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

Antigenotoxicity properties of Copaifera multijuga oleoresin and its chemical marker, the diterpene (-)-copalic acid

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Author(s):
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Alves, Jacqueline Morais [1] ; Leandro, Luis Fernando [1] ; Senedese, Juliana Marques [1] ; de Castro, Pamela Tinti [1] ; Pereira, Daiane Eleuterio [1] ; Resende, Flavia Aparecida [2] ; Campos, Debora Leite [3] ; Mangabeira da Silva, Jonas Joaquim [4] ; Varanda, Eliana Aparecida [3] ; Bastos, Jairo Kenupp [4] ; Ambrosio, Sergio Ricardo [1] ; Tavares, Denise Crispim [1]
Total Authors: 12
Affiliation:
[1] Univ Franca, Dept Ciencias, BR-14404600 Franca, SP - Brazil
[2] Univ Araraquara, Grp Pesquisa Quim Med & Med Regenerat, Araraquara, SP - Brazil
[3] Univ Estadual Paulista, Fac Ciencias Farmaceut Araraquara, Dept Ciencias Biol, Araraquara, SP - Brazil
[4] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, Dept Ciencias Farmaceut, Ribeirao Preto, SP - Brazil
Total Affiliations: 4
Document type: Journal article
Source: JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES; v. 81, n. 5, p. 116-129, 2018.
Web of Science Citations: 5
Abstract

In view of the biological activities and growing therapeutic interest in oleoresin obtained from Copaifera multijuga, this study aimed to determine the genotoxic and antigenotoxic potential of this oleoresin (CMO) and its chemical marker, diterpene (-)-copalic acid (CA). The micronucleus (MN) assay in V79 cell cultures and the Ames test were used for in vitro analyses, as well as MN and comet assays in Swiss mice for in vivo analyses. The in vitro genotoxicity/mutagenicity results showed that either CMO (30, 60, or 120 mu g/ml-MN assay; 0.39-3.12 mg/plate-Ames test) or CA (2.42; 4.84, or 9.7 mu g/ml-MN assay; 0.39-3.12 mg/plate-Ames test) did not induce a significant effect on the frequency of MN and number of revertants, demonstrating an absence of genotoxic and mutagenic activities, respectively, in vitro. In contrast, these natural products significantly reduced the frequency of MN induced by methyl methanesulfonate (MMS), and exerted a marked inhibitory effect against indirect-acting mutagens in the Ames test. In the in vivo test system, animals treated with CMO (6.25 mg/kg b.w.) exhibited a significant decrease in rate of MN occurrence compared to those treated only with MMS. An antigenotoxic effect of CA was noted in the MN test (1 and 2 mg/kg b.w.) and the comet assay (0.5 mg/kg b.w.). Data suggest that the chemical marker of the genus Copaifera, CA, may partially be responsible for the observed chemopreventive effect attributed to CMO exposure. (AU)

FAPESP's process: 09/17237-8 - In vivo and in vitro evaluation of cytotoxic, mutagenic, genotoxic potential and chemopreventive effect of Copaifera langsdorffii oleoresin and copalic acid diterpenoid
Grantee:Jacqueline Morais Alves
Support Opportunities: Scholarships in Brazil - Doctorate
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