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Updated: Aug 16, 2026

Assessing Whole-Body Lipid-Handling Capacity in Mice
Published on: November 24, 2020
Chronic high-fat diet feeding reduces the rate of postprandial triglyceride absorption independent of intestinal
Shwetha K Shetty1, Kelli L Sylvers-Davie1, Brandon S J Davies1
1Department of Biochemistry and Molecular Biology, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, IA, USA.
Abstract:
Pancreatic lipase is the major enzyme responsible for breaking down dietary triglycerides in the intestines. A previous report suggested that intestinal angiopoietin-like 4 (ANGPTL4) might serve as an endogenous inhibitor of pancreatic lipase and thus regulate fat absorption. As Angptl4 expression is reportedly induced by high-fat-diet feeding, we hypothesized that induction of ANGPTL4 by a high-fat diet would lead to an increased inhibition of pancreatic lipase, less breakdown of dietary triglycerides, and ultimately a reduced rate of postprandial triglyceride absorption. To test this hypothesis, we generated intestinal epithelial cell-specific ANGPTL4 knockout mice, fed them diets with varying levels of fat, and measured postprandial triglyceride absorption and intestinal triglyceride lipase activity. As we hypothesized, we found that chronic high-fat feeding reduced the rate of postprandial triglyceride absorption in mice. However, this regulation of postprandial triglyceride absorption appeared to be largely independent of ANGPTL4, as similar decreases were observed in both wild-type and intestinal epithelial cell-specific ANGPTL4 knockout mice. We conclude that there is a mechanism by which chronic high-fat feeding reduces the rate of secretion of dietary triglycerides into the circulation, but that this mechanism does not require intestinal ANGPTL4.
Insights
High-fat diets reduce triglyceride absorption, but not by increasing angiopoietin-like 4 (ANGPTL4) in the intestine. This fat absorption regulation mechanism is independent of ANGPTL4 in mice.
Area of Science:
- Biochemistry
- Physiology
- Molecular Biology
Background:
- Pancreatic lipase hydrolyzes dietary triglycerides.
- Intestinal angiopoietin-like 4 (ANGPTL4) may inhibit pancreatic lipase, regulating fat absorption.
- ANGPTL4 expression increases with high-fat diets.
Purpose of the Study:
- To investigate if ANGPTL4 induction by high-fat diets inhibits pancreatic lipase and reduces triglyceride absorption.
- To determine the role of intestinal ANGPTL4 in regulating postprandial fat absorption.
Main Methods:
- Generated and utilized intestinal epithelial cell-specific ANGPTL4 knockout mice.
- Administered diets with varying fat content.
- Measured postprandial triglyceride absorption and intestinal triglyceride lipase activity.
Main Results:
- Chronic high-fat feeding reduced postprandial triglyceride absorption in mice.
- This reduction in fat absorption occurred similarly in both wild-type and ANGPTL4 knockout mice.
- The regulation of triglyceride absorption was independent of intestinal ANGPTL4.
Conclusions:
- A mechanism exists for reducing dietary triglyceride secretion into circulation after high-fat feeding.
- This regulatory mechanism does not involve intestinal ANGPTL4.
- Intestinal ANGPTL4 is not essential for high-fat diet-induced regulation of fat absorption.
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