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1.
Foods ; 10(7)2021 Jun 24.
Article in English | MEDLINE | ID: mdl-34202539

ABSTRACT

Microalgae are a valuable and innovative emerging source of natural nutrients and bioactive compounds that can be used as functional ingredients in order to increase the nutritional value of foods to improve human health and to prevent disease. The marine microalga Isochrysis galbana has great potential for the food industry as a functional ingredient, given its richness in ω3 long chain-polyunsaturated fatty acids (LC-PUFAs), with high contents of oleic, linoleic, alpha-linolenic acid (ALA), stearidonic, and docosahexaenoic (DHA) acids. This study focuses on the formulation of a functional food by the incorporation of 2% (w/w) of I. galbana freeze-dried biomass and 2% (w/w) of I. galbana ethyl acetate lipidic extract in solid natural yogurts preparation. In the functional yogurt enriched with microalgal biomass, the ω3 LC-PUFA's content increased (to 60 mg/100 g w/w), specifically the DHA content (9.6 mg/100 g ww), and the ω3/ω6 ratio (augmented to 0.8). The in vitro digestion study showed a poor bioaccessibility of essential ω3 LC-PUFAs, wherein linoleic acid (18:2 ω6) presented a bioaccessibility inferior to 10% and no DHA or eicosapentaenoic acid (EPA) was detected in the bioaccessible fraction of the functional yogurts, thus indicating a low accessibility of lipids during digestion. Notwithstanding, when compared to the original yogurt, an added value novel functional yogurt with DHA and a higher ω3 LC-PUFAs content was obtained. The functional yogurt enriched with I. galbana can be considered important from a nutritional point of view and a suitable source of essential FAs in the human diet. However, this needs further confirmation, entailing additional investigation into bioavailability through in vivo assays.

2.
Food Funct ; 9(4): 2051-2069, 2018 Apr 25.
Article in English | MEDLINE | ID: mdl-29589631

ABSTRACT

This study was aimed at investigating the chemical composition (proximate, minerals, fatty acids and phenolic compounds) and the in vitro (antimicrobial, radical scavenging, anti-acetylcholinesterase and protein denaturing activities) and in vivo (anti-diabetic and histo-protective effects in alloxan-induced diabetic mice) biological activities of broad bean pods (BBPs), a food waste by-product material. The results showed that BBPs have high dietary fiber (57.46%), carbohydrate (18.93%) and protein (13.81%) content versus low fat content (<1%) contributing to a low energy value of 139.24 kcal per 100 g. Profiling of fatty acids showed an abundance of the essential polyunsaturated α-linolenic and linoleic acids, exhibiting an excellent nutritional quality as revealed by their low atherogenic and thrombogenic indices and their hypocholesterolemic properties. The methanol extract which exhibited the highest total phenolic, flavonoid and tannin contents was found to be the most active extract in terms of antimicrobial and anti-radical activities. In alloxan-induced diabetic mice, the oral administration of a methanol extract (500 mg per kg bw) attenuated the elevated levels of serum alanine aminotransferase (ALA), aspartate aminotransferase (AST), and alkaline phosphatase activities, and urea, uric acid, and creatinine. It effectively normalized the status of lipid profiles, mitigated oxidative stress through the activation of antioxidant enzymes (CAT, GPx and SOD), and alleviated oxidative stress-mediated histopathological changes in the pancreas, liver, kidney and testis. Compositional analysis by HPLC-PDA-ESI-MS/MS revealed the presence of flavan-3-ols (catechin, epicatechin and their derivatives), flavones (apigenin derivatives) and flavonols (glycosides of quercetin and kaempferol), among others. These findings suggest that BBPs may be an effective functional food for the management of diabetes and its complications.


Subject(s)
Diabetes Mellitus, Experimental/diet therapy , Dietary Supplements , Fruit/chemistry , Hypoglycemic Agents/therapeutic use , Industrial Waste/analysis , Plant Extracts/therapeutic use , Vicia faba/chemistry , Animals , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/economics , Anti-Bacterial Agents/isolation & purification , Anti-Bacterial Agents/therapeutic use , Antioxidants/chemistry , Antioxidants/economics , Antioxidants/isolation & purification , Antioxidants/therapeutic use , Biomarkers/blood , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/pathology , Dietary Supplements/analysis , Disk Diffusion Antimicrobial Tests , Food-Processing Industry/economics , Fruit/economics , Fruit/growth & development , Humans , Hypoglycemic Agents/chemistry , Hypoglycemic Agents/economics , Hypoglycemic Agents/isolation & purification , Industrial Waste/economics , Male , Methanol/chemistry , Mice , Nutritive Value , Oxidative Stress , Plant Extracts/chemistry , Plant Extracts/economics , Plant Extracts/isolation & purification , Random Allocation , Solvents/chemistry , Tunisia , Vicia faba/growth & development
3.
Nat Prod Bioprospect ; 2015 Oct 22.
Article in English | MEDLINE | ID: mdl-26493049

ABSTRACT

The inhibition of α-glucosidase and glucose-6-phosphatase, two enzymes involved in the carbohydrate metabolism, is an important target to control glycaemia on individuals with type 2 diabetes. In this work we report for the first time the inhibition of both enzymes by the antihyperglycemic n-butanol extract from Genista tenera (Fabaceae). This extract decreased α-glucosidase and glucose-6-phosphatase activities to 0.97 and 80.25 %, respectively, being more effective than acarbose, and phlorizin, the positive controls, which reduced enzymes activities only to 17.39 and 96.06 %. Once inflammation and oxidative stress are related to diabetic impairments, the anti-inflammatory activity of the extract was also evaluated, through its inhibitory activity over COX-1 enzyme (47.5 % inhibition). Moreover, after induction of oxidative stress by UV radiation, the viability of irradiated rat liver hepatoma cells exposed to the extract was significantly higher (67.82 %) than that promoted by ascorbic acid, the positive control (45.05 %). In addition, the stability of the extract under gastrointestinal conditions was evaluated by HPLC-DAD-ESI-MS/MS. Flavonoid diglycosides were identified as the main constituents of the extract, and no alterations in the chemical composition nor in the antioxidant activity were observed after in vitro digestion with artificial gastric and pancreatic juices.

5.
J Ethnopharmacol ; 150(2): 718-23, 2013 Nov 25.
Article in English | MEDLINE | ID: mdl-24095697

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Decoctions of the leaves of Annona cherimola Mill. are traditionally used in Azores to treat hypercholesterolemia. Although they are sold and consumed by people in order to improve their health, these are products that cannot be sold with claims for health benefits as they have never been studied scientifically. MATERIALS AND METHODS: The activities of decoctions from Annona cherimola leaves were analysed for the two therapeutic approaches currently used to reduce plasma cholesterol: inhibition of dietary cholesterol uptake and inhibition of HMG-CoA reductase activity. Furthermore, the composition of the decoction was elucidated by LC-MS and the permeability of the active components was analysed using Caco-2 cell monolayers as a model of the intestinal barrier (dietary cholesterol uptake). RESULTS: The chemical composition of the Annona cherimola leaves' extract revealed that rutin was its main component. The in vitro gastrointestinal digestion did not modify the chemical composition of the extract. This extract was able to originate a slight reduction in cholesterol absorption through Caco-2 cells lines and to reduce the HMG-CoA reductase activity in 50% when using 137.3 µg of the extract/mL. Rutin, when used in the same concentration as that found in the extract, was able to reduce cholesterol absorption through Caco-2 cells monolayer in approximately 47%. This flavonoid had an IC50 of 17.85 µM relatively to the HMG-CoA reductase activity. CONCLUSIONS: The traditional use of decoctions from the leaves of Annona cherimola may be justified, at least by the inhibition of HMG-CoA reductase activity.


Subject(s)
Annona , Anticholesteremic Agents/pharmacology , Cholesterol/metabolism , Plant Extracts/pharmacology , Annona/chemistry , Anticholesteremic Agents/chemistry , Caco-2 Cells , Gastric Juice/chemistry , Humans , Hydroxymethylglutaryl CoA Reductases/metabolism , Pancreatic Juice/chemistry , Permeability , Plant Extracts/chemistry , Plant Leaves/chemistry , Rutin/isolation & purification , Rutin/pharmacology
6.
Food Funct ; 4(3): 426-31, 2013 Feb 26.
Article in English | MEDLINE | ID: mdl-23223784

ABSTRACT

Herbal teas are usually complex mixtures of therapeutically active compounds. The present study is focused on the interference of flavonoids on the bioavailability of rosmarinic acid, as these types of compounds are often present together in decoctions of medicinal plants, namely Lamiaceae species. The bioavailability of rosmarinic acid was analysed in the decoction of P. barbatus and in mixtures with apigenin and luteolin. Rosmarinic acid in the herbal tea showed a 43% bioavailability through the Caco-2 cells when luteolin and apigenin were approximately 30 µM each. In the artificial mixtures the bioavailability could be increased to 90% when the concentration of flavonoids was increased to 90 µM. The co-administration of substrates of known intestinal transport systems, Pgp, Oatp and MCT, showed that the extract components not only modulated the activity of these transporters but also their own bioavailability was dependent on them. Our results demonstrate that plant extracts with a high diversity of polyphenol compounds may have higher bioavailability than that predicted by the isolated compounds.


Subject(s)
Apigenin/pharmacology , Beverages , Cinnamates/pharmacokinetics , Depsides/pharmacokinetics , Luteolin/pharmacology , Plant Extracts/pharmacology , Plectranthus/chemistry , Biological Availability , Caco-2 Cells , Humans , Polyphenols/pharmacology , Rosmarinic Acid
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