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1.
J Appl Physiol (1985) ; 94(6): 2375-83, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12611768

ABSTRACT

We hypothesized that, in the airway mucosa, opioids are inhibitory neural modulators that cause an increase in net water absorption in the airway mucosa (as in the gut). Changes in bidirectional water fluxes across ovine tracheal mucosa in response to basolateral application of the opioid peptides beta-endorphin, dynorphin A-(1-8), and [d-Ala(2), d-Leu(5)]-enkephalin (DADLE) were measured. beta-Endorphin and dynorphin A-(1-8) decreased luminal-to-basolateral water fluxes, and dynorphin A-(1-8) and DADLE increased basolateral-to-luminal water flux. These responses were electroneutral. In seven beagle dogs, administration of aerosolized beta-endorphin (1 mg) to the tracheobronchial airways decreased the clearance of radiotagged particles from the bronchi in 1 h from 34.7 to 22.0% (P < 0.001). Naloxone abrogated the beta-endorphin-induced changes in vitro and in vivo. Contrary to our hypothesis, the opioid-induced changes in water fluxes would all lead to a predictable increase in airway surface fluid. The beta-endorphin-induced increases in airway fluid together with reduced bronchial mucociliary clearance may produce procongestive responses when opioids are administered as antitussives.


Subject(s)
Bronchi/physiology , Dynorphins/pharmacology , Enkephalin, Leucine-2-Alanine/pharmacology , Mucociliary Clearance/drug effects , Peptide Fragments/pharmacology , Trachea/physiology , beta-Endorphin/pharmacology , Aerosols , Animals , Dogs , Drug Synergism , In Vitro Techniques , Injections, Intramuscular , Ions , Male , Naloxone/administration & dosage , Narcotic Antagonists/administration & dosage , Sheep , Trachea/metabolism , Water/metabolism , beta-Endorphin/administration & dosage
2.
J Appl Physiol (1985) ; 94(5): 1821-8, 2003 May.
Article in English | MEDLINE | ID: mdl-12547842

ABSTRACT

The ragweed- and histamine-induced decreases in nasal patency in cohorts of ragweed-sensitized and nonsensitized dogs were assessed. The volume of nasal airways (V(NA)) was assessed by acoustic rhinometry and resistance to airflow (R(NA)) by anterior rhinomanometry. Histamine delivered to the nasal passages of five dogs caused a rapid and prolonged increase in R(NA) (0.75 +/- 0.26 to 3.56 +/- 0.50 cmH(2)O. l(-1). min), an effect that was reversed by intranasal delivery of aerosolized phenylephrine. Ragweed challenge in five ragweed-sensitized dogs increased R(NA) from 0.16 +/- 0.02 to 0.53 +/- 0.07 cmH(2)O. l(-1). min and decreased V(NA) from 12.5 +/- 1.9 to 3.9 +/- 0.3 cm(3), whereas administration of saline aerosol neither increased R(NA) nor decreased V(NA). Prior administration of d-pseudoephedrine (30 mg po) attenuated the ragweed-induced increase in R(NA) and decrease in V(NA). Ragweed challenge changed neither R(NA) nor V(NA) in four nonsensitized dogs. Mediator-induced nasal congestion and allergen-induced allergic rhinitis in ragweed-sensitized dogs, which exhibit symptoms similar to human disease, can be used in the evaluation of safety and efficacy of antiallergic activity of potential drugs.


Subject(s)
Nasal Obstruction/physiopathology , Rhinitis, Allergic, Seasonal/physiopathology , Aerosols , Airway Resistance/physiology , Ambrosia/immunology , Animals , Disease Models, Animal , Dogs , Female , Heart Rate/physiology , Histamine/pharmacology , Male , Nasal Decongestants/therapeutic use , Nasal Obstruction/drug therapy , Pollen/immunology , Respiratory Mechanics/physiology , Rhinitis, Allergic, Seasonal/drug therapy , Rhinomanometry
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