Berberine ameliorates nonalcoholic fatty liver disease by decreasing the liver lipid content via reversing the abnormal expression of MTTP and LDLR

被引:29
作者
Chen, Ping [1 ]
Li, Yusheng [2 ]
Xiao, Li [2 ]
机构
[1] Shandong Med Coll, Dept Pharm, Affiliated Hosp, Linyi 276000, Shandong, Peoples R China
[2] Linyi Maternal & Child Hlth Care Hosp, Dept Pharm, 1 Qinghe South Rd, Linyi 276000, Shandong, Peoples R China
关键词
nonalcoholic fatty liver disease; berberine; microsomal triglyceride transfer protein; apolipoprotein B; low-density lipoprotein receptor; TRIGLYCERIDE TRANSFER PROTEIN; MESSENGER-RNA; APOLIPOPROTEIN; PREVALENCE; KINASE; DERIVATIVES; POPULATION; METABOLISM; SECRETION; MECHANISM;
D O I
10.3892/etm.2021.10543
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The global incidence of nonalcoholic fatty liver disease (NAFLD) is increasing. The present study explored the effect and mechanism of berberine (BBR) on NAFLD in rats. Thirty-five Sprague-Dawley rats were randomly divided into the control and NAFLD groups, which were fed a normal diet or high-fat diet, respectively, for 8 weeks. Hematoxylin and eosin staining was performed on liver tissues and establishment of the NAFLD model was confirmed by microscopy. NAFLD rats were subsequently randomly subdivided and treated with saline or BBR for 8 weeks. The liver wet weight of rats in each group was measured, the liver tissue structure was observed by microscopy, and alanine aminotransferase (ALT), aspartate aminotransferase (AST), total cholesterol (TC), triglyceride (TG), fasting blood glucose (FBG), low-density lipoprotein (LDL) and high-density lipoprotein (HDL) levels were detected using a semi-automatic biochemical detector. Reverse transcription-quantitative PCR and western blotting were performed to determine the mRNA and protein expression levels of microsomal triglyceride transfer protein (MTTP), apolipoprotein B and low-density lipoprotein receptor (LDLR). Compared with the control group, the liver wet weight of the NAFLD rats was higher; the liver showed obvious fatty degeneration and liver TG levels increased significantly, as did serum levels of ALT, AST, TC, TG, FBG, HDL and LDL, while expression of MTTP and LDLR significantly decreased. Compared with the saline-treated NAFLD rats, the BBR-treated rats had reduced liver wet weight, improved liver steatosis and a significant decrease in liver TG levels, while ALT, AST, TC, TG, and LDL serum levels significantly decreased and MTTP levels were significantly upregulated. In conclusion, BBR treatment ameliorated the fatty liver induced by a high-fat diet in rats. Furthermore, BBR reversed the abnormal expression of MTTP and LDLR in rats with high-fat diet induced-NAFLD. The present findings suggest that fatty liver could be improved by BBR administration, via reversing the abnormal expression of MTTP and LDLR and inhibiting lipid synthesis.
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页数:8
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共 49 条
[1]   The natural history of nonalcoholic fatty liver disease: A population-based cohort study [J].
Adams, LA ;
Lymp, JF ;
St Sauver, J ;
Sanderson, SO ;
Lindor, KD ;
Feldstein, A ;
Angulo, P .
GASTROENTEROLOGY, 2005, 129 (01) :113-121
[2]   Nonalcoholic fatty liver disease [J].
Adams, LA ;
Angulo, P ;
Lindor, KD .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2005, 172 (07) :899-905
[3]   AMP-activated protein kinase and coordination of hepatic fatty acid metabolism of starved/carbohydrate-refed rats [J].
Assifi, MM ;
Suchankova, G ;
Constant, S ;
Prentki, M ;
Saha, AK ;
Ruderman, NB .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2005, 289 (05) :E794-E800
[4]   Effect of exercise and dietary modification on serum aminotransferase levels in patients with nonalcoholic steatohepatitis [J].
Baba, CS ;
Alexander, G ;
Kalyani, B ;
Pandey, R ;
Rastogi, S ;
Pandey, A ;
Choudhuri, G .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2006, 21 (01) :191-198
[5]   Prevalence of and risk factors for nonalcoholic fatty liver disease: The Dionysos Nutrition and Liver Study [J].
Bedogni, G ;
Miglioli, L ;
Masutti, F ;
Tiribelli, C ;
Marchesini, G ;
Bellentani, S .
HEPATOLOGY, 2005, 42 (01) :44-52
[6]   Pathology of non-alcoholic fatty liver disease [J].
Bedossa, Pierre .
LIVER INTERNATIONAL, 2017, 37 :85-89
[7]   Prevalence of hepatic steatosis in an urban population in the United States: Impact of ethnicity [J].
Browning, JD ;
Szczepaniak, LS ;
Dobbins, R ;
Nuremberg, P ;
Horton, JD ;
Cohen, JC ;
Grundy, SM ;
Hobbs, HH .
HEPATOLOGY, 2004, 40 (06) :1387-1395
[8]   Inhibition of lipid synthesis through activation of AMP kinase: an additional mechanism for the hypolipidemic effects of berberine [J].
Brusq, Jean-Marie ;
Ancellin, Nicolas ;
Grondin, Pascal ;
Guillard, Raphaelle ;
Martin, Sandrine ;
Saintillan, Yannick ;
Issandou, Marc .
JOURNAL OF LIPID RESEARCH, 2006, 47 (06) :1281-1288
[9]   Cohort Study of Non-alcoholic Fatty Liver Disease, NAFLD fibrosis score, and the Risk of Incident Diabetes in a Korean population [J].
Chang, Yoosoo ;
Jung, Hyun-Suk ;
Yun, Kyung Eun ;
Cho, Juhee ;
Cho, Yong Kyun ;
Ryu, Seungho .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2013, 108 (12) :1861-1868
[10]   Berberine ameliorates non-steroidal anti-inflammatory drugs-induced intestinal injury by the repair of enteric nervous system [J].
Chao, Guanqun ;
Ye, Fangxu ;
Yuan, Yuan ;
Zhang, Shuo .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2020, 34 (02) :238-248