Alizarin increase glucose uptake through PI3K/Akt signaling and improve alloxan-induced diabetic mice

Future Med Chem. 2019 Mar;11(5):395-406. doi: 10.4155/fmc-2018-0515. Epub 2019 Jan 16.

Abstract

Aim: Alizarin (AZ), that can be isolated from Rubia cordifolia, has biological activities such as antioxidation and anti-inflammatory. This study aimed to investigate the effect of AZ on glucose and lipid metabolism disorders in alloxan-induced diabetic mice and also explored the effect of AZ on insulin resistance in 3T3-L1 adipocytes.

Results: The research showed that AZ could decrease fasting and postprandial blood glucose, TG, TC and MDA, and it could also increase liver glycogen levels and SOD activity in diabetic mice. AZ could significantly improve the glucose uptake of 3T3-L1 adipocytes under insulin resistance, and could also increase GLUT4 protein expression levels, IRS-1 and Akt protein phosphorylation.

Conclusion: These results showed that AZ has the potential to reduce blood sugar and improve insulin resistance.

Keywords: 3T3-L1; IRS-1/PI3K/Akt; alizarin; diabetes; insulin resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes
  • Alloxan
  • Animals
  • Anthraquinones / administration & dosage
  • Anthraquinones / pharmacology*
  • Anthraquinones / therapeutic use
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / metabolism
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / pharmacology*
  • Hypoglycemic Agents / therapeutic use
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance
  • Male
  • Mice
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects

Substances

  • Anthraquinones
  • Glucose Transporter Type 4
  • Hypoglycemic Agents
  • Insulin Receptor Substrate Proteins
  • alizarin
  • Alloxan
  • Proto-Oncogene Proteins c-akt
  • Glucose