The effects of neuromodulation in a novel obese-prone rat model of detrusor underactivity

被引:8
作者
Gonzalez, Eric J. [1 ]
Grill, Warren M. [1 ,2 ,3 ,4 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Dept Elect & Comp Engn, Durham, NC 27708 USA
[3] Duke Univ, Dept Neurobiol, Durham, NC 27708 USA
[4] Duke Univ, Dept Neurosurg, Durham, NC 27708 USA
基金
美国国家卫生研究院;
关键词
detrusor underactivity; obesity; electrical stimulation; voiding efficiency; SYMPATHETIC-NERVOUS-SYSTEM; VOIDING DYSFUNCTION; STRESS-INCONTINENCE; PUDENDAL AFFERENTS; MICTURITION REFLEX; OVERACTIVE BLADDER; COMPONENT REFLEXES; URINARY RETENTION; FEMALE RAT; INSULIN;
D O I
10.1152/ajprenal.00242.2017
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Obesity is a global epidemic associated with an increased risk for lower urinary tract dysfunction. Inefficient voiding and urinary retention may arise in late-stage obesity when the expulsive force of the detrusor smooth muscle cannot overcome outlet resistance. Detrusor underactivity (DUA) and impaired contractility may contribute to the pathogenesis of nonobstructive urinary retention. We used cystometry and electrical stimulation of peripheral nerves (pudendal and pelvic nerves) to characterize and improve bladder function in urethane-anesthetized obeseprone (OP) and obese-resistant (OR) rats following diet-induced obesity (DIO). OP rats exhibited urinary retention and impaired detrusor contractility following DIO, reflected as increased volume threshold, decreased peak micturition pressure, and decreased voiding efficiency (VE) compared with OR rats. Electrical stimulation of the sensory branch of the pudendal nerve did not increase VE, whereas patterned bursting stimulation of the motor branch of the pudendal nerve increased VE twofold in OP rats. OP rats required increased amplitude of electrical stimulation of the pelvic nerve to elicit bladder contractions, and maximum evoked bladder contraction amplitudes were decreased relative to OR rats. Collectively, these studies characterize a novel animal model of DUA that can be used to determine pathophysiology and suggest that neuromodulation is a potential management option for DUA.
引用
收藏
页码:F815 / F825
页数:11
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