Evaluation of acute oral toxicity of lemon grass oil and citral in albino rats

Adheena Xavier, S. Padma Rani, R. Shankar, A. Nisha, S. Sujith, R. Uma
{"title":"Evaluation of acute oral toxicity of lemon grass oil and citral in albino rats","authors":"Adheena Xavier, S. Padma Rani, R. Shankar, A. Nisha, S. Sujith, R. Uma","doi":"10.31254/phyto.2022.11410","DOIUrl":null,"url":null,"abstract":"Essential oils, which are the plant derived secondary metabolites have been reported for various traditional medicinal applications. Amongst them, lemongrass oil (LGO) derived from Cymbopogon spp. as well as its major constituent citral possess a myriad of therapeutic potentials. The present study has been undertaken to study the adverse effects of LGO and citral on acute oral exposure to Sprague Dawley rats to establish the preliminary safety of these compounds prior to their efficacy evaluation against fatty liver disease. The toxicity study was conducted as per OECD guidelines No. 420. The LGO and citral were solubilized in 1% tween 80 and administered orally in a sequential manner in one animal at 2000 mg/kg (sighting study) followed by four animals (main study). The animals were then monitored for any clinical abnormalities or mortality and body weight gain during the observational period of 14- days, after which the animals were sacrificed and examined for abnormal lesions. LGO was further subjected to gas chromatography-mass spectrometry (GC-MS) analysis to characterize its chemical constituents, which revealed alpha and beta citral as the two major constituents. The rats treated with LGO and citral survived throughout the study period and didn’t exhibit any clinical abnormalities. Moreover, body weight gain was comparable to the vehicle treated rats and necropsy revealed no pathological alterations. Thus, the present study indicated LGO and citral as safe compounds with an LD50 greater than 2000 mg/kg and could be labelled as category 5/unclassified in hazard category of Globally harmonized system for classification of chemicals.","PeriodicalId":22851,"journal":{"name":"The Journal of Phytopharmacology","volume":"37 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Phytopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31254/phyto.2022.11410","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Essential oils, which are the plant derived secondary metabolites have been reported for various traditional medicinal applications. Amongst them, lemongrass oil (LGO) derived from Cymbopogon spp. as well as its major constituent citral possess a myriad of therapeutic potentials. The present study has been undertaken to study the adverse effects of LGO and citral on acute oral exposure to Sprague Dawley rats to establish the preliminary safety of these compounds prior to their efficacy evaluation against fatty liver disease. The toxicity study was conducted as per OECD guidelines No. 420. The LGO and citral were solubilized in 1% tween 80 and administered orally in a sequential manner in one animal at 2000 mg/kg (sighting study) followed by four animals (main study). The animals were then monitored for any clinical abnormalities or mortality and body weight gain during the observational period of 14- days, after which the animals were sacrificed and examined for abnormal lesions. LGO was further subjected to gas chromatography-mass spectrometry (GC-MS) analysis to characterize its chemical constituents, which revealed alpha and beta citral as the two major constituents. The rats treated with LGO and citral survived throughout the study period and didn’t exhibit any clinical abnormalities. Moreover, body weight gain was comparable to the vehicle treated rats and necropsy revealed no pathological alterations. Thus, the present study indicated LGO and citral as safe compounds with an LD50 greater than 2000 mg/kg and could be labelled as category 5/unclassified in hazard category of Globally harmonized system for classification of chemicals.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
柠檬草油和柠檬醛对白化大鼠急性口服毒性的评价
精油是植物衍生的次生代谢产物,已被报道用于各种传统医学应用。其中,从香茅属植物中提取的柠檬草精油(LGO)及其主要成分柠檬醛具有无数的治疗潜力。本研究旨在研究LGO和柠檬醛对Sprague Dawley大鼠急性口服暴露的不良影响,在评估其对脂肪肝疾病的疗效之前,确定这些化合物的初步安全性。毒性研究是按照经合组织第420号准则进行的。将LGO和柠檬醛在80年之间以1%的浓度溶解,并在一只动物中按2000 mg/kg顺序口服(观察研究),然后在四只动物中依次口服(主要研究)。然后在14天的观察期内监测动物的任何临床异常或死亡率和体重增加,之后处死动物并检查异常病变。进一步采用气相色谱-质谱联用(GC-MS)对其化学成分进行表征,发现α和β柠檬醛是其主要成分。用LGO和柠檬醛治疗的大鼠在整个研究期间都存活下来,没有出现任何临床异常。此外,体重增加与给药大鼠相当,尸检未发现病理改变。因此,本研究表明,LGO和柠檬醛是安全的化合物,其LD50大于2000 mg/kg,可以在全球化学品统一分类系统中标记为第5类/未分类的危险类别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Comparison and Efficacy Study of In-house Developed Formulation of Fumaria indica (Pitpapra) Against Expensive Market Alternative Dracaena trifasciata (Prain) Mabb. – Traditional use, pharmacognosy, phytochemistry and pharmacology: A comprehensive review Anti-inflammatory Effects of Carissa spiranum Mediated via Attenuation of Leucocyte Migration Aqueous extract of Alstonia boonei De Wild (Apocynaceae) alleviates bone metabolism disorders induced by oxidised palm oil and sucrose supplementation in rats Evaluation of Immunomodulatory Activities of Clove Powder in Broiler
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1