Abstract
A method is described for preparing isolated rat submandibular acini by collagenase digestion followed by mechanical dispersion. As assessed by Trypan Blue exclusion, phase contrast microscopy, ATP content and release of mucins and lactate dehydrogenase, the acini are morphologically and functionally intact. Secretory function of isolated acini was similar to that of intact tissue in terms of time-course, dose dependence and degree of stimulation of mucin release by adrenergic secretagogues. Mucin release was increased to the same extent (approx. 3-4-fold) by either isoproterenol or noradrenaline at a maximally effective concentration (10 microM). Stimulation of mucin release by isoproterenol (10 microM), noradrenaline (10 microM) or adrenaline (10 microM) was inhibited by propranolol (30 microM) but not by phentolamine (30 microM). Isoproterenol (10 microM) increased both 45Ca2+ uptake and efflux from the acini, which was shown to represent a net release of calcium. However, there was a delay (approx. 10 min) in onset of stimulation of 45Ca2+ mobilization which was not apparent in isoproterenol stimulation of mucin release. Our results indicate that increases in intracellular calcium mobilization in response to a beta-adrenergic secretagogue do not trigger mucin secretion from rat submandibular acini.
MeSH Terms
Animals
Calcium/metabolism,pharmacology
Glycoproteins/metabolism
In Vitro Techniques
Isoproterenol/pharmacology
Kinetics
Male
Methods
Microbial Collagenase
Microscopy, Phase-Contrast
Mucins/metabolism
Norepinephrine/pharmacology
Rats
Rats, Inbred Strains
Submandibular Gland/cytology,drug effects,metabolism
Chemicals
Glycoproteins
Mucins
Microbial Collagenase
Isoproterenol
Calcium
Norepinephrine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
McPherson M A
Dormer R L
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