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Overexpression of small-conductance Ca2+-activated K+ channel 2 attenuates pain-like behavior in female mice with cystitis
Guadalupe Manrique-Maldonado, Xuejiao Sun, Allison L. Marciszyn, Nicolas Montalbetti, Marcelo D. Carattino
Guadalupe Manrique-Maldonado, Xuejiao Sun, Allison L. Marciszyn, Nicolas Montalbetti, Marcelo D. Carattino
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Research Article Nephrology Neuroscience

Overexpression of small-conductance Ca2+-activated K+ channel 2 attenuates pain-like behavior in female mice with cystitis

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Abstract

Small-conductance Ca2+-activated K+ (SK) channels regulate neuronal excitability and act as a feedback mechanism to limit firing during sustained stimulation. In the present study, we demonstrated that SK2 plays an important role in the control of bladder function and visceral pain processing. SK2 channels are expressed in bladder-innervating afferent neurons, and ablation of this subunit results in elevated afferent firing rates in response to physiological levels of bladder distension, supporting a role for SK2 in modulating mechanosensory excitability. Mice overexpressing SK2 exhibit increased bladder capacity and reduced voiding frequency. Furthermore, overexpression of SK2 prevents the onset of pelvic mechanical allodynia and attenuates the exaggerated visceromotor response to bladder distension seen in wild-type mice with chemical cystitis. Thus, SK2 may be a promising target for treating overactive bladder and pain originating from the urinary bladder and other pelvic organs.

Authors

Guadalupe Manrique-Maldonado, Xuejiao Sun, Allison L. Marciszyn, Nicolas Montalbetti, Marcelo D. Carattino

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Figure 6

Voiding behavior of transgenic SK2 mice.

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Voiding behavior of transgenic SK2 mice.
Voiding activity was evaluated ...
Voiding activity was evaluated over a 12-hour time window during the dark phase in freely mobile SK2+/T and WT littermate mice. Saline (SAL) or CYP was administered every other day for a week. (A) Diagram of the system used to assess voiding behavior in awake mice. A filter paper is placed on the bottom of the chamber housing the mouse. The chamber is illuminated from below with UV light, allowing the visualization of the urine spots. Activity is recorded using the top and bottom cameras. (B) Total voided volume during a 12-hour period. (C) Number of voids during a 12-hour period. (D) Average volume per void. Data are shown as the mean ± SEM (WT-SAL, n = 12; WT-CYP, n = 15; SK2+/T-SAL, n = 15; SK2+/T-CYP, n = 14; *P < 0.05, **P < 0.01, Brown-Forsythe and Welch’s ANOVA test followed by Dunnett’s T3 multiple-comparison test).

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