AI Article Synopsis

  • The study evaluated the acute oral toxicity and genotoxicity of essential oil from Croton pulegiodorus leaves (CPLEO), which is known for its biological properties but lacks comprehensive toxicity data.
  • After characterizing CPLEO chemically using GC-MS, the research involved administering varying doses to female mice and monitoring effects on their health, including changes in weight, food and water consumption, and organ conditions.
  • Results revealed an LD of 460.42 mg/kg for acute toxicity, signs of toxicity at certain doses, but no genotoxic effects were found using comet and micronucleus assays, indicating careful dosage is crucial for further testing of CPLEO's benefits.

Article Abstract

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.

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http://dx.doi.org/10.1016/j.toxicon.2024.108147DOI Listing

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