ABSTRACT
Plants with medicinal potential may also produce adverse effects in humans. This seems to be the case for the species Rubus rosifolius, where preliminary studies demonstrated genotoxic effects attributed to extracts obtained from leaves and stems of this plant using on HepG2/C3A human hepatoma cells as a model. Considering the beneficial properties of this plant as an antidiarrheal, analgesic, antimicrobial, and antihypertensive and its effects in the treatment of gastrointestinal diseases, the present study was developed with the aim of determining the cytotoxic and genotoxic potential of extracts of leaves and stems of R. rosifolius in primary without metabolic competence in human peripheral blood mononuclear cells (PBMC). Cell viability analyses at concentrations of between 0.01 and 100 µg/ml of both extracts did not markedly affect cell viability. In contrast, assessment of the genotoxic potential using the comet assay demonstrated significant damage to DNA within PBMC from a concentration of 10 µg/ml in the stem extract, and a clastogenic/aneugenic response without cytokinesis-block proliferation index (CBPI) alterations at concentrations of 10, 20, or 100 µg/ml for both extracts. Under our experimental conditions, the data obtained demonstrated genotoxic and mutagenic effects attributed to extracts from leaves and stems of R. rosifolius in cells in the absence of hepatic metabolism.
Disclosure statement
No potential conflict of interest was reported by the authors.
Author contributions
Ana Paula Oliveira Quadros: Methodology, data curation, statistical analysis, Writing – original draft. Isabel Bragança Baraldi: Methodology, statistical analysis. Marcel Petreanu: Methodology. Rivaldo Niero: Methodology, Resources. Mário Sergio Mantovani: Methodology, Conceptualization, Resources. Isabel O’Neill de Mascarenhas Gaivão: Writing – review and editing. Edson Luis Maistro: Conceptualization, Supervision, Resources, Funding acquisition, Writing – original draft, Writing – review and editing.
Financial support
This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001. Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP – Grant: 2017/24149–4), and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq – Grant: 303604/2021–2).