In Vitro Effect of Combined Hypertonic Saline and Salbutamol on Ciliary Beating Frequency and Mucociliary Transport in Human Nasal Epithelial Cells of Healthy Volunteers and Patients with Cystic Fibrosis.
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BORIS DOI
Publisher DOI
PubMed ID
37196208
Description
Background: Inhalation of hypertonic saline (HS) is standard of care in patients with cystic fibrosis (CF). However, it is unclear if adding salbutamol has-besides bronchodilation-further benefits, for example, on the mucociliary clearance. We assessed this in vitro by measuring the ciliary beating frequency (CBF) and the mucociliary transport rate (MCT) in nasal epithelial cells (NECs) of healthy volunteers and patients with CF. Aims: To investigate the effect of HS, salbutamol, and its combination on (muco)ciliary activity of NECs in vitro, and to assess potential differences between healthy controls and patients with CF. Methods: NECs obtained from 10 healthy volunteers and 5 patients with CF were differentiated at the air-liquid interface and aerosolized with 0.9% isotonic saline ([IS] control), 6% HS, 0.06% salbutamol, or combined HS and salbutamol. CBF and MCT were monitored over 48-72 hours. Results: In NECs of healthy controls, the absolute CBF increase was comparable for all substances, but CBF dynamics were different: HS increased CBF slowly and its effect lasted for an extended period, salbutamol and IS increased CBF rapidly and the effect subsided similarly fast, and HS and salbutamol resulted in a rapid and long-lasting CBF increase. Results for CF cells were comparable, but less pronounced. Similar to CBF, MCT increased after the application of all the tested substances. Conclusion: CBF and MCT of NECs of healthy participants and CBF of patients with CF increased upon treatment with aerosolized IS, HS, salbutamol, or HS and salbutamol, showing a relevant effect for all tested substances. The difference in the CBF dynamics can be explained by the fact that the properties of the mucus are changed differently by different saline concentrations.
Date of Publication
2023-08
Publication Type
article
Subject(s)
600 - Technology::610 - Medicine & health
500 - Science::570 - Life sciences; biology
600 - Technology::620 - Engineering
Keyword(s)
air–liquid interface cell cultures ciliary motility cystic fibrosis inhalation primary ciliary dyskinesia
Language(s)
en
Contributor(s)
Savas, Sibel T | |
Additional Credits
Institut für Angewandte Physik (IAP)
Universitätsklinik für Kinderheilkunde - Pneumologie / Allergologie
Universitätsklinik für Kinderheilkunde
Department for BioMedical Research, Forschungsgruppe Pneumologie (Pädiatrie)
Institut für Anatomie - Rotation Anatomie
Institut für Anatomie
Series
Journal of aerosol medicine and pulmonary drug delivery
Publisher
Mary Ann Liebert
ISSN
1941-2711
Access(Rights)
restricted