Work of adhesion of respiratory tract mucus
| Autor: | Tarun Chandra, Ravivaj S. Pillai, J. Lloyd-Still, Donovan B. Yeates, Irving F. Miller |
|---|---|
| Rok vydání: | 1992 |
| Předmět: |
Pathology
medicine.medical_specialty Adolescent Cystic Fibrosis Physiology Surface Properties Cystic fibrosis chemistry.chemical_compound fluids and secretions Dogs Physiology (medical) Glycerol medicine Animals Humans Child Vapor pressure osmometry Viscosity Osmolar Concentration Sputum Substrate (chemistry) Water respiratory system Apparent viscosity medicine.disease Mucus medicine.anatomical_structure chemistry Respiratory Physiological Phenomena medicine.symptom Rheology Respiratory tract Nuclear chemistry |
| Zdroj: | Journal of applied physiology (Bethesda, Md. : 1985). 72(4) |
| ISSN: | 8750-7587 |
| Popis: | A method was devised to measure the work of adhesion (WA) to a substrate of mucus, a viscoelastic gel, from the measured contact angle of glycerol on a mucus substrate and the known physical properties of a Teflon surface. Fifteen sputum samples from cystic fibrosis (CF) patients were compared with 25 mucus samples from canine tracheal pouches (CP), studied in the hydrated and partially dehydrated states. Apparent viscosity (eta A) and recoverable shear strain (SR) were measured by fluxgate magnetometry, and water content was inferred from vapor pressure osmometry. Na+, K+, and Ca2+ concentrations were measured with specific ion electrodes and Cl- with a chloridimeter. The Cl- concentration of the CP mucus was inversely proportional to its osmolality, and the Cl- concentration of the CP mucus was 102.5 +/- 1.6 meq/l compared with 55.6 +/- 2.5 meq/l for CF sputum. When CP mucus osmolality was increased from 316.0 +/- 5.5 to 430.0 +/- 7.5 mosmol/kg, WA increased from 25.1 +/- 1.8 to 31.1 +/- 1.2 ergs/cm2 and eta A increased from 391 +/- 55 to 622 +/- 121 P, respectively. CF sputum WA was 30.2 +/- 0.6 ergs/cm2, eta A was 1,110 +/- 316 P, and osmolality was 466.0 +/- 14.0 mosmol/kg. The increased WA and eta A of mucus in CF patients may thus be dependent on the hydration of mucus, which is related to the documented Cl- transport defect. |
| Databáze: | OpenAIRE |
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