Physical activity effects on bladder dysfunction in an obese and insulin-resistant murine model
André Matos de Oliveira1, Fernando Mello Froes Fonseca1, Sabrina Thalita Reis1
1Laboratory of Medical Research - LIM 55, Urology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
Physiological Reports
|April 27, 2021
Summary
Physical activity may prevent high-fat diet-induced bladder dysfunction by modulating the insulin signaling pathway. Exercise improved bladder function and insulin pathway gene expression in obese mice.
Area of Science:
- Metabolic Syndrome
- Urology
- Exercise Physiology
Background:
- Obesity and insulin resistance are linked to bladder dysfunction.
- The role of physical activity in mitigating these effects requires further investigation.
Purpose of the Study:
- To examine how physical activity influences bladder function and molecular changes in an obese, insulin-resistant mouse model.
- To investigate the impact of a high-fat diet and physical activity on the insulin signaling pathway in bladder tissue.
Main Methods:
- Wistar rats were divided into four groups based on diet (standard vs. high-fat) and physical activity (swimming vs. sedentary).
- Urodynamic studies (UDS) assessed bladder function.
- Quantitative real-time PCR analyzed gene expression in the insulin pathway (IRS1/IRS2/PI3K/AKT/eNOS).
Main Results:
- Physical activity reduced body weight gain in rats on both standard and high-fat diets.
- The high-fat diet group without physical activity exhibited higher insulin levels, insulin resistance (HOMA-IR), and significant bladder dysfunction (increased micturition frequency, postvoid pressure; decreased capacity, compliance).
- Physical activity was associated with overexpression of the insulin signaling pathway, while a high-fat diet led to its underexpression.
Conclusions:
- The insulin signaling pathway is implicated in high-fat diet-induced bladder dysfunction.
- Physical activity may serve as a protective strategy against diet-induced bladder dysfunction by positively influencing the insulin pathway.


