TY - JOUR
T1 - Electrical activity of the bladder is attenuated by intravesical inhibition of P2X2/3 receptors during micturition in female rats
AU - Salazar, Betsy H.
AU - Hoffman, Kristopher A.
AU - Zhang, Chuan
AU - Kavanagh, Alex
AU - Zhang, Yingchun
AU - Boone, Timothy B.
AU - Munoz, Alvaro
N1 - Funding Information:
• Grant/Fund Support: This study was supported by the Brown Foundation and the Houston Methodist Foundation.
Publisher Copyright:
© 2017 Korean Continence Society.
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Purpose: To simultaneously monitor electrical discharges in various bladder regions and the external urethral sphincter (EUS) during voiding contractions, and to assess the functional role of myogenic modulation of the lower urinary tract (LUT) by ionotropic purinergic receptors containing the P2X3 subunit. Methods: Female Sprague-Dawley rats were anesthetized with urethane, and implanted with a suprapubic catheter for open cystometry. Flexible microelectrodes were placed ventrally in the bladder dome, upper bladder, lower bladder, and bladder base, along with the middle section of the exposed EUS. Intravesical P2X3-containing receptors were blocked with AF-323, a specific P2X3-P2X2/3 receptor antagonist. A digital electrophysiology amplifier was used to record electrical and cystometric signals throughout the LUT. Results: Electrical activity in the LUT started before effective voiding contractions. Bladder pressure and electrical waveforms showed consistent out-of-phase activity when compared with the recordings made at the EUS. This pattern was also observed during voiding contractions in the presence of AF-353, supporting the hypothesis that during bladder distension, activation of P2X3-containing receptors is required for voiding contractions. Furthermore, the inhibition of P2X3-containing receptors significantly decreased the amplitude of electrical signals in the urinary bladder, but not the base or EUS. Conclusions: Our results provide novel information about the regulation of the micturition process by P2X3-containing receptors located in the inner layers of the bladder.
AB - Purpose: To simultaneously monitor electrical discharges in various bladder regions and the external urethral sphincter (EUS) during voiding contractions, and to assess the functional role of myogenic modulation of the lower urinary tract (LUT) by ionotropic purinergic receptors containing the P2X3 subunit. Methods: Female Sprague-Dawley rats were anesthetized with urethane, and implanted with a suprapubic catheter for open cystometry. Flexible microelectrodes were placed ventrally in the bladder dome, upper bladder, lower bladder, and bladder base, along with the middle section of the exposed EUS. Intravesical P2X3-containing receptors were blocked with AF-323, a specific P2X3-P2X2/3 receptor antagonist. A digital electrophysiology amplifier was used to record electrical and cystometric signals throughout the LUT. Results: Electrical activity in the LUT started before effective voiding contractions. Bladder pressure and electrical waveforms showed consistent out-of-phase activity when compared with the recordings made at the EUS. This pattern was also observed during voiding contractions in the presence of AF-353, supporting the hypothesis that during bladder distension, activation of P2X3-containing receptors is required for voiding contractions. Furthermore, the inhibition of P2X3-containing receptors significantly decreased the amplitude of electrical signals in the urinary bladder, but not the base or EUS. Conclusions: Our results provide novel information about the regulation of the micturition process by P2X3-containing receptors located in the inner layers of the bladder.
KW - Electrophysiology
KW - Lower urinary tract symptoms
KW - Purinergic P2X receptor antagonists
KW - Urinary bladder
KW - Urination
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U2 - 10.5213/inj.1734998.499
DO - 10.5213/inj.1734998.499
M3 - Article
AN - SCOPUS:85038926522
SN - 2093-4777
VL - 21
SP - 259
EP - 269
JO - International Neurourology Journal
JF - International Neurourology Journal
IS - 4
ER -