Selenium-biofortified corn peptides: Attenuating concanavalin A-Induced liver injury and structure characterization

被引:37
作者
Guo, Danjun [1 ,2 ]
Zhang, Yan [1 ,2 ]
Zhao, Juanjuan [1 ,2 ]
He, Hui [1 ,2 ]
Hou, Tao [1 ,2 ]
机构
[1] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Peoples R China
[2] Huazhong Agr Univ, Key Lab Environm Correlat Dietol, Minist Educ, Wuhan 43000, Hubei, Peoples R China
关键词
Selenium-biofortified corn peptides; Concanavalin A; Antioxidant ability; Hepatoprotective effect; Structure characterization; CHAIN AMINO-ACIDS; ANTIOXIDANT ACTIVITY; IN-VITRO; SU DERIVATIVES; PURIFICATION; HEPATITIS; PROTEIN; IDENTIFICATION; PREVENTION; MEDICINE;
D O I
10.1016/j.jtemb.2018.09.010
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
The relationship between hepatoprotective effects of selenium-biofortified corn (Zea mays Linn) peptides (SeCPs) and its antioxidant ability was evaluated and the structure of SeCPs was identified. SeCPs and corn peptides (CPs) both had good antioxidant ability, and the effect of SeCPs was significantly higher than CPs within a certain concentration range (P<0.05). Additionally, animal experiments indicated that SeCPs (200 mg/kg) had a significantly protective effect against concanavalin A (Con A) induced hepatic lesions, as it significantly declined glutamic-pyruvic transaminase (AST), alanine transaminase (ALT) activities, tumor necrosis factor alpha (TNF-a), interferon (IFN)-gamma contents in serum, and malondialdehyde (MDA) contents in liver (P<0.05). Superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities in liver were also significantly increased by SeCPs (P<0.05). The amino acid composition of SeCPs with Mw < 1 kDa was mainly glutamic acid (Glu, 31.18%), leucine (Leu, 21.06%) and alanine (Ala, 13.26%). According to the retention time, the amino acid sequences of 8 selenium-biofortified corn peptides and 29 selenium-free corn peptides were identified. Our results illustrated that the mechanisms of SeCPs against Con A induced hepatic injury in mice may be related to its antioxidant ability and reduction of lipid peroxidation, inhibiting the release of immune factors, such as TNF-alpha and IFN-gamma.
引用
收藏
页码:57 / 64
页数:8
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