Cross-organ sensitization between the prostate and bladder in an experimental rat model of lipopolysaccharide (LPS)-induced chronic pelvic pain syndrome

• Published in: BMC urology Vol. 21; no. 1; p. 113
• Main Authors: Aydogdu, Ozgu, Gocun, Pinar Uyar, Aronsson, Patrik, Carlsson, Thomas, Winder, Michael
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 21-08-2021; BioMed Central; BMC
• Subjects: Animal experimentation; Animals; Bladder; Chronic pain; Chronic Pain - physiopathology; Contractility; CPPS; Cystitis - physiopathology; Cytokines; Disease Models, Animal; Experiments; Farmakologi och toxikologi; Inflammation; Intravenous administration; Laparotomy; Lipopolysaccharide (LPS); Lipopolysaccharides; LUTS; Male; Metabolism; Methacholine; Mitogens; Overactive bladder; Pain; Pelvic pain; Pelvic Pain - physiopathology; Pelvis; Pharmacology and Toxicology; Prostate; Prostate - innervation; Prostate - pathology; Prostate - physiopathology; Prostatitis; Prostatitis - physiopathology; Rats; Rats, Sprague-Dawley; Receptors, Cholinergic - physiology; Receptors, Muscarinic - physiology; Sensory neurons; Software; Syndrome; Tumor necrosis factor-TNF; Urinary Bladder - innervation; Urinary Bladder - pathology; Urinary Bladder - physiopathology; Urinary Bladder, Overactive - etiology; Urinary incontinence; Urination; Urine; Urology; United States > US; Sweden; Bladder; Overactive bladder; LUTS; Prostate; CPPS; Lipopolysaccharide (LPS)
• ISSN: 1471-2490; 1471-2490
• DOI: 10.1186/s12894-021-00882-9

The aim of the current study was to investigate the effects of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) on bladder function via prostate-to-bladder cross-sensitization in a rat model of lipopolysaccharide (LPS)-induced prostate inflammation.
Male rats were intraprostatically injected with LPS or saline, serving as control. Micturition parameters were examined in a metabolic cage 10 or 14 days later. Subsequently, to evaluate bladder function, cystometry was performed. Micturition cycles were induced by saline infusion and cholinergic and purinergic contractile responses were measured by intravenous injection with methacholine and ATP, respectively. Thereafter, the prostate and bladder were excised and assessed histopathologically for possible inflammatory changes.
Metabolic cage experiments showed increased urinary frequency in rats with LPS-induced CP/CPPS. Cystometry showed a significant increase in the number of non-voiding contractions, longer voiding time and lower compliance in CP/CPPS animals compared to controls. Induction of CP/CPPS led to significantly reduced cholinergic and purinergic bladder contractile responses. Histopathological analysis demonstrated prostatic inflammation in CP/CPPS animals. There were no significant differences between the groups regarding the extent or the grade of bladder inflammation. Prostate weight was not significantly different between the groups.
The present study shows that prostate-to-bladder cross-sensitization can be triggered by an infectious focus in the prostate, giving rise to bladder overactivity and alterations in both afferent and efferent signalling. Future studies are required to fully understand the underlying mechanisms.