Evidence map›Paper›PMID 41926225›Full record

ArticleThe Journal of clinical investigation2026

Therapeutic potential of synergistic mucociliary clearance for cystic fibrosis airways by β-adrenergic plus cholinergic agonists.

Nam Soo Joo, Susan E Birket, Johnathan D Keith, Juan P Ianowski, Xiaojie Luan, Jacquelyn Spano, Jennifer B Bollyky, Marissa N Dobry, Juan R Sabater, Ryan W Williams and 3 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Nam Soo JooThe Cystic Fibrosis Research Laboratory and.
Susan E BirketDepartment of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Johnathan D KeithDepartment of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Juan P IanowskiDepartment of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Xiaojie LuanDepartment of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Jacquelyn SpanoCenter for Excellence in Pulmonary Biology, Stanford University, Stanford, California, USA.
Jennifer B BollykyDepartment of Medicine and.
Marissa N DobryInnovative Medicines Accelerator Program, Stanford University, Stanford, California, USA.
Juan R SabaterFriedman Advanced Research Institute, Mount Sinai Medical Center, Miami, Florida, USA.
Ryan W WilliamsDepartment of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
John F EngelhardtDivision of Pulmonary, Allergy and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jeffrey J WineThe Cystic Fibrosis Research Laboratory and.
Carlos E MillaCenter for Excellence in Pulmonary Biology, Stanford University, Stanford, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucociliary clearance (MCC) is an innate defense mechanism that normally keeps airways clean but is dysfunctional in cystic fibrosis (CF) and other muco-obstructive pulmonary diseases. Previously we discovered that activating adenyl cyclase in combination with a cholinergic agonist increased MCC velocity (MCCV) synergistically in ex vivo WT and CF ferret and WT piglets. For what we believe is the first time, we show in vivo synergistic MCC using FDA approved β-adrenergic and cholinergic drugs delivered to the apical surface of WT and CF rats and a CF sheep model. Also, a single dose of the combined drugs is tolerated by humans. As for mechanisms, via ex vivo experiments, we show the combined agonists increased net fluid secretion mainly by stimulating gland secretion and by inhibiting surface absorption, consequently increasing airway surface liquid depth. They also increased net base secretion and increased ciliary beat frequency. Additional ex vivo and in vitro experiments show that the combined agonists had additive effects when combined with highly effective CF transmembrane conductance regulator modulator therapy. The synergistic increase in MCCV induced by this combination of agonists offers therapeutic potential for treating muco-obstructive pulmonary diseases, including CF.

Indexed as

Adrenergic beta-AgonistsCholinergic AgonistsCystic FibrosisMucociliary ClearanceAnimalsCystic Fibrosis Transmembrane Conductance RegulatorDrug SynergismFerretsHumansMaleRatsSheepSwineAdrenergic beta-AgonistsCholinergic AgonistsCystic Fibrosis Transmembrane Conductance RegulatorCell biologyChloride channelsClinical ResearchEpithelial transport of ions and waterPharmacologyPulmonology

Identifiers

PMID41926225
PMCPMC13221217

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.