Related Experiment Videos
Nutrient absorption
D F Nutting1, N S Kumar, R J St Hilaire
1University of Tennessee-Memphis, Department of Medicine 38163, USA.
Current Opinion in Clinical Nutrition and Metabolic Care
|December 10, 1999
Summary
Recent advances reveal that endoplasmic reticulum-to-Golgi transport limits lipid absorption. Apolipoprotein B aids particle movement, while peptide transporters absorb modified peptides and leptin receptors in the intestine modulate body mass.
Area of Science:
- Nutrient absorption
- Lipid metabolism
- Molecular biology
Background:
- Endoplasmic reticulum-to-Golgi transport is a critical step in lipid absorption.
- Apolipoprotein B's role in chylomicron formation and transport is under investigation.
- Drug bioavailability can be enhanced through esterification, but absorption mechanisms require clarification.
- Leptin's systemic effects may involve direct modulation of intestinal nutrient absorption.
- Gene regulation of apolipoprotein B differs between the liver and intestine.
Purpose of the Study:
- To investigate the rate-limiting step in lipid absorption.
- To elucidate the function of Apolipoprotein B in lipid particle transport.
- To explore the absorption pathways for modified peptides and drugs.
- To identify novel roles for leptin in the gastrointestinal tract.
- To compare the gene regulation of apolipoprotein B in different tissues.
Main Methods:
- Kinetics of triacylglycerol appearance in cellular compartments and lymph.
- Analysis of chylomicron-sized lipid particle formation and transport.
- In vitro studies using human ileal mucosa.
- Investigation of peptide and drug absorption using peptide transporters.
- Assessment of leptin receptor presence and function in intestinal mucosa.
Main Results:
- Endoplasmic reticulum-to-Golgi transport appears to be the rate-limiting step for lipid absorption.
- Apolipoprotein B is essential for the transport of lipid particles from the endoplasmic reticulum to the Golgi, not their initial formation.
- Fatty acylation of peptides and esterification of acyclovir with valine do not prevent absorption via peptide transporters.
- Human intestinal mucosa possesses leptin receptors, and leptin inhibits galactose absorption.
- The enhancer element for the apolipoprotein B gene is located significantly farther from its structural gene in the intestine compared to the liver.
Conclusions:
- Lipid absorption is regulated by the rate of transport between the endoplasmic reticulum and Golgi apparatus.
- Apolipoprotein B plays a crucial role in the post-formation trafficking of lipid particles.
- Peptide transporters are capable of absorbing modified peptides and esterified drugs.
- Leptin may directly influence nutrient absorption and body mass regulation via intestinal receptors.
- Tissue-specific differences in apolipoprotein B gene regulation exist, particularly concerning enhancer element location.