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   <dc:title>A synergic GLP-1/Acylethanolamide-based combined therapy for MAFLD: Studies in rat models</dc:title>
   <dc:creator>De Ceglia, Marialuisa</dc:creator>
   <dc:creator>Tovar, Rubén</dc:creator>
   <dc:creator>Rodríguez-Pozo, Miguel</dc:creator>
   <dc:creator>Vargas, Antonio</dc:creator>
   <dc:creator>Gavito, Ana L.</dc:creator>
   <dc:creator>Suárez-Pérez, Juan</dc:creator>
   <dc:creator>Baixeras-Llano, Elena</dc:creator>
   <dc:creator>Rodriguez de Fonseca, Fernando</dc:creator>
   <dc:creator>Decara, Juan</dc:creator>
   <dc:subject>Obesidad</dc:subject>
   <dc:subject>Receptores de hormonas</dc:subject>
   <dc:subject>Metabolismo</dc:subject>
   <dc:subject>Hígado -- Enfermedades</dc:subject>
   <dcterms:abstract>Obesity remains a major epidemic in developed countries, with metabolic-associated fatty liver disease (MAFLD)&#xd;
as one of its main hepatic consequences. Pharmacological treatments for MAFLD are limited, but modulation of&#xd;
glucagon-like peptide-1 (GLP-1) or acylethanolamide signalling offers promising therapeutic potential, while&#xd;
exerting anti-obesity effects. This study evaluated the effects of a combined therapy using a dual ligand targeting&#xd;
peroxisome proliferator-activated receptor alpha (PPARα) and peripheral cannabinoid receptor 1 (CB1) (OLHHA,&#xd;
acting as a PPARα agonist and CB1 antagonist) in combination with the GLP-1 receptor agonist liraglutide. Our&#xd;
aim was to assess their potential as a multitarget therapy to ameliorate liver dysfunction in an obesity animal&#xd;
model. In Wistar rats, we evaluated the effects of administering 3 mg/kg OLHHA and 25 µg/kg liraglutide, both&#xd;
acutely and chronically (daily for 42 days), in the context of exposure to a high-fat/high-fructose diet. Although&#xd;
both OLHHA and liraglutide individually ameliorated certain hepatic alterations induced by MAFLD, our findings&#xd;
demonstrate that their combined administration was significantly more effective in promoting body weight loss,&#xd;
improving lipid profiles and transaminase levels, and exerting robust antisteatotic effects in obese rats. This&#xd;
enhanced efficacy was evidenced by a marked reduction in hepatic fat content, downregulation of lipogenesisrelated enzymes, and upregulation of proteins involved in lipid oxidation. Moreover, OLHHA, either alone or&#xd;
in combination with liraglutide, efficiently restored redox balance disrupted by MAFLD in obese rats.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-28T11:49:29Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-28T11:49:29Z</dcterms:available>
   <dcterms:created>2025-10-28T11:49:29Z</dcterms:created>
   <dcterms:issued>2025</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Ceglia M, Tovar R, Rodríguez-Pozo M, Vargas A, Gavito A, Suárez J, Baixeras E, Rodríguez de Fonseca F, Decara J. A synergic GLP-1/Acylethanolamide-based combined therapy for MAFLD: Studies in rat models. Biochemical Pharmacology. 2025;242(3):117364. https://doi.org/10.1016/j.bcp.2025.117364</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/40477</dc:identifier>
   <dc:identifier>10.1016/j.bcp.2025.117364</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:rights>Atribución 4.0 Internacional</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
</qdc:qualifieddc>
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