Related Experiment Video
Updated: Apr 18, 2026

The 4-vessel Sampling Approach to Integrative Studies of Human Placental Physiology In Vivo
Published on: August 2, 2017
Insulin therapy and fetoplacental vascular function in gestational diabetes mellitus
Luis Sobrevia1, Rocío Salsoso, Tamara Sáez
1Cellular and Molecular Physiology Laboratory (CMPL), Division of Obstetrics and Gynaecology, School of Medicine, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile; University of Queensland Centre for Clinical Research (UQCCR), Faculty of Medicine and Biomedical Sciences, University of Queensland, Herston, Queensland, Australia; Department of Physiology, Faculty of Pharmacy, Universidad de Sevilla, Seville, Spain.
New Findings:
What is the topic of this review? This review focuses on the effects of insulin therapy on fetoplacental vasculature in gestational diabetes mellitus and the potentiating effects of adenosine on this therapy. What advances does it highlight? This review highlights recent studies exploring a potential functional link between insulin receptors and their dependence on adenosine receptor activation (insulin-adenosine axis) to restore placental endothelial function in gestational diabetes mellitus. Gestational diabetes mellitus (GDM) is a disease that occurs during pregnancy and is associated with maternal and fetal hyperglycaemia. Women with GDM are treated via diet to control their glycaemia; however, a proportion of these patients do not achieve the recommended values of glycaemia and are subjected to insulin therapy until delivery. Even if a diet-treated GDM pregnancy leads to normal maternal and newborn glucose levels, fetoplacental vascular dysfunction remains evident. Thus, control of glycaemia via diet does not prevent GDM-associated fetoplacental vascular and metabolic alterations. We review the available information regarding insulin therapy in the context of its potential consequences for fetoplacental vascular function in GDM. We propose the possibility that insulin therapy to produce normoglycaemia in the mother and newborn may require additional therapeutic measures to restore the normal metabolic condition of the vascular network in GDM. A role for A1 and A2A adenosine receptors and insulin receptors A and B as well as a potential functional link in the cell signalling associated with the activation of these receptors is proposed. This possibility could be helpful for the planning of strategies, including adenosine receptor-improved insulin therapy, for the treatment of GDM patients, thereby promoting the wellbeing of the growing fetus, newborn and mother.
Insights
Insulin therapy for gestational diabetes mellitus (GDM) may not fully restore fetoplacental vasculature. Combining insulin with adenosine receptor activation could improve placental function and maternal-fetal health.
Area of Science:
- Reproductive biology
- Endocrinology
- Vascular physiology
Background:
- Gestational diabetes mellitus (GDM) causes maternal and fetal hyperglycemia.
- Insulin therapy is used when diet fails, but fetoplacental vascular dysfunction persists.
- GDM-associated vascular alterations impact maternal and fetal well-being.
Purpose of the Study:
- To review insulin therapy effects on fetoplacental vasculature in GDM.
- To explore adenosine's potentiating effects on insulin therapy.
- To highlight the insulin-adenosine axis in restoring placental function.
Main Methods:
- Literature review of studies on insulin therapy in GDM.
- Analysis of the role of insulin and adenosine receptors in placental vasculature.
- Exploration of potential functional links in cell signaling pathways.
Main Results:
- Insulin therapy normalizes maternal and newborn glucose but not fetoplacental vascular function.
- A functional link between insulin and adenosine receptors (insulin-adenosine axis) is proposed.
- A1 and A2A adenosine receptors and insulin receptors A and B are implicated.
Conclusions:
- Insulin therapy alone may be insufficient for GDM-related vascular issues.
- Additional therapies, like adenosine receptor modulation, are needed.
- Targeting the insulin-adenosine axis may enhance GDM treatment and improve outcomes.
Related Concept Videos
Diabetes Mellitus: Type 2 and Gestational
Pathophysiology of Diabetes
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
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...
Dipeptidyl Peptidase 4 Inhibitors
Type I Diabetes II: Pathophysiology
Diabetes Mellitus: Introduction

