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Molecular analysis of the role of the tachykinins in pain reward and anxiety
Reference
NEU15439
Principal Investigator / Supervisor
Professor John Quinn
Co-Investigators /
Co-Supervisors
Professor Stephen Hunt
Institution
University of Liverpool
Department
Human Anatomy and Cell Biology
Funding type
Research
Value (£)
290,564
Status
Completed
Type
Research Grant
Start date
01/01/2002
End date
01/01/2006
Duration
48 months
Abstract
The substance P (NK1) receptor is important in pain, anxiety and reward behaviours. Good receptor antagonists are not available for mice and although the NK1 receptor is widely expressed in the CNS, the areas modulating these different behaviours are unclear. We propose therefore a molecular and behavioural analysis using over-expression of the human NK1 (hNK1) gene from its own promoter in a bacterial artificial chromosome construct. We will i) replace the mouse NK1 receptor by the hNK1 receptor. ii) Over-express the hNK1 receptor gene to assess behavioural changes. iii) Flank exon 2 of the hNK1 gene with lox-P sites prior to transgenic delivery in NK1 null mice to allow targeted deletion of the hNK1 receptor. (Joint with grant 31/NEU15440).
Summary
unavailable
Committee
Closed Committee - Biochemistry & Cell Biology (BCB)
Research Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
Neurone (NEU) [2000]
Funding Scheme
X – not Funded via a specific Funding Scheme
Associated awards:
NEU15440 Molecular analysis of the role of the tachykinins in pain reward and anxiety
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