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Effect of Telmisartan in the Oxidative Stress Components Induced by Ischemia Reperfusion in Rats

The therapeutic effects of telmisartan, an angiotensin II receptor antagonist and a peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist, have been demonstrated in several disorders. It has antioxidant and immune response modulator properties and has shown promising results in the treatment...

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Detalles Bibliográficos
Autores principales: Rodríguez-Lara, Simón Quetzalcoatl, Trujillo-Rangel, Walter Angel, Castillo-Romero, Araceli, Totsuka-Sutto, Sylvia Elena, Garcia-Cobián, Teresa Arcelia, Cardona-Muñoz, Ernesto German, Miranda-Díaz, Alejandra Guillermina, Ramírez-Lizardo, Ernesto Javier, García-Benavides, Leonel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636510/
https://www.ncbi.nlm.nih.gov/pubmed/31354899
http://dx.doi.org/10.1155/2019/1302985
Descripción
Sumario:The therapeutic effects of telmisartan, an angiotensin II receptor antagonist and a peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist, have been demonstrated in several disorders. It has antioxidant and immune response modulator properties and has shown promising results in the treatment of an ischemia/reperfusion (I/R) lesion. In this study, a skeletal muscle (right gastrocnemius muscle) I/R lesion was induced in rats and different reperfusion times (1 h, 24 h, 72 h, 7-day, and 14-day subgroups) were assessed. Furthermore, levels of oxidative markers such as enzymatic scavengers (catalase (CAT) and superoxide dismutase (SOD)) and metabolites (nitrates and 8-oxo-deoxyguanosine) were determined. The degree of tissue injury (total lesioned fibers and inflammatory cell count) was also evaluated. We observed an increase in CAT and SOD expression levels under telmisartan treatment, with a decrease in injury and oxidative biomarker levels in the 72 h, 7-day, and 14-day subgroups. Telmisartan reduced oxidative stress and decreased the damage of the I/R lesion.