Hepatoprotective Effect of Loquat Leaf Flavonoids in PM2.5-Induced Non-Alcoholic Fatty Liver Disease via Regulation of IRs-1/Akt and CYP2E1/JNK Pathways

Int J Mol Sci. 2018 Oct 1;19(10):3005. doi: 10.3390/ijms19103005.

Abstract

Ambient air particulate matter (PM) represents a class of heterogeneous substances present in polluted air, which contains many harmful components. Exposure to ambient particulate matter in fine rages (PM2.5) is associated with non-alcoholic fatty liver disease (NAFLD). Loquat Leaf possesses pharmacological actions on NAFLD. As the main biological active ingredients, the potential therapeutic role of total flavonoids (TF) isolated from Loquat Leaf in PM2.5-induced NAFLD model remains unclear. The present study was designed to explore the hepatoprotective effect of TF in PM2.5-induced NAFLD mice with its related mechanisms of action. Mice were exposed to PM2.5 to induce NAFLD, and body weight, the ratio of liver to body weight, and blood lipids increased significantly compared with the control group. It was found that TF significantly reduced the above parameters in PM2.5-induced NAFLD mice. TF treatment alleviated oxidative stress by preventing the accumulation of oxidative product malondialdehyde (MDA) and by strengthening the anti-oxidative capacity of superoxide dismutase (SOD). TF was also found to reduce the alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activity in the PM2.5 group. In addition, TF repaired the PM2.5-induced decline of insulin receptor substrate-1 (IRs-1) and protein kinase B (Akt) phosphorylation. Meanwhile, the data showed TF suppressed the expression of cytochrome P450 2E1(CYP2E1) and the phosphorylation of c-jun N-terminal kinase (JNK) in PM2.5-induced NAFLD. Taken together, these findings show that TF alleviate PM2.5-induced NAFLD via regulation of IRs-1/Akt and CYP2E1/JNK pathways, which may have potential for further development as novel therapeutic agents for NAFLD.

Keywords: CYP2E1/JNK; IRs/Akt; Loquat Leaf; PM2.5; insulin resistance; non-alcoholic fatty liver disease; oxidative stress; total flavonoids.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Cytochrome P-450 CYP2E1 / metabolism*
  • Eriobotrya / chemistry*
  • Flavonoids / chemistry
  • Flavonoids / pharmacology
  • Flavonoids / therapeutic use*
  • Insulin Receptor Substrate Proteins / metabolism*
  • Insulin Resistance
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Lipid Metabolism / drug effects
  • Liver / drug effects
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Models, Biological
  • Non-alcoholic Fatty Liver Disease / chemically induced
  • Non-alcoholic Fatty Liver Disease / drug therapy*
  • Non-alcoholic Fatty Liver Disease / pathology
  • Organ Size / drug effects
  • Oxidative Stress / drug effects
  • Particulate Matter
  • Plant Leaves / chemistry
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction

Substances

  • Flavonoids
  • Insulin Receptor Substrate Proteins
  • Particulate Matter
  • Protective Agents
  • Cytochrome P-450 CYP2E1
  • Proto-Oncogene Proteins c-akt
  • JNK Mitogen-Activated Protein Kinases