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Toxicogenetic profile of the monoterpene alpha-terpineol on normal and tumor eukaryotic cells.

Authors :
Negreiros HA
Fontele SBC
Batista FA
Farias MG
Silva FCCD
Nascimento MLLBD
Moura KG
Correa LS
Pereira ARS
Lopes LO
Ferreira PMP
Mendes AN
Gonçalves JCR
Melo-Cavalcante AAC
Sousa JMCE
Source :
Drug and chemical toxicology [Drug Chem Toxicol] 2024 Jul; Vol. 47 (4), pp. 427-435. Date of Electronic Publication: 2023 Mar 13.
Publication Year :
2024

Abstract

Alpha-terpineol is a monoterpene alcohol found in essential oils from medicinal plants with some well-known pharmacological activities and widely used in cosmetics. However, the toxicological effects and additional pharmacological activities need to be clarified. Thus, the study evaluated the toxic, cytotoxic, genotoxic, hemolytic, and oxidative potential of alpha-terpineol in non-clinical bioassays. Different concentrations of alpha-terpineol were used in bioassays, including MTT (50, 100, 200, and 400 μg/mL), Artemia salina (6.25-400 μg/mL), Allium cepa (10, 50, and 100 μg/mL), comet assay (100, 200, and 500 μg/mL), cytokinesis-block micronucleus (100, 250, and 500 μg/mL), confocal microscopy for apoptosis quantification (100 and 500 μg/mL), hemolysis and Saccharomyces cerevisiae central disk test (10, 35, and 75 μg/mL). For the MTT test, alpha-terpineol was more cytotoxic on melanoma murine B16-F10 cells rather than macrophages. For A. salina test, alpha-terpineol showed LC <subscript>50</subscript> of 68.29 and 76.36 μg/mL for 24 h and 48 h of exposure time, respectively. Meanwhile, alpha-terpineol was also cytotoxic to meristematic cells, which revealed inhibition of cellular division and mutagenic action by formation of bridges and delayed anaphases. The compound increased damage index and frequency of damage corroborated by the presence of micronuclei, bridges and nuclear buds at 500 μg/mL, but it caused neither hemolysis, oxidative damage on the S. cerevisiae nor cell death in normal fibroblasts. The findings indicate alpha-terpineol has cytotoxic potential by cytogenetic and molecular mechanisms associated with apoptosis and probable target effects against melanoma cells.

Details

Language :
English
ISSN :
1525-6014
Volume :
47
Issue :
4
Database :
MEDLINE
Journal :
Drug and chemical toxicology
Publication Type :
Academic Journal
Accession number :
36912194
Full Text :
https://doi.org/10.1080/01480545.2023.2188440