Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Comparative study of the cytotoxicity and genotoxicity of kaurenoic acid and its semi-synthetic derivatives methoxy kaurenoic acid and kaurenol in CHO-K1cells

Full text
Author(s):
Cano, Bruno Limonti ; Moreira, Monique Rodrigues ; Goulart, Mirian Oliveira ; dos Santos Goncalves, Natalia ; Sola Veneziani, Rodrigo Cassio ; Bastos, Jairo Kenupp ; Ambrosio, Sergio Ricardo ; dos Santos, Raquel Alves
Total Authors: 8
Document type: Journal article
Source: Food and Chemical Toxicology; v. 102, p. 102-108, APR 2017.
Web of Science Citations: 1
Abstract

The diterpene kaurenoic acid (KA) has vasorelaxant, antimicrobial, anti-tumoural and anti-leishmanial effects. Semi-synthetic derivatives were obtained to achieve more satisfactory responses. The assessment of genotoxicity is part of the toxicological evaluation of therapeutic compound candidates. The present study investigated the cytotoxicity and genotoxicity of KA and its semi-synthetic derivatives methoxy kaurenoic acid (MKA) and kaurenol (KRN) using the CHO-K1 cell line. The cytotoxicity evaluation demonstrated that treatments with 200 and 400 mu M KA reduced cellular proliferation to 36.5 and 4.43%, respectively, and that 100 and 200 mu M KA reduced the survival fraction (SF) to 48.1 and 5.5%, respectively. MKA and KRN at concentrations of 400 mu M reduced proliferation to 81 and 86.8%, respectively, while 100 and 200 mu M KRN reduced the SF to 50%, and 200 mu M MKA reduced the SF to 74%. No genotoxicity was observed for KA or MKA. However, 100 mu M KRN increased the DNA damage index, as detected by comet assay, although a micronucleus assay did not confirm these data. The results demonstrated that KA and its semi-synthetic derivative MKA were not genotoxic when tested at non-cytotoxic concentrations, but KRN was genotoxic at the highest concentration that was tested, as demonstrated by the comet assay. (C) 2017 Elsevier Ltd. All rights reserved. (AU)

FAPESP's process: 11/13630-7 - Chemical and pharmacological validation of extracts and active compounds of Copaifera species
Grantee:Jairo Kenupp Bastos
Support Opportunities: Research Projects - Thematic Grants