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논문 기본 정보

자료유형
학술저널
저자정보
Jae Yun Han (Chosun University) Sun Hee Park (Chosun University) Ji Hye Yang (Chosun University) Mi Gwang Kim (Chosun University) Seung Sik Cho (Mokpo National University) Goo Yoon (Mokpo National University) Seung Hoon Cheon (Chonnam National University) Sung Hwan Ki (Chosun University)
저널정보
한국독성학회 Toxicological Research Toxicological Research Vol.30 No.1
발행연도
2014.3
수록면
19 - 25 (7page)

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초록· 키워드

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Licochalcone (LC), a major phenolic retrochalcone from licorice, has anti-inflammatory activity. This study investigated the effects of licochalcone A (LCA) and licochalcone E (LCE) on Liver X receptor-α (LXRα)-mediated lipogenic gene expression and the molecular mechanisms underlying those effects. LCA and LCE antagonized the ability of LXRα agonists (T0901317 or GW3965) to increase sterol regulatory element binding protein-1c (SREBP-1c) expression and thereby inhibited target gene expression (e.g., FAS and ACC) in HepG2 cells. Moreover, treatment with LCA and LCE impaired LXRα/RXRα-induced CYP7A1-LXRE-luciferase (CYP7A1) transactivation. The AMPK-Sirt1 signaling pathway is an important regulator of energy metabolism and, therefore, a potential therapeutic target for metabolic diseases, including hepatic steatosis. We found here that LCE increased AMPK phosphorylation and Sirt1 expression. We conclude that LC inhibits SREBP-1c-mediated hepatic lipogenesis via activation of the AMPK/Sirt1 signaling pathway.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2015-510-001344001