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Cited 57 time in webofscience Cited 58 time in scopus
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Green tea changes serum and liver metabolomic profiles in mice with high-fat diet-induced obesity

Authors
Lee, Lan-SookChoi, Ji HeaSung, Mi JeongHur, Jin-YoungHur, Haeng JeonPark, Jong-DaeKim, Young-ChanGu, Eun-JiMin, ByungjinKim, Hyun-Jin
Issue Date
Apr-2015
Publisher
WILEY
Keywords
Acetyl-CoA acyltransferase 2; Fatty acid beta-oxidation; Green tea; Metabolomics; Obesity
Citation
MOLECULAR NUTRITION & FOOD RESEARCH, v.59, no.4, pp 784 - 794
Pages
11
Indexed
SCI
SCIE
SCOPUS
Journal Title
MOLECULAR NUTRITION & FOOD RESEARCH
Volume
59
Number
4
Start Page
784
End Page
794
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/17321
DOI
10.1002/mnfr.201400470
ISSN
1613-4125
1613-4133
Abstract
Scope: Green tea (GT) consumption helps to prevent and control obesity by stimulating hepatic lipid metabolism. However, GT-induced changes in serum and liver metabolomes associated with the anti-obesity effects are not clearly understood. The aim of this study was to identify and validate metabolomic profiles in the livers and sera of GT-fed obese mice to elucidate the relationship between GT consumption and obesity prevention. Methods and results: Serum and liver metabolites were analyzed in mice fed normal diet, high-fat diet (HFD), HFD with GT, and HFD with crude catechins, using LC-quadrupole TOF MS. The addition of 1% GT to HFD reduced adipose tissue and the levels of blood triglycerides, glucose, insulin, and leptin elevated in HFD-fed mice. We proposed an HFD-induced obesity pathway and validated it by investigating the key regulatory enzymes of mitochondrial beta-oxidation: carnitine palmitoyltransferase-1 and -2, acyl-coenzyme A dehydrogenase, and acetylcoenzyme A acyltransferase. The results showed that HFD-induced abnormal mitochondrial beta-oxidation was moderated by the consumption of caffeine-and theanine-enriched GT. Conclusion: Results of LC/MS-based metabolomic analysis of obese mice showed changes associated with abnormal lipid and energy metabolism, which were alleviated by GT intake, indicating the mechanism underlying the anti-obesity effects of GT.
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