Evidence map›Paper›PMID 22505670›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2012

β-Adrenergic agonists differentially regulate highly selective and nonselective epithelial sodium channels to promote alveolar fluid clearance in vivo.

Charles A Downs, Lisa H Kriener, Ling Yu, Douglas C Eaton, Lucky Jain, My N Helms

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.0field-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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Effects of βScientific reports · 2020
    Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Alveolar nonselective channels are ASIC1a/α-ENaC channels and contribute to AFC.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
  9. Article
  10. Review
  11. Oxidized glutathione (GSSG) inhibits epithelial sodium channel activity in primary alveolar epithelial cells.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  12. Article
  13. NADPH oxidases in lung health and disease.Antioxidants & redox signaling · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. Estradiol activates epithelial sodium channels in rat alveolar cells through the G protein-coupled estrogen receptor.American journal of physiology. Lung cellular and molecular physiology · 2013
    Article
  18. Cholinergic regulation of epithelial sodium channels in rat alveolar type 2 epithelial cells.American journal of physiology. Lung cellular and molecular physiology · 2013
    Article
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Charles A DownsDepartment of Physiology, School of Medicine, Emory University, Atlanta, GA, USA.
Lisa H Kriener
Ling Yu
Douglas C Eaton
Lucky Jain
My N Helms
Emory University · USChildren's Healthcare of Atlanta · US

Funding

REGULATION OF SODIUM IN TIGHT EPITHELIAR37DK037963 · NIDDK · EMORY UNIVERSITY · PI EATON, DOUGLAS C. · 2002 to 2011
$3.8M
Regulation of Lung Sodium ChannelsR01HL063306 · NHLBI · EMORY UNIVERSITY · PI JAIN, LUCKY · 2001 to 2011
$3.1M
Redox regulation of alveolar fluid balanceR00HL092226 · NHLBI · EMORY UNIVERSITY · PI HELMS, MY N. · 2010 to 2012
$740k
NHLBI NIH HHS 5R00HL092226-04NHLBI NIH HHS 5R01HL063306-09NHLBI NIH HHS R00 HL092226NHLBI NIH HHS R01 HL063306NIDDK NIH HHS 5R37DK037963-25
6 · The paper itself

Abstract

β-Adrenergic receptors (β-AR) increase epithelial sodium channel (ENaC) activity to promote lung fluid clearance. However, the effect of selective β-AR agonist on highly selective cation (HSC) channels or nonselective cation (NSC) channels in alveolar type 1 (T1) and type 2 (T2) cells is unknown. We hypothesized that stimulation with β(1)-AR agonist (denopamine) or β(2)-AR agonist (terbutaline) would increase HSC and/or NSC channel activity in alveolar epithelial cells. We performed single-channel measurements from T1 and T2 cells accessed from rat lung slices. Terbutaline (20 μM) increased HSC ENaC activity (open probability, NP(o)) in T1 (from 0.96 ± 0.61 to 1.25 ± 0.71, n = 5, P <0.05) and T2 cells (from 0.28 ± 0.14 to 1.0 ± 0.30, n = 8, P = 0.02). Denopamine (20 μM) increased NSC NP(o) in T1 cells (from 0.34 ± 0.09 to 0.63 ± 0.14, n = 7, P = 0.02) and in T2 cells (from 0.47 ± 0.09 to 0.68 ± 0.10, P = 0.004). In vivo X-ray imaging of lung fluid clearance and ICI 118,551 selective inhibition of β(2)-ARs confirmed patch-clamp findings. cAMP concentrations increased following treatment with denopamine or terbutaline (n = 3, P < 0.002). The effects of systemic (intraperitoneal, IP) and local (intratracheal, IT) modes of delivery on lung fluid clearance were assessed. IT delivery of denopamine promoted alveolar flooding, whereas IP delivery promoted delayed fluid clearance. In summary, β-AR agonists differentially regulate HSC and NSC in T1 and T2 cells to promote lung fluid clearance in vivo, and the mode of drug delivery is critical for maximizing β-AR agonist efficacy.

Indexed as

Adrenergic beta-AgonistsAnimalsCyclic AMPDrug Administration RoutesEpithelial CellsEpithelial Sodium ChannelsEthanolaminesFemaleIon TransportLungMaleMiceMice, Inbred BALB CPatch-Clamp TechniquesPulmonary AlveoliRatsAdrenergic beta-AgonistsCyclic AMPdenopamineEpithelial Sodium ChannelsEthanolaminesReceptors, Adrenergic, betaSodiumTerbutaline

Identifiers

PMID22505670
PMCPMC3379040
OpenAlexW2125325789

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.