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Acid lipase in rat intestinal mucosa: physiological parameters
1Department of Medicine, University of Tennessee, Memphis 38163.
Biochimica Et Biophysica Acta
|April 17, 1990
Summary
A novel acid-active lipase in rat intestinal mucosa may explain how dietary fats are processed. This enzyme, primarily lysosomal, is most active in the proximal intestine, suggesting a role in fat absorption.
Area of Science:
- Gastroenterology
- Biochemistry
- Cell Biology
Background:
- Up to 50% of dietary triacylglycerol bypasses lymphatic absorption in the intestine.
- This suggests an alternative pathway for fatty acid transport, potentially involving mucosal lipases and portal vein circulation.
Purpose of the Study:
- To characterize a novel acid-active lipase identified in rat intestinal mucosa.
- To investigate the enzyme's cellular localization, activity, and potential role in triacylglycerol metabolism.
Main Methods:
- Assay of acid lipase activity using a radiolabeled triolein emulsion at pH 5.8.
- Differential centrifugation of mucosal homogenates to isolate cellular organelles.
- Sequential release of cells from villi using citrate and EDTA.
- Enzyme activity assessment across intestinal segments and villus height.
- Chromatographic analysis using Sepharose 6B and assessment of detergent effects.
Main Results:
- The acid-active lipase exhibited peak activity in the proximal intestinal quarter and the upper villus regions.
- The enzyme was predominantly localized within the lysosomal fraction.
- Lingual lipase was excluded as the precursor via esophageal diversion.
- Bile salts significantly stimulated lipase activity (3-5 fold), while other detergents were mostly inhibitory.
- Chromatography indicated the enzyme forms mixed micelles with SDS and taurocholate.
Conclusions:
- A distinct, intrinsic mucosal acid lipase exists in the rat intestine, primarily of lysosomal origin.
- Its localization suggests a significant role in the disposal and processing of mucosal triacylglycerol.
- This enzyme may contribute to the alternative portal vein transport of fatty acids.