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https://www.selleckchem.com/pr....oducts/ll37-human.ht
After 3 months, MI led to left ventricular (LV) hypertrophy, with systolic and diastolic dysfunction, and increased oxidative stress and inflammatory mediators. OJ intake reduced LV cavity and improved systolic and diastolic function. The OJ animals presented lower activity of glutathione peroxidase and higher expression of heme-oxygenase-1 (HO-1). OJ attenuated CR in infarcted rats and HO-1 may be play an important role in this process. OJ attenuated CR in infarcted rats and HO-1 may be play an important role in this process. Athero

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