Evaluation of Acute and Subacute Toxicity and LC-MS/MS Compositional Alkaloid Determination of the Hydroethanolic Extract of Dysphania ambrosioides (L.) Mosyakin and Clemants Flowers

• Published in: Toxins Vol. 14; no. 7; p. 475
• Main Authors: Kandsi, Fahd, Lafdil, Fatima Zahra, Elbouzidi, Amine, Bouknana, Saliha, Miry, Achraf, Addi, Mohamed, Conte, Raffaele, Hano, Christophe, Gseyra, Nadia
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 12.07.2022; MDPI
• Subjects: Acute toxicity; Alkaloids; Alzheimer's disease; Aspartate aminotransferase; Body weight; Cultural heritage; Drug dosages; Dysphania ambrosioides; Enzymes; Evaluation; Flowers; Food consumption; Food intake; Glycoproteins; Hepatocytes; Herbal medicine; Inflammation; Investigations; Kidneys; LC-MS/MS; Liver; Medicinal plants; Metabolism; Metabolites; Mexican tea; Nervous system; Organ weight; Parameter identification; Permeability; Pharmacokinetics; Phytochemicals; Subacute toxicity; Toxicity; Urea; Water consumption
• ISSN: 2072-6651; 2072-6651
• DOI: 10.3390/toxins14070475

Dysphania ambrosioides (L.) Mosyakin and Clemants is a medicinal plant that has traditionally been used to cure a range of diseases. There has been no thorough investigation of the potential toxicity of this plant. The objective of this study is to assess the acute and subacute toxicity of D. ambrosioides hydroethanolic extract (DAHE), as well as it alkaloids composition, utilizing LC-MS/MS analysis. An in silico approach was applied to determine pharmacokinetic parameters and to predict the toxicity of D. ambrosioides identified alkaloids. A 14-day treatment with a single oral dose of 1–7 g/kg was carried out to investigate acute toxicity. DAHE was given orally at dosages of 5, 50, and 500 mg/kg for 15 days in the subacute toxicity investigation, and body weight and biochemical parameters were evaluated. Livers, kidneys, lungs, and heart were examined histologically. Chromatographic investigation revealed the existence of nine alkaloids, with N-formylnorgalanthamine being the most prevalent. The oral LD50 value of DAHE was found to be 5000 mg/kg in an acute toxicity study. No variations were observed with respect to food intake, water consumption, mortality, or body and organ weight in the subacute toxicity study. On the other hand, DAHE (500 mg/kg) significantly enhanced alanineaminotransferase, aspartate aminotransferase, and urea. Liver and kidney histological examinations revealed modest infiltration of hepatocyte trabeculae by inflammatory cells in the liver and slight alteration in the kidney histoarchitecture. According to our findings, DAHE exhibits low to moderate toxicity.