Department of Clinical Analyses, Toxicology and Food Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Avenida Do Café S/nº, Ribeirão Preto, São Paulo, 14040-903, Brazil; Department of Biology, School of Life Sciences, Federal University of Technology, P.M.B. 704, Akure, Ondo State, Nigeria; Department of Zoology and Environmental Biology, Faculty of Sciences, Ekiti State University, Ado-Ekiti, Ekiti State, Nigeria.
Department of Clinical Analyses, Toxicology and Food Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Avenida Do Café S/nº, Ribeirão Preto, São Paulo, 14040-903, Brazil.
Food Chem Toxicol. 2022 Jul;165:113189. doi: 10.1016/j.fct.2022.113189. Epub 2022 May 28.
The toxicity of D. tripetala fruit extract to mice was investigated using data obtained from lipidomic analyses, comet and Acetylcholinesterase (AChE) assays. Mice (n = 8) were exposed for 30 days via oral gavage to vehicle (5% Tween 80) (negative control), D. tripetala extract (100, 200 and 400 mg/kg) and 40 mg/kg methyl methanesulfonate (MMS) (positive control). The profile of compounds in the fruit extract was analyzed using gas chromatography-mass spectrometry. Out of the total of 32 compounds identified, considerable amount of established insecticidal compounds such as 2-phenylnitroethane, cis-vaccenic acid, linalool and linoleic acid were detected. Fruit extract did not induce DNA damage relative to negative control. Percentage gain in body weights differed significantly across the four weeks. Significantly highest and lowest brain AChE activity was observed in animals exposed to 200 and 400 mg/kg D. tripetala, respectively. Fruit extract modulated the brain phospholipid profile due to significant fold changes of 48 lipid species out of the total of 280 lipid species. High number of differentially expressed phosphatidylcholine (PC) species and significant levels of phosphatidylethanolamine (PE) at 400 mg/kg suggests that activation of inflammation and methylation pathways are the most plausible mechanisms of D. tripetala toxicity to mouse brain tissue.
采用脂质组学分析、彗星和乙酰胆碱酯酶 (AChE) 测定的结果,研究了三齿棱果提取物对小鼠的毒性。将 8 只小鼠(n=8)通过口服灌胃暴露于 30 天,给予载体(5%吐温 80)(阴性对照)、三齿棱果提取物(100、200 和 400mg/kg)和 40mg/kg 甲磺酸甲酯(MMS)(阳性对照)。使用气相色谱-质谱法分析了水果提取物中化合物的图谱。在所鉴定的 32 种化合物中,检测到相当数量的已确定的杀虫化合物,如 2-苯硝基乙烷、顺式-维库酸、芳樟醇和亚油酸。与阴性对照相比,果实提取物未诱导 DNA 损伤。在四周内,体重增加百分比存在显著差异。在暴露于 200 和 400mg/kg 三齿棱果的动物中,观察到脑 AChE 活性显著最高和最低。由于总共有 280 种脂质中 48 种脂质发生了显著的倍数变化,因此果实提取物调节了脑磷脂谱。高水平的差异表达的磷脂酰胆碱(PC)种类和 400mg/kg 时显著的磷脂酰乙醇胺(PE)水平表明,炎症和甲基化途径的激活是三齿棱果对小鼠脑组织毒性的最可能机制。