Literature DB >> 7208157

Lingual lipase: an important lipase in the digestion of dietary lipids in cystic fibrosis?

B Fredrikzon, L Bläckberg.   

Abstract

A convenient lipase assay that discriminates between pancreatic and lingual lipase activities was developed to describe some properties of the triglyceride-hydrolyzing activities of lingual lipase (from von Ebners glands) and pancreatic lipase. Secretion of lingual lipase is stimulated by feeding. Gastric contents collected postyprandially from patients with cystic fibrosis (CF) contained lipase activity which is probably secreted from pharyngeal tissues. Also, duodenal contents from CF patients contained lipase activity with properties very close to those found in gastric contents from CF patients and controls. Apparently, the serous glands responsible for the secretion of lingual lipase is less affected than the exocrine pancrease in this disease. During fat balance experiments, CF patients utilized around 40% of the dietary lipids and more than 50% of milk lipids given as a test meal were hydrolyzed in the duodenum within 2 hr. In these patients with severe pancreatic insufficiency, we suggest that the lingual lipase is responsible for a considerable proportion of triglyceride hydrolysis. This hydrolysis starts in the stomach and continues in duodenum.

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Year:  1980        PMID: 7208157     DOI: 10.1203/00006450-198012000-00026

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  10 in total

Review 1.  Rationale of modern dietary recommendations in cystic fibrosis.

Authors:  J M Littlewood; A MacDonald
Journal:  J R Soc Med       Date:  1987       Impact factor: 5.344

Review 2.  Gastrointestinal tract and nutrition in cystic fibrosis: pathophysiology.

Authors:  J A Dodge
Journal:  J R Soc Med       Date:  1986       Impact factor: 5.344

3.  Cystic fibrosis.

Authors:  M B Mearns
Journal:  Arch Dis Child       Date:  1985-03       Impact factor: 3.791

4.  Lingual lipase in cystic fibrosis. Quantitation of enzyme activity in the upper small intestine of patients with exocrine pancreatic insufficiency.

Authors:  C K Abrams; M Hamosh; V S Hubbard; S K Dutta; P Hamosh
Journal:  J Clin Invest       Date:  1984-02       Impact factor: 14.808

5.  Influence of antacid and formulation on effectiveness of pancreatic enzyme supplementation in cystic fibrosis.

Authors:  C Braggion; G Borgo; P Faggionato; G Mastella
Journal:  Arch Dis Child       Date:  1987-04       Impact factor: 3.791

6.  Antiviral and antibacterial lipids in human milk and infant formula.

Authors:  J A Dodge; F A Sagher
Journal:  Arch Dis Child       Date:  1991-02       Impact factor: 3.791

7.  Pancreatic function and gene deletion F508 in cystic fibrosis.

Authors:  G Borgo; G Mastella; P Gasparini; A Zorzanello; R Doro; P F Pignatti
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

8.  Cystic fibrosis in adolescents and adults.

Authors:  A R Penketh; A Wise; M B Mearns; M E Hodson; J C Batten
Journal:  Thorax       Date:  1987-07       Impact factor: 9.139

9.  Relation between gastric emptying rate and rate of intraluminal lipolysis.

Authors:  B D Maes; Y F Ghoos; B J Geypens; M I Hiele; P J Rutgeerts
Journal:  Gut       Date:  1996-01       Impact factor: 23.059

10.  Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency.

Authors:  N Peretti; V Marcil; E Drouin; E Levy
Journal:  Nutr Metab (Lond)       Date:  2005-05-03       Impact factor: 4.169

  10 in total

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