Related Experiment Video
Updated: Jun 5, 2025

09:34
Uptake of New Lipid-coated Nanoparticles Containing Falcarindiol by Human Mesenchymal Stem Cells
Published on: February 9, 2019
8.9K
Smart control lipid-based nanocarriers for fine-tuning gut hormone secretion
Yining Xu1,2,3,4, Cécilia Bohns Michalowski1, Jackie Koehler5,6
1Louvain Drug Research Institute, Advanced Drug Delivery and Biomaterials, Université catholique de Louvain, 1200 Brussels, Belgium.
Science Advances
|December 13, 2024
Summary
Lipid nanocarriers activate gut hormone release, offering a new noninvasive strategy for metabolic dysfunction. This nanotechnology approach modulates multiple endogenous hormones for therapeutic benefits.
Area of Science:
- Gastroenterology and Endocrinology
- Nanotechnology
- Metabolic Disease Research
Background:
- Modulating gastrointestinal hormones is a key strategy for metabolic dysfunction.
- Enteroendocrine cells (EECs) play a crucial role in gut endocrine function.
Purpose of the Study:
- To investigate the potential of lipid nanocarriers to modulate endogenous gastrointestinal hormone release.
- To explore the therapeutic applications of nanotechnology in managing metabolic dysfunction.
Main Methods:
- Utilized mouse and human knock-in/knockout intestinal organoids.
- Formulated lipid nanocarriers using commercial lipid excipients.
- Studied effects in wild-type, dysglycemic, and gut Gcg knockout mice.
Main Results:
- Lipid nanocarriers activated nutrient-sensitive receptors on EECs.
- Demonstrated release of GLP-1, GIP, and PYY from K and L cells.
- Excipient type, formulation, and nanocarrier properties modulated biological effects.
Conclusions:
- Nanotechnology offers a promising, noninvasive therapeutic approach for metabolic dysfunction.
- Modulating multiple endogenous hormones via lipid nanocarriers is feasible.
- This strategy presents a patient-friendly and cost-effective method for hormone modulation.
Related Concept Videos
Glucagon-like Receptor Agonists
298
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
298
Hormonal Regulation
43.1K
Hormones regulate a significant portion of digestion through activation of the neuroendocrine system. The neuroendocrine system of digestion contains many different hormones all with multiple functions that are both, directly and indirectly, involved in digestion.
43.1K

