Use this URL to cite or link to this record in EThOS:
Title: Modulation of nerve growth factor receptor expression in the urothelium and its relevance to ketmine induced cystitis
Author: Kidger, Elizabeth Anne
ISNI:       0000 0004 5357 0082
Awarding Body: University of Hull and the University of York
Current Institution: University of Hull
Date of Award: 2014
Availability of Full Text:
Access from EThOS:
Access from Institution:
Ketamine-induced cystitis (KIC) is a form of bladder pain syndrome (BPS) that usually arises following recreational abuse. Urothelial expression of the p75 low-affinity nerve growth factor receptor (NGFR) has been implicated in the aetiopathology of BPS. The aim of this project was to examine the expression of NGFR in urothelium and KIC and to identify modulators of NGFR expression. From the literature, candidate modulators identified were: ketamine, the transcriptional regulator Early growth response (Egr-1), glucocorticoids, cytokines, brain derived neurotrophic factor (BDNF) and ibuprofen, a non-steroidal anti-inflammatory drug. Immunoperoxidase labelling and semi-quantitative analysis was performed on normal and KIC surgical specimens for NGFR and Egr-1. Cell and organ culture systems were developed from which NGFR transcript and protein expression were assessed following exposure to the candidate modulators. NGFR was expressed by basal cells in all normal urothelial samples and extended suprabasally in KIC samples. A case study revealed widespread urothelial destruction and a non-patent urachal remnant with normal NGFR basal expression, in comparison to NGFR suprabasal extension in Von Brunn’s nests, which were patent with the luminal surface of the bladder. Using an in vitro approach NGFR transcript was most highly expressed by proliferating normal human urothelial cell cultures and was immunolocalised basally in differentiated cell sheets and organ cultures. Glucocorticoids, cytokines, BDNF and Egr-1 did not modulate NGFR expression. Cell death inducing concentrations of ibuprofen, ketamine or G418 up-regulated NGFR transcript and protein in cell and organ cultures. This study supports a urinary-mediated urothelial damage process in KIC and implicates NGFR upregulation in the pathogenesis. Ketamine and other toxins are able to directly up-regulate expression of NGFR in the urothelium and this study has laid the foundation for future exploration of the role of NGFR in the urothelial damage response.
Supervisor: Southgate, Jennifer; Baker, Simon C. Sponsor: Not available
Qualification Name: Thesis (M.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: Medicine