An Overview to the Health Benefits of Seaweeds Consumption
Abstract
:1. Introduction
2. Main Bioactive Compounds of Seaweeds
2.1. Phaeophyceae
2.2. Rhodophyta
2.3. Chlorophyta
3. The Health Benefits of Seaweed Bioactive Compounds
3.1. Nutraceutical Applications
3.2. Biomedical Applications
3.3. Pharmaceutical Applications
3.4. Cosmetics
4. Seaweeds Extracts in Industrial Applications
4.1. Agriculture
4.2. Animal Feed
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Data Availability Statement
Conflicts of Interest
References
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Type of Algae | Isolated Compounds | Type of Compound | Reference |
---|---|---|---|
Phaeophyceae | Laminaran | Polysaccharide of glucose | [26,41,42] |
Fucoidan | Sulphated polysaccharide | [28,29,30,31] | |
Alginic acid | Polysaccharide | [38,39] | |
Phlorotannin | Polyphenolic compound | [48,49,50,51,52] | |
Fucoxanthin | Pigment | [22,23,24,25] |
Type of Algae | Isolated Compounds | Type of Compound | Reference |
---|---|---|---|
Rhodophyta | Carrageenans Agar | Sulphated polysaccharides | [7,65,66] |
Sesquiterpenes | Mixture of polysaccharide agarose and small molecules Terpenes | [69,70,71,72] | |
Diterpenes | Terpenes | [63,64] | |
Triterpenes | Terpenes | [63,64] |
Type of Algae | Isolated Compounds | Type of Compound | Reference |
---|---|---|---|
Chlorophyta | Ulvan | Sulphated polysaccharides | [87,88,89] |
Palmitic acid | Saturated fatty acid | [87,88,89] | |
Linoleic acid | Polyunsaturated fatty acid | [78,80] | |
Chlorophylls (a and b) | Pigments | [77] | |
Carotenoids (β-carotene and xanthophylls) | Pigments | [77] |
Seaweed | Main Bioactive Compound | Property | Biotechnological Application | Reference |
---|---|---|---|---|
Phaeaophyceae | ||||
Laminaria hyperborea | Alginate | Biodegradability, biocompatibility, non-toxic behaviour | Cosmetics, pharmaceutical and food industries as stabilizers | [18,40] |
Ascophyllum nodosum | ||||
Ecklonia radiata | ||||
Durvillaea sp. | ||||
Lessonia sp. | ||||
Sargassum sp. | ||||
Scytothalia dorycarpa | ||||
Cystophora subfarcinata | ||||
Sargassum linearifolium | ||||
Macrocystis pyrifera | Alginate | Biodegradability, biocompatibility, non-toxic behaviour | Cosmetics as a thickening agent | [36] |
Phlorotannins | Antioxidant activity | Cosmetics for preventing skin aging | [90] | |
Ecklonia cava | Phlorotannins | Anticancer, antioxidant, anti-inflammatory, antiviral activities and antihypertensive effects. | Pharmaceutical and nutraceutical industries | [49,50,53] |
Eisenia arborea | Phlorotannins | Antiallergic effects | Pharmaceutical industry | [62] |
Eisenia bicyclis | Phlorotannins | Antidiabetic, antioxidant, antitumor, anti-inflammatory, and anticancer activities | Pharmaceutical and medical industries | [61] |
Ecklonia kurome | ||||
Ecklonia stolonifera | ||||
Pelvetia siliquosa | ||||
Ishige okamurae | ||||
Fucus vesiculosus | Phlorotannins | Anti-inflammatory and antioxidant properties | Cosmetics, to produce make-up and sunscreens | [91] |
Fucus evanescens | Fucoidans | Anticoagulant activity | Potential substitute to heparin | [92,93] |
Laminaria cichorioides | ||||
Rhodophyta | ||||
Chondrus pinnulatus | λ-carrageenan and κ-carrageenan | High viscosity in drinks; antitumoral property | Food industry (production of drinks, e.g., milk and chocolate) and pharmaceutical industry | [7,73] |
Chondrus armatus | ||||
Chondrus yendoi | ||||
Kappaphycus striatum | κ-carrageenan | Antitumoral activity against human nasopharynx carcinoma, human gastric carcinoma, and cervical cancer cell lines | Pharmaceutical industry | [94] |
Kappaphycus alvarezii | κ-carrageenan and agar | Antioxidant properties | Cosmetics and nutraceutical industry | [68,95] |
Gracilaria edulis | Agar Phenolic, flavonoid, and alkaloid compounds | Antidiabetic, antioxidant, antimicrobial, anticoagulant, anti-inflammatory, and antitumoral activities; hypoglycaemic activity | Pharmaceutical industry | [74,96,97,98] |
Laurencia catarinensis | Halogenated metabolites | Antitumoral activity | Pharmaceutical industry | [99] |
Laurencia obtuse | Diterpene and sesquiterpene | Actions against different cancer cell lines (KB, HepG2 and MCF-7) | Pharmaceutical industry | [99] |
Griffithsia sp. | Griffith (Protein) | Antiviral activity against MERS-CoV-2 virus and SARS-CoV-2 glycoprotein | Pharmaceutical industry | [100,101] |
Chlorophyta | ||||
Caulerpa racemosa | Phenolic compounds and flavonoids | Antioxidant, scavenging, anti-proliferative activities of cancer line cells | Pharmaceutical and nutraceutical industries | [102,103] |
Ulva lactuca | Ulvan | Antioxidant activity, antimicrobial and photocatalytic activities | Food industry (the whole body is used as salad) and industrial industry (production of biogas and biodiesel) | [83,103,104,105,106] |
Ulva rigida | Ulvan | Antigenotoxic activity in human lymphocytes; hypoglycaemic effect in vivo experiment | Pharmaceutical industry | [107,108] |
Ulva fasciata | Ulvan | Antioxidant and good mechanical properties; antiviral property | Industrial industry to develop bioplastics; pharmaceutical industry | [109,110] |
Preclinical Trial | Cell Lines Surveyed | Dosage (µg/mL) | Effect | Reference |
---|---|---|---|---|
Antitumoral activity of carregaagenans and oligosaccharide fractions of carregaagenans from Kappaphycus striatum | Human nasopharyngeal carcinoma (KB), human gastric carcinoma (BGC) and human hela carcinoma (Hela) | 500, 250, 125 | The results of bioassay showed that the fraction F1 exhibits relatively higher antitumor activity against three cancer cells in vitro than polysaccharides | [94] |
Antitumoral activity of ethanol:water extracts and ethanol:chloroform extracts of Laurencia papillosa | Jurkat cancer cells | 25–1000 | The number of the viable cells is decreased with ethanol:chloroform extract with IC50 value of 57.77 µg/mL is (more cytotoxic than the ethanol:water extract with IC50 value of 121.642 µg/mL) | [99] |
Antitumoral activity of three sesquiterpenes (12-hydroxy isolaurene 8,11-dihydro-12-hydroxy isolaurene and isolauraldehyde) obtained from extract of the red alga Laurencia obtusa. | Ehrlich cells (Ehrlich ascites Carcinoma, EAC) | 25, 50, 100 | Isolauraldehyde proved to have the highest cytotoxic activity (83.1%) followed by compound 2 (79.9%) | [140] |
Antitumoral activity of ethanolic extract of Gracilaria edulis | Ehrlich ascites tumour (EAT) cells from mice | 0–100 | EAT cells viability was close to 65% At 50 μg/mL dose and the maximum decrease of 15% was observed at 100 μg/mL | [97] |
Antigenotoxicity activity of Ulva rigida crude extracts on human lymphocytes and protective effects on chemotherapeutic agent mitomycine-C. | In vitro human lymphocytes | 10, 20, 40 | Genotoxic activity in human lymphocyte cell culture was not high, while Ulva ridiga extracts significantly decreased the number of chromosomal aberrations, the frequencies of sister chromatid exchange and micronuclei, compared with the cell culture treated with chemotherapeutic agent mitomycine-C | [107] |
Activation of LXRα or LXRβ (nuclear receptor) from polysaccharide extracts of Sargassum fusiforme | Human microglia cells (CHME3) from University Paris-Sud, France and in vivo from mice used as model of survey for AD | 1, 3, 5 | In vitro CHME3 cells showed a significantly activation of LXRβ but not LXRα with dose of 5 µg/mL. In vivo test showed after ten weeks LXR activation in the central nervous system, evidenced by a cerebral induction of LXR response genes | [145] |
Protection against Aβ- induced neurotoxicity in PC12 cells trough isolated phlorotannins from Eisenia bicyclis | Rat pheochromocytoma cells (PC12 cells) obtained from American Type Culture Collection (ATCC) | 2.5, 5, 10, 20 | 7-phloroeckol and phlorofucofuroeckol A have been shown to be potent neuroprotective agents | [147] |
Protection against hydrogen peroxide (H2O2)-induced damage trough sulfated polysaccharides from Codium fragile | Monkey kidney fibroblasts (Vero cells) Zebrafish embyos | 12.5, 25, 50 | In vivo and in vitro tests showed the potential of polysaccharides extracted as neurorepair in animals | [149] |
Seaweed | Compound Extracted | Cell Lines/Animals Surveyed | Route of Administration | Dosage (µg/mL) | Effect | Reference |
---|---|---|---|---|---|---|
Laminaria cichorioides (Phaeophyceae) | Sulphated fucan | Human plasma | The lyophilized crude polysaccharide was dissolved in human plasma | 10, 30, 50 | In vitro anticoagulant activity | [92] |
Fucus evanescens (Phaeophyceae) | Fucoidans | Human plasma Rat plasma | Intravenous Injection | 125, 250, 500, 1000 | In vitro and in vivo anticoagulant activity | [93] |
Sargassum fulvellum (Phaeophyceae) | Phlorotannins, grasshopper ketone, fucoidan and polysaccharides | Mice | Oral administration | Based on weight of mice | Antioxidant, anticancer, anti-inflammatory, antibacterial, and anticoagulant activities | [153] |
Gracilaria edulis (Rhodophyceae) | Phenolic, Flavonoid and Alkaloid compounds | Bovine serum albumin (protein) | The extracts were tested on the protein | 20, 40, 60, 80, 100, 120 | Hypoglycaemic activity | [98] |
Ulva rigida (Chlorophyceae) | Ethanolic extract | Twenty-four male Wistar rats | Oral administration | 500 mL of water with extracts in 2% wt/vol as drinking water for exposed groups per each day (from 3 to 30 days). | In vivo anti-hyperglycaemic, antioxidative and genotoxic/antigenotoxic activities | [108] |
Griffithsia sp. (Rhodophyceae) | Griffithsin (protein) | MERS-CoV and SARS-CoV glycoproteins | The extracts were tested on the proteins | 0.125, 0.25, 0.5, 1, 2 | Antiviral activity against MERS-CoV virus and SARS-CoV glycoprotein | [100] |
Saccharina japonica (Phaeophyceae) | polysaccharides | SARS-CoV-2 S-protein | The extracts were tested on the protein | 50–500 | In vitro inhibition to SARS-CoV-2 | [164] |
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Lomartire, S.; Marques, J.C.; Gonçalves, A.M.M. An Overview to the Health Benefits of Seaweeds Consumption. Mar. Drugs 2021, 19, 341. https://doi.org/10.3390/md19060341
Lomartire S, Marques JC, Gonçalves AMM. An Overview to the Health Benefits of Seaweeds Consumption. Marine Drugs. 2021; 19(6):341. https://doi.org/10.3390/md19060341
Chicago/Turabian StyleLomartire, Silvia, João Carlos Marques, and Ana M. M. Gonçalves. 2021. "An Overview to the Health Benefits of Seaweeds Consumption" Marine Drugs 19, no. 6: 341. https://doi.org/10.3390/md19060341
APA StyleLomartire, S., Marques, J. C., & Gonçalves, A. M. M. (2021). An Overview to the Health Benefits of Seaweeds Consumption. Marine Drugs, 19(6), 341. https://doi.org/10.3390/md19060341