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Effects of verapamil on bladder instability induced by partial outflow obstruction in rat.

作者信息

Saito M, Kondo A

机构信息

Department of Urology, Nagoya University School of Medicine, Japan.

出版信息

Int Urol Nephrol. 1998;30(5):543-52. doi: 10.1007/BF02550542.

DOI:10.1007/BF02550542
PMID:9934794
Abstract

BACKGROUND

Overactivity of the detrusor due to benign prostatic hyperplasia may be induced by hyperpermeability of the smooth muscle cell membrane to calcium. We investigated the effect of verapamil, a calcium channel blocker, on detrusor function in outflow obstructed and control rat bladders.

METHODS

Verapamil was injected intravenously via a catheter inserted into the internal jugular vein in doses of 0.5, 1.0, 2.0, 4.0, and 10.0 mg/kg in rat bladders with and without partial outflow obstruction under urethane anaesthesia. The intravesical pressure was monitored continuously. We measured the tidal voided urine volume, the voiding pressure, the pressure at which micturition was induced, and the end-point pressure of micturition.

RESULTS

The tidal voided urine volume was significantly decreased in the obstructed bladders before administration of verapamil. Verapamil had similar effects in cystometric parameters in obstructed and control bladders. Verapamil increased the tidal voided urine volume, the pressure at which micturition was induced, and the end-point pressure of micturition, and reduced the voiding in obstructed and control bladders. Verapamil at doses of 4.0 mg/kg or higher induced significant arrhythmia.

CONCLUSIONS

Verapamil reduced the contractile force of the bladder and increased the capacity and residual urine volume in both normal and obstructed bladders. Thus, although calcium channel blockers such as verapamil may be effective in treating a hyperactive bladder, they may have adverse cardiovascular effects.

摘要

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Effect of partial outlet obstruction of the rat urinary bladder on the response to alterations in the concentrations of potassium and calcium.大鼠膀胱部分出口梗阻对钾和钙浓度变化反应的影响
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J Urol. 1993 Sep;150(3):1045-51. doi: 10.1016/s0022-5347(17)35683-5.
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