The hypothesis by Doggett and Harrison, according to which alpha-amylase is the pathogenic factor of the exocrinopathy in cystic fibrosis (C.F.), is investigated. No elevation of alpha-amylase in sweat and serum of C.F. patients, as compared with controls of similar age, is observed. It is concluded
Ultramicro-electrophoresis of protein in sweat from patients with cystic fibrosis of the pancreas and controls
✍ Scribed by Claus-P. Schröder; Hinderk M. Emrich
- Publisher
- Springer
- Year
- 1978
- Tongue
- English
- Weight
- 527 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0340-6997
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✦ Synopsis
46 sweat-samples from 32 children with cystic fibrosis of the pancreas (C.F.) and 35 samples from 23 control-children were collected with glass micro-capillaries. Protein was determined by ultramicro-electrophoresis.
Results:
- protein was detected in 48% of the samples (c.f. and controls). 2. at ph 2.3, c.f.-sweat showed at least one more band than control-sweat. 3. at ph 8.9, c.f.-sweat occasionally showed one more band than the control-group. 4. at ph 2.3, more protein was found at the electrophoresis start point using c.f.-sweat, whereas at ph 8.9 the opposite was found. 5. at ph 2.3, protein was found in fewer samples than at ph 8.9. the "c.f.-factor" is postulated to represent a basic polyelectrolyte which induces the following pathogenic mechanisms: a) aggregation of proteins giving rise to a high viscosity of secretions, such as saliva. b) binding to the cell-membrane of the glandular epithelium, thus inducing a disturbance of active nacl-reabsorption (e.g. by reduction of luminal passive na+-influx).
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