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Cardiovasc Toxicol ; 22(1): 35-51, 2022 01.
Artículo en Inglés | MEDLINE | ID: mdl-34655413

RESUMEN

The beneficial effect of curcumin (CU) on dietary AGEs (dAGEs) involves blocking the overexpression of proinflammatory cytokine genes in the heart and kidney tissues of experimental mice. The animals were divided into six groups (n = 6/group) and were fed a heat-exposed diet (dAGEs) with or without CU for 6 months. Their blood pressure (BP) was monitored by a computerized tail-cuff BP-monitoring system. The mRNA and protein expression levels of proinflammatory genes were analyzed by RT-PCR and western blot, respectively. A marked increase in BP (108 ± 12 mmHg vs 149 ± 15 mmHg) accompanied by a marked increase in the heart and kidney weight ratio was noted in the dAGE-fed mice. Furthermore, the plasma levels of proinflammatory molecules (C5a, ICAM-1, IL-6, MCP-1, IL-1ß and TNF-α) were found to be elevated (3-fold) in dAGE-fed mice. mRNA expression analysis revealed a significant increase in the expression levels of inflammatory markers (Cox-2, iNOS, and NF-κB) (3-fold) in cardiac and renal tissues of dAGE-fed mice. Moreover, increased expression of RAGE and downregulation of AGER-1 (p < 0.001) were noticed in the heart and kidney tissues of dAGE-fed mice. Interestingly, the dAGE-induced proinflammatory genes and inflammatory responses were neutralized upon cotreatment with CU. The present study demonstrates that dietary supplementation with CU has the ability to neutralize dAGE-induced adverse effects and alleviate proinflammatory gene expression in the heart and kidney tissues of experimental mice.


Asunto(s)
Antiinflamatorios/farmacología , Curcumina/farmacología , Citocinas/metabolismo , Dieta/efectos adversos , Productos Finales de Glicación Avanzada/toxicidad , Mediadores de Inflamación/metabolismo , Riñón/efectos de los fármacos , Lisina/análogos & derivados , Miocardio/metabolismo , Alimentación Animal , Animales , Colágeno/metabolismo , Citocinas/genética , Regulación de la Expresión Génica , Riñón/inmunología , Riñón/metabolismo , Riñón/patología , Lisina/toxicidad , Masculino , Ratones , Miocardio/inmunología , Miocardio/patología , Receptor para Productos Finales de Glicación Avanzada/genética , Receptor para Productos Finales de Glicación Avanzada/metabolismo
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