Mice Fed a High-Cholesterol Diet Supplemented with Quercetin-3-Glucoside Show Attenuated Hyperlipidemia and Hyperinsulinemia Associated with Differential Regulation of PCSK9 and LDLR in their Liver and Pancreas

Mol Nutr Food Res. 2018 May;62(9):e1700729. doi: 10.1002/mnfr.201700729. Epub 2018 Apr 23.

Abstract

Scope: Hepatic LDL receptor (LDLR) and proprotein convertase subtilisin/kexin type 9 (PCSK9) regulate the clearance of plasma LDL-cholesterol (LDL-C): LDLR promotes it, and PCSK9 opposes it. These proteins also express in pancreatic β cells. Using cultured hepatocytes, we previously showed that the plant flavonoid quercetin-3-glucoside (Q3G) inhibits PCSK9 secretion, stimulated LDLR expression, and enhanced LDL-C uptake. Here, we examine whether Q3G supplementation could reverse the hyperlipidemia and hyperinsulinemia of mice fed a high-cholesterol diet, and how it affects hepatic and pancreatic LDLR and PCSK9 expression.

Methods and results: For 12 weeks, mice are fed a low- (0%) or high- (1%) cholesterol diet (LCD or HCD), supplemented or not with Q3G at 0.05 or 0.1% (w/w). Tissue LDLR and PCSK9 is analyzed by immunoblotting, plasma PCSK9 and insulin by ELISA, and plasma cholesterol and glucose by colorimetry. In LCD-fed mice, Q3G has no effect. In HCD-fed mice, it attenuates the increase in plasma cholesterol and insulin, accentuates the decrease in plasma PCSK9, and increases hepatic and pancreatic LDLR and PCSK9. In cultured pancreatic β cells, however, it stimulates PCSK9 secretion.

Conclusion: In mice, dietary Q3G could counter HCD-induced hyperlipidemia and hyperinsulinemia, in part by oppositely modulating hepatic and pancreatic PCSK9 secretion.

Keywords: LDLR; PCSK9; high-cholesterol diet; mice; quercetin glycoside.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cholesterol, Dietary / adverse effects
  • Dietary Supplements / adverse effects
  • Gene Expression Regulation
  • Glucose Transporter Type 2 / agonists
  • Glucose Transporter Type 2 / antagonists & inhibitors
  • Glucose Transporter Type 2 / genetics
  • Glucose Transporter Type 2 / metabolism
  • Hyperinsulinism / blood
  • Hyperinsulinism / metabolism
  • Hyperinsulinism / pathology
  • Hyperinsulinism / prevention & control
  • Hyperlipidemias / blood
  • Hyperlipidemias / metabolism
  • Hyperlipidemias / pathology
  • Hyperlipidemias / prevention & control*
  • Hypolipidemic Agents / administration & dosage
  • Hypolipidemic Agents / adverse effects
  • Hypolipidemic Agents / therapeutic use*
  • Insulin Resistance
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / pathology
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Mice, Inbred C57BL
  • Non-alcoholic Fatty Liver Disease / blood
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Non-alcoholic Fatty Liver Disease / pathology
  • Non-alcoholic Fatty Liver Disease / prevention & control
  • Organ Specificity
  • Pancreas / metabolism*
  • Pancreas / pathology
  • Proprotein Convertase 9 / blood
  • Proprotein Convertase 9 / genetics
  • Proprotein Convertase 9 / metabolism*
  • Quercetin / administration & dosage
  • Quercetin / adverse effects
  • Quercetin / analogs & derivatives*
  • Quercetin / therapeutic use
  • Receptors, LDL / genetics
  • Receptors, LDL / metabolism*

Substances

  • Cholesterol, Dietary
  • Glucose Transporter Type 2
  • Hypolipidemic Agents
  • Receptors, LDL
  • Slc2a2 protein, mouse
  • isoquercitrin
  • Quercetin
  • Pcsk9 protein, mouse
  • Proprotein Convertase 9