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

Author:

Rodrigues Albuquerque Edilson1ORCID,Ratti da Silva Gustavo1ORCID,de Abreu Braga Fernanda2ORCID,Pelegrini Silva Ester2ORCID,Sposito Negrini Karina2ORCID,Rodrigues Fracasso Julia Amanda3ORCID,Pires Guarnier Lucas4ORCID,Jacomassi Ezilda5ORCID,Ribeiro-Paes João Tadeu6ORCID,da Silva Gomes Roberto7ORCID,Gasparotto Junior Arquimedes8ORCID,Lívero Francislaine Aparecida dos Reis29ORCID

Affiliation:

1. Laboratory of Preclinical Research of Natural Products, Post Graduate Program in Animal Science with Emphasis on Bioactive Products, Universidade Paranaense, Umuarama, Brazil

2. Laboratory of Preclinical Research of Natural Products, Paranaense University, Umuarama, Brazil

3. School of Dentistry, São Paulo State University, Araçatuba, Brazil

4. Department of Genetic, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil

5. Laboratory of Preclinical Research of Natural Products, Post Graduate Program in Medicinal Plants and Phytotherapeutics in Basic Attention, Paranaense University, Umuarama, Brazil

6. Department of Biotechnology, São Paulo State University, Assis, São Paulo, Brazil

7. Department of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, USA

8. Laboratory of Cardiovascular Pharmacology, Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Brazil

9. Laboratory of Cardiometabolic Pharmacology, Federal University of Paraná, Curitiba, Brazil

Abstract

Metabolic-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. Pereskia grandifolia has shown potential as an alternative treatment, but its effectiveness against liver disease remains unexplored. This research aims to determine the hepatoprotective properties of P. grandifolia 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 P. grandifolia. Initially, an in vitro 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 P. grandifolia 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-), P. grandifolia (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. P. grandifolia 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, P. grandifolia effectively reversed these changes, highlighting its potential as a therapeutic agent. These findings emphasize the significance of P. grandifolia in mitigating hepatic consequences associated with various risk factors.

Funder

Coordenadoria de Pós-Graduação

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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