Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
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
View: Text | PDF
Research Article Nephrology Neuroscience

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

  • Text
  • PDF
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

×

Figure 1

SK2 channels are expressed in bladder sensory neurons.

Options: View larger image (or click on image) Download as PowerPoint
SK2 channels are expressed in bladder sensory neurons.
(A) RT-PCR confir...
(A) RT-PCR confirms the expression of transcripts for SK1 (Kcnn1), SK2 (Kcnn2), and SK3 (Kcnn3) in dorsal root ganglia (DRG) (lines 2–5). Actin (Actb) served as a positive control for reverse transcription and amplification. Expected PCR product sizes are shown. Negative control reactions included GoTaq, primers, and DMSO, but not sample (lines 6–9). Representative of 3 experiments. (B) Kcnn2 is expressed in bladder-innervating DRG neurons. Immuno-FISH was performed in fresh-frozen sections of DRG (L6–S1) harvested from mice injected into the bladder wall with cholera toxin β subunit (CTb) conjugated to Alexa Fluor 555. A rabbit anti-CTb antibody and a secondary goat anti-rabbit antibody conjugated with Cy3 were used to identify bladder sensory neurons (red). Bottom: 4-fold magnification of a CTb-labeled neuron in box (i). No signal was visible with the negative control probe (not shown). Scale bar: 50 μm. (C) Quantitative analysis of expression for Kcnn2 and Asic3 in bladder sensory neurons. Percentage of neurons expressing Kcnn2, or Kcnn2 and Asic3, is shown (n = 187 bladder-innervating neurons from 8 L6–S1 DRG from 4 mice).

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts