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In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida

One of the main bioactive compounds of interest from the Ulva species is the sulfated polysaccharide ulvan, which has recently attracted attention for its anticancer properties. This study investigated the cytotoxic activity of ulvan polysaccharides obtained from Ulva rigida in the following scenari...

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Autores principales: García-Márquez, Jorge, Moreira, Bruna Rodrigues, Valverde-Guillén, Piedad, Latorre-Redoli, Sofía, Caneda-Santiago, Candela T., Acién, Gabriel, Martínez-Manzanares, Eduardo, Marí-Beffa, Manuel, Abdala-Díaz, Roberto T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222840/
https://www.ncbi.nlm.nih.gov/pubmed/37242444
http://dx.doi.org/10.3390/ph16050660
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author García-Márquez, Jorge
Moreira, Bruna Rodrigues
Valverde-Guillén, Piedad
Latorre-Redoli, Sofía
Caneda-Santiago, Candela T.
Acién, Gabriel
Martínez-Manzanares, Eduardo
Marí-Beffa, Manuel
Abdala-Díaz, Roberto T.
author_facet García-Márquez, Jorge
Moreira, Bruna Rodrigues
Valverde-Guillén, Piedad
Latorre-Redoli, Sofía
Caneda-Santiago, Candela T.
Acién, Gabriel
Martínez-Manzanares, Eduardo
Marí-Beffa, Manuel
Abdala-Díaz, Roberto T.
author_sort García-Márquez, Jorge
collection PubMed
description One of the main bioactive compounds of interest from the Ulva species is the sulfated polysaccharide ulvan, which has recently attracted attention for its anticancer properties. This study investigated the cytotoxic activity of ulvan polysaccharides obtained from Ulva rigida in the following scenarios: (i) in vitro against healthy and carcinogenic cell lines (1064sk (human fibroblasts), HACAT (immortalized human keratinocytes), U-937 (a human leukemia cell line), G-361 (a human malignant melanoma), and HCT-116 (a colon cancer cell line)) and (ii) in vivo against zebrafish embryos. Ulvan exhibited cytotoxic effects on the three human cancer cell lines tested. However, only HCT-116 demonstrated sufficient sensitivity to this ulvan to make it relevant as a potential anticancer treatment, presenting an LC(50) of 0.1 mg mL(−1). The in vivo assay on the zebrafish embryos showed a linear relationship between the polysaccharide concentration and growth retardation at 7.8 hpf mL mg(−1), with an LC(50) of about 5.2 mg mL(−1) at 48 hpf. At concentrations near the LC(50), toxic effects, such as pericardial edema or chorion lysis, could be found in the experimental larvae. Our in vitro study supports the potential use of polysaccharides extracted from U. rigida as candidates for treating human colon cancer. However, the in vivo assay on zebrafish indicated that the potential use of ulvan as a promising, safe compound should be limited to specific concentrations below 0.001 mg mL(−1) since it revealed side effects on the embryonic growth rate and osmolar balance.
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spelling pubmed-102228402023-05-28 In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida García-Márquez, Jorge Moreira, Bruna Rodrigues Valverde-Guillén, Piedad Latorre-Redoli, Sofía Caneda-Santiago, Candela T. Acién, Gabriel Martínez-Manzanares, Eduardo Marí-Beffa, Manuel Abdala-Díaz, Roberto T. Pharmaceuticals (Basel) Article One of the main bioactive compounds of interest from the Ulva species is the sulfated polysaccharide ulvan, which has recently attracted attention for its anticancer properties. This study investigated the cytotoxic activity of ulvan polysaccharides obtained from Ulva rigida in the following scenarios: (i) in vitro against healthy and carcinogenic cell lines (1064sk (human fibroblasts), HACAT (immortalized human keratinocytes), U-937 (a human leukemia cell line), G-361 (a human malignant melanoma), and HCT-116 (a colon cancer cell line)) and (ii) in vivo against zebrafish embryos. Ulvan exhibited cytotoxic effects on the three human cancer cell lines tested. However, only HCT-116 demonstrated sufficient sensitivity to this ulvan to make it relevant as a potential anticancer treatment, presenting an LC(50) of 0.1 mg mL(−1). The in vivo assay on the zebrafish embryos showed a linear relationship between the polysaccharide concentration and growth retardation at 7.8 hpf mL mg(−1), with an LC(50) of about 5.2 mg mL(−1) at 48 hpf. At concentrations near the LC(50), toxic effects, such as pericardial edema or chorion lysis, could be found in the experimental larvae. Our in vitro study supports the potential use of polysaccharides extracted from U. rigida as candidates for treating human colon cancer. However, the in vivo assay on zebrafish indicated that the potential use of ulvan as a promising, safe compound should be limited to specific concentrations below 0.001 mg mL(−1) since it revealed side effects on the embryonic growth rate and osmolar balance. MDPI 2023-04-28 /pmc/articles/PMC10222840/ /pubmed/37242444 http://dx.doi.org/10.3390/ph16050660 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
García-Márquez, Jorge
Moreira, Bruna Rodrigues
Valverde-Guillén, Piedad
Latorre-Redoli, Sofía
Caneda-Santiago, Candela T.
Acién, Gabriel
Martínez-Manzanares, Eduardo
Marí-Beffa, Manuel
Abdala-Díaz, Roberto T.
In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida
title In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida
title_full In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida
title_fullStr In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida
title_full_unstemmed In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida
title_short In Vitro and In Vivo Effects of Ulvan Polysaccharides from Ulva rigida
title_sort in vitro and in vivo effects of ulvan polysaccharides from ulva rigida
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222840/
https://www.ncbi.nlm.nih.gov/pubmed/37242444
http://dx.doi.org/10.3390/ph16050660
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