Study on the Cytotoxic, Genotoxic and Clastogenic Potential of Attalea phalerata Mart. ex Spreng. Oil Pulp In Vitro and In Vivo Experimental Models

Attalea phalerata Mart. ex Spreng. (Arecaceae), popularly known as "bacuri", is used in Brazilian folk medicine. Its oil is used orally to relieve pulmonary congestion and joint pain. In topical applications, it is applied as an effective hair tonic and anti-dandruff. The in natura pulp an...

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Published inPloS one Vol. 11; no. 10; p. e0165258
Main Authors Freitas de Lima, Fernando, Lima Tolouei Menegati, Sara Emilia, Karenina Traesel, Giseli, Souza de Araújo, Flávio Henrique, Honaiser Lescano, Caroline, Moraes Peixoto, Sara, Mao Silva, Felipe Ariel, Heredia Vieira, Silvia Cristina, do Carmo Vieira, Maria, Oesterreich, Silvia Aparecida
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 20.10.2016
Public Library of Science (PLoS)
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Summary:Attalea phalerata Mart. ex Spreng. (Arecaceae), popularly known as "bacuri", is used in Brazilian folk medicine. Its oil is used orally to relieve pulmonary congestion and joint pain. In topical applications, it is applied as an effective hair tonic and anti-dandruff. The in natura pulp and its nuts are used as food because of its nutritional value. Despite its use in folk medicine, there is a lack of data regarding its in vivo/in vitro cytotoxic/genotoxic and clastogenic effects. Therefore, in this study, we evaluated the cytotoxic, genotoxic and clastogenic effects of Attalea phalerata Mart. ex Spreng. oil (APMO) in vitro and in vivo. For the analysis of cytotoxic potential, the Artemia salina and MTT (3-(4,5-dimethizzol-zyl)-2,5-diphenyltetrazolium bromide) assays were performed. Possible cytotoxic, genotoxic and clastogenic effects of APMO intake were determined by performing the comet and micronucleus assays. Male and female Wistar rats were orally treated with doses of 125, 250, 500 or 1000 mg.kg-1 of the APMO daily for 28 consecutive days (four weeks). The results showed that the APMO did not induce cell death in the experiments of Artemia salina and MTT, indicating that it has no cytotoxicity. The APMO did not cause significant damage to the DNA of the rats in the four doses used when compared to the negative control group (saline + Tween® 80). The APMO did not present any significant increase in micronucleated polychromatic erythrocytes (MNPCEs) for the four tested doses. When compared to the positive control group, all groups (comet and micronucleus tests) were statistically different. These data suggest that the administration of Attalea phalerata Mart oil. ex Spreng does not cause cytotoxicity, genotoxicity and clastogenicity in experimental models in vitro and in vivo following oral administration in this study.
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Conceptualization: FFL SELTM GKT MCV SAO. Data curation: FFL SELTM GKT FHSA CHL MCV SAO. Formal analysis: FFL SELTM GKT SAO. Funding acquisition: MCV. Investigation: FFL SELTM GKT FHSA CHL SMP FAMS SCHV MCV SAO. Methodology: FFL SELTM GKT FHSA CHL MCV SAO. Project administration: SAO. Resources: CHL MCV SAO. Software: FFL SELTM GKT FHSA CHL MCV SAO. Supervision: MCV SAO. Validation: FFL SELTM GKT FHSA CHL SMP FAMS SCHV. Visualization: FFL SELTM GKT MCV SAO. Writing – original draft: FFL SELTM GKT MCV SAO. Writing – review & editing: FFL SELTM GKT MCV SAO.
Competing Interests: The authors have declared that no competing interests exist.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0165258