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Updated: Jun 22, 2026

A Zebrafish Model of Diabetes Mellitus and Metabolic Memory
Published on: February 28, 2013
Prevention of diabetes in hypertensive patients: results and implications from the VALUE trial
Ming-Sheng Zhou1, Ivonne Hernandez Schulman
1Division of Nephrology and Hypertension, Vascular Biology Institute, Nephrology-Hypertension Section, Veterans Affairs Medical Center and , University of Miami Miller School of Medicine, Miami, FL 33125, USA.
Abstract:
A growing number of experimental and clinical studies have provided evidence indicating that pharmacological blockade of the renin-angiotensin system (RAS) by either angiotensin-converting enzyme inhibitors or angiotensin type 1 receptor blockers reduces the incidence of new onset type 2 diabetes in subjects with hypertension and/or cardiovascular disease, independently of antihypertensive and cardiovascular protective effects. The beneficial effects of RAS inhibition on the development of diabetes have been largely attributed to improvements in peripheral insulin sensitivity and glucose metabolism. This review focuses on recent experimental and clinical evidence supporting the role of RAS inhibition in the reduction of new onset type 2 diabetes and the mechanisms that may be involved.
Insights
Pharmacological blockade of the renin-angiotensin system (RAS) reduces new type 2 diabetes incidence in patients with cardiovascular disease. RAS inhibition improves insulin sensitivity and glucose metabolism, offering protective effects beyond blood pressure control.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Pharmacology
Background:
- The renin-angiotensin system (RAS) plays a crucial role in cardiovascular and metabolic regulation.
- Pharmacological inhibition of the RAS is a cornerstone in managing hypertension and cardiovascular disease.
- Emerging evidence suggests a link between RAS blockade and reduced incidence of type 2 diabetes.
Purpose of the Study:
- To review recent experimental and clinical evidence on the role of RAS inhibition in preventing new-onset type 2 diabetes.
- To explore the underlying mechanisms by which RAS blockade influences glucose metabolism and insulin sensitivity.
Main Methods:
- Systematic review of preclinical studies investigating RAS components and glucose homeostasis.
- Analysis of clinical trial data and observational studies evaluating RAS inhibitors (ACE inhibitors, ARBs) and diabetes incidence.
- Examination of mechanistic studies focusing on insulin signaling pathways and glucose uptake.
Main Results:
- Consistent evidence shows that ACE inhibitors and angiotensin type 1 receptor blockers (ARBs) decrease new-onset type 2 diabetes risk.
- These benefits are observed in patients with hypertension and/or cardiovascular disease, independent of blood pressure reduction.
- RAS inhibition appears to improve peripheral insulin sensitivity and enhance glucose metabolism.
Conclusions:
- Pharmacological RAS blockade is a promising strategy for diabetes prevention in at-risk populations.
- Improved insulin sensitivity and glucose metabolism are key mechanisms mediating the anti-diabetic effects of RAS inhibitors.
- Further research is warranted to fully elucidate the complex interplay between the RAS and metabolic health.
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