TY - JOUR
T1 - Impaired micturition reflex caused by acute selective dorsal or ventral root(s) rhizotomy in anesthetized rats
AU - Liao, Jiuan Miaw
AU - Cheng, Chen Li
AU - Lee, Shin Da
AU - Chen, Gin Den
AU - Chen, Kuo Jung
AU - Yang, Chao Hsun
AU - Pan, Shwu Fen
AU - Chen, Mei Jung
AU - Huang, Pei Chen
AU - Lin, Tzer Bin
PY - 2006
Y1 - 2006
N2 - Purpose: To clarify the contributions of parasympathetic inputs and outputs to the micturition reflex. Materials and Methods: Intra-vesical pressure (IVP), external urethral sphincter electromyogram (EMG), pelvic afferent nerve activities (PANA), and pelvic efferent nerve activities (PENA) as well as the time-derived IVP (dIVP, an index of bladder contractility) were evaluated in intact and acute dorsal or ventral root(s) rhizotomized (DRX and VRX, respectively) rats. Results: In DRX rats, when compared with that in intact stage, the voiding frequency was decreased (75 ± 15% of intact, P <0.05, n = 8), while the threshold pressure to trigger voiding contractions was significantly increased (187 ± 75% of intact, P <0.05, n = 8). In addition, several insufficient contractions (5.3 ± 3.5 contractions/voiding, P <0.05, n = 8) occurred in ahead of each voiding contraction. On the other hand, in VRX rats, the peak and rebound IVP were significantly decreased (90 ± 3.5% and 75 ± 11.3% of intact, P <0.01, n = 8), while the threshold pressure was not affected (102 ± 11% of intact, P = NS, n = 8). The time-derived parameters were significantly decreased in VRX (peak dIVP, 78 ± 10.2%, rebound dIVP, 75 ± 15.6%, minimal dIVP, 68 ± 14% of intact, P <0.01, n = 8) but only peak dIVP was decreased (85 ± 11% of intact, P <0.01, n = 8) in DRX rats. Conclusion: Acute selective DRX and VRX rat can be an animal model to investigate peripheral neural control in micturition functions.
AB - Purpose: To clarify the contributions of parasympathetic inputs and outputs to the micturition reflex. Materials and Methods: Intra-vesical pressure (IVP), external urethral sphincter electromyogram (EMG), pelvic afferent nerve activities (PANA), and pelvic efferent nerve activities (PENA) as well as the time-derived IVP (dIVP, an index of bladder contractility) were evaluated in intact and acute dorsal or ventral root(s) rhizotomized (DRX and VRX, respectively) rats. Results: In DRX rats, when compared with that in intact stage, the voiding frequency was decreased (75 ± 15% of intact, P <0.05, n = 8), while the threshold pressure to trigger voiding contractions was significantly increased (187 ± 75% of intact, P <0.05, n = 8). In addition, several insufficient contractions (5.3 ± 3.5 contractions/voiding, P <0.05, n = 8) occurred in ahead of each voiding contraction. On the other hand, in VRX rats, the peak and rebound IVP were significantly decreased (90 ± 3.5% and 75 ± 11.3% of intact, P <0.01, n = 8), while the threshold pressure was not affected (102 ± 11% of intact, P = NS, n = 8). The time-derived parameters were significantly decreased in VRX (peak dIVP, 78 ± 10.2%, rebound dIVP, 75 ± 15.6%, minimal dIVP, 68 ± 14% of intact, P <0.01, n = 8) but only peak dIVP was decreased (85 ± 11% of intact, P <0.01, n = 8) in DRX rats. Conclusion: Acute selective DRX and VRX rat can be an animal model to investigate peripheral neural control in micturition functions.
KW - Cystometry
KW - Electromyogram
KW - Motor
KW - Sensory
KW - Spinal cord
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U2 - 10.1002/nau.20220
DO - 10.1002/nau.20220
M3 - Article
C2 - 16496396
AN - SCOPUS:33646499657
SN - 0733-2467
VL - 25
SP - 283
EP - 289
JO - Neurourology and Urodynamics
JF - Neurourology and Urodynamics
IS - 3
ER -