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Cited 4 time in webofscience Cited 4 time in scopus
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Persimmon Water Extract Suppresses Hepatic Lipotoxicity by Regulating Lipid Metabolites

Authors
Kang, Jin YongLee, UkPark, Seon KyeongKim, Jong MinKim, Min JiMoon, Jong HyunLee, Hyo LimJeong, Hye RinPark, Hyo WonKim, Chul-WooKim, Mahn-JoHeo, Ho Jin
Issue Date
Jul-2022
Publisher
한국식품영양과학회
Keywords
Diospyros kaki; hepatic lipotoxicity; lysophosphatidylcholine; nonalcoholic fatty liver disease
Citation
Journal of Medicinal Food, v.25, no.7, pp 710 - 721
Pages
12
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Medicinal Food
Volume
25
Number
7
Start Page
710
End Page
721
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/1066
DOI
10.1089/jmf.2022.K.0021
ISSN
1096-620X
1557-7600
Abstract
This study was performed to investigate the effects of persimmon (Diospyros kaki) on high-fat diet (HFD)-induced hepatic lipotoxicity. The compounds of persimmon water extract (PWE) were identified as gallic acid, glucogallin, 1-O-Galloyl-(2-O-acetyl)-glu, and trihydroxy-octadecadienoic acid. The PWE was ingested by C57BL/6 mice with an HFD for 8 weeks. The PWE improved glucose tolerance and suppressed weight gain by inhibiting increases in the weight of liver and adipose tissues. The results of serum biomarker analysis showed that PWE suppressed biomarkers such as liver injury and dyslipidemia. In ex vivo tests, reduction of oxidative stress and improvement of mitochondrial dysfunction were confirmed in the liver of PWE groups. In a molecular study, it was confirmed that PWE decreased lipid accumulation, insulin resistance, inflammation, and apoptosis in the liver. Finally, in a metabolite analysis of liver tissue using ultra-high performance liquid chromatography with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS), it was confirmed that PWE has an effect on lipid metabolism. In particular, PWE reduced phosphatidylcholines (PCs) and lysophosphatidylcholines (lysoPCs). Notably, it is presumed that the reduction of lysoPCs and PCs in the PWE group is related to the improvement of liver dysfunction due to lipotoxicity.
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