Nitric oxide modulates blood-brain barrier permeability during infections with an inactivated bacterium

Neuroreport. 1995 Aug 21;6(12):1629-32. doi: 10.1097/00001756-199508000-00010.

Abstract

The objective of the present investigation was to study the involvement of NO in regulating the permeability of the blood-brain barrier (BBB) during infections, since NOS is known to be induced following infections. The administration of inactivated Escherichia coli (a source of lipopolysaccharide) or poly (I:C), an interferon inducer, to rats increased the permeability of BBB significantly. This increase was found to be potentiated in the presence of L-arginine, a substrate for NOS, while D-arginine had no such effect. N-nitro L-arginine methyl ester, an inhibitor of NOS, and dexamethasone, an inhibitor of NOS induction, blocked the E. coli-induced effects. These results suggest that during infections, NOS inductions causes the release of large quantities of NO, resulting in increased BBB permeability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine / analogs & derivatives
  • Arginine / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Escherichia coli
  • Infections / drug therapy*
  • Male
  • NG-Nitroarginine Methyl Ester
  • Nitric Oxide / pharmacology*
  • Permeability / drug effects*
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors

Substances

  • Enzyme Inhibitors
  • Nitric Oxide
  • Arginine
  • NG-Nitroarginine Methyl Ester