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Updated: May 28, 2026

Differentiated Mouse Adipocytes in Primary Culture: A Model of Insulin Resistance
Published on: February 17, 2023
The renin-angiotensin system: a link between obesity, inflammation and insulin resistance
N S Kalupahana1, N Moustaid-Moussa
1Obesity Research Center, The University of Tennessee, Knoxville, TN 37996-4588, USA.
Abstract:
The renin-angiotensin system (RAS) is classically known for its role in regulation of blood pressure, fluid and electrolyte balance. Recently, several local RASs in organs such as brain, heart, pancreas and adipose tissue have also been identified. Evidence from clinical trials suggests that in addition to anti-hypertensive effects, pharmacological inhibition of RAS also provides protection against the development of type-2 diabetes. Moreover, animal models with targeted inactivation of RAS genes exhibit improved insulin sensitivity and are protected from high-fat diet-induced obesity and insulin resistance. Because there is evidence for RAS overactivation in obesity, it is possible that RAS is a link between obesity and insulin resistance. This review summarizes the evidence and mechanistic insights on the associations between RAS, obesity and insulin resistance, with special emphasis on the role of adipose tissue RAS in the pathogenesis of metabolic derangements in obesity.
Insights
The renin-angiotensin system (RAS) links obesity and insulin resistance. Inhibiting RAS improves insulin sensitivity and protects against obesity-related metabolic issues, particularly via adipose tissue RAS.
Area of Science:
- Endocrinology
- Metabolic Physiology
Background:
- The renin-angiotensin system (RAS) classically regulates blood pressure and fluid balance.
- Local RAS have been identified in various organs, including adipose tissue.
- RAS overactivation is observed in obesity, suggesting a link to insulin resistance.
Purpose of the Study:
- To review evidence and mechanistic insights on the association between RAS, obesity, and insulin resistance.
- To highlight the role of adipose tissue RAS in obesity-related metabolic dysfunction.
Main Methods:
- Review of clinical trial evidence.
- Analysis of animal model studies with targeted RAS gene inactivation.
- Examination of mechanistic insights into RAS involvement in metabolic derangements.
Main Results:
- Pharmacological RAS inhibition shows anti-hypertensive and anti-diabetic effects.
- Targeted RAS gene inactivation improves insulin sensitivity in animal models.
- Evidence suggests RAS overactivation in obesity contributes to insulin resistance.
Conclusions:
- The RAS plays a significant role in the pathogenesis of obesity and insulin resistance.
- Adipose tissue RAS is a key factor in metabolic derangements associated with obesity.
- Targeting RAS may offer therapeutic strategies for obesity and type-2 diabetes.
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