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Long-term alcohol consumption increases matrix metalloproteinase-2 activity in rat aorta
C R Partridge1, H W Sampson, R Forough
1Department of Medical Physiology, Texas A&M University, College Station 77843, USA.
Life Sciences
|September 30, 1999
Summary
Chronic alcohol consumption increases matrix metalloproteinase-2 (MMP-2) activity, leading to extracellular matrix degradation and vascular remodeling in female rats. This suggests a pathway for alcohol-induced cardiovascular disease.
Area of Science:
- Cardiovascular Science
- Toxicology
- Biochemistry
Background:
- Vascular remodeling, driven by altered extracellular matrix (ECM) degradation, is key in cardiovascular diseases like hypertension.
- While alcohol is a known cardiovascular risk factor, its specific impact on vascular remodeling requires further investigation.
Purpose of the Study:
- To investigate the effect of chronic alcohol consumption on matrix metalloproteinase-2 (MMP-2) activity.
- To explore MMP-2 as a potential mediator of alcohol-induced large vessel remodeling.
Main Methods:
- Female rats were fed diets with ethanol, a pair-fed control, or a standard diet.
- Blood alcohol levels were monitored weekly.
- Aortic MMP activity was assessed using gelatin zymography at 2, 4, and 72 weeks.
- Aortic ECM composition, specifically elastic fibers, was analyzed histochemically.
Main Results:
- Long-term (72 weeks) alcohol consumption significantly increased aortic MMP-2 activity.
- Short-term alcohol consumption (2 and 4 weeks) did not affect MMP-2 activity.
- Histochemical analysis revealed distinct disruption of elastic fibers in aortas of long-term alcohol-fed rats.
Conclusions:
- Chronic alcohol consumption up-regulates MMP-2 activity in rat aortas.
- This MMP-2 upregulation is associated with the degradation of vascular elastin.
- Long-term alcohol intake contributes to vascular remodeling by altering ECM composition.

