Ameliorative effects of bone marrow derived pancreatic progenitor cells on hyperglycemia and oxidative stress in diabetic rats

Acta Histochem. 2018 Jul;120(5):412-419. doi: 10.1016/j.acthis.2018.05.001. Epub 2018 May 8.

Abstract

The present study aimed to investigate the effects of Bone marrow derived pancreatic progenitor cells (BM- PPCs) in diabetic rats. It was conducted on 30 adult male Sprague-Dawley rats weighing 200-220 g. They were divided into three groups: (a) Group 1 was the control group; (b) Group 2 was the diabetic (induced diabetic by a single intraperitoneal (IP) injection of streptozotocin (STZ) (60 mg/kg) and (c) Group 3 was the treated (received injection of 2.5 X 106 BM- PPCs via the tail vein twice with a 21-day time interval). The blood glucose level was estimated weekly, the oxidative stress and insulin gene expression were evaluated at the end of the experiment. Pancreatic tissue histopathology was performed. The insulin immuno-histochemical reaction was applied to the islets. The blood glucose level was reduced in the treated group over time till reaching its acceptable level whereas it was increased in the diabetic group. The oxidative stress was decreased in the treated group compared to the diabetic one. The treated group showed increased expression of the insulin gene compared to the diabetic group. The immune-histochemical analysis of insulin showed an increased number and size of pancreatic islets in the treated group compared to the diabetic one. Thus, the twofold injection of BM- PPCs could restore the normal beta-cell morphology and function.

Keywords: Diabetes mellitus; Gene expression; Insulin; Mesenchymal stem cells.

MeSH terms

  • Animals
  • Diabetes Mellitus* / chemically induced
  • Flow Cytometry
  • Hyperglycemia / therapy*
  • Insulin / genetics
  • Insulin / metabolism
  • Islets of Langerhans / cytology*
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Oxidative Stress
  • Rats
  • Rats, Sprague-Dawley
  • Reference Standards
  • Stem Cells*

Substances

  • Insulin