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Acute toxicity studies of extracts from Lavandula angustifolia mill

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dc.contributor.author Jian, Mariana
dc.contributor.author Nacu, Viorel
dc.contributor.author Cotelea, Tamara
dc.contributor.author Organ, Adina
dc.contributor.author Cojocaru-Toma, Maria
dc.contributor.author Kulcițki, Veaceslav
dc.date.accessioned 2023-05-10T09:03:37Z
dc.date.available 2023-05-10T09:03:37Z
dc.date.issued 2023
dc.identifier.citation JIAN, Mariana, NACU, Viorel, COTELEA, Tamara, et al. Acute toxicity studies of extracts from Lavandula angustifolia mill. In: Cells and Tissues Transplantation. Actualities and Perspectives: the materials of the national scientific conf. with internat. participation, Chișinău: CEP Medicina. 2023, p. 54. ISBN 978-9975-82-313-5. en_US
dc.identifier.isbn 978-9975-82-313-5
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/24237
dc.description.abstract Introduction. Fine lavender (Lavandula angustifolia Mill., LA) is a valuable plant, broadly cultivated for essencial oil production. LA extracts display a broad spectrum of pharmacological activities, including antioxidant, sedative, anti-inflammatory and antimicrobial properties. The use of LA extracts as food additives requires a thorough investigation of their toxicity profile. We report in the current comunication preclinical acute toxicity studies of a LA ethanolic extract. Material și methods. Wistar rats (n=42) of both sexes, with a body weight of 200 - 400 g, aged approximately 3 months, were used for the acute toxicity study. Acute toxicity was modeled by intragastric administration of LA extract solution by gavage to outbred rats. The LA extract was administered in doses of: control group, group I - 500 mg/kg; II - 1000 mg/kg; III - 1500 mg/kg; IV - 3000 mg/kg; V - 4000mg/kg; VI – 5000 mg/kg. After 14 days, the animals were euthanized and blood was collected with the study of biochemical indices (total protein, albumin, urea, creatinine, AST, ALT). Results. Acute toxicity studies demonstrated that after internal administration of LA extract to rats in doses of 500 mg/kg, 1000 mg/kg; 1500 mg/kg, 3000 mg/kg, 4000 mg/kg, 5000 mg/kg no death of animals. LA extract was established as a relatively harmless biologically active substance (LD50 being >5000 mg/kg). the harmlessness of the LA extract was confirmed by the study of the peripheral blood picture in the animals of the group treated with the LA extract with the administrable dose of 500 mg/kg and 5000 mg/kg in which the level of biochemical indices did not change. Conclusion. LA extracts in doses of 500 mg/kg - 5000 mg/kg do not produce changes in biochemical parameters and can be considered harmless. Acknowledgements: This work has been funded by ANCD, project “New products with preventive and therapeutic potential basing on natural products of vegetal origin and modern methods of organic synthesis”, code 20.80009.8007.03. en_US
dc.language.iso en en_US
dc.publisher CEP Medicina en_US
dc.relation.ispartof „Cells and tissues transplantation. Actualities and perspectives” dedicated to the 10th anniversary of the founding of the Human Tissue and Cells Bank and to the 15th anniversary of the founding of the Laboratory of Tissue Engineering and Cells Culture of Nicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldova, March 17-18th 2023, Chisinau, Republic of Moldova en_US
dc.title Acute toxicity studies of extracts from Lavandula angustifolia mill en_US
dc.type Other en_US


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