Evidence map›Paper›PMID 21454249›Full record

ArticleAmerican journal of physiology. Renal physiology2011

Coupled ATP and potassium efflux from intercalated cells.

J David Holtzclaw, Ryan J Cornelius, Lori I Hatcher, Steven C Sansom

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Renal NaAmerican journal of physiology. Renal physiology · 2019
    Article
  6. Article
  7. Article
  8. ENaC activity in the cortical collecting duct of HKαAmerican journal of physiology. Renal physiology · 2017
    Article
  9. Article
  10. New perspective of ClC-Kb/2 Cl- channel physiology in the distal renal tubule.American journal of physiology. Renal physiology · 2016
    Review
  11. Review
  12. Chemical and Physical Sensors in the Regulation of Renal Function.Clinical journal of the American Society of Nephrology : CJASN · 2015
    Review
  13. Dietary potassium and the renal control of salt balance and blood pressure.Pflugers Archiv : European journal of physiology · 2015
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Regulation of BK-α expression in the distal nephron by aldosterone and urine pH.American journal of physiology. Renal physiology · 2013
    Article
  20. Bicarbonate promotes BK-α/β4-mediated K excretion in the renal distal nephron.American journal of physiology. Renal physiology · 2012
    Article
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

4 authors at 2 institutions in 1 country.

J David HoltzclawDepartment of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska 68198-5850, USA.
Ryan J Cornelius
Lori I Hatcher
Steven C Sansom
University of Nebraska at Omaha · USUniversity of Nebraska Medical Center · US

Funding

TRP channels in statin reversal of diabetic nephropathyR01DK073070 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SANSOM, STEVEN · 2006 to 2009
$1.2M
NEW ASSAY FOR ERYTHROCYTE HEMATOPOIETIC ACTIVITYR43DK049461 · NIDDK · BACUS LABORATORIES, INC. · PI BACUS, JAMES W · 1995 to 1995
–
NIDDK NIH HHS R01 DK073070NIDDK NIH HHS R01 DK49461NIDDK NIH HHS R01 DK73070
6 · The paper itself

Abstract

Increased flow in the distal nephron induces K secretion through the large-conductance, calcium-activated K channel (BK), which is primarily expressed in intercalated cells (IC). Since flow also increases ATP release from IC, we hypothesized that purinergic signaling has a role in shear stress (τ; 10 dynes/cm(2)) -induced, BK-dependent, K efflux. We found that 10 μM ATP led to increased IC Ca concentration, which was significantly reduced in the presence of the P(2) receptor blocker suramin or calcium-free buffer. ATP also produced BK-dependent K efflux, and IC volume decrease. Suramin inhibited τ-induced K efflux, suggesting that K efflux is at least partially dependent on purinergic signaling. BK-β4 small interfering (si) RNA, but not nontarget siRNA, decreased ATP secretion and both ATP-dependent and τ-induced K efflux. Similarly, carbenoxolone (25 μM), which blocks connexins, putative ATP pathways, blocked τ-induced K efflux and ATP secretion. Compared with BK-β4(-/-) mice, wild-type mice with high distal flows exhibited significantly more urinary ATP excretion. These data demonstrate coupled electrochemical efflux between K and ATP as part of the mechanism for τ-induced ATP release in IC.

Indexed as

Adenosine TriphosphateAnimalsBlotting, WesternCalciumImmunohistochemistryMiceMice, KnockoutNephronsPotassiumPotassium Channels, Calcium-ActivatedRNA, Small InterferingStatistics, NonparametricAdenosine TriphosphateCalciumPotassiumPotassium Channels, Calcium-ActivatedRNA, Small Interfering

Identifiers

PMID21454249
PMCPMC3119139
OpenAlexW2109508889

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.