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Updated: Dec 21, 2025

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Published on: August 28, 2020
Neurophysiological control of urinary bladder storage and voiding-functional changes through development and
Youko Ikeda1,2
1School of Medicine, Renal-Electrolyte Division, University of Pittsburgh, A1219 Scaife Hall, Pittsburgh, PA, 15261, USA. yoi4@pitt.edu.
Understanding the neural control of the lower urinary tract (LUT) is crucial. This review details the development of bladder control from birth and the impact of congenital anomalies on urinary function.
Area of Science:
- Neuroscience
- Urology
- Developmental Biology
Background:
- The lower urinary tract (LUT) requires coordinated parasympathetic, sympathetic, and somatic nerve activity for urine storage and expulsion.
- Neonates initially lack voluntary bladder control, which develops as central nervous system (CNS) connections form.
- Congenital defects can impair LUT function, leading to conditions like urinary tract infections and kidney disease.
Purpose of the Study:
- To review current knowledge on the neurophysiological regulation of the LUT during human and animal development.
- To explore the consequences of congenital anomalies on LUT neural function.
Main Methods:
- Literature review of neurophysiological studies on LUT development.
- Analysis of animal models and human developmental data.
- Examination of congenital anomaly impacts on LUT neural regulation.
Main Results:
- Limited research exists on neonatal and postnatal LUT neurophysiological development compared to adult models.
- Congenital anomalies significantly affect the development of continence and voiding functions.
- Understanding developmental neuroregulation is key to addressing LUT dysfunction.
Conclusions:
- Further research is needed on the developmental neurophysiology of the LUT.
- Early identification and understanding of congenital anomalies are vital for preventing secondary urinary tract conditions.
- This review synthesizes current knowledge to guide future research and clinical practice.
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