Allelochemical Potential of Smilax fluminensis Steud. (Smilacaceae) Leaves: Investigation of the Effects on Germination, Seedling Development and Cellular Alterations
Lucas Santos Azevedo, Thaís Paula Rodrigues Gonçalves, Gabriela Cristina Ferreira Mota, Mariana Guerra de Aguilar, Lúcia Pinheiro Santos Pimenta, Ana Hortência Fonsêca Castro, Luciana Alves Rodrigues dos Santos LimaAgrochemicals are used worldwide in food production, but their use varies between countries due to the damage observed to nature and human health. Allelopathy is the primary pathway of chemical communication in plants, interfering with biome development through stimulation and/or inhibition mechanisms. Therefore, this study aimed to assess the biological activities of the ethanol extract (EE) and fractions of S. fluminensis leaves on monocotyledonous and eudicotyledonous models. The EE was obtained by percolation with ethanol, and the hexane (HEXF), dichloromethane (DCMF), ethyl acetate (EAF), and hydroethanol (HEF) fractions were obtained by liquid–liquid partition. The phytochemical characterization was performed by 1H nuclear magnetic resonance (NMR). The allelopathic activity was evaluated on Allium cepa (onion) and Lactuca sativa (lettuce) seeds. The cytotoxic, genotoxic, and antigenotoxic effects on A. cepa meristematic cells were analyzed in vitro. Aliphatic compounds, saponins, and flavonoids derived from quercetin and kaempferol were characterized in the samples. All samples decreased the vigor, germination rate, and germination speed index (GSI) of A. cepa seeds. In contrast, they did not alter the vigor and viability of L. sativa seeds, but decreased the GSI, except for HEF. The samples inhibited the epicotyl and root growth of A. cepa and L. sativa, except HEXF, which stimulated the growth of epicotyls (750 µg/mL) and roots (750 and 1000 µg/mL). The cytotoxic assays showed that the EE and HEXF had cytotoxic action at low concentrations, and no sample showed a genotoxic effect. The following samples exhibited an antigenotoxic effect after pretreatment with atrazine (ATZ): EE (125 and 750 µg/mL), HEXF (750 and 1000 µg/mL), DCMF (125, 250, and 1000 µg/mL), EAF (at all tested concentrations), and HEF (125, 250, and 750 µg/mL). Furthermore, the EAF at 125 and 500 µg/mL and HEF at 125 µg/mL demonstrated the potential to reverse genetic damage induced by glyphosate (GLY).