Influence of N-acetylcysteine on oxidative stress in slow-twitch soleus muscle of heart failure rats

• Autor(a) principal: Martinez, Paula Felippe [UNESP]
• Data de Publicação: 2015
• Outros Autores: Bonomo, Camila [UNESP], Guizoni, Daniele Mendes [UNESP], Oliveira Junior, Silvio Assis [UNESP], Damatto, Ricardo Luiz [UNESP], Cezar, Marcelo Diarcadia Mariano [UNESP], Lima, Aline Regina Ruiz [UNESP], Pagan, Luana Urbano [UNESP], Seiva, Fabio Rodrigues, Fernandes, Denise Castro, Laurindo, Francisco Rafael Martins, Novelli, Ethel Lourenzi Barbosa [UNESP], Matsubara, Luiz Shiguero [UNESP], Zornoff, Leonardo Antonio Mamede [UNESP], Okoshi, Katashi [UNESP], Okoshi, Marina Politi [UNESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://www.karger.com/Article/FullText/369683; http://hdl.handle.net/11449/128297
• topic: Heart failure; Skeletal muscle; NADPH oxidase; Myocardial infarction; N-acetylcysteine; Reactive oxygen species

Background: Chronic heart failure is characterized by decreased exercise capacity with early exacerbation of fatigue and dyspnea. Intrinsic skeletal muscle abnormalities can play a role in exercise intolerance. Causal or contributing factors responsible for muscle alterations have not been completely defined. This study evaluated skeletal muscle oxidative stress and NADPH oxidase activity in rats with myocardial infarction (MI) induced heart failure. Methods and Results: Four months after MI, rats were assigned to Sham, MI-C (without treatment), and MI-NAC (treated with N-acetylcysteine) groups. Two months later, echocardiogram showed left ventricular dysfunction in MI-C; NAC attenuated diastolic dysfunction. In soleus muscle, glutathione peroxidase and superoxide dismutase activity was decreased in MI-C and unchanged by NAC. 3-nitrotyrosine was similar in MI-C and Sham, and lower in MI-NAC than MI-C. Total reactive oxygen species (ROS) production was assessed by HPLC analysis of dihydroethidium (DHE) oxidation fluorescent products. The 2-hydroxyethidium (EOH)/DHE ratio did not differ between Sham and MI-C and was higher in MI-NAC. The ethidium/DHE ratio was higher in MI-C than Sham and unchanged by NAC. NADPH oxidase activity was similar in Sham and MI-C and lower in MI-NAC. Gene expression of p47(phox) was lower in MI-C than Sham. NAC decreased NOX4 and p22(phox) expression. Conclusions: We corroborate the case that oxidative stress is increased in skeletal muscle of heart failure rats and show for the first time that oxidative stress is not related to increased NADPH oxidase activity.