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Activation of Nrf2/HO-1 by Peptide YD1 Attenuates Inflammatory Symptoms through Suppression of TLR4/MYyD88/NF-κB Signaling Cascade
被引:26
|作者:
Rahman, Md Saifur
[1
,2
]
Alam, Md Badrul
[3
]
Kim, Young Kyun
[1
]
Madina, Mst Hur
[4
]
Fliss, Ismail
[2
]
Lee, Sang Han
[3
]
Yoo, Jin Cheol
[1
]
机构:
[1] Chosun Univ, Dept Pharm, Coll Pharm, Gwangju 501759, South Korea
[2] Laval Univ, Dept Food Sci, Fac Agr & Food Sci, Quebec City, PQ G1V 0A6, Canada
[3] Kyungpook Natl Univ, Dept Food Sci & Biotechnol, Daegu 702701, South Korea
[4] Laval Univ, Dept Phytol, Fac Agr & Food Sci, Quebec City, PQ G1V 0A6, Canada
关键词:
anti-inflammation;
YD1;
peptide drug;
NF-kappa B;
RAW;
264.7;
TLR-4;
MyD88;
AKT;
NF-KAPPA-B;
ANTIOXIDANT ACTIVITIES;
OXIDATIVE STRESS;
MACROPHAGES;
LIPOPOLYSACCHARIDE;
RESPONSES;
TLR4;
MAPK;
AMYLOLIQUEFACIENS;
EXPRESSION;
D O I:
10.3390/ijms22105161
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In this study, we investigate the immunomodulatory effects of a novel antimicrobial peptide, YD1, isolated from Kimchi, in both in vitro and in vivo models. We establish that YD1 exerts its anti-inflammatory effects via up-regulation of the Nrf2 pathway, resulting in the production of HO-1, which suppresses activation of the NF-kappa B pathway, including the subsequent proinflammatory cytokines IL-1 beta, IL-6, and TNF-alpha. We also found that YD1 robustly suppresses nitric oxide (NO) and prostaglandin E2 (PGE(2)) production by down-regulating the expression of the upstream genes, iNOS and COX-2, acting as a strong antioxidant. Collectively, YD1 exhibits vigorous anti-inflammatory and antioxidant activity, presenting it as an interesting potential therapeutic agent.
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页数:14
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