The effect of Chinese medicine Pu-Ren-Dan on pancreatic angiogenesis in high fat diet/streptozotocin-induced diabetic rats

Indian J Pharmacol. 2013 Nov-Dec;45(6):556-62. doi: 10.4103/0253-7613.121364.

Abstract

Objectives: The islet vascular system is critical for β-cell function. This study investigated the antidiabetic effect of the Chinese Pu-Ren-Dan (PRD) recipe by regulating the pancreatic angiogenic factors in T2DM rats.

Materials methods: High fat diet/streptozotocin-induced obese type-2 diabetes mellitus rats were developed and treated with PRD for 4 weeks. Then glucolipid metabolism, insulin secretion, pancreatic blood flow, ultrastructure of islet β-cell, histological changes of islet and protein expressions of pancreatic angiogenic factors were investigated.

Results: PRD-reduced T2DM rats' body weight and blood glucose level resisted the lipid metabolism disturbance, and ameliorated the insulin resistance and β-cell function. In addition, the histological and morphological studies proved that PRD could maintain the normal distribution of endocrine cell in islet and normal ultrastructure of β cell. An increased pancreatic blood flow was observed after the PRD treatment. In the investigation of pancreatic angiogenic factors, PRD inhibited the decreased expression of VEGF and Ang-1, and reversed the reduction of VEGFR2 and Tie2 phosphorylation in T2DM rats; the Ang-2 and TGFβ expression were up-regulated by PRD while PKC was activated; endostatin and angiostatin were down-regulated by PRD.

Conclusions: The results suggest that increasing VEGF expression, regulating VEGF/VEGFR2 signaling, stimulating Ang-1/Tie-2 signaling pathway, and inhibiting PKC-TGFβ signaling and antiangiogenic factors might be the underlying mechanism of PRD's antidiabetic effect.

Keywords: Pancreatic angiogenic factors; traditional Chinese medicine Pu-Ren-Dan; type-2 diabetes mellitus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / physiopathology*
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Diet, High-Fat*
  • Drugs, Chinese Herbal
  • Insulin / metabolism
  • Insulin Secretion
  • Male
  • Neovascularization, Pathologic / prevention & control*
  • Pancreas / blood supply
  • Pancreas / drug effects*
  • Phosphorylation
  • Rats
  • Rats, Wistar
  • Receptor, TIE-2 / metabolism
  • Streptozocin
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • Blood Glucose
  • Drugs, Chinese Herbal
  • Insulin
  • Streptozocin
  • Receptor, TIE-2
  • Vascular Endothelial Growth Factor Receptor-2