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dc.contributor.author
Marques, Patrice
dc.contributor.author
Villarroel Vicente, Carlos
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Collado, Aida
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García, Ainhoa
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Vila, Laura
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Duplan, Isabelle
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Hennuyer, Nathalie
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Garibotto, Francisco Matías
dc.contributor.author
Enriz, Ricardo Daniel
dc.contributor.author
Dacquet, Catherine
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Staels, Bart
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Piqueras, Laura
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Cortes, Diego
dc.contributor.author
Sanz, María Jesús
dc.contributor.author
Cabedo, Nuria
dc.date.available
2023-12-06T14:28:07Z
dc.date.issued
2023-01
dc.identifier.citation
Marques, Patrice; Villarroel Vicente, Carlos; Collado, Aida; García, Ainhoa; Vila, Laura; et al.; Anti-inflammatory effects and improved metabolic derangements in ob/ob mice by a newly synthesized prenylated benzopyran with pan-PPAR activity; Academic Press Ltd - Elsevier Science Ltd; Pharmacological Research; 187; 1-2023; 1-14
dc.identifier.issn
1043-6618
dc.identifier.uri
http://hdl.handle.net/11336/219488
dc.description.abstract
Background and purpose: Selective peroxisome proliferator-activated receptors (PPARs) are widely used to treat metabolic complications; however, the limited effect of PPARα agonists on glucose metabolism and the adverse effects associated with selective PPARγ activators have stimulated the development of novel pan-PPAR agonists to treat metabolic disorders. Here, we synthesized a new prenylated benzopyran (BP-2) and evaluated its PPAR-activating properties, anti-inflammatory effects and impact on metabolic derangements. Experimental approach: BP-2 was used in transactivation assays to evaluate its agonism to PPARα, PPARβ/δ and PPARγ. A parallel-plate flow chamber was employed to investigate its effect on TNFα-induced leukocyte-endothelium interactions. Flow cytometry and immunofluorescence were used to determine its effects on the expression of endothelial cell adhesion molecules (CAMs) and chemokines and p38-MAPK/NF-κB activation. PPARs/RXRα interactions were determined using a gene silencing approach. Analysis of its impact on metabolic abnormalities and inflammation was performed in ob/ob mice. Key results: BP-2 displayed strong PPARα activity, with moderate and weak activity against PPARβ/δ and PPARγ, respectively. In vitro, BP-2 reduced TNFα-induced endothelial ICAM-1, VCAM-1 and fractalkine/CX3CL1 expression, suppressed mononuclear cell arrest via PPARβ/δ-RXRα interactions and decreased p38-MAPK/NF-κB activation. In vivo, BP-2 improved the circulating levels of glucose and triglycerides in ob/ob mice, suppressed T-lymphocyte/macrophage infiltration and proinflammatory markers in the liver and white adipose tissue, but increased the expression of the M2-like macrophage marker CD206. Conclusion and implications: BP-2 emerges as a novel pan-PPAR lead candidate to normalize glycemia/triglyceridemia and minimize inflammation in metabolic disorders, likely preventing the development of further cardiovascular complications.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Academic Press Ltd - Elsevier Science Ltd
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.subject
ANTI-INFLAMMATORY EFFECTS
dc.subject
GW501516 OR ENDUROBOL (PUBCHEM CID: 9803963)
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METABOLIC DISORDERS
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MOLECULAR MODELING
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OB/OB MICE
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PPAR
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PRENYLATED BENZOPYRAN
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ROSIGLITAZONE (PUBCHEM CID: 77999)
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WY-14,643 OR PIRINIXIC ACID (PUBCHEM CID: 5694)
dc.subject.classification
Química Orgánica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Anti-inflammatory effects and improved metabolic derangements in ob/ob mice by a newly synthesized prenylated benzopyran with pan-PPAR activity
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2023-12-05T15:04:18Z
dc.journal.volume
187
dc.journal.pagination
1-14
dc.journal.pais
Estados Unidos
dc.description.fil
Fil: Marques, Patrice. Universidad de Valencia; España
dc.description.fil
Fil: Villarroel Vicente, Carlos. Universidad de Valencia; España
dc.description.fil
Fil: Collado, Aida. Universidad de Valencia; España
dc.description.fil
Fil: García, Ainhoa. Universidad de Valencia; España
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Fil: Vila, Laura. Hospital Clinico Universitario de Valencia; España
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Fil: Duplan, Isabelle. University Of Lille.; Francia
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Fil: Hennuyer, Nathalie. University Of Lille.; Francia
dc.description.fil
Fil: Garibotto, Francisco Matías. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto Multidisciplinario de Investigaciones Biológicas de San Luis. Universidad Nacional de San Luis. Facultad de Ciencias Físico Matemáticas y Naturales. Instituto Multidisciplinario de Investigaciones Biológicas de San Luis; Argentina
dc.description.fil
Fil: Enriz, Ricardo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto Multidisciplinario de Investigaciones Biológicas de San Luis. Universidad Nacional de San Luis. Facultad de Ciencias Físico Matemáticas y Naturales. Instituto Multidisciplinario de Investigaciones Biológicas de San Luis; Argentina
dc.description.fil
Fil: Dacquet, Catherine. No especifíca;
dc.description.fil
Fil: Staels, Bart. University Of Lille.; Francia
dc.description.fil
Fil: Piqueras, Laura. Universidad de Valencia; España
dc.description.fil
Fil: Cortes, Diego. Universidad de Valencia; España
dc.description.fil
Fil: Sanz, María Jesús. Universidad de Valencia; España
dc.description.fil
Fil: Cabedo, Nuria. Universidad de Valencia; España
dc.journal.title
Pharmacological Research
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.phrs.2022.106638
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