Evidence map›Paper›PMID 21697543›Full record

ArticleAmerican journal of physiology. Cell physiology2011

Large-conductance voltage- and Ca2+-activated K+ channels regulate human detrusor smooth muscle function.

Kiril L Hristov, Muyan Chen, Whitney F Kellett, Eric S Rovner, Georgi V Petkov

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
11.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 88 citations in OpenAlex.

  1. Gene Therapy With URO-902 (pVAX/The Journal of urology · 2025
    Trial
  2. Review
  3. Review
  4. Review
  5. The BK channel-NS1619 agonist complex reveals molecular insights into allosteric activation gating.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. New targets for overactive bladder-ICI-RS 2109.Neurourology and urodynamics · 2020
    Review
  12. Article
  13. Detrusor Smooth Muscle KFrontiers in physiology · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Kiril L HristovDepartment of Pharmaceutical and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, Columbia, 29208, USA.
Muyan Chen
Whitney F Kellett
Eric S Rovner
Georgi V Petkov
University of South Carolina · USMedical University of South Carolina · US

Funding

BK Channel Function and Regulation in Urinary Bladder Smooth MuscleR01DK084284 · NIDDK · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI PETKOV, GEORGI V · 2009 to 2013
$1.6M
Regulation of Urinary Bladder Smooth Muscle by K+ ChannelsR21DK083687 · NIDDK · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI PETKOV, GEORGI V · 2010 to 2011
$393k
NIDDK NIH HHS DK-083687NIDDK NIH HHS DK-084284NIDDK NIH HHS R01 DK084284
6 · The paper itself

Abstract

The large-conductance voltage- and Ca(2+)-activated K(+) (BK) channel is expressed in many smooth muscle types, but its role in human detrusor smooth muscle (DSM) is unclear. With a multidisciplinary approach spanning channel molecules, single-channel activity, freshly isolated human DSM cells, intact DSM preparations, and the BK channel specific inhibitor iberiotoxin, we elucidated human DSM BK channel function and regulation. Native human DSM tissues were obtained during open surgeries from patients with no preoperative history of overactive bladder. RT-PCR experiments on single human DSM cells showed mRNA expression of BK channel α-, β(1)-, and β(4)-subunits. Western blot and immunocytochemistry confirmed BK channel α, β(1), and β(4) protein expression. Native human BK channel properties were described using the perforated whole cell configuration of the patch-clamp technique. In freshly isolated human DSM cells, BK channel blockade with iberiotoxin inhibited a significant portion of the total voltage step-induced whole cell K(+) current. From single BK channel recordings, human BK channel conductance was calculated to be 136 pS. Voltage-dependent iberiotoxin- and ryanodine-sensitive transient BK currents were identified in human DSM cells. In current-clamp mode, iberiotoxin inhibited the hyperpolarizing membrane potential transients and depolarized the cell resting membrane potential. Isometric DSM tension recordings revealed that BK channels principally control the contractions of isolated human DSM strips. Collectively, our results indicate that BK channels are fundamental regulators of DSM excitability and contractility and may represent new targets for pharmacological or genetic control of urinary bladder function in humans.

Indexed as

AdultAgedAged, 80 and overCells, CulturedFemaleGene Expression RegulationHumansLarge-Conductance Calcium-Activated Potassium ChannelsMaleMiddle AgedMuscle ContractionMuscle, SmoothMyocytes, Smooth MusclePeptidesProtein SubunitsTissue Culture TechniquesiberiotoxinLarge-Conductance Calcium-Activated Potassium ChannelsPeptidesProtein SubunitsToxins, Biological

Identifiers

PMID21697543
PMCPMC3191561
OpenAlexW2085548554

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.