English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  TRANSGENIC OVEREXPRESSION OF CORTICOTROPIN RELEASING HORMONE PROVIDES PARTIAL PROTECTION AGAINST NEURODEGENERATION IN AN IN VIVO MODEL OF ACUTE EXCITOTOXIC STRESS

Hanstein, R., Lu, A., Wurst, W., Holsboer, F., Deussing, J. M., Clement, A. B., et al. (2008). TRANSGENIC OVEREXPRESSION OF CORTICOTROPIN RELEASING HORMONE PROVIDES PARTIAL PROTECTION AGAINST NEURODEGENERATION IN AN IN VIVO MODEL OF ACUTE EXCITOTOXIC STRESS. Neuroscience, 156(3), 712-721.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Hanstein, R., Author
Lu, A.1, Author           
Wurst, W.2, Author           
Holsboer, F.3, Author           
Deussing, J. M.4, Author           
Clement, A. B., Author
Behl, C.2, Author           
Affiliations:
1AG Almeida, Osborne, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607141              
2Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137              
3Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607139              
4AG Deussing, Jan, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607145              

Content

show
hide
Free keywords: CRH; BDNF; excitotoxicity; neuroprotection
 Abstract: Corticotropin releasing hormone (CRH) is the central modulator of the mammalian hypothalamic-pituitaryadrenal (HPA) axis. In addition, CRH affects other processes in the brain including learning, memory, and synaptic plasticity. Moreover, CRH has been shown to play a role in nerve cell survival under apoptotic conditions and to serve as an endogenous neuroprotectant in vitro. Employing mice over-expressing murine CRH in the CNS, we observed a differential response of CRH-overexpressing mice (CRH-COEhom-Nes) to acute excitotoxic stress induced by kainate compared with controls (CRH-COEcon-Nes). Interestingly, CRH-overexpression reduced the duration of epileptic seizures and prevented kainate-induced neurodegeneration and neuro-inflammation in the hippocampus. Our findings highlight a neuroprotective action of CRH in vivo. This neuroprotective effect was accompanied by increased levels of brain-derived neurotrophic factor (BDNF) in CRH-COEhom-Nes mice, suggesting a potential role for BDNF in mediating CRH-induced neuroprotective actions against acute excitotoxicity in vivo. (C) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.

Details

show
hide
Language(s): eng - English
 Dates: 2008-10-15
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 395621
ISI: 000260508100027
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Neuroscience
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 156 (3) Sequence Number: - Start / End Page: 712 - 721 Identifier: ISSN: 0306-4522