No abstract

RESUMO:A infusão das folhas de Plantago major (Plantaginaceae), conhecida como tansagem ou transagem, é usada como antibiótica, antiinflamatória, anti-séptica, anti-térmica, na prevenção de tumores e no tratamento de neoplasias. Este efeito é atribuído aos flavonóides encontrados em diversas espécies do gênero Plantago. O presente estudo objetivou avaliar os potenciais efeitos, tóxico e mutagênico, do extrato bruto hidroalcoólico de folhas de P. major, por meio dos testes in vivo de Allium cepa e do micronúcleo. Para o ensaio biológico vegetal, meristemas de raízes de A. cepa foram usados para o preparo de lâminas através da técnica de esmagamento. No ensaio do micronúcleo foram analisadas lâminas de células de medula óssea de roedores. As análises estatísticas seguiram o teste de Tukey (p<0,05) para o ensaio de Allium cepa e teste de Scott-Knott (p<0,05) para o ensaio do micronúcleo. Os resultados do teste de Allium cepa demonstram que houve redução significativa no índice de germinação em todas as concentrações testadas. P. major provoca alteração no ciclo celular pela inibição da divisão das células, como indica o índice mitótico. Os índices de efeitos clastogênico e aneugênico demonstram que, além de não determinar aumento de aberrações cromossômicas, o que indica ausência de ação genotóxica, P. major possui atividade anti-genotóxica. Os resultados do teste do micronúcleo reforçam a sugestão de que o extrato de P.major não possui atividade mutagênica, entretanto provoca alterações na divisão celular.Palavras-chave: mutagênese, tansagem, plantas medicinais, Allium cepa, micronúcleo ABSTRACT: Evaluation of the cytotoxic and genotoxic potential of Plantago major L. in test systems in vivo. The infusion of leaves of Plantago major (Plantaginaceae), known as "tansagem" or "transagem", is used as antibiotic, anti-inflammatory, anti-septic, anti-thermal in the prevention of tumors and in the treatment of neoplasms. This effect is attributed to the flavonoids found in diverse species of the genus Plantago. The present study aimed to evaluate the potential toxic and mutagenic effects of the crude hydroalcoholic extract from P. major leaves by means of in vivo tests with Allium cepa and micronucleus. For the plant biological assay, meristems of A. cepa roots were used for the preparation of slides by adopting the crushing technique. In the micronucleus assay, slides of bone marrow cells from rodents were analyzed. Statistical analyses were carried out according to Tukey's test (ρ<0.05) for the Allium cepa assay and Scott-Knott test (ρ<0.05) for the micronucleus assay. Results of the A. cepa test demonstrate that there was a significant reduction in the germination index at all tested concentrations. P. major causes alteration in the cell cycle by inhibiting the division of cells, as indicated by the mitotic index. The indexes of clastogenic and aneugenic effects show that, in addition to not determining the increase in chromosomal aberrations, which indicates the absence of genotoxic action, P. major has anti-genotoxi...

The objective of this study was to investigate changes in enzymatic activity and gene expression related to antioxidant defense in two passion fruit cultivars (FB100 and FB200) exposed to aluminum. The specific activity of superoxide dismutase (SOD), catalase and ascorbate peroxidase were analyzed, in addition to their relative expression pattern. The characterization of gene expression was achieved by semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) technique followed by densitometric analysis. Plants were irrigated every two days with a nutrient solution: pH 6; pH 4; 0.2 and 2.0 mM Al (pH 4). The leaves were collected at the times 0 h, 2 days, 5 days and 10 days. The analysis of the potential oxidative stress induced by aluminum demonstrated increased expression of catalase and superoxide dismutase gene, and only on the cultivar FB100 this increase was accompanied by an increase of SOD enzymatic activity, which indicates its higher efficiency on the removal of reactive oxygen species (ROS) compared to cultivar FB200.

ABSTRACT-Functional genomic analyses require intact RnA; however, Passiflora edulis leaves are rich in secondary metabolites that interfere with RnA extraction primarily by promoting oxidative processes and by precipitating with nucleic acids. this study aimed to analyse three RnA extraction methods, Concert ™ Plant RnA Reagent (Invitrogen, Carlsbad, CA, uSA), tRIzol ® Reagent (Invitrogen) and tRIzol ® Reagent (Invitrogen)/ice -commercial products specifically designed to extract RNA, and to determine which method is the most effective for extracting RnA from the leaves of passion fruit plants. In contrast to the RnA extracted using the other 2 methods, the RnA extracted using tRIzol ® Reagent (Invitrogen) did not have acceptable A260/A280 and A260/A230 ratios and did not have ideal concentrations. Agarose gel electrophoresis showed a strong dnA band for all of the Concert ™ method extractions but not for the tRIzol ® and tRIzol ® /ice methods. the tRIzol ® method resulted in smears during electrophoresis. due to its low levels of dnA contamination, ideal A260/A280 and A260/A230 ratios and superior sample integrity, RnA from the tRIzol ® /ice method was used for reverse transcription-polymerase chain reaction (Rt-PCR), and the resulting amplicons were highly similar. We conclude that tRIzol ® /ice is the preferred method for RnA extraction for P. edulis leaves.

Cereus jamacaru D.C. (mandacaru) is a cactus used as food and in the traditional medicine. In the present study, hydroalcoholic extract of C. jamacaru was evaluated for its chemical composition, antioxidant activity, cytotoxic and anti-cytotoxic effects in human lymphocytes and sarcoma 180 cells in vitro by MTT assay and antitumoral, mutagenic and cytotoxic effects on mice sarcoma-induced in vivo. Phytochemical characterization showed positive reactions for coumarin, flavanol and tyramine and total flavonoid content of 0.51 µg/mL. C. jamacaru showed antioxidant activity following DPPH (EC50 = 427.74 µg/mL), ABTS (EC50 = 270.57 µg/mL) and Fe2+ chelating ions assays (EC50 = 41.18 µg/mL). C. jamacaru induced significant decrease of sarcoma 180 viability at 24 h and 48 h of treatment, did not induce cytotoxicity in human lymphocytes and inhibits the cytotoxicity of cisplatin in vitro. Following in vivo assays, C. jamacaru promoted tumor reduction (86.07% of tumor inhibition), without inducing mutagenic or cytotoxic damage on mice blood cells. We propose that phenolic and alkaloid compounds in the extract are related to antioxidant activity, increasing its ability in metal chelating activity and promoting anti-cytotoxic activity against cisplatin, as well as these compounds may act on the cell cycle of the tumor cells in vitro and in vivo, leading to anticancer effects and tumor reduction.