸟类、哺乳动物等。尽管它对昆虫有选择性的作用模式,但一些体内和体外研究也表明对非目标无脊椎动物和脊椎动物有毒性。最初,在蜜蜂身上观察到新烟碱类毒性,蜜蜂是作物的重要传粉昆虫。后来,研究报告称,新烟碱类残留物的积累导致水生动物的死亡,包括盐沼和淡水蚊子、卤虾、跳蚤和小龙虾。吡虫啉暴露导致果蝇幼虫发育中断。此外,在提高土壤肥力方面发挥关键作用的蚯蚓也受到啶虫脒、噻虫胺、吡虫啉、烯啶虫胺和噻虫脒的严重影响。除此之外,在鸟类等脊椎动物中也观察到了毒理学影响,吡虫啉、噻虫胺、啶虫脒和噻虫脒会导致生殖、代谢和形态改变。同样,吡虫啉和啶虫脒会导致鳃、脑和肝功能障碍,并导致胚胎死亡。即使在新烟碱类药物的选择性作用之后,在许多体内研究中也报道了哺乳动物毒性的例子。在各种研究中观察到吡虫啉对家兔的DNA损伤和肝脏功能障碍。在最近的一项研究中,吡虫啉暴露导致水牛骨髓间充质细胞的DNA损伤和氧化应激。此外,由于不同的新烟碱类化合物,在小鼠和大鼠模型中观察到许多神经毒性、生殖毒性、免疫毒性、遗传毒性和细胞毒性。许多使用哺乳动物细胞系的体外研究也确定了新烟碱类暴露的潜在风险。因此,本综述汇集了不同类型新烟碱类农药对非目标无脊椎动物和脊椎动物的各种毒性研究,包括对接触新烟碱类杀虫剂的哺乳动物造成的几种毒性。
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引用次数: 0
Acute and Repeated Dose 28-Day Oral Toxicity Studies of Phlorotannin Rich Fraction of Sargassum tenerrimum, A Marine Brown Algae 富绿鞣酸马尾藻(一种海洋褐藻)急性和重复剂量28天口服毒性研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/31390
N. G V, Chitra Vellapandian
Sargassum tenerrimum is a marine brown algae rich in phlorotannins, a class of marine polyphenols with significant biological activities. The present study aimed to prepare a phlorotannin-rich fraction from S. tenerrimum (PST) and evaluate its acute and subacute oral toxicity in Wistar albino rats according to the procedures and methods of the OECD test guidelines for acute and repeated dose 28-day oral toxicity studies. S. tenerrimum powder was extracted with ethanol and further fractionated with ethylacetate, 1-butanol, and water. The ethyl acetate fraction was found to have the highest total phlorotannin concentration and was evaluated for its safety. In the acute oral toxicity study, a single dose of PST at 2000 mg/kg body weight did not result in any treatment-related clinical symptoms of toxicity or mortality. Therefore, the median lethal dose (LD50) of PST was identified as greater than 2000 mg/kg. The subacute oral toxicity investigation at 200, 400, and 800 mg/kg doses administered for 28 days with a 14-day recovery period revealed no treatment-related adverse clinical symptoms or mortality/morbidity. The treated animals exhibited normal weight gain, feed intake and did not result in clinically significant toxicity as measured by clinical blood chemistry and hematological markers. Gross and histological examinations of selected tissues did not reveal any notable adverse alterations associated with the intervention. Under the study's findings, the LD50 for PST was determined to be >2000 mg/kg b.wt. and No Observed Adverse Effect Level (NOAEL) to be 800 mg/kg rat b.wt.
细叶马尾藻是一种富含根皮黄酮的海洋褐藻,根皮黄酮是一类具有重要生物活性的海洋多酚。本研究旨在根据经合组织急性和重复剂量28天口服毒性研究试验指南的程序和方法,从藤毒中制备富含根皮藤素的组分,并评估其对Wistar白化大鼠的急性和亚急性口服毒性。用乙醇提取S.tenemum粉末,并用乙酸乙酯、1-丁醇和水进一步分馏。发现乙酸乙酯部分具有最高的总根皮藤素浓度,并对其安全性进行了评估。在急性口服毒性研究中,单剂量2000 mg/kg体重的PST不会导致任何与治疗相关的毒性或死亡临床症状。因此,PST的中位致死剂量(LD50)被确定为大于2000 mg/kg。在为期14天的恢复期内,以200、400和800 mg/kg剂量给药28天的亚急性口服毒性调查显示,没有出现与治疗相关的不良临床症状或死亡率/发病率。经治疗的动物表现出正常的体重增加和采食量,并且通过临床血液化学和血液学标志物测量,没有导致临床显著的毒性。所选组织的大体和组织学检查没有发现任何与干预相关的显著不良变化。根据研究结果,PST的LD50被确定为>2000 mg/kg b.wt,无观察到的不良反应水平(NOAEL)为800 mg/kg大鼠b.wt。
{"title":"Acute and Repeated Dose 28-Day Oral Toxicity Studies of Phlorotannin Rich Fraction of Sargassum tenerrimum, A Marine Brown Algae","authors":"N. G V, Chitra Vellapandian","doi":"10.18311/ti/2023/v30i1/31390","DOIUrl":"https://doi.org/10.18311/ti/2023/v30i1/31390","url":null,"abstract":"Sargassum tenerrimum is a marine brown algae rich in phlorotannins, a class of marine polyphenols with significant biological activities. The present study aimed to prepare a phlorotannin-rich fraction from S. tenerrimum (PST) and evaluate its acute and subacute oral toxicity in Wistar albino rats according to the procedures and methods of the OECD test guidelines for acute and repeated dose 28-day oral toxicity studies. S. tenerrimum powder was extracted with ethanol and further fractionated with ethylacetate, 1-butanol, and water. The ethyl acetate fraction was found to have the highest total phlorotannin concentration and was evaluated for its safety. In the acute oral toxicity study, a single dose of PST at 2000 mg/kg body weight did not result in any treatment-related clinical symptoms of toxicity or mortality. Therefore, the median lethal dose (LD50) of PST was identified as greater than 2000 mg/kg. The subacute oral toxicity investigation at 200, 400, and 800 mg/kg doses administered for 28 days with a 14-day recovery period revealed no treatment-related adverse clinical symptoms or mortality/morbidity. The treated animals exhibited normal weight gain, feed intake and did not result in clinically significant toxicity as measured by clinical blood chemistry and hematological markers. Gross and histological examinations of selected tissues did not reveal any notable adverse alterations associated with the intervention. Under the study's findings, the LD50 for PST was determined to be >2000 mg/kg b.wt. and No Observed Adverse Effect Level (NOAEL) to be 800 mg/kg rat b.wt.","PeriodicalId":23205,"journal":{"name":"Toxicology International","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47804778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessment of the Protective Effects of Selenium and Zinc against Potassium Dichromate Induced Thyrotoxicity in Preimplanted Wistar albinos Rats 硒和锌对预植入Wistar白化大鼠重铬酸钾致甲状腺毒性保护作用的评价
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/24528
Anfal Fedala, O. Adjroud, Asma Saouli, Imène Salah
Hexavalent chromium is an environmental pollutant considered to be an endocrine-disrupting metal. Selenium and zinc are essential trace elements, known to play a crucial role in thyroid homeostasis. The purpose of the current work is to investigate the effects of potassium dichromate (K₂Cr₂O7) administrated subcutaneously (s.c) on the 3rd day of pregnancy in preimplanted rats by using graded doses (10, 50, 100 mg/kg, s.c) or K₂Cr₂O7 (10 mg/kg, s.c) in association with Selenium (0.3 mg/kg, s.c) and Zinc chloride (20 mg/kg, s.c). The hormonal profile, apoptosis induction and histological changes in thyroids were evaluated. Our main findings showed that K₂Cr₂O7 promoted hypothyroidism with a significant decrease in plasma T3 and T4 levels (P<0.001), while plasma TSH level increased significantly (P<0.001), in addition, a hypertrophy of the thyroid was noted (P<0.01). Moreover, K2Cr2O7 (10 mg/kg, s.c) induced apoptosis via the caspase 3 pathway (P<0.001) and altered the gland histoarchitecture. The co-treatment with Se or ZnCl₂ has ameliorated the hormonal status and restored partially the thyroid histoarchitecture. We concluded that the administration of Selenium and Zinc can prevent the hazardous effects of potassium dichromate on the hormonal and histological status of the thyroid gland in preimplanted Wistar albino rats.
六价铬是一种环境污染物,被认为是一种干扰内分泌的金属。硒和锌是必需的微量元素,已知在甲状腺稳态中起着至关重要的作用。当前工作的目的是研究重铬酸钾(K₂Cr₂O7)在预植入大鼠妊娠第3天通过分级剂量(10、50、100mg/kg,皮下注射)或K₂Cr₂O7(10 mg/kg,皮下注射)与硒(0.3 mg/kg,皮下滴注)和氯化锌(20 mg/kg,皮下灌注)的联合作用。评估甲状腺的激素谱、细胞凋亡诱导和组织学变化。我们的主要发现表明₂Cr₂O7促进甲状腺功能减退,血浆T3和T4水平显著降低(P<0.001),而血浆TSH水平显著升高(P<001),此外,甲状腺肥大(P<0.01)。此外,K2Cr2O7(10mg/kg,s.c)通过胱天蛋白酶3途径诱导细胞凋亡(P<0.001),并改变腺体组织结构。Se或ZnCl的共处理₂ 改善了激素状态,部分恢复了甲状腺组织结构。我们得出的结论是,硒和锌的给药可以防止重铬酸钾对植入前Wistar白化大鼠甲状腺激素和组织学状态的有害影响。
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引用次数: 0
An Updated Review on Taxonomy and Chemotaxonomy 分类学和化学分类学的最新进展
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/32123
Sunayana Mali, R. Yadav, V. Gauttam, Jyotiram A. Sawale
Taxonomy is a discipline of study that deals with the identification, naming, and categorization of plants. The word taxonomy is derived from the Greek words taxis, which means arrangement, and nomos, which means law. The Convention on Biological Diversity's administration and implementation is supported by the taxonomy's identification and enumeration of its constituent parts. Chemotaxonomy, also known as chemosystematics, is the endeavour to categorise and identify organisms (initially plants) based on biochemical compositional differences and similarities. About 10-25% species of the total over 400,000 species present on the planet Earth are used for human welfare. Plants and their habitats are destroyed for human benefit, and thus, valuable diversity is lost without understanding the utility. The classification and identification of organisms based on verifiable differences and similarities in their biochemical compositions are known as chemotaxonomy, sometimes known as chemosystematics. There are several methods for taxonomizing organisms. Chemotaxonomy-based plant selection is a prerequisite for successful natural product research. The rise of chemotaxonomy is mainly due to the advancement in analytical techniques for chemical analysis that can detect even trace amounts of chemical compounds. The current methodology, particularly for plants, is chemotaxonomy. In a nutshell, the biochemical makeup of plants and animals is used to classify them biologically based on similarities and differences. In this brief overview, problems associated with biodiversity and the use of modern tools to resolve these issues are discussed. In this review, the various plant drugs are discussed related to their various morphology, phytogeography, chemotaxonomy and taxonomy.
分类学是一门研究植物识别、命名和分类的学科。单词分类学来源于希腊语单词taxis,意思是排列,nomos,意思是法律。《生物多样性公约》的管理和实施得到了分类学对其组成部分的识别和列举的支持。化学分类学,也称为化学系统学,是根据生物化学成分的差异和相似性对生物体(最初是植物)进行分类和鉴定的努力。地球上40多万种物种中,约有10-25%的物种用于人类福利。为了人类的利益,植物及其栖息地被破坏,因此,在不了解其效用的情况下,宝贵的多样性被丧失。基于生物化学组成的可验证差异和相似性对生物体进行分类和鉴定,称为化学分类学,有时称为化学系统学。对生物进行分类有几种方法。基于化学分类学的植物选择是成功进行天然产物研究的先决条件。化学分类学的兴起主要是由于用于化学分析的分析技术的进步,该技术甚至可以检测微量化合物。目前的方法,特别是对植物来说,是化学分类学。简而言之,植物和动物的生物化学组成被用来根据相似性和差异对它们进行生物学分类。在这篇简短的综述中,讨论了与生物多样性相关的问题以及使用现代工具来解决这些问题。本文就各种植物药物的形态、植物地理学、化学分类学和分类学等方面进行了综述。
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引用次数: 0
Cassia tora Mitigates Aluminium Chloride Induced Alterations in Pro-inflammatory Cytokines, Neurotransmitters, and Beta-amyloid and Tau Protein Markers in Wistar Rats 决明子减轻氯化铝诱导的Wistar大鼠促炎细胞因子、神经递质、β -淀粉样蛋白和Tau蛋白标记物的改变
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-03-20 DOI: 10.18311/ti/2023/v30i1/30863
V. Bhargava, A. Netam, Rambir Singh, Poonam Sharma
Background and Aim: Exposure to Aluminium (Al) has been reported to cause neurotoxicity in laboratory animals. Amyloid-β (Aβ) plaque formation, tau protein hyperphosphorylation, and neuroinflammation have been indicated as the possible mechanism of Al-induced neurodegeneration. The present study aimed to understand the mechanism of aluminium chloride (AlCl3)-induced neurotoxicity in Wistar rats and to assess the neuroprotective effect of methanolic extract of Cassia tora leaves (MECT). Material and Methods: Seventy-two male Wistar rats were randomly divided into nine groups. AlCl3 (100 mg/kg bw) and MECT (300 mg/kg bw) were given orally by gavage and memantine (MEM) was administered intraperitoneally (20 mg/kg bw) to rats, daily for 60 days. The spatial learning memory and recognition memory were evaluated using the Morris Water Maze (MWM) test. The levels of oxidative stress, neurotransmitter markers, pro-inflammatory markers, Aβ proteins plaques formation and tau protein hyperphosphorylation were evaluated. Histopathology of brain tissue was performed to assess the extent of tissue damage on AlCl3 exposure. Results: MECT significantly improved cognitive behaviours in AlCl3-exposed rats during the MWM test. Treatment with MECT resulted in a significant recovery of antioxidant enzyme function, the activity of neurotransmitter markers and pro-inflammatory cytokine levels. MECT prevented the aggregation of Aβ proteins and tau protein phosphorylation. Also, it inhibited the loss of neuronal integrity in the cortex and hippocampus regions of the brain in AlCl3-exposed rats. Conclusion: The findings demonstrate that a methanolic extract of Cassia tora leaves ameliorated AlCl3-induced neurodegeneration in Wistar rats.
背景和目的:有报道称,在实验动物中暴露于铝(Al)会引起神经毒性。淀粉样蛋白-β (Aβ)斑块形成、tau蛋白过度磷酸化和神经炎症已被认为是铝诱导的神经变性的可能机制。本研究旨在了解氯化铝(AlCl3)诱导Wistar大鼠神经毒性的机制,并评价决明子叶甲醇提取物(MECT)的神经保护作用。材料与方法:雄性Wistar大鼠72只,随机分为9组。大鼠灌胃给予AlCl3 (100 mg/kg bw)和MECT (300 mg/kg bw),腹腔注射美金刚(MEM) (20 mg/kg bw),连续60 d。采用Morris水迷宫(MWM)测验评价空间学习记忆和识别记忆。评估氧化应激、神经递质标志物、促炎标志物、Aβ蛋白斑块形成和tau蛋白过度磷酸化水平。通过脑组织组织病理学来评估AlCl3暴露对脑组织的损伤程度。结果:MECT在MWM试验中显著改善了alcl3暴露大鼠的认知行为。MECT治疗可显著恢复抗氧化酶功能、神经递质标志物活性和促炎细胞因子水平。MECT阻止了Aβ蛋白的聚集和tau蛋白的磷酸化。此外,它还能抑制暴露于alcl3的大鼠大脑皮层和海马区神经元完整性的丧失。结论:决明子叶甲醇提取物对alcl3诱导的Wistar大鼠神经变性有改善作用。
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引用次数: 0
Impact of DEHP Toxicity on Testis of Rat Leading to Disruption of Testis Histology DEHP毒性对大鼠睾丸组织破坏的影响
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-02-07 DOI: 10.18311/ti/2022/v29i4/30294
K. Gouri, P. Sinha
Di (2-ethyl hexyl) Phthalate (DEHP) is one of the plasticizers widely used in the manufacturing of plastics to make it flexible and durable. Present study is focussed to observe the deleterious effects of DEHP on male reproductive system of animals. For this, 1000 mg/kg body wt. of DEHP was administered to different groups of male Wistar rat for 2, 4, 6 and 8 weeks. After each interval, rats were sacrificed and histological alterations in testis of rats were observed. On hormonal assay, testosterone level decreased significantly in DEHP exposed groups. The histological structure of the testis was also observed to be disrupted significantly with increasing duration of DEHP exposure. Organisation of seminiferous tubule was found distorted and disoriented showing large gaps between them along with degenerated epithelium. Evident changes in morphology of spermatozoa were seen with gradual loss of head and tail structure. Decrease in the number of Leydig cells and sertoli cells were also found suggesting DEHP as a potent toxicant for male reproductive system.
邻苯二甲酸二(2-乙基己基)酯(DEHP)是塑料制造中广泛使用的增塑剂之一,可使塑料具有柔韧性和耐用性。本研究旨在观察DEHP对动物雄性生殖系统的有害影响。为此,在不同组雄性Wistar大鼠中分别给予1000 mg/kg体重的DEHP,为期2、4、6和8周。每隔一段时间处死大鼠,观察大鼠睾丸组织学变化。激素测定显示,DEHP暴露组睾酮水平明显下降。随着DEHP暴露时间的增加,睾丸的组织学结构也被观察到明显破坏。精小管组织扭曲,方向混乱,其间间隙大,上皮变性。精子形态变化明显,头尾结构逐渐丧失。间质细胞和支持细胞数量减少,表明DEHP是男性生殖系统的一种强毒性物质。
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引用次数: 0
Pharmaceutical Drugs in Aquatic Environment and their Toxic Effect on Pangasius sp. : An Overview 水生环境中的药物及其对Pangasius sp.的毒性作用综述
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-02-07 DOI: 10.18311/ti/2022/v29i4/30376
B. Vijaya Geetha, K. Shreenidhi, Varshini Anand, H. Savithakshini, S. Subashini
One of the fastest-growing freshwater fish varieties is the Pangasius sp., which has a great capability for production and export growth. When Pangasius sp. is exposed to substances such as diclofenac, phenol, quinolones, sulfonamides, and tetracycline, even at low environmental exposure levels the fish tissue can develop chronic risk, genetic abnormalities, and histopathological changes. They come into contact with these antibiotics mostly through the discharge of pharmaceutical industry effluents, which contain antibiotic residues that are not been completely eliminated by wastewater treatment, thereby posing environmental concerns when released into aquatic ecosystems. The main objective of this review paper is to study the effect of the concentration of pharmaceutical drugs, farming techniques, and various substitutes for antibiotics that can be utilized to enhance the growth performance of Pangasius sp. Few studies conducted on toxicity demonstrated that increased mucus production in the gills and intestines, histological abnormalities in the liver and skin, and impaired immunoglobulin production have all been linked to sublethal phenol concentrations in fish. The consumption of these contaminated Pangasius sp. can raise various human health concerns. Therefore, exposure of Pangasius sp. to the detrimental pharmaceutical drug from industrial effluent must be held serious concern. Further research is required to conserve human health and the ecosystem.
生长最快的淡水鱼品种之一是Pangasius sp.,它具有强大的生产和出口增长能力。当Pangasius sp.暴露于双氯芬酸、苯酚、喹诺酮类、磺酰胺类和四环素等物质时,即使在低环境暴露水平下,鱼类组织也会出现慢性风险、遗传异常和组织病理学变化。它们主要通过排放制药工业废水接触这些抗生素,这些废水中含有未经废水处理完全消除的抗生素残留物,因此在释放到水生生态系统中时会引起环境问题。这篇综述论文的主要目的是研究药物浓度、养殖技术和各种抗生素替代品对提高Pangasius sp.生长性能的影响。很少有关于毒性的研究表明,鳃和肠的粘液分泌增加,肝脏和皮肤的组织学异常,以及免疫球蛋白产生受损都与鱼类体内亚致死性苯酚浓度有关。食用这些受污染的Pangasius sp.会引起各种人类健康问题。因此,必须严重关注Pangasius sp.暴露于工业废水中的有害药物。需要进一步的研究来保护人类健康和生态系统。
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引用次数: 0
Safety and Anti-Fatigue Activity of Ayurvedic Formulation Sramahara Mahaakaasaya - A Pre-Clinical Study 阿育吠陀配方Sramahara Mahaakaasaya的安全性和抗疲劳活性-临床前研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2023-02-07 DOI: 10.18311/ti/2022/v29i4/30296
Bidhan Mahajon, A. Ramamurthy, Rupashri Nath, M. Gautam, Neeladrisingha Das, P. Roy
An experimental evaluation of anti-fatigue activity of Shramahara Mahaakashaaya (SM) and its applicability in sports medicine has been systematically evaluated. Aqueous, ethanolic and petroleum ether extracts of SM granules (200mg/kg) were studies for light-dark model test for assessment anti-anxiety effect, rota-rod test for assessment of the effect on muscle tone and muscle balance, weight loaded forced swimming test for assessment of anti-fatigue activity. The acute toxicity study of SM granules has also been evaluated as per the OECD 423. SM granules showed significant anti-fatigue activity in different experimental models and found safe up to 2000mg/kg body weight dose. The results provide an important basis for considering Shramahara Mahaakashaaya (SM) as an alternative medicine having anti-fatigue effects which can be further included in the sports medicine.
本文系统评价了Shramahara Mahaakashaaya (SM)抗疲劳活性的实验评价及其在运动医学中的适用性。研究SM颗粒水、醇、石油醚提取物(200mg/kg)抗焦虑作用的光暗模型试验、肌张力和肌肉平衡作用的旋转杆试验、抗疲劳活性的负重强迫游泳试验。SM颗粒的急性毒性研究也根据OECD 423进行了评估。SM颗粒在不同的实验模型中显示出明显的抗疲劳活性,且在2000mg/kg体重剂量下是安全的。本研究结果为将沙摩原Mahaakashaaya (SM)作为一种具有抗疲劳作用的替代药物,进一步纳入运动医学提供了重要依据。
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引用次数: 0
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Toxicology International
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