87 research outputs found

    Molecular actions of hypocholesterolaemic compounds from edible mushrooms

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    Cholesterol levels are strictly regulated to maintain its homeostasis; therefore, if it is not absorbed with the diet, the cholesterol biosynthetic pathway is enhanced and vice versa. Nowadays, the commonly prescribed therapeutic treatments for hypocholesterolemic patients are targeted toward the reduction of both cholesterol intestinal absorption and/or its endogenous biosynthesis. But, when hypercholesterolemia is still moderate the consumption of food products with cholesterol-lowering capacities is more desirable than using drugs. Marketed foods supplemented with hypocholesterolemic compounds are only inhibiting mechanisms for cholesterol absorption (i.e. phytosterols and cereal β-glucans). However, certain fungal extracts obtained from edible mushrooms might be able to modulate cholesterol levels by both strategies, pharmaceutical drugs and functional foods. In vitro and in vivo studies indicated that fungal sterols down-regulated genes involved in cholesterol homeostasis (such as Srebf2 and Nr1h4 (FXR)) and other specific mushroom extracts (β-glucans and other water-soluble compounds) also stimulated transcriptional profiles similar to simvastatin or ezetimibe (two hypocholesterolemic drugs). These and other observations suggested that the hypocholesterolemic effect of mushroom extracts could be due to transcriptional and post-transcriptional modulations besides other indirect effectsThis research was supported by national R+D program from the Spanish Ministry of Science and Innovation (projects AGL2010-21537 and AGL2014-56211-R) and the regional program from the Community of Madrid, Spain (S2013/ABI-2728

    Antiviral activities of Boletus edulis, Pleurotus ostreatus and Lentinus edodes extracts and polysaccharide fractions against Herpes simplex virus type 1

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    Deposited with permissionAntiviral properties of water and methanol extracts from Lentinus edodes, Boletus edulis and Pleurotus ostreatus were evaluated against herpes simplex virus type 1 (HSV-1). Pre-treatment of Vero cells with 75 mg·ml-1 water extracts before virus addition, inhibited 60% of the virus infection and its addition during the virus adsorption period inhibited it up to 80%. Moreover, the mushrooms water extracts were able to significantly inhibit the in vitro virus replication, showing the concentration of a substance required to reduce plaque number in Vero cells by 50% (IC50) values from 26.69 mg·ml-1 to 35.12 mg·ml-1. Methanol extracts exhibited a lower antiviral activity in all cases. In order to identify the type of compounds responsible for the antiviral activity, the low molecular weight (LMW) and high molecular weight (HMW) fractions were evaluated. The activity was found to correlate with the β-glucans present in the polysaccharide fractions, which showed higher antiviral activity than the complete water extracts except for B. edulis where other compounds (probably chitin-binding lectins) might have contributed to the observed activity.This work was also supported by the ALIBIRD-CM S2009/AGR-1469 regional program from the Comunidad de Madrid (Spain

    Revalorization of low-quality truffles using SFE to obtain aromatic and flavoring extracts

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    Esta investigación ha contado con el apoyo de la beca Ibercaja-CAI Estancias de Investigación número CA 1/20trufflerevalorizationsupercritical fluidsarom

    Testing edible mushrooms to inhibit the pancreatic lipase activity by an in vitro digestion model

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    This is the peer reviewed version of the following article: Palanisamy, M. Testing edible mushrooms to inhibit the pancreatic lipase activity by an in vitro digestion model (2012) International Journal of Food Science and Technology, 47 (5), pp. 1004-1010., which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2621.2011.02934.x. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archivingOne of the strategies in prevention or treatment of obesity is altering metabolism of lipids by inhibition of dietary fat absorption. The extracts obtained with methanol, water and methanol:water (1:1) from 21 mushroom species were screened as potential sources of pancreatic lipase (PL) inhibitors using a standardised in vitro test. Lepiota procera methanol:water (1:1) extracts showed the highest inhibition activity closely followed by Grifola frondosa, Pleurotus eryngii and Lyophyllum shimeji. Other mushroom strains such as Morchella conica, Marasmius oreades, Lentinula edodes, Amanita ponderosa and Boletus edulis also showed a certain inhibitory activity. However, when the PL inhibitory activity was evaluated using an in vitro digestion model mimicking gut conditions, none of the selected mushroom extracts were able to inhibit PL activity. On the contrary, stimulation of the lipase activity levels was observed and it was not due to endogenous mushroom lipases activitiesThe research was supported by the European Union within the 7th framework programme (7FM-PEOPLE-2009-IIF project 251285), ALIBIRD-CM S2009 ⁄AGR-1469 regional program from the Community of Madrid (Spain) and AGL2010-21537 national R+D program from the Spanish Ministry of Science and Innovatio

    Pressurized water extraction of β-glucan enriched fractions with bile acids-binding capacities obtained from edible mushrooms

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    This is the peer reviewed version of the following article: Biotechnology Progress 30.2 (2014): 391-400, which has been published in final form at http://dx.doi.org/10.1002/btpr.1865.  This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archivingA pressurized water extraction (PWE) method was developed in order to extract β-glucans with bile acids-binding capacities from cultivated mushrooms (Agaricus bisporus, Lentinula edodes and Pleurotus ostreatus) to be used as supplements to design novel foods with hypocholesterolemic properties. Extraction yields were higher in individual than sequential extractions being the optimal extraction parameters: 200ºC, 5 cycles of 5 min each at 10.3 MPa. The crude polysaccharide (PSC) fractions, isolated from the PWE extracts contained mainly β-glucans (including chitooligosaccharides deriving from chitin hydrolysis), -glucans and other PSCs (hetero-/proteo-glucans) depending on the extraction temperature and mushroom strain considered. The observed bile acids-binding capacities of some extracts were similar to a β-glucan enriched fraction obtained from cereals.The research was supported by the European Union within the 7th framework programme (7FM-PEOPLE-2009-IIF project 251285), ALIBIRD-CM S2009/AGR-1469 regional program from the Community of Madrid (Spain) and AGL2010-21537 national R+D program from the Spanish Ministry of Science and Innovation. CTICH is also acknowledged for the cultivation and supplying of the mushrooms fruiting bodie

    RNA-Seq, bioinformatic identification of potential microRNA-like small RNAs in the edible mushroom Agaricus bisporus and experimental approach for their validatiol

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    Although genomes from many edible mushrooms are sequenced, studies on fungal micro RNAs (miRNAs) are scarce. Most of the bioinformatic tools are designed for plants or animals, but the processing and expression of fungal miRNAs share similarities and differences with both kingdoms. Moreover, since mushroom species such as Agaricus bisporus (A. bisporus, white button mushroom) are frequently consumed as food, controversial discussions are still evaluating whether their miRNAs might or might not be assimilated, perhaps within extracellular vesicles (i.e., exosomes). Therefore, the A. bisporus RNA-seq was studied in order to identify potential de novo miRNA-like small RNAs (milRNAs) that might allow their later detection in diet. Results pointed to 1 already known and 37 de novo milRNAs. Three milRNAs were selected for RT-qPCR experiments. Precursors and mature milRNAs were found in the edible parts (caps and stipes), validating the predictions carried out in silico. When their potential gene targets were investigated, results pointed that most were involved in primary and secondary metabolic regulation. However, when the human transcriptome is used as the target, the results suggest that they might interfere with important biological processes related with cancer, infection and neurodegenerative disease

    Sterol enriched fractions obtained from Agaricus bisporus fruiting bodies and by-products by compressed fluid technologies (PLE and SFE)

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    This is the author’s version of a work that was accepted for publication in Innovative Food Science and Emerging Technologies. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Innovative Food Science and Emerging Technologies, 18, (2013) DOI: 10.1016/j.ifset.2013.01.007Ergosterol, ergosta7,22 dienol, ergosta 5,7 dienol, fungisterol, ergosta-4,7,2-trien-3-ona and ergosta-4,6,8(14),22-tetraen-3-ona were the fungal sterols detected in Agaricus bisporus mushrooms after optimization of a sterol extraction method. Their concentration ranged from 3.1 to 11.2 mg/g dw depending on the strain, casing soil, flush number, developmental stage and sporophore tissue analyzed. Two methods were optimized to obtain sterol enriched extracts from A. bisporus fruiting bodies using pressurized liquid extraction (PLE) and supercritical fluid extraction (SFE). PLE using ethanol as solvent at 10.7 MPa (50 C and 100 C) after 5 cycles of 5 min extraction (mixing in the extraction cell the sample with sand in a ratio 1:4) yielded extracts with respectively 5 and 2.9% sterols. Using SFE-CO2 at 40 C and 9 to 30 MPa fractions containing 60% of sterols were obtained. Both technologies could be also utilized to extract sterols from mushroom by-products (the lower part of the stipe) as a method for their valorization. Industrial relevance In this work, two environmentally friendly methods (SFE and PLE) to obtain sterol enriched fractions from Agaricus bisporus mushrooms were optimized. Extractions from both the complete fruiting body and the lower part of the stipe (usually discarded as a by-product during harvesting) yielded extracts with high ergosterol (and derivatives) content that could be used as functional ingredients to design novel foods with hypocholesterolemic properties since fungal sterols are able to reduce cholesterol levels in serum as plant phytosterols. Moreover, if the mushroom by-products are utilized as starting material, this application can be an interesting alternative method for the commercial valorization of this residueThe research was supported by the European Union within the 7th Framework Program (7FM-PEOPLE-2009-IIF project 251285), ALIBIRDCMS2009/ AGR-1469 Regional Programfromthe Community ofMadrid (Spain) and AGL2010-21537 National R+D Program from the Spanish Ministry of Science and Innovation
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