Carnosine prevents Aβ-induced oxidative stress and inflammation in microglial cells: a key role of TGF-β1
journal contributionposted on 07.03.2019 by Giuseppe Caruso, Claudia G. Fresta, Nicolò Musso, Mariaconcetta Giambirtone, Margherita Grasso, Simona F. Spampinato, Sara Merlo, Filippo Drago, Giuseppe Lazzarino, Maria Angela Sortino, Susan M. Lunte, Filippo Caraci
Any type of content formally published in an academic journal, usually following a peer-review process.
By using an in vitro model of AD, we showed that carnosine prevents Aβ-induced oxidative stress in BV-2 microglial cells by decreasing the expression of iNOS and NADPH oxidase and the concentrations of nitric oxide and superoxide anion. Carnosine is also able to decrease the secretion of pro-inﬂammatory cytokines, simultaneously rescuing IL-10 levels and increasing the synthesis and the release of TGF-β1. Carnosine, through its multimodal mechanism of action, might represent a new pharmacological tool to yield neuroprotection in AD.