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Updated: May 15, 2026

Quantification of Atherosclerosis in Mice
Published on: June 12, 2019
Rosuvastatin reduced deep vein thrombosis in ApoE gene deleted mice with hyperlipidemia through non-lipid lowering
K A Patterson1, X Zhang, S K Wrobleski
1Unit for Laboratory Animal Medicine, University of Michigan, Ann Arbor, MI 48103, USA.
Introduction:
Statins, particularly rosuvastatin, have recently become relevant in the setting of venous thrombosis. The objective of this study was to study the non-lipid lowering effects of rosuvastatin in venous thrombosis in mice with hyperlipidemia.
Materials And Methods:
An inferior vena cava ligation model of venous thrombosis in mice was utilized. Saline or 5mg/kg of rosuvastatin was administered by gavage 48hs previous to thrombosis. Blood, the inferior vena cava, thrombus, and liver were harvested 3, 6hours, and 2days post-thrombosis. Thrombus weight, inflammatory markers, and plasminogen activator inhibitor-1 expression and plasma levels were measured. Also, neutrophil migration to the IVC was assessed.
Results:
Rosuvastatin significantly decreased thrombus weight, plasminogen activator inhibitor-1 expression and plasma levels, expression of molecules related to the interleukin-6 pathway, and neutrophil migration into the vein wall.
Conclusions:
This work supports the beneficial effects of rosuvastatin on venous thrombosis in mice with hyperlipidemia, due to its non-lipid lowering effects.
Insights
Rosuvastatin effectively reduced venous thrombosis in hyperlipidemic mice by inhibiting inflammation and neutrophil migration, independent of its lipid-lowering effects. This study highlights rosuvastatin
Area of Science:
- Pharmacology
- Thrombosis Research
- Cardiovascular Science
Background:
- Statins, specifically rosuvastatin, are gaining attention for their role in managing venous thrombosis.
- Hyperlipidemia is a known risk factor for developing venous thrombosis.
- Understanding non-lipid-lowering effects of statins is crucial for optimizing treatment strategies.
Purpose of the Study:
- To investigate the non-lipid-lowering effects of rosuvastatin on venous thrombosis.
- To evaluate rosuvastatin's impact on thrombosis in a mouse model of hyperlipidemia.
Main Methods:
- Utilized an inferior vena cava ligation model to induce venous thrombosis in hyperlipidemic mice.
- Administered rosuvastatin (5mg/kg) or saline via gavage 48 hours prior to thrombosis induction.
- Assessed thrombus weight, inflammatory markers, plasminogen activator inhibitor-1 (PAI-1) levels, and neutrophil migration.
Main Results:
- Rosuvastatin significantly reduced thrombus weight.
- Decreased expression and plasma levels of plasminogen activator inhibitor-1 (PAI-1).
- Inhibited neutrophil migration into the vein wall and reduced expression of interleukin-6 pathway molecules.
Conclusions:
- Rosuvastatin demonstrates beneficial effects in mitigating venous thrombosis in hyperlipidemic mice.
- These protective effects are attributed to rosuvastatin's non-lipid-lowering mechanisms.
- Supports the therapeutic potential of rosuvastatin beyond cholesterol reduction in thrombosis management.
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