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Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model

At present, there is a growing interest in finding new non-toxic anti-inflammatory drugs to treat inflammation, which is a key pathology in the development of several diseases with considerable mortality. Sulforaphane (SFN), a bioactive compound derived from Brassica plants, was shown to be promisin...

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Autores principales: Yepes-Molina, Lucía, Pérez-Jiménez, María Isabel, Martínez-Esparza, María, Teruel, José A., Ruiz-Alcaraz, Antonio J., García-Peñarrubia, Pilar, Carvajal, Micaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878270/
https://www.ncbi.nlm.nih.gov/pubmed/35216054
http://dx.doi.org/10.3390/ijms23041940
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author Yepes-Molina, Lucía
Pérez-Jiménez, María Isabel
Martínez-Esparza, María
Teruel, José A.
Ruiz-Alcaraz, Antonio J.
García-Peñarrubia, Pilar
Carvajal, Micaela
author_facet Yepes-Molina, Lucía
Pérez-Jiménez, María Isabel
Martínez-Esparza, María
Teruel, José A.
Ruiz-Alcaraz, Antonio J.
García-Peñarrubia, Pilar
Carvajal, Micaela
author_sort Yepes-Molina, Lucía
collection PubMed
description At present, there is a growing interest in finding new non-toxic anti-inflammatory drugs to treat inflammation, which is a key pathology in the development of several diseases with considerable mortality. Sulforaphane (SFN), a bioactive compound derived from Brassica plants, was shown to be promising due to its anti-inflammatory properties and great potential, though its actual clinical use is limited due to its poor stability and bioavailability. In this sense, the use of nanocarriers could solve stability-related problems. In the current study, sulforaphane loaded into membrane vesicles derived from broccoli plants was studied to determine the anti-inflammatory potential in a human-macrophage-like in vitro cell model under both normal and inflammatory conditions. On the one hand, the release of SFN from membrane vesicles was modeled in vitro, and two release phases were stabilized, one faster and the other slower due to the interaction between SFN and membrane proteins, such as aquaporins. Furthermore, the anti-inflammatory action of sulforaphane-loaded membrane vesicles was demonstrated, as a decrease in interleukins crucial for the development of inflammation, such as TNF-α, IL-1β and IL-6, was observed. Furthermore, these results also showed that membrane vesicles by themselves had anti-inflammatory properties, opening the possibility of new lines of research to study these vesicles, not only as carriers but also as active compounds.
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spelling pubmed-88782702022-02-26 Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model Yepes-Molina, Lucía Pérez-Jiménez, María Isabel Martínez-Esparza, María Teruel, José A. Ruiz-Alcaraz, Antonio J. García-Peñarrubia, Pilar Carvajal, Micaela Int J Mol Sci Article At present, there is a growing interest in finding new non-toxic anti-inflammatory drugs to treat inflammation, which is a key pathology in the development of several diseases with considerable mortality. Sulforaphane (SFN), a bioactive compound derived from Brassica plants, was shown to be promising due to its anti-inflammatory properties and great potential, though its actual clinical use is limited due to its poor stability and bioavailability. In this sense, the use of nanocarriers could solve stability-related problems. In the current study, sulforaphane loaded into membrane vesicles derived from broccoli plants was studied to determine the anti-inflammatory potential in a human-macrophage-like in vitro cell model under both normal and inflammatory conditions. On the one hand, the release of SFN from membrane vesicles was modeled in vitro, and two release phases were stabilized, one faster and the other slower due to the interaction between SFN and membrane proteins, such as aquaporins. Furthermore, the anti-inflammatory action of sulforaphane-loaded membrane vesicles was demonstrated, as a decrease in interleukins crucial for the development of inflammation, such as TNF-α, IL-1β and IL-6, was observed. Furthermore, these results also showed that membrane vesicles by themselves had anti-inflammatory properties, opening the possibility of new lines of research to study these vesicles, not only as carriers but also as active compounds. MDPI 2022-02-09 /pmc/articles/PMC8878270/ /pubmed/35216054 http://dx.doi.org/10.3390/ijms23041940 Text en © 2022 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
Yepes-Molina, Lucía
Pérez-Jiménez, María Isabel
Martínez-Esparza, María
Teruel, José A.
Ruiz-Alcaraz, Antonio J.
García-Peñarrubia, Pilar
Carvajal, Micaela
Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
title Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
title_full Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
title_fullStr Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
title_full_unstemmed Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
title_short Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
title_sort membrane vesicles for nanoencapsulated sulforaphane increased their anti-inflammatory role on an in vitro human macrophage model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878270/
https://www.ncbi.nlm.nih.gov/pubmed/35216054
http://dx.doi.org/10.3390/ijms23041940
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