Journal of Applied Physiology Journal of Applied Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


J Appl Physiol (April 27, 2006). doi:10.1152/japplphysiol.01264.2005
This Article
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
101/2/486    most recent
01264.2005v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kim, J.-S.
Right arrow Articles by Rubin, B. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kim, J.-S.
Right arrow Articles by Rubin, B. K.
Submitted on October 2, 2005
Accepted on April 21, 2006

Vasoactive intestinal peptide stimulates mucus secretion, but nitric oxide has no effect on mucus secretion in the ferret trachea

Jung-Soo Kim1, Kosuke Okamoto1, Shinobu Arima1, and Bruce K. Rubin1*

1 Pediatrics, Wake Forest University School of Medicine, Winston Salem, North Carolina, United States

* To whom correspondence should be addressed. E-mail: brubin{at}wfubmc.edu.

Vasoactive intestinal peptide (VIP) and nitric oxide (NO) are neurotransmitters involved in the regulation of bronchial and pulmonary vascular tone. Published studies of the effects of VIP on airway mucus secretion have yielded conflicting results. The purpose of this study was to determine the effect of VIP on mucus secretion in the ferret trachea and if this effect was influenced by NO. We used a sandwich enzyme-linked lectin assay to measure mucin secretion and a turbidimetric assay to measure lysozyme (serous cell) secretion from ferret tracheal segments. VIP 10-7 M increased mucin secretion over 2 hours. VIP (10-9 to 10-5 M) stimulated mucin secretion in a dose-dependent fashion. VIP-induced mucin secretion was partially blocked by a VIP receptor antagonist (a chimeric VIP-PACAP analog, VRA) at a 10-fold excess concentration. At all concentrations tested, neither N-nitroarginine methyl ester, an inhibitor of nitric oxide synthase, nor S-nitroso-N-acetyl-penicillamine, an NO donor, had any significant effect on constitutive or VIP-induced mucus secretion. We conclude that VIP stimulated mucin and lysozyme secretion was both time-dependent and dose-dependent and that NO neither stimulates nor inhibits mucus secretion in the ferret trachea.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 1948 by the American Physiological Society.