Hepatoprotective Effect of Oyster Peptide on Alcohol-Induced Liver Disease in Mice
Wang, Xueqin1,2,3; Yu, Huahua1,2,3; Xing, Ronge1,2,3; Li, Pengcheng1,2,3
刊名INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
2022-08-01
卷号23期号:15页码:15
关键词oyster peptide alcohol-induced liver diseases hepatoprotective effect oxidative stress inflammatory response
DOI10.3390/ijms23158081
通讯作者Li, Pengcheng(pcli@qdio.ac.cn)
英文摘要Alcohol-induced liver disease (ALD) has become one of the major global health problems, and the aim of this study was to investigate the characterization of the structure as well as the hepatoprotective effect and mechanism of oyster peptide (OP, MW < 3500 Da) on ALD in a mouse model. The results demonstrate that ethanol administration could increase the activities of aspartate aminotransferase (AST), alanine transaminase (ALT), gamma-Glutamyl transferase (GGT), reactive oxygen species (ROS), malondialdehyde (MDA), and triglycerides (TG), as well as increase the interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and tumor necrosis factor (TNF-alpha) levels (p < 0.01), and reduce the activity of superoxide dismutase (SOD) and the concentration of glutathione (GSH). Those changes were significantly reversed by the application of different doses of OP. Furthermore, the mRNA expressions of nuclear factor elythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), and quinone oxidoreductase1 (NQO1) were significantly up-regulated in OP groups, and the mRNA expressions of nuclear factor kappa-light chain enhancer of B cells (NF-kappa B), TNF-alpha, and IL-6 were markedly reduced in OP groups compared to that of the model group. Thus, OP had a significant protective effect on ALD through the enhancement of the in vivo antioxidant ability and the inhibition of the inflammatory response as possible mechanisms of action, which therefore suggests that OP might be useful as a natural source to protect the liver from alcohol damage.
资助项目Key Projects for Major Projects on the Transformation of Old and Novel Kinetic Energy of Shandong Province[2020-1220] ; STS Project of the Chinese Academy of Sciences[2021T3038]
WOS研究方向Biochemistry & Molecular Biology ; Chemistry
语种英语
出版者MDPI
WOS记录号WOS:000839141400001
内容类型期刊论文
源URL[http://ir.qdio.ac.cn/handle/337002/179898]  
专题海洋研究所_实验海洋生物学重点实验室
通讯作者Li, Pengcheng
作者单位1.Pilot Natl Lab Marine Sci & Technol Qingdao, Lab Marine Drugs & Bioprod, 1 Wenhai Rd, Qingdao 266237, Peoples R China
2.Chinese Acad Sci, Ctr Ocean Megasci, Inst Oceanol, Shandong Prov Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
3.Chinese Acad Sci, Ctr Ocean Megasci, Inst Oceanol, Qingdao 266071, Peoples R China
推荐引用方式
GB/T 7714
Wang, Xueqin,Yu, Huahua,Xing, Ronge,et al. Hepatoprotective Effect of Oyster Peptide on Alcohol-Induced Liver Disease in Mice[J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,2022,23(15):15.
APA Wang, Xueqin,Yu, Huahua,Xing, Ronge,&Li, Pengcheng.(2022).Hepatoprotective Effect of Oyster Peptide on Alcohol-Induced Liver Disease in Mice.INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,23(15),15.
MLA Wang, Xueqin,et al."Hepatoprotective Effect of Oyster Peptide on Alcohol-Induced Liver Disease in Mice".INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 23.15(2022):15.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace