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Updated: Jan 31, 2026

Minimizing Hypoxia in Hippocampal Slices from Adult and Aging Mice
Published on: July 2, 2020
Aspirin treatment does not increase microhemorrhage size in young or aged mice
Sandy Chan1, Morgan Brophy1, Nozomi Nishimura1
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America.
Insights
Aspirin does not increase the size of brain microhemorrhages in aging mice. This study suggests aspirin is safe for use in older individuals, even with potential bleeding risks.
Area of Science:
- Neuroscience
- Pharmacology
- Gerontology
Background:
- Microhemorrhages are common in aging brains and linked to cognitive decline and neurodegenerative diseases like Alzheimer's.
- Chronic aspirin use is prevalent in older adults, reducing risks of stroke and heart attack.
- Concerns exist that aspirin may worsen brain bleeds by prolonging hemorrhage size.
Purpose of the Study:
- To investigate the effect of aspirin on cortical microhemorrhage size in young and aged mice.
- To compare aspirin's impact on bleeding with other anticoagulants like heparin.
Main Methods:
- Femtosecond laser ablation was used to induce controlled microhemorrhages in mouse arterioles.
- Red blood cell and plasma penetration were measured in young and aged mice, with and without aspirin treatment.
- Aspirin dosage was administered via drinking water; heparin was given intravenously.
Main Results:
- Aspirin treatment did not significantly alter microhemorrhage size in either young or aged mice compared to controls.
- The average hematoma diameter was similar across control, aspirin-treated young, and aspirin-treated aged mice.
- In contrast, heparin treatment led to a significant increase in hematoma diameter.
Conclusions:
- Aspirin does not exacerbate bleeding from cortical microhemorrhages.
- These findings support the safety of chronic aspirin therapy in older individuals regarding brain microhemorrhage size.
- Aspirin's safety profile appears favorable compared to other anticoagulants like heparin in this context.
Abstract:
Microhemorrhages are common in the aging brain and are thought to contribute to cognitive decline and the development of neurodegenerative diseases, such as Alzheimer's disease. Chronic aspirin therapy is widespread in older individuals and decreases the risk of coronary artery occlusions and stroke. There remains a concern that such aspirin usage may prolong bleeding after a vessel rupture in the brain, leading to larger bleeds that cause more damage to the surrounding tissue. Here, we aimed to understand the influence of aspirin usage on the size of cortical microhemorrhages and explored the impact of age. We used femtosecond laser ablation to rupture arterioles in the cortex of both young (2-5 months old) and aged (18-29 months old) mice dosed on aspirin in their drinking water and measured the extent of penetration of both red blood cells and blood plasma into the surrounding tissue. We found no difference in microhemorrhage size for both young and aged mice dosed on aspirin, as compared to controls (hematoma diameter = 104 +/- 39 (97 +/- 38) μm in controls and 109 +/- 25 (101 +/- 28) μm in aspirin-treated young (aged) mice; mean +/- SD). In contrast, young mice treated with intravenous heparin had an increased hematoma diameter of 136 +/- 44 μm. These data suggest that aspirin does not increase the size of microhemorrhages, supporting the safety of aspirin usage.
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