Purinergic signalling: therapeutic developments

G Burnstock - Frontiers in pharmacology, 2017 - frontiersin.org
Purinergic signalling, ie, the role of nucleotides as extracellular signalling molecules, was
proposed in 1972. However, this concept was not well accepted until the early 1990's when …

Purinergic signalling in the urinary tract in health and disease

G Burnstock - Purinergic signalling, 2014 - Springer
Purinergic signalling is involved in a number of physiological and pathophysiological
activities in the lower urinary tract. In the bladder of laboratory animals there is …

Novel insights into the mechanism of cyclophosphamide-induced bladder toxicity: chloroacetaldehyde's contribution to urothelial dysfunction in vitro

KA Mills, R Chess-Williams, C McDermott - Archives of Toxicology, 2019 - Springer
The clinical use of cyclophosphamide and ifosfamide is limited by a resultant bladder toxicity
which has been attributed to the metabolite acrolein. Another metabolite chloroacetaldehyde …

The therapeutic potential of purinergic signalling

G Burnstock - Biochemical pharmacology, 2018 - Elsevier
This review is focused on the pathophysiology and therapeutic potential of purinergic
signalling. A wide range of diseases are considered, including those of the central nervous …

Signalling molecules in the urothelium

M Winder, G Tobin, D Zupančič… - BioMed research …, 2014 - Wiley Online Library
The urothelium was long considered to be a silent barrier protecting the body from the toxic
effects of urine. However, today a number of dynamic abilities of the urothelium are well …

A systematic review of therapeutic approaches used in experimental models of interstitial cystitis/bladder pain syndrome

T Kuret, D Peskar, A Erman, P Veranič - Biomedicines, 2021 - mdpi.com
Interstitial cystitis/bladder pain syndrome (IC/BPS) is a multifactorial, chronic bladder
disorder with limited therapeutic options currently available. The present review provides an …

Uroprotective mechanisms of natural products against cyclophosphamide-induced urinary bladder toxicity: A comprehensive review

I Sherif - Acta Scientiarum Polonorum Technologia Alimentaria, 2020 - food.actapol.net
One of the widely used anticancer drugs for the treatment of various neoplasms is
cyclophosphamide (CYP). The inactive prodrug CYP is metabolized by cytochrome P450 …

Research findings on overactive bladder

PB Patra, S Patra - Current urology, 2015 - karger.com
Several physiopathologic conditions lead to the manifestation of overactive bladder (OAB).
These conditions include ageing, diabetes mellitus, bladder outlet obstruction, spinal cord …

Inhibition of NMDAR reduces bladder hypertrophy and improves bladder function in cyclophosphamide induced cystitis

M Liu, S Shen, DM Kendig, S Mahavadi… - The Journal of …, 2015 - auajournals.org
Purpose: We examined the role of NMDAR in the regulation of bladder hypertrophy and
function in a rat model of cyclophosphamide induced cystitis. Materials and Methods: Cystitis …

Hypersensitivity of bladder low threshold, wide dynamic range, afferent fibres following treatment with the chemotherapeutic drugs cyclophosphamide and ifosfamide

KA Mills, EJ West, L Grundy, C McDermott… - Archives of …, 2020 - Springer
The cytotoxic drugs cyclophosphamide (CPO) and ifosfamide (IFO) cause toxic urological
effects due to the production of urinary metabolites that cause bladder inflammation. This …