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Molecular analysis of the role of the tachykinins in pain reward and anxiety

ReferenceNEU15439
Principal Investigator / Supervisor Professor John Quinn
Co-Investigators /
Co-Supervisors
Professor Stephen Hunt
Institution University of Liverpool
DepartmentHuman Anatomy and Cell Biology
Funding typeResearch
Value (£) 290,564
StatusCompleted
TypeResearch Grant
Start date 01/01/2002
End date 01/01/2006
Duration48 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 TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative Neurone (NEU) [2000]
Funding SchemeX – not Funded via a specific Funding Scheme
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