Immunomodulatory effect of the purine nucleoside inosine following spinal cord contusion injury in rat
Study design: In vivo study using a moderate spinal cord contusion injury (SCI) model in adult rat. Objective: To assess the immunomodulatory effects of the purine nucleoside inosine on macrophage/microglia activation at and near the lesion site and in white matter areas remote from the injury epice...
Gespeichert in:
Veröffentlicht in: | Spinal cord 2008-01, Vol.46 (1), p.39-44 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Study design:
In vivo
study using a moderate spinal cord contusion injury (SCI) model in adult rat.
Objective:
To assess the immunomodulatory effects of the purine nucleoside inosine on macrophage/microglia activation at and near the lesion site and in white matter areas remote from the injury epicenter.
Setting:
Department of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY, USA.
Methods:
Animals (
N
=56) were injured using a moderate SCI at T9–T10 spinal level and were divided into three groups, depending on treatment paradigm. Rats received either intraperitoneal or subcutaneous injections of inosine (
N
=28) or vehicle (
N
=28). Spinal cord tissue was processed for ED-1 immunoreactivity and the volume fraction of ED-1
+
profiles was calculated using the Cavalieri method and unbiased stereology.
Results:
The volume fraction of ED-1
+
profiles within gray and lateral white matter regions at and around the lesion site was significantly reduced only following a twice daily-6 week treatment course, compared with vehicle controls, and white matter areas remote from the lesion were unaffected by all inosine treatment paradigms.
Conclusions:
Continued subcutaneous delivery of inosine, beginning 15-min post-SCI and persisting throughout the survival period of 6 weeks exerted immunomodulatory effects at and around the lesion site. |
---|---|
ISSN: | 1362-4393 1476-5624 |
DOI: | 10.1038/sj.sc.3102057 |