Decreased astrocytic GFAP expression in streptozotocin-induced diabetes after gliotoxic lesion in the rat brainstem

Arq Bras Endocrinol Metabol. 2013 Aug;57(6):431-6. doi: 10.1590/s0004-27302013000600004.

Abstract

Objective: The aim of this study was to evaluate the effect of diabetic hyperglycemia on astrocyte function, estimated by means of glial fibrillary acidic protein - GFAP - immunohistochemical expression.

Materials and methods: Adult male rats received a single intravenous injection of streptozotocin (50 mg/kg) and were submitted 10 days later to a single injection of 10 microlitres 0.1% EB solution or 0.9% saline solution into the cisterna pontis. Ten microliters of 0.1% EB or 0.9% saline solution were also injected in non-diabetic rats. Animals were anesthetized and perfused through the heart 15 and 31 days after EB or saline injection, and brainstem sections were collected for ultrastructural analysis and GFAP immunohistochemical staining.

Results: The GFAP brown-stained areas were evaluated by colorimetry using a computerized image analysis system and the results have shown that diabetes hindered the increase of GFAP astrocyte expression in the EB-injected group compared to non-diabetic animals. However, diabetes did not affect GFAP response in the saline-injected group or in control animals.

Conclusion: Streptozotocin-induced diabetic condition reduced astrocytic GFAP expression following gliotoxic injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Astrocytes / metabolism*
  • Blood Glucose / metabolism*
  • Brain Stem / drug effects
  • Brain Stem / pathology*
  • Diabetes Mellitus, Experimental / pathology*
  • Disease Models, Animal
  • Ethidium / toxicity
  • Glial Fibrillary Acidic Protein / adverse effects
  • Glial Fibrillary Acidic Protein / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Rats
  • Rats, Wistar
  • Streptozocin

Substances

  • Blood Glucose
  • Glial Fibrillary Acidic Protein
  • Streptozocin
  • Ethidium