Departamento de Bioquímica, Centro de Biociências, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil.
Instituto de Química, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Toxicon. 2024 Nov 28;251:108147. doi: 10.1016/j.toxicon.2024.108147. Epub 2024 Oct 19.
Essential oils obtained from Croton pulegiodorus leaf are renowned for their biological activities; however, data on their toxicity are limited. Therefore, this study aimed to evaluate the acute oral toxicity and genotoxicity of a C. pulegiodorus leaf essential oil (CPLEO). Chemical characterization of CPLEO was conducted by gas chromatography coupled to mass spectrometry (GC-MS). In vitro assay was performed to verify the hemolytic capacity of the oil in mice erythrocytes. Next, an acute oral toxicity study was conducted on female mice at CPLEO doses of 2000, 1000, 500, 250, 100, and 50 mg/kg. Hematological, biochemical, and histopathological markers were assessed in mice from groups were no death occurred. Relative consumption of water and food and the weight of animals and their organs were also recorded. Finally, a genotoxicity analysis was performed using the micronucleus and comet assays. The extraction yield of CPLEO was 1.149% and its major compounds were ascaridole (23.18%), eucalyptol (17.20%), camphor (14.20%), p-cymene (7.91%), α-terpineol (4.69%), and isobornyl acetate (4.57%). CPLEO showed a hemolytic effect only at high concentrations (185.5-1000 mg/mL). It showed acute oral toxicity in mice with a LD of 460.42 mg/kg. CPLEO (50-250 mg/kg) caused some significant changes in hematological and biochemical parameters. Histopathological evaluation indicated alterations in liver and kidneys but transaminases, urea and creatinine levels remained like the negative control. CPLEO administration impaired weight gain and reduced water and food consumption. Finally, it was not genotoxic by both comet and micronucleus tests. The results highlight the need for attention when choosing doses to evaluate the bioactivities of CPLEO.
从巴豆叶中提取的精油以其生物活性而闻名;然而,关于其毒性的数据有限。因此,本研究旨在评估巴豆叶精油(CPLEO)的急性口服毒性和遗传毒性。通过气相色谱-质谱联用(GC-MS)对 CPLEO 进行化学特征分析。在体外试验中,验证了该油在小鼠红细胞中的溶血能力。接下来,对 2000、1000、500、250、100 和 50mg/kg 剂量的 CPLEO 对雌性小鼠进行急性口服毒性研究。在未发生死亡的组中评估了小鼠的血液学、生化和组织病理学标志物。还记录了相对水和食物消耗以及动物及其器官的重量。最后,通过微核和彗星试验进行了遗传毒性分析。CPLEO 的提取产率为 1.149%,其主要化合物为ascaridole(23.18%)、桉油醇(17.20%)、樟脑(14.20%)、对伞花烃(7.91%)、α-松油醇(4.69%)和异丁酸冰片酯(4.57%)。CPLEO 仅在高浓度(185.5-1000mg/mL)下显示溶血作用。它在小鼠中表现出急性口服毒性,LD 为 460.42mg/kg。CPLEO(50-250mg/kg)导致一些血液学和生化参数的显著变化。组织病理学评估表明肝脏和肾脏发生了变化,但转氨酶、尿素和肌酐水平与阴性对照相似。CPLEO 给药会影响体重增加,并减少水和食物的消耗。最后,彗星和微核试验均未显示其遗传毒性。这些结果强调在选择剂量评估 CPLEO 的生物活性时需要注意。