Potential signalling pathways underlying corticotrophin-releasing hormone-mediated neuroprotection from excitotoxicity in rat hippocampus
Article first published online: 21 JAN 2002
Journal of Neurochemistry
Volume 80, Issue 3, pages 416–425, February 2002
How to Cite
Elliott-Hunt, C. R., Kazlauskaite, J., Wilde, G. J. C., Grammatopoulos, D. K. and Hillhouse, E. W. (2002), Potential signalling pathways underlying corticotrophin-releasing hormone-mediated neuroprotection from excitotoxicity in rat hippocampus. Journal of Neurochemistry, 80: 416–425. doi: 10.1046/j.0022-3042.2001.00712.x
- Issue published online: 21 JAN 2002
- Article first published online: 21 JAN 2002
- Received May 30, 2001; revised manuscript received October 8, 2001; accepted October 31, 2001.
- corticotrophin-releasing hormone (CRH);
- mitogen-activating protein kinase (MAPK);
In several neurological disorders including cerebral ischaemia, glutamate has been implicated as a neurotoxic agent in the mechanisms leading to neuronal cell death. The role of corticotrophin-releasing hormone (CRH), the 41-amino acid peptide, which activates the HPA axis in response to stressful stimuli, remains controversial. In this study, we report that CRH in low physiological concentrations (2 pm), prevented glutamate-induced neurotoxicity via receptor-mediated mechanisms when administered to organotypic hippocampal cultures both during and after the glutamate-induced insult. Detailed investigations on the mechanisms mediating this neuroprotective effect showed that activation of the adenylate cyclase pathway and induction of MAP kinase phosphorylation mediate the CRH action. In addition we showed that CRH can inhibit the phosphorylation of JNK/SAPK by glutamate. Most importantly, we showed that CRH can afford neuroprotection against neurotoxicity up to 12 h following the insult, suggesting that CRH is acting at a late stage in the neuronal death cycle, and this might be important in the development of novel neuroprotective agents in order to improve neuronal survival following the insult.