Studies in several tissues have demonstrated CF (cystic fibrosis)-related abnormalities in autonomic regulation of tissue function. Among these are an increased sensitivity to cholinergic agents and a decreased sensitivity to beta-adrenergic agents. If CF mucous glands also have increased sensitivity to cholinergic agonists, then the resulting increased mucus secretion might contribute to the bronchial pathophysiology observed in these patients. However, a previous study (Mangos, J Dent Res 60, 797, 1981) utilizing a serous human salivary gland--the parotid--came to just the opposite conclusion with regard to CF-related abnormalities in autonomic control. Hence, it is important to determine how the regulation of human mucous salivary gland function is affected in CF. This proposal utilizes measurements of stimulation induced changes in intracellular elemental concentrations to test for CF-related changes in sensitivity to parasympathomimetic and sympathomimetic agents. Elemental concentrations in different intracellular organelles in human labial glands incubated in vitro under different experimental conditions will be measured using X-ray microanalysis. Temporal and spatial concentration dependencies following gland stimulation with cholinergic and adrenergic agonists will be analyzed using appropriate coding and computer assisted analysis of variance techniques. Spatial dependencies will also be analyzed using digital imaging techniques. The in vitro results will not only allow statistical tests for altered sensitivities to cholinergic and adrenergic agonists, but also for disease related changes in resting intracellular elemental concentrations as previously reported for the parotid gland. Moreover, the present study will extend previous findings by allowing a determination of the intracellular organelles in which the concentration changes occur. In addition, use of Co-EDTA will provide an objective method for detecting cells injured in the preparatory procedure, and the use of the variable osmols (defined as the sum of Na + K + C1) will allow an estimation of disease and stimulation related changes in osmotic driving forces. Most importantly, the use of human labial gland tissues obtained by biopsy from patients with CF will maximize the likelihood that the results will be relevant to CF.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK035975-03
Application #
3234275
Study Section
Oral Biology and Medicine Study Section (OBM)
Project Start
1985-08-01
Project End
1989-07-31
Budget Start
1987-08-01
Budget End
1988-07-31
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Dentistry/Oral Hygn
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Izutsu, K T; Cantino, M E; Johnson, D E (1994) A review of electron probe X-ray microanalysis studies of salivary gland cells. Microsc Res Tech 27:71-9
Izutsu, K; Wilkinson, L; Oda, D et al. (1991) Comparison of elemental concentrations in the acinar cells of the human labial salivary gland. Arch Oral Biol 36:727-35
Mei, L; Roeske, W R; Izutsu, K T et al. (1990) Characterization of muscarinic acetylcholine receptors in human labial salivary glands. Eur J Pharmacol 176:367-70
Izutsu, K T; Ensign, W Y; Ramsey, B W et al. (1989) Potassium release in labial glands from controls and patients with cystic fibrosis. Lab Invest 60:158-60
Izutsu, K; Ensign, W; Ramsey, B et al. (1988) Autonomic regulation of potassium release from human labial salivary glands in vitro. Arch Oral Biol 33:519-23