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- Synthesis and the in vitro evaluation of antitumor activity of novel thiobenzanilidesPublication . Álvaro Martins, Maria Joao; Railean, Violeta; Martins, Filomena; Machuqueiro, Miguel; Pacheco, Rita; Santos, SusanaCancer is a generic term for a large group of diseases that are the second-leading cause of death worldwide, accounting for nearly 10 million deaths in 2020. Melanoma is a highly aggressive skin tumor with an increasing incidence and poor prognosis in the metastatic stage. Breast cancer still stands as one of the major cancer-associated deaths among women, and diagnosed cases are increasing year after year worldwide. Despite the recent therapeutic advances for this type of cancer, novel drugs and treatment strategies are still urgently needed. In this paper, the synthesis of 18 thiobenzanilide derivatives (17 of them new) is described, and their cytotoxic potential against melanoma cells (A375) and hormone-dependent breast cancer (MCF-7) cells is evaluated using the MTT assay. In the A375 cell line, most of the tested thiobenzanilides derivatives showed EC50 values in the order of mu M. Compound 17 was the most promising, with an EC50 (24 h) of 11.8 mu M. Compounds 8 and 9 are also interesting compounds that deserve to be further improved. The MCF-7 cell line, on the other hand, was seen to be less susceptible to these thiobenzanilides indicating that these compounds show different selectivity towards skin and breast cancer cells. Compound 15 showed the highest cytotoxic potential for MCF-7 cells, with an EC50 (24 h) of 43 mu M, a value within the range of the EC50 value determined for tamoxifen (30.0 mu M). ADME predictions confirm the potential of the best compounds. Overall, this work discloses a new set of thiobenzanilides that are worth being considered as new scaffolds for the further development of anticancer agents.
- Effect of food preparations on in vitro bioactivities and chemical components of fucus vesiculosusPublication . André, Rebeca; Guedes, Laura; Melo, Ricardo; Ascensão, Lia; Pacheco, Rita; Vaz, Pedro D.; Serralheiro, Maria LuisaFucus vesiculosus is a brown macroalgae used in food and generally considered safe to be consumed, according to EU Directive (EC 258/97). The aim of this study is to analyze the e_ect of food preparation on F.vesiculosus of di_erent origins on what concerns its chemical constituents and final bioactivities. The aqueous extract of the seaweeds were obtained at di_erent temperatures, similar to food preparation and then purified by SPE. The compound identification was carried out by Liquid Chromatography High Resolution Mass Spectrometry (LC-HRMS/MS) and algae extracts microstructure were observed by Scanning Electron Microscopy (SEM). The activities were determined by using antioxidant activity, inhibition of acetylcholinesterase (AChE) and 3-hidroxi-3-methyl-glutaril-CoA (HMG-CoA) reductase (HMGR) together with Caco-2 cells line simulating the intestinal barrier. The activity of AChE and the HMGR were inhibited by the extracts giving IC50 values of 15.0 _ 0.1 _g/mL and 4.2 _ 0.1 _g/mL, respectively and 45% of the cholesterol permeation inhibition. The main compounds identified were phlorotannins and peptides derivatives. The mode of preparation significantly influenced the final bioactivities. Moreover, the in vitro results suggest that the preparation of F. vesiculosus as a soup could have hypercholesterolemia lowering effect.
- Melanin: production from cheese bacteria, chemical characterization, and biological activitiesPublication . Ferraz, Ana Rita; Pacheco, Rita; Vaz, Pedro D.; Pintado, C. M. B. S.; Ascensão, Lia; Serralheiro, Maria LuisaPigments are compounds of importance to several industries, for instance, the food industry, where they can be used as additives, color intensifiers, and antioxidants. As the current trend around the world is shifting to the use of eco-friendly commodities, demand for natural dyes is increasing. Melanins are pigments that are produced by several microorganisms. Pseudomonas putida ESACB 191, isolated from goat cheese rind, was described as a brown pigment producer. This strain produces a brown pigment via the synthetic Mueller-Hinton Broth. This brown compound was extracted, purified, analyzed by FTIR and mass spectrometry, and identified as eumelanin. The maximum productivity was 1.57 mg/L/h. The bioactivity of eumelanin was evaluated as the capacity for scavenging free radicals (antioxidant activity), EC50 74.0 & PLUSMN; 0.2 mu g/mL, and as an acetylcholinesterase inhibitor, with IC50 575 & PLUSMN; 4 mu g/mL. This bacterial eumelanin did not show cytotoxicity towards A375, HeLa Kyoto, HepG2, or Caco2 cell lines. The effect of melanin on cholesterol absorption and drug interaction was evaluated in order to understand the interaction of melanin present in the cheese rind when ingested by consumers. However, it had no effect either on cholesterol absorption through an intestinal simulated barrier formed by the Caco2 cell line or with the drug ezetimibe.
- Exploring the Hypocholesterolemic Potential of a Fucus vesiculosus Extract: Omic Insights into Molecular Mechanisms at the Intestinal LevelPublication . Rebeca, André; Pacheco, Rita; Santos, Hugo M.; Serralheiro, Maria LuisaHigh blood cholesterol levels are a major risk factor for cardiovascular diseases. A purified aqueous extract of Fucus vesiculosus, rich in phlorotannins and peptides, has been described for its potential to inhibit cholesterol biosynthesis and intestinal absorption. In this work, the effect of this extract on intestinal cells' metabolites and proteins was analysed to gain a deeper understanding of its mode of action on lipids' metabolism, particularly concerning the absorption and transport of exogenous cholesterol. Caco-2 cells, differentiated into enterocytes, were exposed to the extract, and analysed by untargeted metabolomics and proteomics. The results of the metabolomic analysis showed statistically significant differences in glutathione content of cells exposed to the extract compared to control cells, along with an increased expression of fatty acid amides in exposed cells. A proteomic analysis showed an increased expression in cells exposed to the extract compared to control cells of FAB1 and NPC1, proteins known to be involved in lipid metabolism and transport. To the extent of our knowledge, this study is the first use of untargeted metabolomics and a proteomic analysis to investigate the effects of F. vesiculosus on differentiated Caco-2 cells, offering insights into the molecular mechanism of the extract’s compounds on intestinal cells.
- Mechanism of action and the biological activities of Nigella sativa oil componentsPublication . Silva, André Filipe C.; Haris, Parvez I.; Serralheiro, Maria Luisa; Pacheco, RitaNigella sativa seeds oil is consumed because of its health benefits. Although the oil has been studied for its properties and composition, these effects are often associated with its major compound thymoquinone, and less has been reported about the other components' contributions to the pharmacological properties and mechanism of action. The present study aimed to evaluate the oil compounds' antioxidant and anti-tumour activities, and its effect on molecular targets associated with the claimed health effects. A wide a range of biochemical and biophysical techniques were used to understand the biological activities of the oil components. Compounds such as thymoquinone and volatile monoterpenes such as alpha-thujene, alpha-pynene, sabinene and 3-carene were identified by using GC-MS. Similar high antioxidant activities were obtained for the oil and its non-volatile (NV) fraction, with enzymes inhibition and cytotoxic activity against MCF-7 and A375 cells the oil showed a strong effect but not its NV fraction. Analysis of A375 cells' proteome in contact with the oil showed increased expression of proteins POTEF and HSP 90-b suggesting that the oil's antitumor effect was due to apoptosis and cellular stress. FT-IR studies in two model proteins in contact with the oil allowed oil compounds-protein interactions to be recognized and also showed that volatiles stabilized proteins. Therefore, not only thymoquinone but also the volatile monoterpenes were important for the diversity of properties, and therefore modifications in the chemical composition of the oil, as an outcome of storage or even food preparation, may affect its biological activity.
- Phenolic profile and biological activities of decoctions from Santolina impressa, a Portuguese endemic speciesPublication . Rodrigues, Ana M.; Fale, Pedro; Madeira, Paulo; Pacheco, Rita; Florêncio, Maria Helena; Ascensão, Lia; Serralheiro, Maria LuisaSantolina impressa Hoffmanns & Link is an aromatic Asteraceae species endemic to the southwest of Portugal. It is used in folk medicine as an herbal tea for gastrointestinal ailments and mouthwash antiseptic. The present study aimed to relate the chemical composition of decoctions from the aerial parts S. impressa with their antiacetylcholinesterase, antioxidant, antimicrobial and cytotoxic activities, in an attempt to explain the traditional use of this species. LC–MS/MS analysis identified chlorogenic acid and cynarin as the main components. Antimicrobial activity of the extracts was investigated against two cariogenic bacteria:- Streptococcus sobrinus and Streptococcus mutans, and these decoctions were not cytotoxic towards Caco-2 and HepG2 cell lines. Decoctions from capitula and stems/leaves showed high AChE inhibition, with IC50 values of 328 μg/mL and 579 μg/mL, respectively. The antioxidant activity measured using the DPPH radical scavenging assay showed an EC50 of 14.7 μg/mL and 12.9 μg/mL for capitula and stems/leaves extracts, respectively. The biological activities were kept constant after in vitro digestive process and the HPLC analysis did not indicate changes in the extract’s chemical composition. The results may explain the traditional use of S. impressa decoctions for digestive problems and as a mouthwash antiseptic.
- Nanoformulation of seaweed eisenia bicyclis in albumin nanoparticles targeting cardiovascular diseases: In vitro and in vivo evaluationPublication . Pinto, Sofia; Gaspar, Maria Manuela; Ascensão, Lia; Faísca, Pedro; Reis, Catarina; Pacheco, RitaNatural products, especially those derived from seaweeds, are starting to be seen as effective against various diseases, such as cardiovascular diseases (CVDs). This study aimed to design a novel oral formulation of bovine albumin serum nanoparticles (BSA NPs) loaded with an extract of Eisenia bicyclis and to validate its beneficial health effects, particularly targeting hypercholesterolemia and CVD prevention. Small and well-defined BSA NPs loaded with Eisenia bicyclis extract were successfully prepared exhibiting high encapsulation efficiency. Antioxidant activity and cholesterol biosynthesis enzyme 3-hydroxy-3 methylutaryl coenzyme A reductase (HMGR) inhibition, as well as reduction of cholesterol permeation in intestinal lining model cells, were assessed for the extract both in free and nanoformulated forms. The nanoformulation was more efficient than the free extract, particularly in terms of HMGR inhibition and cholesterol permeation reduction. In vitro cytotoxicity and in vivo assays in Wistar rats were performed to evaluate its safety and overall effects on metabolism. The results demonstrated that the Eisenia bicyclis extract and BSA NPs were not cytotoxic against human intestinal Caco-2 and liver HepG2 cells and were also safe after oral administration in the rat model. In addition, an innovative approach was adopted to compare the metabolomic profile of the serum from the animals involved in the in vivo assay, which showed the extract and nanoformulation's impact on CVD-associated key metabolites. Altogether, these preliminary results revealed that the seaweed extract and the nanoformulation may constitute an alternative natural dosage form which is safe and simple to produce, capable of reducing cholesterol levels, and consequently helpful in preventing hypercholesterolemia, the main risk factor of CVDs.
- Molecular-level changes induced by hydroxycinnamic acid derivatives in HepG2 cell line: comparison with pravastatinPublication . RESSAISSI, Asma; Pacheco, Rita; Serralheiro, Maria LuisaHydroxycinnamic acid derivatives are an important class of polyphenols found in fruits, vegetables, and medicinal plants and widely consumed in human diet. In the present work, alterations of HepG2 cells biochemical profile under the effect of four hydroxycinnamic acid derivatives (caffeic acid, m-coumaric acid, chlorogenic acid and rosmarinic acid) relatively to the effect of pravastatin, a drug often prescribed to inhibit HMG-CoA reductase enzyme, the regulator enzyme in the cholesterol biosynthesis pathway, were reported. The application of FTIR spectroscopy in combination with multivariate analysis by PCA showed a similarity between pravastatin and the four hydroxycinnamic acid derivatives in metabolite profile modification expressed by various changes in proteins region, the phosphate region which mainly corresponds to nucleic acids as well as in lipids regions. FTIR structural analysis in the amide I region, using resolution enhancement methods, such as second derivative and amide I deconvolution method, revealed significant decrease in alpha-helix/random coil and intermolecular beta-sheet decreased while intramolecular beta-sheet in treated cells showed an increase. It was also noticed that the intracellular cholesterol as well as esterified ingredients such as cholesterol esters in the cell membrane decreased. Moreover, principal component analysis (PCA) of the spectral data showed that the compounds and pravastatin were well separated from untreated cells showing a different mode of action on HepG2 treated cells for each compound.
- Brown algae potential as a functional food against hypercholesterolemia: reviewPublication . André, Rebeca; Pacheco, Rita; Bourbon, Mafalda; Serralheiro, Maria LuisaBrown algae have been part of the human diet for hundreds of years, however, in recent years, commercial and scientific interest in brown algae has increased due to the growing demand for healthier diet by the world population. Brown algae and its metabolites, such as carotenoids, polysaccharides, phlorotannins, and proteins, have been associated with multiple beneficial health effects for different diseases, such as cardiovascular diseases, one of the main causes of death in Europe. Since high blood cholesterol levels are one of the major cardiovascular risks, this review intends to provide an overview of current knowledge about the anti-hypercholesterolemic effect of different brown algae species and/or their isolated compounds.
- Cholesterol transporter proteins in HepG2 cells can be modulated by phenolic compounds present in Opuntia ficus-indica aqueous solutionsPublication . RESSAISSI, Asma; ATTIA, Nebil; Pacheco, Rita; Fale, Pedro; Serralheiro, Maria LuisaIncreased blood cholesterol is a risk factor for atherosclerotic cardiovascular disease. This study tested the hypothesis that phenolic compounds can modulate the level of cholesterol transporters including Niemann-Pick C1-like 1 (NPC1L1) and ATP-binding cassette transporters in liver cells. HepG2 cells, used as a model of hepatocytes, showed a decrease in the abundance of cholesterol transporters comparatively to the control when treated with the Opuntia ficus-indica's cladodes decoction. The decrease was between 13-70%, 25-60%, 9-60% and 23-60% for NPC1L1, ABCA1, ABCG5 and ABCG8 transporters, respectively, when using between 0.15 and 0.35 mg/mL of decoction in the culture medium. FTIR analysis showed changes in the amount of RNA, which may be the cause of the decrease in the level of several proteins. These in vitro results pave the way to a molecular explanation for the decoction of cladodes effect on cholesterol levels as it reduced the membrane cholesterol transporter proteins, NPC1L1, ABCG5/ABCG8 and ABCA1, in HepG2 cells.