Evidence map›Paper›PMID 11230516›Full record

ArticleThe Journal of physiology2001

Functional inhibition of native volume-sensitive outwardly rectifying anion channels in muscle cells and Xenopus oocytes by anti-ClC-3 antibody.

D Duan, J Zhong, M Hermoso, C M Satterwhite, C F Rossow, W J Hatton, I Yamboliev, B Horowitz, J R Hume

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Cl⁻ channels in smooth muscle cells.Pflugers Archiv : European journal of physiology · 2014
    Review
  7. Article
  8. The ClC-3 chloride channel and osmoregulation in the European sea bass, Dicentrarchus labrax.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2013
    Article
  9. Flufenamic acid as an ion channel modulator.Pharmacology & therapeutics · 2013
    Review
  10. Phenomics of cardiac chloride channels.Comprehensive Physiology · 2013
    Review
  11. Chloride channels in stroke.Acta pharmacologica Sinica · 2013
    Review
  12. Article
  13. Article
  14. Review
  15. Activation of volume regulated chloride channels protects myocardium from ischemia/reperfusion damage in second-window ischemic preconditioning.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2011
    Article
  16. 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

9 authors at 1 institution in 1 country.

D DuanCentre of Biomedical Research Excellence, Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557-0046, USA.
J Zhong
M Hermoso
C M Satterwhite
C F Rossow
W J Hatton
I Yamboliev
B Horowitz
J R Hume
University of Nevada, Reno · US

Funding

IONIC AND PHARMACOLOGICAL REGULATION OF VASCULAR CELLSR37HL049254 · NHLBI · UNIVERSITY OF NEVADA RENO · PI HUME, JOSEPH R · 1998 to 2007
$2.7M
IONIC AND PHARMACOLOGICAL REGULATION OF VASCULAR CELLSR01HL049254 · NHLBI · UNIVERSITY OF NEVADA RENO · PI HUME, JOSEPH R · 1993 to 1998
–
NHLBI NIH HHS HL 49254NHLBI NIH HHS R01 HL049254NHLBI NIH HHS R37 HL049254PHS HHS P2015581
6 · The paper itself

Abstract

Intracellular dialysis of NIH/3T3 cells with a commercially available anti-ClC-3 polyclonal antibody (Ab) for approximately 30 min completely inhibited expressed guinea-pig ClC-3 currents (IgpClC-3), while intracellular dialysis with antigen-preabsorbed anti-ClC-3 Ab failed to affect IgpClC-3. Anti-ClC-3 Ab was used as a selective probe to examine the relationship between endogenous ClC-3 expression and native volume-sensitive outwardly rectifying anion channels (VSOACs) in guinea-pig cardiac cells, canine pulmonary arterial smooth muscle cells (PASMCs) and Xenopus laevis oocytes. Intracellular dialysis or injection of anti-ClC-3 Ab abolished native VSOAC function in cardiac cells and PASMCs and significantly reduced VSOACs in oocytes. In contrast, native VSOAC function was unaltered by antigen-preabsorbed anti-ClC-3 Ab. It is suggested that endogenous ClC-3 represents a major molecular entity responsible for native VSOACs in cardiac and smooth muscle cells and Xenopus oocytes. Anti-ClC-3 Ab should be a useful experimental tool to directly test the relationship between endogenous ClC-3 expression and native VSOAC function, and help resolve existing controversies related to the regulation and physiological role of native VSOACs in a wide variety of different cells.

Indexed as

3T3 CellsAnimalsAnionsAntibodiesChloride ChannelsFemaleInjectionsIon ChannelsMiceMuscle, Smooth, VascularMyocardiumOocytesXenopus laevisAnionsAntibodiesChloride ChannelsClC-3 channelIon Channels

Identifiers

PMID11230516
PMCPMC2278470
OpenAlexW2153335059

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.