Artigo Acesso aberto Produção Nacional Revisado por pares

Effects of aerobic exercise training in oxidative metabolism and mitochondrial biogenesis markers on prefrontal cortex in obese mice

2022; BioMed Central; Volume: 14; Issue: 1 Linguagem: Inglês

10.1186/s13102-022-00607-x

ISSN

2052-1847

Autores

Matheus Santos de Sousa Fernandes, Felipe J. Aidar, Anderson Apolônio da Silva Pedroza, Severina Cássia de Andrade Silva, Gabriela Carvalho Jurema Santos, Rafael dos Santos Henrique, Filipe Manuel Clemente, Ana Filipa Silva, Raphael Fabrício de Souza, Diorginis José Soares Ferreira, Georgian Bădicu, Claúdia Jacques Lagranha, Hadi Nobarı,

Tópico(s)

Regulation of Appetite and Obesity

Resumo

Abstract Background To evaluate the effects of 8 weeks of Aerobic Physical Training (AET) on the mitochondrial biogenesis and oxidative balance in the Prefrontal Cortex (PFC) of leptin deficiency-induced obese mice (ob/ob mice). Methods Then, the mice were submitted to an 8-week protocol of aerobic physical training (AET) at moderate intensity (60% of the maximum running speed). In the oxidative stress, we analyzed Malonaldehyde (MDA) and Carbonyls, the enzymatic activity of Superoxide Dismutase (SOD), Catalase (CAT) and Glutathione S Transferase (GST), non-enzymatic antioxidant system: reduced glutathione (GSH), and Total thiols. Additionally, we evaluated the gene expression of PGC-1α SIRT-1, and ATP5A related to mitochondrial biogenesis and function. Results In our study, we did not observe a significant difference in MDA ( p = 0.2855), Carbonyl’s ( p = 0.2246), SOD ( p = 0.1595), and CAT ( p = 0.6882) activity. However, the activity of GST ( p = 0.04), the levels of GSH ( p = 0.001), and Thiols ( p = 0.02) were increased after 8 weeks of AET. Additionally, there were high levels of PGC-1α ( p = 0.01), SIRT-1 ( p = 0.009), and ATP5A ( p = 0.01) gene expression after AET in comparison with the sedentary group. Conclusions AET for eight weeks can improve antioxidant defense and increase the expression of PGC-1α, SIRT-1, and ATP5A in PFC of ob/ob mice.

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