Glycation increases the permeability of proteins across the blood-nerve and blood-brain barriers

Brain Res Mol Brain Res. 1994 Apr;23(1-2):157-62. doi: 10.1016/0169-328x(94)90222-4.

Abstract

Our previous investigations have demonstrated increased permeability across the blood-nerve barrier of human plasma albumin after glycation with D-glucose [J.F. Poduslo and G.L. Curran, Proc. Natl. Acad. Sci. USA, 89 (1992) 2218-2222]. In the present investigation, the generality of this observation was evaluated by measuring the permeability coefficient-surface area product (PS) after correction for the residual plasma volume (Vp) across the blood-nerve barrier (BNB), as well as the blood-brain barrier (BBB), for nerve growth factor (NGF) and human IgG after in vitro glycation with D-glucose using an i.v. bolus injection technique in the cannulated brachial vein and artery of normal adult rats. Glycated proteins (gNGF and gIgG) had significantly decreased circulating plasma half-lives compared to the non-glycated proteins. The PS across the BNB obtained for gNGF was significantly increased compared to NGF with a 2.0-fold increase observed after 8 weeks of glycation and a 5.1-fold increase at 21 weeks of glycation. The Vp measurement for NGF and gNGF across the BNB was not significantly different at 8 weeks of glycation but was 1.3-fold greater at 21 weeks of glycation. The PS across the BBB for gNGF was about 2-fold greater than NGF with a glycation time of 8 weeks and 3.2-3.6-fold greater with a glycation time of 21 weeks for six different brain regions. No changes were observed in the Vp for any of the brain regions for gNGF compared to NGF. The PS across the BNB for gIgG compared to IgG was significantly greater with a 4.1-fold relative increase and no significant difference in the Vp values.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blood-Brain Barrier*
  • Brain / anatomy & histology
  • Brain / metabolism*
  • Glycoproteins / pharmacokinetics*
  • Glycosylation
  • Half-Life
  • Immunoglobulin G / metabolism*
  • Male
  • Nerve Growth Factors / pharmacokinetics*
  • Organ Specificity
  • Permeability
  • Protein Processing, Post-Translational
  • Rats
  • Rats, Sprague-Dawley
  • Sciatic Nerve / blood supply
  • Sciatic Nerve / metabolism*

Substances

  • Glycoproteins
  • Immunoglobulin G
  • Nerve Growth Factors