Efficacy of AdipoDren® in Reducing Interleukin-1-Induced Lymphatic Endothelial Hyperpermeability
Identifieur interne : 001125 ( Main/Exploration ); précédent : 001124; suivant : 001126Efficacy of AdipoDren® in Reducing Interleukin-1-Induced Lymphatic Endothelial Hyperpermeability
Auteurs : Valerio Ciccone [Italie] ; Martina Monti [Italie] ; Giulia Antonini [Italie] ; Luisa Mattoli [Italie] ; Michela Burico [Italie] ; Francesca Marini [Italie] ; Anna Maidecchi [Italie] ; Lucia Morbidelli [Italie]Source :
- Journal of Vascular Research [ 1018-1172 ] ; 2016.
Descripteurs français
- KwdFr :
- Catalase (métabolisme), Cellules cultivées, Cellules endothéliales (), Cellules endothéliales (métabolisme), Cyclooxygenase 2 (métabolisme), Endothélium lymphatique (), Endothélium lymphatique (métabolisme), Endothélium lymphatique (physiopathologie), Endothélium vasculaire (), Endothélium vasculaire (métabolisme), Extraits de plantes (pharmacologie), Humains, Interleukine-1 bêta (pharmacologie), Jonctions serrées (), Jonctions serrées (métabolisme), Lymphoedème (métabolisme), Lymphoedème (physiopathologie), Lymphoedème (traitement médicamenteux), NADPH oxidase (métabolisme), Occludine (métabolisme), Perméabilité capillaire (), Protéine-1 de la zonula occludens (métabolisme), Préparations à base de plantes (pharmacologie), Relation dose-effet des médicaments, Rutoside (pharmacologie), Superoxide dismutase-1 (métabolisme), Survie cellulaire ().
- MESH :
- métabolisme : Catalase, Cellules endothéliales, Cyclooxygenase 2, Endothélium lymphatique, Endothélium vasculaire, Jonctions serrées, Lymphoedème, NADPH oxidase, Occludine, Protéine-1 de la zonula occludens, Superoxide dismutase-1.
- pharmacologie : Extraits de plantes, Interleukine-1 bêta, Préparations à base de plantes, Rutoside.
- physiopathologie : Endothélium lymphatique, Lymphoedème.
- traitement médicamenteux : Lymphoedème.
- Cellules cultivées, Cellules endothéliales, Endothélium lymphatique, Endothélium vasculaire, Humains, Jonctions serrées, Perméabilité capillaire, Relation dose-effet des médicaments, Survie cellulaire.
English descriptors
- KwdEn :
- Capillary Permeability (drug effects), Catalase (metabolism), Cell Survival (drug effects), Cells, Cultured, Cyclooxygenase 2 (metabolism), Dose-Response Relationship, Drug, Endothelial Cells (drug effects), Endothelial Cells (metabolism), Endothelium, Lymphatic (drug effects), Endothelium, Lymphatic (metabolism), Endothelium, Lymphatic (physiopathology), Endothelium, Vascular (drug effects), Endothelium, Vascular (metabolism), Humans, Interleukin-1beta (pharmacology), Lymphedema (drug therapy), Lymphedema (metabolism), Lymphedema (physiopathology), NADPH Oxidase (metabolism), Occludin (metabolism), Plant Extracts (pharmacology), Plant Preparations (pharmacology), Rutin (pharmacology), Superoxide Dismutase-1 (metabolism), Tight Junctions (drug effects), Tight Junctions (metabolism), Zonula Occludens-1 Protein (metabolism).
- MESH :
- chemical , metabolism : Catalase, Cyclooxygenase 2, NADPH Oxidase, Occludin, Superoxide Dismutase-1, Zonula Occludens-1 Protein.
- drug effects : Capillary Permeability, Cell Survival, Endothelial Cells, Endothelium, Lymphatic, Endothelium, Vascular, Tight Junctions.
- drug therapy : Lymphedema.
- metabolism : Endothelial Cells, Endothelium, Lymphatic, Endothelium, Vascular, Lymphedema, Tight Junctions.
- chemical , pharmacology : Interleukin-1beta, Plant Extracts, Plant Preparations, Rutin.
- physiopathology : Endothelium, Lymphatic, Lymphedema.
- Cells, Cultured, Dose-Response Relationship, Drug, Humans.
Abstract
Lymphatic leakage can be seen as a detrimental phenomenon associated with fluid retention and deposition as well as gain of weight. Moreover, lymphatic dysfunction is associated with an inflammatory environment and can be a substrate for other health conditions. A number of treatments can ameliorate lymphatic vasculature: natural substances have been used as treatment options particularly suitable for their consolidated effectiveness and safety profile. Here we report the protective effect of AdipoDren®, an association of a series of plant-derived natural complexes, on lymphatic endothelium permeability promoted by interleukin-1 beta (IL-1β) and the associated molecular mechanisms. AdipoDren® demonstrated a protective effect on dermal lymphatic endothelial cell permeability increased by IL-1β. Reduced permeability was due to the maintenance of tight junctions and cell-cell localisation of occludin and zonula occludens-1 (ZO-1). Moreover, AdipoDren® reduced the expression of the inflammatory key element cyclooxygenase-2 (COX-2), while not altering the levels of endothelial and inducible nitric oxide synthases (eNOS and iNOS). The upregulation of antioxidant enzymatic systems (catalase and superoxide dismutase-1, SOD-1) and the downregulation of pro-oxidant markers (p22 phox subunit of NADPH oxidase) were also evident. In conclusion, AdipoDren® would be useful to ameliorate conditions of altered lymphatic vasculature and to support the physiological functionality of the lymphatic endothelium.
Url:
DOI: 10.1159/000452798
PubMed: 27923233
PubMed Central: 5348734
Affiliations:
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Le document en format XML
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<term>Catalase (metabolism)</term>
<term>Cell Survival (drug effects)</term>
<term>Cells, Cultured</term>
<term>Cyclooxygenase 2 (metabolism)</term>
<term>Dose-Response Relationship, Drug</term>
<term>Endothelial Cells (drug effects)</term>
<term>Endothelial Cells (metabolism)</term>
<term>Endothelium, Lymphatic (drug effects)</term>
<term>Endothelium, Lymphatic (metabolism)</term>
<term>Endothelium, Lymphatic (physiopathology)</term>
<term>Endothelium, Vascular (drug effects)</term>
<term>Endothelium, Vascular (metabolism)</term>
<term>Humans</term>
<term>Interleukin-1beta (pharmacology)</term>
<term>Lymphedema (drug therapy)</term>
<term>Lymphedema (metabolism)</term>
<term>Lymphedema (physiopathology)</term>
<term>NADPH Oxidase (metabolism)</term>
<term>Occludin (metabolism)</term>
<term>Plant Extracts (pharmacology)</term>
<term>Plant Preparations (pharmacology)</term>
<term>Rutin (pharmacology)</term>
<term>Superoxide Dismutase-1 (metabolism)</term>
<term>Tight Junctions (drug effects)</term>
<term>Tight Junctions (metabolism)</term>
<term>Zonula Occludens-1 Protein (metabolism)</term>
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<term>Cellules cultivées</term>
<term>Cellules endothéliales ()</term>
<term>Cellules endothéliales (métabolisme)</term>
<term>Cyclooxygenase 2 (métabolisme)</term>
<term>Endothélium lymphatique ()</term>
<term>Endothélium lymphatique (métabolisme)</term>
<term>Endothélium lymphatique (physiopathologie)</term>
<term>Endothélium vasculaire ()</term>
<term>Endothélium vasculaire (métabolisme)</term>
<term>Extraits de plantes (pharmacologie)</term>
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<term>Jonctions serrées ()</term>
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<term>Lymphoedème (métabolisme)</term>
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<term>Préparations à base de plantes (pharmacologie)</term>
<term>Relation dose-effet des médicaments</term>
<term>Rutoside (pharmacologie)</term>
<term>Superoxide dismutase-1 (métabolisme)</term>
<term>Survie cellulaire ()</term>
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<term>Cyclooxygenase 2</term>
<term>NADPH Oxidase</term>
<term>Occludin</term>
<term>Superoxide Dismutase-1</term>
<term>Zonula Occludens-1 Protein</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Capillary Permeability</term>
<term>Cell Survival</term>
<term>Endothelial Cells</term>
<term>Endothelium, Lymphatic</term>
<term>Endothelium, Vascular</term>
<term>Tight Junctions</term>
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<term>Endothelium, Lymphatic</term>
<term>Endothelium, Vascular</term>
<term>Lymphedema</term>
<term>Tight Junctions</term>
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<term>Cellules endothéliales</term>
<term>Cyclooxygenase 2</term>
<term>Endothélium lymphatique</term>
<term>Endothélium vasculaire</term>
<term>Jonctions serrées</term>
<term>Lymphoedème</term>
<term>NADPH oxidase</term>
<term>Occludine</term>
<term>Protéine-1 de la zonula occludens</term>
<term>Superoxide dismutase-1</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Extraits de plantes</term>
<term>Interleukine-1 bêta</term>
<term>Préparations à base de plantes</term>
<term>Rutoside</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Interleukin-1beta</term>
<term>Plant Extracts</term>
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<term>Rutin</term>
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<keywords scheme="MESH" qualifier="physiopathologie" xml:lang="fr"><term>Endothélium lymphatique</term>
<term>Lymphoedème</term>
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<term>Humains</term>
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<term>Perméabilité capillaire</term>
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<front><div type="abstract" xml:lang="en"><p>Lymphatic leakage can be seen as a detrimental phenomenon associated with fluid retention and deposition as well as gain of weight. Moreover, lymphatic dysfunction is associated with an inflammatory environment and can be a substrate for other health conditions. A number of treatments can ameliorate lymphatic vasculature: natural substances have been used as treatment options particularly suitable for their consolidated effectiveness and safety profile. Here we report the protective effect of AdipoDren®, an association of a series of plant-derived natural complexes, on lymphatic endothelium permeability promoted by interleukin-1 beta (IL-1β) and the associated molecular mechanisms. AdipoDren® demonstrated a protective effect on dermal lymphatic endothelial cell permeability increased by IL-1β. Reduced permeability was due to the maintenance of tight junctions and cell-cell localisation of occludin and zonula occludens-1 (ZO-1). Moreover, AdipoDren® reduced the expression of the inflammatory key element cyclooxygenase-2 (COX-2), while not altering the levels of endothelial and inducible nitric oxide synthases (eNOS and iNOS). The upregulation of antioxidant enzymatic systems (catalase and superoxide dismutase-1, SOD-1) and the downregulation of pro-oxidant markers (p22 phox subunit of NADPH oxidase) were also evident. In conclusion, AdipoDren® would be useful to ameliorate conditions of altered lymphatic vasculature and to support the physiological functionality of the lymphatic endothelium.</p>
</div>
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<name sortKey="Mattoli, Luisa" sort="Mattoli, Luisa" uniqKey="Mattoli L" first="Luisa" last="Mattoli">Luisa Mattoli</name>
<name sortKey="Monti, Martina" sort="Monti, Martina" uniqKey="Monti M" first="Martina" last="Monti">Martina Monti</name>
<name sortKey="Morbidelli, Lucia" sort="Morbidelli, Lucia" uniqKey="Morbidelli L" first="Lucia" last="Morbidelli">Lucia Morbidelli</name>
</country>
</tree>
</affiliations>
</record>
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