Qushi Huayu Decoction Inhibits Hepatic Lipid Accumulation by Activating AMP-Activated Protein Kinase In Vivo and In Vitro
Autor: | Wen-jing Wang, Jinghua Peng, Qin Feng, Lin Xu, Ya-jun Tang, Yu-quan Zhang, Yi-Yang Hu, Cheng Huang, Xiao-jun Gou, Sheng-xi Meng |
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Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: |
chemistry.chemical_classification
medicine.medical_specialty Article Subject Fatty liver AMPK Fatty acid lcsh:Other systems of medicine Biology medicine.disease lcsh:RZ201-999 Endocrinology Complementary and alternative medicine chemistry AMP-activated protein kinase In vivo Internal medicine Nonalcoholic fatty liver disease medicine biology.protein lipids (amino acids peptides and proteins) Carbohydrate-responsive element-binding protein Protein kinase A Research Article |
Zdroj: | Evidence-Based Complementary and Alternative Medicine, Vol 2013 (2013) Evidence-based Complementary and Alternative Medicine : eCAM |
ISSN: | 1741-427X |
DOI: | 10.1155/2013/184358 |
Popis: | Qushi Huayu Decoction (QHD), a Chinese herbal formula, has been proven effective on alleviating nonalcoholic fatty liver disease (NAFLD) in human and rats. The present study was conducted to investigate whether QHD could inhibit hepatic lipid accumulation by activating AMP-activated protein kinase (AMPK)in vivoandin vitro. Nonalcoholic fatty liver (NAFL) model was duplicated with high-fat diet in rats and with free fatty acid (FFA) in L02 cells. Inin vivoexperimental condition, QHD significantly decreased the accumulation of fatty droplets in livers, lowered low-density lipoprotein cholesterol (LDL-c), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) levels in serum. Moreover, QHD supplementation reversed the HFD-induced decrease in the phosphorylation levels of AMPK and acetyl-CoA carboxylase (ACC) and decreased hepatic nuclear protein expression of sterol regulatory element-binding protein-1 (SREBP-1) and carbohydrate-responsive element-binding protein (ChREBP) in the liver. Inin vitro, QHD-containing serum decreased the cellular TG content and alleviated the accumulation of fatty droplets in L02 cells. QHD supplementation reversed the FFA-induced decrease in the phosphorylation levels of AMPK and ACC and decreased the hepatic nuclear protein expression of SREBP-1 and ChREBP. Overall results suggest that QHD has significant effect on inhibiting hepatic lipid accumulation via AMPK pathwayin vivoandin vitro. |
Databáze: | OpenAIRE |
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