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Illustratively, BPC 157 may interfere with NO-system activities (Sikiric et al., 2014) and counteract harmful events, arising from either NO-blockade (L-NAME-application) or L-arginine (NOS-substrate-application) (Sikiric et al., 2014)
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These findings collectively underscore the broad therapeutic potential of targeting the Nrf2 system within astrocytes to mitigate oxidative damage and ferroptosis in PD
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