Evidence map›Paper›PMID 24396055›Full record

ArticleThe Journal of physiology2014

Purinergic inhibitory regulation of murine detrusor muscles mediated by PDGFRα+ interstitial cells.

Haeyeong Lee, Byoung H Koh, Lauren E Peri, Kenton M Sanders, Sang Don Koh

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Defining the molecular fingerprint of bladder and kidney fibroblasts.American journal of physiology. Renal physiology · 2023
    Review
  10. Article
  11. Review
  12. Vascular mechanotransduction.Physiological reviews · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Role of detrusor PDGFRαScientific reports · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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 1 institution in 1 country.

Haeyeong LeeDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, 1664 N. Virginia St MS 0352, Reno, NV 89557, USA. skoh@medicine.nevada.edu.
Byoung H Koh
Lauren E Peri
Kenton M Sanders
Sang Don Koh
University of Nevada, Reno · US

Funding

Molecular and Functional Mechanisms of Purinergic Relaxation in Detrusor MuscleR01DK098388 · NIDDK · UNIVERSITY OF NEVADA RENO · PI KOH, SANG DON · 2013 to 2017
$1.6M
NIDDK NIH HHS R01 DK098388
6 · The paper itself

Abstract

Purines induce transient contraction and prolonged relaxation of detrusor muscles. Transient contraction could be due to activation of inward currents in smooth muscle cells, but the mechanism of purinergic relaxation has not been determined. We recently reported a new class of interstitial cells in detrusor muscles and showed that these cells could be identified with antibodies against platelet-derived growth factor receptor-α (PDGFRα(+) cells). The current density of small conductance Ca(2+)-activated K(+) (SK) channels in these cells is far higher (∼100 times) than in smooth muscle cells. Thus, we examined purinergic receptor (P2Y) mediated SK channel activation as a mechanism for purinergic relaxation. P2Y receptors (mainly P2ry1 gene) were highly expressed in PDGFRα(+) cells. Under voltage clamp conditions, ATP activated large outward currents in PDGFRα(+) cells that were inhibited by blockers of SK channels. ATP also induced significant hyperpolarization under current clamp conditions. A P2Y1 agonist, MRS2365, mimicked the effects of ATP, and a P2Y1 antagonist, MRS2500, inhibited ATP-activated SK currents. Responses to ATP were largely abolished in PDGFRα(+) cells of P2ry1(-/-) mice, and no response was elicited by MRS2365 in these cells. A P2X receptor agonist had no effect on PDGFRα(+) cells but, like ATP, activated transient inward currents in smooth muscle cells (SMCs). A P2Y1 antagonist decreased nerve-evoked relaxation. These data suggest that purines activate SK currents via mainly P2Y1 receptors in PDGFRα(+) cells. Our findings provide an explanation for purinergic relaxation in detrusor muscles and show that there are no discrete inhibitory nerve fibres. A dual receptive field for purines provides the basis for inhibitory neural regulation of excitability.

Indexed as

Adenosine DiphosphateAdenosine TriphosphateAnimalsDeoxyadenine NucleotidesElectric StimulationMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutMuscle RelaxationMuscle, SmoothPurinergic P2Y Receptor AgonistsPurinergic P2Y Receptor AntagonistsReceptor, Platelet-Derived Growth Factor alphaReceptors, Purinergic P2Y1Small-Conductance Calcium-Activated Potassium Channels2-iodo-N(6)-methyl-(N)-methanocarba-2'-deoxyadenosine-3',5'-bisphosphateAdenosine DiphosphateAdenosine TriphosphateDeoxyadenine Nucleotides(N)-methanocarba-2MeSADPPurinergic P2Y Receptor AgonistsPurinergic P2Y Receptor AntagonistsReceptor, Platelet-Derived Growth Factor alphaReceptors, Purinergic P2Y1Small-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID24396055
PMCPMC3961087
OpenAlexW1506803793

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.