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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 7

Chronic cystitis and afferent function.

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Chronic cystitis and afferent function.
(A) Apparent bladder capacity fo...
(A) Apparent bladder capacity for WT and SK2+/T mice treated with saline (SAL) or cyclophosphamide (CYP). Urinary bladders were infused at a rate of 15 μL/min until the intravesical pressure reached 40 cmH2O. Apparent bladder capacity represents the volume required to increase the intravesical pressure to 40 cmH2O. (B) Mean afferent nerve discharge frequency at 40 cmH2O for WT and SK2+/T mice treated with SAL or CYP. (C and E) Normalized afferent discharge as a function of intravesical pressure for bladders of WT (C) and SK2+/T mice (E) treated with SAL or CYP. No difference in bladder afferent discharge was observed between mice treated with SAL versus CYP. Data are expressed as the mean ± SEM (WT-SAL, n = 8; WT-CYP, n = 9; SK2+/T-SAL, n = 6; SK2+/T-CYP, n = 6). (D and F) Bladder capacity as a function of intravesical pressure for bladders of WT (D) and SK2+/T mice (F) treated with SAL or CYP. Data are shown as the mean ± SEM (WT-SAL, n = 8; WT-CYP, n = 9; SK2+/T-SAL, n = 6; SK2+/T-CYP, n = 6; 2-way ANOVA, *P < 0.05).

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