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Updated: Jun 12, 2025

The Forced Swim Test as a Model of Depressive-like Behavior
Published on: March 2, 2015
Escitalopram can reverse co-occurring depression and overactive bladder induced by corticosterone in rats
Gongyue Liu1, Zhonghan Zhou1, Xin Liu2
1School of Rehabilitation of Capital Medical University, Department of Urology, China Rehabilitation Research Center, Beijing, China; China Rehabilitation Science Institute, Beijing, China; Urological and Pelvic Floor Rehabilitation Center, Beijing Bo'ai Hospital, Beijing, China.
Objectives:
This study aimed to investigate the effects of escitalopram, a selective serotonin reuptake inhibitor (SSRI), on depressive symptoms and bladder function in a rat model of coexisting depression and overactive bladder (OAB) induced by corticosterone (CORT).
Materials And Methods:
Depression and OAB were induced in 30 female Sprague-Dawley rats via subcutaneous CORT injections (20 mg/kg/day for 14 days). After treatment with escitalopram (10 mg/kg/day), solifenacin (10 mg/kg/day), mirabegron (1 mg/kg/day), or saline(1 ml/kg/day) for 14 days, behavioral tests (Novel Object Recognition Task [NORT] and Tail Suspension Test [TST]) and cystometric analysis were performed to assess depressive symptoms and bladder dysfunction.
Results:
Treatment with escitalopram significantly reversed depressive symptoms, as indicated by the NORT index and immobility time in TST. Cystometry showed that escitalopram improved bladder parameters, including bladder capacity (BC), inter-contraction interval (ICI), and bladder compliance, to a greater extent than CORT + saline, with values restored to those of the control group. In contrast, neither solifenacin nor mirabegron showed significant improvements in these parameters.
Conclusion:
Escitalopram effectively alleviates both depressive symptoms and bladder dysfunction in a rat model of coexisting depression and OAB. These findings suggest that escitalopram may offer a promising dual-acting therapeutic approach for patients with both conditions. Further studies are required to examine its long-term efficacy and safety in clinical practice.
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