Related Experiment Video
Updated: Mar 17, 2026

Author Spotlight: Exploring the Impact of Reduced Resistance Exercise Volume on Metabolic Health
Published on: December 1, 2023
Dual Effect of Rosuvastatin on Glucose Homeostasis Through Improved Insulin Sensitivity and Reduced Insulin Secretion
Vishal A Salunkhe1, Inês G Mollet1, Jones K Ofori1
1Unit of Islet Cell Exocytosis, Dept Clinical Sciences Malmö, Lund University Diabetes Centre, Lund University CRC 91-11, SUS Malmö, Jan Waldenströms gata 35, 205 02 Malmö, Sweden.
Abstract:
Statins are beneficial in the treatment of cardiovascular disease (CVD), but these lipid-lowering drugs are associated with increased incidence of new on-set diabetes. The cellular mechanisms behind the development of diabetes by statins are elusive. Here we have treated mice on normal diet (ND) and high fat diet (HFD) with rosuvastatin. Under ND rosuvastatin lowered blood glucose through improved insulin sensitivity and increased glucose uptake in adipose tissue. In vitro rosuvastatin reduced insulin secretion and insulin content in islets. In the beta cell Ca(2+) signaling was impaired and the density of granules at the plasma membrane was increased by rosuvastatin treatment. HFD mice developed insulin resistance and increased insulin secretion prior to administration of rosuvastatin. Treatment with rosuvastatin decreased the compensatory insulin secretion and increased glucose uptake. In conclusion, our data shows dual effects on glucose homeostasis by rosuvastatin where insulin sensitivity is improved, but beta cell function is impaired.
Insights
Statins like rosuvastatin improve insulin sensitivity but impair pancreatic beta cell function, potentially increasing diabetes risk. Further research is needed to understand these dual effects on glucose homeostasis.
Area of Science:
- Biochemistry
- Endocrinology
- Pharmacology
Background:
- Statins are widely used for cardiovascular disease (CVD) management.
- A known side effect of statin therapy is an increased incidence of new-onset diabetes.
- The precise cellular mechanisms underlying statin-induced diabetes remain unclear.
Purpose of the Study:
- To investigate the cellular mechanisms by which rosuvastatin affects glucose homeostasis.
- To examine the impact of rosuvastatin on insulin sensitivity and beta cell function in mice on normal and high-fat diets.
Main Methods:
- Mice on normal diet (ND) and high-fat diet (HFD) were treated with rosuvastatin.
- In vitro studies assessed rosuvastatin's effects on pancreatic islets and beta cell function.
- Measurements included blood glucose levels, insulin sensitivity, glucose uptake, insulin secretion, and beta cell calcium signaling.
Main Results:
- Rosuvastatin improved insulin sensitivity and increased glucose uptake in adipose tissue under ND conditions.
- In vitro, rosuvastatin impaired beta cell insulin secretion and insulin content, affecting calcium signaling and granule density.
- In HFD mice, rosuvastatin reduced compensatory insulin secretion while enhancing glucose uptake, despite pre-existing insulin resistance.
Conclusions:
- Rosuvastatin exhibits dual effects on glucose homeostasis: it enhances insulin sensitivity but impairs pancreatic beta cell function.
- These findings highlight a potential mechanism for statin-associated diabetes, emphasizing the need for careful patient monitoring.
More Related Videos
08:13Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test OGTT and Insulin Tolerance Test ITT
Published on: January 7, 2018
08:03Glucose Uptake Measurement and Response to Insulin Stimulation in In Vitro Cultured Human Primary Myotubes
Published on: June 25, 2017
Related Concept Videos
Oral Hypoglycemic Agents: Biguanides and Glitazones
Lipid-Lowering Drugs: Statins and Miscellaneous Agents
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
Acarbose and miglitol are...
Dipeptidyl Peptidase 4 Inhibitors
Oral Hypoglycemic Agents: Glinides
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...