Aloe-emodin exerts cholesterol-lowering effects by inhibiting proprotein convertase subtilisin/kexin type 9 in hyperlipidemic rats

• 作者: Han-qi Sun Jing Guo Juan Hu Ke-yu Liu Peng-zhou Hang Yu-yang Zheng Zhen-li Su Zhi-min Du
• 来源期刊: 中国药理学报（英文版）
• 关键词: aloe-emodin hyperlipidemia cholesterol PCSK9 LDL receptor HepG2 cells atorvastatin
• 年，卷（期）: 2020,（8）
• 页码范围: 1085-1092
• 页数: 8页
• 语种: 英文

摘要

Hyperlipidemia (HPL) characterized by metabolic disorder of lipids and cholesterol is one of the important risk factors for cardiovascular diseases.Proprotein convertase subtilisin/kexin type 9 (PCSKg) is a potent circulating regulator of LDL through its ability to induce degradation of the low-density lipoprotein cholesterol receptor (LDLR) in the lysosome of hepatocytes.Aloeemodin (AE) is one of potentially bioactive components of Chinese traditional medicine Daming capsule.In this study we evaluated the HPL-lowering efficacy of AE in both in vivo and in vitro HPL models.High-fat diet-induced rats were treated with AE (100 mg/kg per day,ig) for 6 weeks.We found that AE administration significantly decreased the levels of total cholesterol (TC) and LDL in the serum and liver tissues.Moreover,AE administration ameliorated HPL-induced hepatic lipid aggregation.But AE administration did not significantly inhibit HMG-CoA reductase activity in the liver of HPL rats.A cellular model of HPL was established in human hepatoma (HepG2) cells treated with cholesterol (20 μg/mL) and 25-hydroxycholesterol (2 μg/mL),which exhibited markedly elevated cholesterol levels.The increased cholesterol levels could be reversed by subsequent treatment with AE (30 μM).In both the in vivo and in vitro HPL models,we revealed that AE selectively suppressed the sterol-regulatory element-binding protein-2 (SREBP-2) and hepatocyte nuclear factor (HNF)1α-mediated PCSK9 signaling,which in turn upregulated LDL receptor (LDLR) and promoted LDL uptake.This study demonstrates that AE reduces cholesterol content in HPL rats by inhibiting the hepatic PCSKg/LDLR pathway.