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Sustained Administration of β-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres
Published on: November 5, 2016
Clinical approaches to preserve beta-cell function in diabetes
1Endocrine Service and Diabetes and Heart Center of the Heart Institute, Hospital das, Clinicas of The University of São Paulo Medical School, São Paulo, SP 05403-000, Brazil. bernarwaj@globo.com
Type 2 diabetes involves progressive beta-cell loss. Treatments like GLP-1 receptor agonists and DPP-4 inhibitors help preserve beta-cell function and mass, improving glucose homeostasis.
Area of Science:
- Endocrinology
- Metabolic Diseases
Background:
- Type 2 diabetes (DM2) is characterized by progressive decline in pancreatic beta-cell function and mass.
- At diagnosis, islet function is approximately 50% of normal, with significant beta-cell mass reduction due to accelerated apoptosis.
Purpose of the Study:
- To review interventions aimed at preserving beta-cell function and mass in type 2 diabetes.
- To highlight the role of incretin-based therapies in managing DM2.
Main Methods:
- Review of existing literature on type 2 diabetes pathophysiology and treatment strategies.
- Focus on interventions impacting beta-cell secretion and survival, including incretin hormone pathways.
Main Results:
- Short-term improvements in beta-cell secretion are achieved with weight loss, metformin, sulfonylureas, and insulin.
- Long-term beta-cell preservation is demonstrated with intensive insulin therapy, antiapoptotic drugs (glitazones), and glucagon-like peptide-1 receptor agonists (GLP-1 mimetics) or enhancers.
Conclusions:
- Incretin hormones, particularly GLP-1, play a crucial role in glucose homeostasis.
- GLP-1 mimetics (exenatide, liraglutide) and DPP-4 inhibitors (sitagliptin, vildagliptin) are approved and effective treatments for type 2 diabetes, preserving beta-cell function.
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