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Bridging the Gap: Exploring the Preclinical Potential of Pereskia grandifolia in Metabolic‐Associated Fatty Liver Disease

dc.contributor.authorAlbuquerque, Edilson Rodrigues
dc.contributor.authorda Silva, Gustavo Ratti
dc.contributor.authorde Abreu Braga, Fernanda
dc.contributor.authorSilva, Ester Pelegrini
dc.contributor.authorNegrini, Karina Sposito
dc.contributor.authorFracasso, Julia Amanda Rodrigues [UNESP]
dc.contributor.authorGuarnier, Lucas Pires
dc.contributor.authorJacomassi, Ezilda
dc.contributor.authorRibeiro-Paes, João Tadeu [UNESP]
dc.contributor.authorda Silva Gomes, Roberto
dc.contributor.authorGasparotto, Arquimedes
dc.contributor.authordos Reis Lívero, Francislaine Aparecida
dc.contributor.editorBashar Saad
dc.date.accessioned2026-04-16T20:54:05Z
dc.date.issued2023-01-01
dc.description.abstractMetabolic-associated fatty liver disease (MAFLD) is a complex condition characterized by steatosis and metabolic disturbances. Risk factors such as diabetes, cigarette smoking, and dyslipidaemia contribute to its development and progression. Effective and safe therapies for MAFLD are urgently needed. <i>Pereskia grandifolia</i> has shown potential as an alternative treatment, but its effectiveness against liver disease remains unexplored. This research aims to determine the hepatoprotective properties of <i>P. grandifolia</i> using a model of MAFLD. The study was carried out through various phases to assess the safety and efficacy of the ethanol-soluble fraction of <i>P. grandifolia</i>. Initially, an <i>in vitro</i> assay was performed to assess cell viability. This was followed by an acute toxicity test conducted in rats to determine the safety profile of the extract. Subsequently, the anti-inflammatory properties of <i>P. grandifolia</i> were examined in macrophages. For the MAFLD study, diabetic Wistar rats were made diabetic and exposed to a high fat diet and cigarette smoke, for 4 weeks. During the last 2 weeks, the rats were orally given either the vehicle (negative control group; C-), <i>P. grandifolia</i> (30, 100, and 300 mg/kg), or insulin in addition to simvastatin. A basal group of rats not exposed to these risk factors was also assessed. Blood samples were collected to measure cholesterol, triglycerides, glucose, ALT, and AST levels. Liver was assessed for lipid and oxidative markers, and liver histopathology was examined. <i>P. grandifolia</i> showed no signs of toxicity. It demonstrated anti-inflammatory effects by inhibiting phagocytosis and macrophage spreading. The MAFLD model induced liver abnormalities, including increased AST, ALT, disrupted lipid profile, oxidative stress, and significant hepatic damage. However, <i>P. grandifolia</i> effectively reversed these changes, highlighting its potential as a therapeutic agent. These findings emphasize the significance of <i>P. grandifolia</i> in mitigating hepatic consequences associated with various risk factors.
dc.description.affiliationLaboratory of Preclinical Research of Natural Products, Post Graduate Program in Animal Science with Emphasis on Bioactive Products, Universidade Paranaense, Umuarama, Brazil unipar.br
dc.description.affiliationLaboratory of Preclinical Research of Natural Products, Paranaense University, Umuarama, Brazil unipar.br
dc.description.affiliationSchool of Dentistry, São Paulo State University, Araçatuba, Brazil unesp.br
dc.description.affiliationDepartment of Genetic, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil usp.br
dc.description.affiliationLaboratory of Preclinical Research of Natural Products, Post Graduate Program in Medicinal Plants and Phytotherapeutics in Basic Attention, Paranaense University, Umuarama, Brazil unipar.br
dc.description.affiliationDepartment of Biotechnology, São Paulo State University, Assis, São Paulo, Brazil unesp.br
dc.description.affiliationDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, USA ndsu.edu
dc.description.affiliationLaboratory of Cardiovascular Pharmacology, Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Brazil ufgd.edu.br
dc.description.affiliationLaboratory of Cardiometabolic Pharmacology, Federal University of Paraná, Curitiba, Brazil ufpr.br
dc.description.affiliationUnespSchool of Dentistry, São Paulo State University, Araçatuba, Brazil unesp.br
dc.description.affiliationUnespDepartment of Biotechnology, São Paulo State University, Assis, São Paulo, Brazil unesp.br
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1165817254
dc.identifier.dimensionspub.1165817254
dc.identifier.doi10.1155/2023/8840427
dc.identifier.issn1741-427X
dc.identifier.issn1741-4288
dc.identifier.orcid0000-0001-5773-9912
dc.identifier.orcid0000-0001-7224-8898
dc.identifier.orcid0000-0002-7294-7469
dc.identifier.orcid0000-0003-3553-534X
dc.identifier.orcid0000-0002-0733-1975
dc.identifier.orcid0000-0003-0967-8427
dc.identifier.orcid0000-0002-7645-5891
dc.identifier.orcid0000-0002-8075-9716
dc.identifier.orcid0000-0003-3433-5098
dc.identifier.pmcidPMC10653969
dc.identifier.pmid38026733
dc.identifier.urihttps://hdl.handle.net/11449/322110
dc.publisherWiley
dc.relation.ispartofEvidence-based Complementary and Alternative Medicine; n. 1; v. 2023; p. 8840427
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleBridging the Gap: Exploring the Preclinical Potential of Pereskia grandifolia in Metabolic‐Associated Fatty Liver Disease
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublicationc3f68528-5ea8-4b32-a9f4-3cfbd4bba64d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências e Letras, Assis

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