The high prevalence of diabetes and obesity encourages research for the development of α-glucosidase inhibitors from natural sources. This study evaluated the activity of fractions obtained from Protium spruceanum branches. Anti-α-glucosidase activity was investigated in vitro using 4-nitrophenyl-α-D-glucopyranoside as the substrate, while free-radical scavenging activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2’-azinobis-3-ethylbenzotiazoline-6-sulfonic acid (ABTS) assays. Furthermore, a model of oxidative stress promoted by H2O2 in fibroblasts was employed, and cell viability was determined by sulforhodamine B. Fractions inhibited α-glucosidase activity effectively, highlighting the hydromethanolic fraction (HMF). Quercitrin, isolated from the HMF, was identified by spectroscopy and quantified by a validated high performance liquid chromatography with diode array detector (HPLC-DAD) method and exhibited free radical scavenging activity comparable to the HMF. However, this flavonoid showed low anti-α-glucosidase effect, suggesting a synergism effect among several components of the HMF. This proposal is also supported by the docking results obtained by PyRx software. The compounds present in the HMF showed a noncompetitive inhibition at the in silico simulation. Finally, the HMF also protected fibroblasts against cell death induced by oxidative stress. This is the first evidence of the capacity of P. spruceanum branches to inhibit α-glucosidase activity and to counteract oxidative stress. These results encourage the use of this Brazilian plant against hyperglycemia-correlated diseases.

The optimized analytical methodology described herein is based on an ion exchange column and an H3PO4 solution (pH 2.24) as the mobile phase, with a flow rate of 0.4 mL min-1 and refractive index detection (RID). On applying the methodology, it was possible to identify 7 products obtained from the oxidation of glycerol with an analysis time of 27 min. The developed method was validated through the evaluation of a series of analytical parameters. The results obtained were evaluated considering the peak area and peak height. The analytical curves showed a correlation coefficient of ≥ 0.986. The coefficient of variation values obtained were ≤ 3.60% for instrumental precision, ≤ 19.36% for intermediate precision in LOQ (1.25 µg mL-1) and ≤ 17.93% for repeatability in LOQ (1.25 µg mL-1) and different days. The limit of quantification established for all compounds was 1.25 µg mL-1 obtained through the parameters of the analytical curve. The accuracy of the method showed recovery values of 85.6 to 112.3% for real fortified sample at 3 concentration levels. Two different samples of glycerol oxidation products were applied to the validated methodology; one obtained from AuNP/SiO2 as catalyst (conversion of 62.42%), and other using AuNP/MWCNT (conversion of 89.5%).

Este trabalho objetivou quantificar a variação do comprimento total e massa corporal para pós-larvas de Sardinella janeiro e determinar as equações de correção para o cálculo do comprimento total e da massa corporal a partir de espécimes preservados. Os peixes foram submetidos aleatoriamente a cinco métodos de preservação (congelamento - 20º C, formalina 2,5% e 5%, álcool 70% e 95%), e medidos o comprimento total (CT) e pesado a massa corporal (P) antes da preservação, e 5, 15, 30 e 60 dias após a preservação. Foram observadas perdas significantes no comprimento total e na massa corporal durante os cinco primeiro dias após a preservação, prosseguindo em menor intensidade até o 30º dia na maioria dos métodos. Exceções foram observadas para a massa corporal em congelamento e formalina 5%, com perdas ocorrendo mesmo depois de 30 dias de preservação. O grau de perdas para comprimento total e massa corporal foi significativamente dependente do tamanho dos peixes, com os menores indivíduos sofrendo as maiores perdas. O comprimento total e massa corporal de indivíduos frescos podem ser retro-calculados usando equações que descrevem a relação entre indivíduos frescos e após 60 dias de preservação para a maioria dos métodos, exceto para a massa corporal em congelamento.

This work aims to quantify the variation in total length and body mass for the early-juvenile Brazilian herring Sardinella janeiro and to determine total length and body mass correction equation to allow fresh measures to be calculated from preserved ones. Fishes were randomly assigned to one of five preservation methods (freezing at - 20º C, 2.5% and 5% formalin, 70% and 95% ethanol), and measured for total length (TL) and body mass (W) before preservation, and on days 5, 15, 30, and 60 after storage. Significant reductions in total length and body mass occurred during the first 5 days after preservation and continued to contract significantly at a lesser rate through 30 days in most methods. Exceptions were shown for body mass in freezing and 5% formalin, where the greatest losses occurred after 30 days of preservation. The degree of shrinkage for total length and body mass was very much dependent on fish size, with smaller specimens shrinking more than larger ones. The fresh total length and body mass can be back-calculated using equations that describe the relationship between fresh and preserved individuals after 60 days storage for all methods except for body mass in freezing.