نمایش مختصر رکورد

dc.contributor.authorYaghoubi, Maedehen_US
dc.contributor.authorMousavi*, Zahraen_US
dc.contributor.authorRastegar, Tayebehen_US
dc.contributor.authorAmin, Gholamrezaen_US
dc.date.accessioned1399-07-08T22:08:39Zfa_IR
dc.date.accessioned2020-09-29T22:08:39Z
dc.date.available1399-07-08T22:08:39Zfa_IR
dc.date.available2020-09-29T22:08:39Z
dc.date.issued2019-04-01en_US
dc.date.issued1398-01-12fa_IR
dc.date.submitted2018-05-26en_US
dc.date.submitted1397-03-05fa_IR
dc.identifier.citationYaghoubi, Maedeh, Mousavi*, Zahra, Rastegar, Tayebeh, Amin, Gholamreza. (2019). Safety Assessment of Arctium lappa L. Fruit Extract in Female Wistar Rats: Acute and Repeated Oral Toxicity Studies. Research Journal of Pharmacognosy, 6(2), 39-48. doi: 10.22127/rjp.2019.84317en_US
dc.identifier.issn2345-4458
dc.identifier.issn2345-5977
dc.identifier.urihttps://dx.doi.org/10.22127/rjp.2019.84317
dc.identifier.urihttp://www.rjpharmacognosy.ir/article_84317.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/126004
dc.description.abstract<strong>Background and objectives: </strong><em>Arctium lappa</em> belonging to the Compositae (Asteraceae) family has been used as a medicinal and nutritional supplement in the world. The fruits, leaves and roots of the plant are well-known for their pharmaceutical effects. Toxicity of the fruit's extract in female rats was investigated in the present study. <strong>Methods: </strong>To assess the toxicity profile of <em>Arctium lappa</em> fruit extract (ALFE), it was administered to rats by gavage in acute and repeated models. The animals were divided into two groups: control and test groups<strong>.</strong> In the acute toxicity model, 1000 and 5000 mg/kg ALFE were administered to the animals. Toxic symptoms, body weight, death and abnormal behaviors were observed for 14 days. In the repeated toxicity model, ALFE (300 mg/kg) was daily administered for 4 weeks. Biochemical and histopathological changes were assessed and compared with the control group. Statistical significance was determined by one-way analyses of variance, followed by the Tukey test using GraphPad Prism 6. <strong>Results: </strong>No mortality was noticed in the acute test; therefore, the oral LD<sub>50</sub> value determined in the female rats was greater than 5000 mg/kg. In the repeated test, the animals received ALFE (300 mg/kg) and no mortality was observed. The hematology and serum chemistry parameters showed no statistically significant changes.  The histopathological studies revealed evidences of microscopic lesions in two main organs lungs and small intestine. <strong>Conclusion: </strong>The results indicated that the oral acute toxicity of ALFE in the rats was of a low order with LD<sub>50</sub> being more than 5000 mg/kg. Moreover, they revealed slight tissue damage to several organs when sub-chronically administered at a dose of 300 mg/kg.<br /> <strong> </strong>en_US
dc.format.extent1302
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisher- The Iranian Society of Pharmacognosy - Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofResearch Journal of Pharmacognosyen_US
dc.relation.isversionofhttps://dx.doi.org/10.22127/rjp.2019.84317
dc.subjectAcuteen_US
dc.subjectArctium lappa Len_US
dc.subjectsubchronicen_US
dc.subjecttoxicity testen_US
dc.subjectWistar ratsen_US
dc.subjectToxicityen_US
dc.titleSafety Assessment of Arctium lappa L. Fruit Extract in Female Wistar Rats: Acute and Repeated Oral Toxicity Studiesen_US
dc.typeTexten_US
dc.typeOriginal paperen_US
dc.contributor.departmentDepartment of Pharmacology & Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Pharmacology & Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Pharmacognosy, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran. Department of Pharmacognosy, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.en_US
dc.citation.volume6
dc.citation.issue2
dc.citation.spage39
dc.citation.epage48
nlai.contributor.orcid0000-0002-8197-9075


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