详细信息
The anti-fatigue effect of the Auxis thazard oligopeptide via modulation of the AMPK/PGC-1α pathway in mice ( SCI-EXPANDED收录 EI收录) 被引量:22
文献类型:期刊文献
英文题名:The anti-fatigue effect of the Auxis thazard oligopeptide via modulation of the AMPK/PGC-1α pathway in mice
作者:Qu, Yushan[1];Ji, Hongwu[1,2,3,4,5];Song, Wenkui[1];Peng, Shuo[1];Zhan, Suhong[1];Wei, Liuyi[1];Chen, Ming[1];Zhang, Di[1];Liu, Shucheng[1,2,3,4,5,6]
机构:[1]Guangdong Ocean Univ, Coll Food Sci & Technol, Zhanjiang 524088, Peoples R China;[2]Guangdong Prov Key Lab Aquat Prod Proc & Safety, Zhanjiang 524088, Peoples R China;[3]Guangdong Prov Engn Lab Marine Biol Prod, Zhanjiang 524088, Peoples R China;[4]Guangdong Prov Engn Technol Res Ctr Marine Food, Zhanjiang 524088, Peoples R China;[5]Guangdong Higher Educ Inst, Key Lab Adv Proc Aquat Prod, Zhanjiang 524088, Peoples R China;[6]Dalian Polytech Univ, Collaborat Innovat Ctr Seafood Deep Proc, Dalian 116034, Peoples R China
年份:2022
卷号:13
期号:3
起止页码:1641
外文期刊名:FOOD & FUNCTION
收录:SCI-EXPANDED(收录号:WOS:000746911600001)、、EI(收录号:20220711651111)、Scopus(收录号:2-s2.0-85124438185)、WOS
基金:This work was co-supported by the National Key Research and Development Program (2019YFD0902004) and the Guangdong Innovation Team of Seafood Green Processing Technology (2019KCXTD011).
语种:英文
外文摘要:The Auxis thazard oligopeptide (ATO) was obtained by papain digestion and ultrafiltration membrane separation, and its anti-fatigue effects and mechanisms were evaluated using animal experiments on Kunming mice. Compared with the negative control group, the ATO extended the time to exhaustion in mice in a forced swim test by 0.81-1.62 times. Liver glycogen levels were significantly increased by 0.6-1.63 times and muscle glycogen levels were increased by 9.52-10.02%; the levels of lactic acid (16.46-17.21%) and urea nitrogen (34.88-41.91%) decreased. The ATO also increased antioxidant activity, reduced malondialdehyde levels (18.00-35.79%) in the liver and myocardium, and increased the gene and protein expression of AMPK and PGC-1 alpha in fatigued mice. These results indicate that the ATO exerts an anti-fatigue effect via improving energy metabolism and decreasing oxidative stress.
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