“… Peptide/protein hydrolysate | Oxidative stress model | Cellular mechanism of action | Ref |
WSREEQEREE and ADIYTEEAGR from walnut protein | UV-radiation-induced mouse skin aging | Suppressed NF-κB signaling pathway by preventing the activation of IκB and p-65 proteins, downregulated gene expression of interleukins (IL)-1β and IL-6, inhibited MMP-1 activity and enhanced the expression of TGF-β and procollagen type I. | [ 155 ] |
GAGLPGKRER from Pinctada fucata protein hydrolysates | UV-radiation-induced mouse skin aging | Inhibited CAT, glutathione system and SOD activities, halted lipid peroxidation and suppressed UV-radiation-induced skin aging | [ 86 , 130 ] |
PELDW, WPDHW, FGYDWW, and YLHFW isolated from Spanish Mackerel muscle | H 2 O 2 -generated plasmid DNA damage | Inhibited DNA damage by boosting the antioxidant status and preventing uncoiling and strand break | [ 156 ] |
MQIFVK, MASVPTK, EMVELPLR and VVLIGDSGVGK derived from pine nut | H 2 O 2 -challenged HepG2 cells and D-galactose-induced premature aging in mouse | Improved the viability of HepG2 cells, and suppressed lipid peroxidation and enhanced antioxidant status by increasing SOD and GPx activity in mouse | [ 84 ] |
LEPVIGT derived from porcine plasma | H 2 O 2 -induced oxidative stress in HepG2 cells | Protected HepG2 cells via Keap1-Nrf2-ARE signaling pathway | [ 103 ] |
FYY and DW derived from lantern fish protein | D-galactose-induced aging | Suppressed lipid peroxidation level and expression of endothelial nitric oxide synthase, and improved memory impairment by elevating brain-derived neurotrophic factor | [ 92 ] |
DVEDLEAGLAK and EITSLAPSTM from golden cuttlefish | High fat Caenorhabditis elegans | Prevented oxidative damage via upregulation of mRNA expression of DAF-16 signaling pathway-regulated genes (sod-3, catalase (cat-1) and ctl-1)) | [ 54 ] |
AYI, AYL, DREI and DREL from Jiuzao | 2,2′-Azobis(2-methylpropanimidamidine)-stressed HepG2 cells | inhibited ROS generation, elevated SOD, CAT and GPx gene expression and improved the viability of HepG2 cells via Keap1-Nrf2-ARE signaling pathway | [ ... |
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