Desenvolvimento e validacáo de metodologia analitica por espectrofotometria no visÍvel para quantificacäo de taninos totais na casca do caule de Simarouba amara Aubl

The stem bark of Simarouba amara Aubl., Simaroubaceae, is widely used in Brazilian folk medicine and in many countries of Central and South America for the treatment of malaria, intestinal parasites, diarrhea, anemia and fever. Although quassinoids are considered chemotaxonomic markers of the species, the unavailability of commercialization standards stay as a challenge for its quality control. Therefore, the purpose of this study was the development and validation of an analytical methodology by spectrophotometry to quantify the total tannin content from stem bark of S. amara, since this class of metabolites is one of the most abundant and representative in the species. The proposed method was based on quantification at 760 nm after addition of Folin-Ciocalteu reagent and its validation included all parameters recommended by the RE 899. The results showed that the proposed method was adequately developed and validated, and it is an useful analytical tool for the quality control of S. amara. © 2015, Sociedade de Investigacoes Florestais. All rights reserved

Sesquiterpene lactones isolated from indigenous Middle Eastern plants inhibit tumor promoter-induced transformation of JB6 cells

<p>Abstract</p> <p>Background</p> <p>Sesquiterpene lactones (SL) are plant secondary metabolites that are known for their anti-fungal, anti-bacterial, anti-inflammatory, and anti-tumor properties. Considering that several SL-derived drugs are currently in cancer clinical trials, we have tested two SL molecules, 3-β-methoxy-iso-seco-tanapartholide (β-tan) isolated from <it>Achillea falcata</it> and salograviolide A (Sal A) isolated from <it>Centaurea ainetensis</it>, for their anti-tumor properties. We used the mouse epidermal JB6P + cells as a model for tumor promotion and cellular transformation. Key players that are involved in cellular transformation and tumorigenesis are the AP-1 and NF-κB transcription factors; therefore, we assessed how β-tan and Sal A modulate their signaling pathways in JB6P + cells.</p> <p>Methods</p> <p>The effects of β-tan and Sal A on the growth of normal and neoplastic keratinocytes and on the tumor promotion-responsive JB6P + cells were determined using the MTT assay. Anchorage-independent cell growth transformation assays were used to evaluate the anti-tumor promoting properties of these SL molecules in JB6P + cells and dual luciferase reporter assays and western blot analysis were used to investigate their effects on tumor promoter-induced AP-1 and NF-κB activities and protein levels of key AP-1 and NF-кB target genes.</p> <p>Results</p> <p>β-tan and Sal A selectively inhibited tumor promoter-induced cell growth and transformation of JB6P + cells at concentrations that do not affect JB6P + and primary keratinocytes basal cell growth. In addition, both molecules reduced basal and tumor promoter-induced NF-κB transcriptional activities, differentially regulated basal and tumor promoter-induced AP-1 transcriptional activities, and modulated key players of the AP-1 and NF-κB signaling pathways.</p> <p>Conclusions</p> <p>These results highlight the anti-tumor promoting properties of β-tan and Sal A. These SL molecules isolated from two plant species native to the Middle East may provide opportunities for complementary medicine practices.</p