Brain Oxidative Stress During Experimental Sepsis Is Attenuated by Simvastatin Administration

During sepsis, brain damage is associated with oxidative stress due to overproduction of reactive oxygen species (ROS). Although there are recent reports about the benefits of statins in experimental sepsis and endotoxemia in peripheral organs, little is known about their effects in the CNS. Here, w...

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Veröffentlicht in:Molecular neurobiology 2017-11, Vol.54 (9), p.7008-7018
Hauptverfasser: Catalão, Carlos Henrique Rocha, Santos-Júnior, Nilton Nascimento, da Costa, Luís Henrique Angenendt, Souza, Anderson Oliveira, Alberici, Luciane Carla, Rocha, Maria José Alves
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Sprache:eng
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Zusammenfassung:During sepsis, brain damage is associated with oxidative stress due to overproduction of reactive oxygen species (ROS). Although there are recent reports about the benefits of statins in experimental sepsis and endotoxemia in peripheral organs, little is known about their effects in the CNS. Here, we investigated the antioxidant properties of simvastatin and its possible neuroprotective role during experimental sepsis. Male Wistar rats (250–300 g) were submitted to cecal ligation and puncture (CLP, n  = 34) or remained as non-manipulated (naive, n  = 34). Both groups were treated by gavage with simvastatin (20 mg/kg) or an equivalent volume of saline. The animals submitted to CLP were treated 4 days before and 48 h after surgery. One animal group was decapitated and the blood and brain were collected to quantify plasma levels of cytokines and assess astrogliosis and apoptosis in the prefrontal cortex and hippocampus. Another group was perfused with PBS (0.01 M), and the same brain structures were dissected to analyze oxidative damage. The CLP rats treated with simvastatin showed a reduction in nitric oxide ( P  
ISSN:0893-7648
1559-1182
DOI:10.1007/s12035-016-0218-3