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자료유형
학술저널
저자정보
김선기 (세종대학교) 김병권 (세종대학교) 김규민 (세종대학교) 황성순 (세종대학교)
저널정보
대한내분비학회 Endocrinology and Metabolism Endocrinology and Metabolism Vol.31 No.4
발행연도
2016.1
수록면
500 - 504 (5page)

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Nonalcoholic fatty liver disease (NAFLD) is one of the causes of fatty liver, occurring when fat is accumulated in the liver withoutalcohol consumption. NAFLD is the most common liver disorder in advanced countries. NAFLD is a spectrum of pathology involvinghepatic steatosis with/without inflammation and nonalcoholic steatohepatitis with accumulation of hepatocyte damage and hepaticfibrosis. Recent studies have revealed that NAFLD results in the progression of cryptogenic cirrhosis that leads to hepatocarcinomaand cardiovascular diseases such as heart failure. The main causes of NAFLD have not been revealed yet, metabolic syndromesincluding obesity and insulin resistance are widely accepted for the critical risk factors for the pathogenesis of NAFLD. Nuclearreceptors (NRs) are transcriptional factors that sense environmental or hormonal signals and regulate expression of genes, involvedin cellular growth, development, and metabolism. Several NRs have been reported to regulate genes involved in energy andxenobiotic metabolism and inflammation. Among various NRs, farnesoid X receptor (FXR) is abundantly expressed in the liver anda key regulator to control various metabolic processes in the liver. Recent studies have shown that NAFLD is associated with inappropriatefunction of FXR. The impact of FXR transcriptional activity in NAFLD is likely to be potential therapeutic strategy, butstill requires to elucidate underlying potent therapeutic mechanisms of FXR for the treatment of NAFLD. This article will focus thephysiological roles of FXR and establish the correlation between FXR transcriptional activity and the pathogenesis of NAFLD.

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