Platelet-rich plasma improves impaired glucose hemostasis, disrupted insulin secretion, and pancreatic oxidative stress in streptozotocin-induced diabetic rat

Growth Factors. 2019 Dec;37(5-6):226-237. doi: 10.1080/08977194.2020.1735382. Epub 2020 Mar 10.

Abstract

Our study aimed to investigate the effects of platelet-rich plasma (PRP) on impaired glucose homeostasis, disrupted islet insulin secretion, and pancreatic oxidative status in streptozotocin (STZ)-diabetic rats. A total of 64 Sprague-Dawley male were randomized to four groups including controls, diabetes, control-PRP, and diabetes-PRP. The rats received the PRP (0.5 ml/kg, SC injection) twice weekly for 4 weeks. Plasma glucose and insulin levels, pancreatic oxidative stress markers and islet insulin secretion and content were measured. Compared with the control group, in the diabetic group, increased plasma glucose and malondialdehyde (MDA) levels and decreased plasma insulin level, islet insulin secretion, pancreatic superoxide dismutase (SOD), and catalase activities were observed. PRP treatment significantly reduced plasma glucose and MDA levels and enhanced plasma insulin, antioxidant enzyme activity, islet insulin secretion, and content in the diabetic rats. These findings showed that PRP can improve pancreatic islet insulin secretion, pancreatic oxidative stress and regulate plasma insulin and glucose levels in diabetic rats.

Keywords: PRP; diabetic rat; islet insulin secretion; oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / analysis
  • Biomarkers / metabolism
  • Blood Glucose / analysis
  • Catalase / metabolism
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / therapy*
  • Disease Models, Animal
  • Glucose / metabolism*
  • Glucose Tolerance Test
  • Hemostasis
  • Insulin / metabolism*
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Islets of Langerhans / metabolism
  • Male
  • Malondialdehyde / analysis
  • Oxidative Stress
  • Pancreas / metabolism*
  • Pancreas / physiopathology
  • Platelet-Rich Plasma*
  • Rats
  • Rats, Sprague-Dawley
  • Streptozocin
  • Superoxide Dismutase / metabolism

Substances

  • Antioxidants
  • Biomarkers
  • Blood Glucose
  • Insulin
  • Intercellular Signaling Peptides and Proteins
  • Malondialdehyde
  • Streptozocin
  • Catalase
  • Superoxide Dismutase
  • Glucose