Related Experiment Video
Updated: May 17, 2026

An In Ovo Model for Testing Insulin-mimetic Compounds
Published on: April 23, 2018
New avenues for the pharmacological management of type 2 diabetes: an update
Thomas Cuny1, Bruno Guerci, Bertrand Cariou
1University of Nancy I, Department of Endocrinology, University Hospital of Nancy-Brabois, 54511 Vandoeuvre-Les-Nancy, France.
Abstract:
Type 2 diabetes mellitus (T2DM) is one of the most troubling chronic disease regarding the huge number of new cases diagnosed annually worldwide. Currently available oral antidiabetic drugs (OADs) attempt to correct the underlying pathophysiological dysfunctions leading to T2DM: insulin resistance for the insulin sensitizers (metformin and thiazolidinediones), and impaired insulin secretion for the insulin secretagogues (sulfonylureas, glinides and more recently incretin mimetics). Incretin-based therapies include GLP-1 receptor agonists that provide pharmacologic levels of GLP-1 receptor stimulation beyond those that would occur from the action of the native hormone alone, and dipeptidyl-peptidase-4 (DPP-4) inhibitors that preserve endogenous GLP-1 by decreasing its degradation by the DPP-4 enzyme. In 2012, the development of new OADs aims to target untapped pathophysiological aspects of the disease (kidney homeostasis, glucagon signalling, chronic low-grade inflammation) for tailoring glycaemic control in T2DM. SGLT-2 inhibitors are the most advanced new OADs that lower HbA1C by increasing glycosuria and lead to a moderate weight loss. Although there is genuine hope that the range of OADs can be extended, a long-term evaluation of side effects and true clinical benefits is necessary.
Insights
New oral antidiabetic drugs (OADs) target type 2 diabetes mellitus (T2DM) by addressing insulin resistance and secretion. Emerging therapies like SGLT-2 inhibitors offer novel approaches for glycemic control, with ongoing evaluation of long-term benefits.
Area of Science:
- Endocrinology
- Pharmacology
- Metabolic Diseases
Background:
- Type 2 diabetes mellitus (T2DM) is a global chronic disease with increasing prevalence.
- Current oral antidiabetic drugs (OADs) target insulin resistance and impaired insulin secretion.
- Incretin-based therapies, including GLP-1 receptor agonists and DPP-4 inhibitors, modulate incretin hormone action.
Purpose of the Study:
- To review current and emerging oral antidiabetic drug (OAD) therapies for type 2 diabetes mellitus (T2DM).
- To discuss novel therapeutic targets for T2DM management.
- To highlight the role of SGLT-2 inhibitors as advanced OADs.
Main Methods:
- Review of existing literature on oral antidiabetic drugs.
- Analysis of pathophysiological targets for T2DM treatment.
- Discussion of emerging drug classes and their mechanisms.
Main Results:
- Established OADs address insulin resistance (metformin, thiazolidinediones) and secretion (sulfonylureas, glinides, incretin mimetics).
- Incretin-based therapies enhance GLP-1 action or preserve endogenous GLP-1.
- SGLT-2 inhibitors lower HbA1C by promoting glycosuria and induce moderate weight loss.
Conclusions:
- New OAD development in 2012 focuses on kidney homeostasis, glucagon signaling, and inflammation.
- SGLT-2 inhibitors represent a significant advancement in T2DM treatment.
- Long-term evaluation of side effects and clinical benefits of new OADs is crucial.
Related Concept Videos
Diabetes: Management and Pharmacotherapy
Insulin remains the cornerstone of treatment for most patients with type 1 and many...
Diabetes Mellitus: Type 2 and Gestational
Type II Diabetes I: Introduction
Type II Diabetes II: Pathophysiology
Diabetes Mellitus: Overview and Type I Subtype
Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks and destroys the insulin-producing beta cells in the pancreas. As a result, the body is unable to produce sufficient insulin, and individuals with...
Type II Diabetes Mellitus III: Clinical Manifestations and Diagnosis