As creatine has not shown significant antioxidant activity against hydrogen

peroxide (H2O2), these findings also demonstrate creatine’s selective antioxidant capacity. Sestili et al. [4] postulated a direct antioxidant role for creatine in cells exposed to various oxidative agents. These authors demonstrated that creatine in doses similar to those found in plasma after supplementation exerts cytoprotective antioxidant activity in three different cell lines against three different oxidative agents: H2O2, OONO- and t-butyl hydroperoxide (tB-OOH), an organic peroxide widely used in a variety of oxidation processes. Furthermore, cytoprotection was observed independent of the anti-oxidative state of the cell, as evaluated by the antioxidant enzymes catalase and glutathione peroxidase, which suggests a direct interaction between creatine and oxidizing agents and/or free radicals. In humans, creatine Autophagy inhibitor synthesis appears to occur mainly in the liver [13], an organ that requires vast amounts of OICR-9429 solubility dmso generated energy to perform its various functions. The high metabolic rate of the liver (200 kcal/kg of tissue per day)

is directly associated with the high flow of electrons in the mitochondrial respiratory chain [14]. However, some of these electrons are diverted to produce reactive oxygen species (ROS). Several authors have demonstrated that the liver undergoes increased oxidative stress following exercise [14, 15]. Thus, we sought to investigate the effects of CrS on oxidative balance, injury and liver antioxidant defense https://www.selleckchem.com/products/Temsirolimus.html mechanisms during exercise in a laboratory model. The aims of this study were to: 1) determine whether creatine supplementation increased liver creatine stores and 2) determine whether creatine supplementation improved markers of liver oxidative stress following exercise training. Methods Animals and treatment Forty 90-day-old male Wistar rats

were given free access to water and food. The animals were housed in collective polyethylene cages measuring 37.0 × 31.0 × 16.0 cm with 5 animals per cage, all under controlled conditions of temperature (22°C) and light/dark cycle (12 h/12 h). The experiment was submitted to and approved by the Animal Experimentation Ethics Committee at the University of Taubaté – UNITAU, São Paulo State, Brazil (register Cytidine deaminase CEEA / UNITAU n° 018/08). Exercise training was performed and creatine supplementation given over eight weeks with animals allocated into four groups of ten animals in each group: control group (C), sedentary rats that received a balanced control diet; creatine control group (CCr), sedentary rats that received a balanced diet supplemented with 2% creatine; trained group (T), rats that were subjected to a training protocol and received a balanced diet; and supplemented trained group (TCr), rats that were subjected to a training protocol and received a balanced diet supplemented with 2% creatine.