Interleukin-1 beta exacerbates hypoxia-induced neuronal damage, but attenuates toxicity produced by simulated ischaemia and excitotoxicity in rat organotypic hippocampal slice cultures

Citation
Ak. Pringle et al., Interleukin-1 beta exacerbates hypoxia-induced neuronal damage, but attenuates toxicity produced by simulated ischaemia and excitotoxicity in rat organotypic hippocampal slice cultures, NEUROSCI L, 305(1), 2001, pp. 29-32
Citations number
16
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROSCIENCE LETTERS
ISSN journal
03043940 → ACNP
Volume
305
Issue
1
Year of publication
2001
Pages
29 - 32
Database
ISI
SICI code
0304-3940(20010601)305:1<29:IBEHND>2.0.ZU;2-N
Abstract
Using organotypic hippocampal slice cultures we have investigated the actio ns of Interleukin-1 (IL-1) in a number of injury paradigms. Low concentrati ons of IL-1 potentiated hypoxia-induced neurodegeneration whilst high conce ntrations had no effect. In contrast, higher concentrations of IL-1 were st rongly neuroprotective in models of combined oxygen/glucose deprivation and Nmethyl-D-aspartate toxicity, but no potentiation was observed at low IL-1 concentrations. Both protective and toxic effects of IL-1 were fully antag onized by IL-1 receptor antagonist. These data demonstrate that the effects of IL-1 on neutronal injury are complex, and may be directly related to th e injury paradigm studied. (C) 2001 Elsevier Science Ireland Ltd. All right s reserved.