Obesity, characterized by chronic low-grade inflammation, promotes cardiac structural and functional abnormalities. This study evaluated the therapeutic potential of lycopene in attenuating obesity-induced cardiac remodeling, based on its antioxidant and anti-inflammatory properties and its ability to inhibit matrix metalloproteinase-2 (MMP-2) activation, thereby preserving myocardial collagen integrity. Male Wistar rats were fed a high-sugar, high-fat (HSF) diet to induce obesity and cardiac remodeling. After the onset of cardiac dysfunction, animals received lycopene supplementation (10 mg/kg/day) for 10 weeks. The HSF diet caused metabolic disturbances, including hypertension, increased adiposity, and insulin resistance, accompanied by myocardial remodeling, inflammation, and elevated MMP-2 activity. Lycopene supplementation reversed insulin resistance, mitigated myocardial remodeling, and improved both systolic and diastolic cardiac function. It also reduced inflammatory markers (TNF-α, IL-6, NF-κB, TLR-4), decreased MMP-2 activation, and enhanced TIMP-2 and type I collagen expression. Lycopene demonstrated cardioprotective and anti-inflammatory effects in obesity-induced cardiac remodeling. By targeting inflammation and extracellular matrix degradation, lycopene may serve as an effective adjunctive therapeutic approach for preventing or treating obesity-related cardiac disorders.
Lycopene's Role in Mitigating Obesity-Induced Cardiac Remodeling: Insights Into Inflammatory and MMP-2 Pathways.
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作者:de Silva Carol Cristina Vagula de Almeida, Ferron Artur Junio Togneri, Francisqueti-Ferron Fabiane Valentini, da Silva Alexandre Ribeiro, Bazan Silmeia Garcia Zanati, Garcia Jéssica Leite, de Campos Dijon Henrique Salomé, Costa Mariane Róvero, Dantas Daniele, da Silva Heloysa Amaral, das Chagas Silva Janaina Paixão, de Lopes Giselle Pinto Faria, Polegato Bertha Furlan, Correa Camila Renata, Moreto Fernando, Ferreira Ana Lucia Anjos
| 期刊: | Molecular Nutrition & Food Research | 影响因子: | 4.200 |
| 时间: | 2026 | 起止号: | 2026 Jan;70(2):e70395 |
| doi: | 10.1002/mnfr.70395 | ||
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