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Urinary Bladder Distention Evoked Visceromotor Responses as a Model for Bladder Pain in Mice
Published on: April 27, 2014
Responses of acrylamide-treated rat bladders
E Nurullahoglu-Atalik1, N Okudan, M Belviranli
1Department of Pharmacology, Necmettin Erbakan University, Konya, Turkey.
Bratislavske Lekarske Listy
|December 21, 2012
Summary
Acrylamide (ACR) exposure in rats impaired urinary bladder function and caused significant tissue damage. This study highlights ACR
Area of Science:
- Toxicology
- Urology
- Pharmacology
Background:
- Acrylamide (ACR) is an industrial chemical and a food contaminant.
- ACR is a known neurotoxicant, reproductive toxicant, and carcinogen in animal models.
- Its effects on the urinary bladder, particularly concerning contractile responses and tissue integrity, require further investigation.
Purpose of the Study:
- To investigate the impact of ACR exposure on rat urinary bladder contractility.
- To assess ACR's influence on receptor-dependent (carbachol) and receptor-independent (KCl) contractions.
- To examine potential gender-specific differences in ACR-induced urinary bladder effects.
Main Methods:
- Rats of both genders were administered ACR daily for 90 days at doses of 2 mg/kg/d (ACR-I) or 5 mg/kg/d (ACR-II).
- Control groups received no ACR treatment.
- Urinary bladder responses to cumulative concentrations of carbachol and KCl were measured and analyzed.
Main Results:
- ACR treatment significantly increased the EC50 values for both carbachol and KCl, indicating reduced bladder sensitivity.
- No significant changes were observed in the maximal contractile responses to carbachol or KCl.
- Histopathological examination revealed increased edema, inflammation, fibrosis, and epithelial damage in ACR-treated bladders compared to controls.
Conclusions:
- ACR exposure induces significant urinary bladder injury in rats.
- The functional and structural damage suggests a detrimental effect of ACR on bladder physiology.
- These findings underscore the potential risks associated with ACR exposure to the urinary system.

