Aspirin treatment does not increase microhemorrhage size in young or aged mice
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 s...
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Published in | PloS one Vol. 14; no. 1; p. e0204295 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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04.01.2019
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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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AbstractList | 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. 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) [mu]m in controls and 109 +/- 25 (101 +/- 28) [mu]m in aspirin-treated young (aged) mice; mean +/- SD). In contrast, young mice treated with intravenous heparin had an increased hematoma diameter of 136 +/- 44 [mu]m. These data suggest that aspirin does not increase the size of microhemorrhages, supporting the safety of aspirin usage. |
Audience | Academic |
Author | Schaffer, Chris B Chan, Sandy Nishimura, Nozomi Brophy, Morgan |
AuthorAffiliation | Institut d’Investigacions Biomediques de Barcelona, SPAIN Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America |
AuthorAffiliation_xml | – name: Institut d’Investigacions Biomediques de Barcelona, SPAIN – name: Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America |
Author_xml | – sequence: 1 givenname: Sandy surname: Chan fullname: Chan, Sandy organization: Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America – sequence: 2 givenname: Morgan surname: Brophy fullname: Brophy, Morgan organization: Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America – sequence: 3 givenname: Nozomi surname: Nishimura fullname: Nishimura, Nozomi organization: Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America – sequence: 4 givenname: Chris B orcidid: 0000-0002-7800-9596 surname: Schaffer fullname: Schaffer, Chris B organization: Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30608925$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s10143_021_01675_2 crossref_primary_10_1177_0271678X19899377 crossref_primary_10_3390_brainsci13071108 |
Cites_doi | 10.1055/s-0034-1384631 10.1038/nmeth844 10.1161/STROKEAHA.114.006620 10.1161/CIRCULATIONAHA.111.035972 10.1016/j.mad.2015.08.006 10.1016/j.amepre.2014.11.005 10.1161/01.STR.0000196991.03618.31 10.1371/journal.pone.0065663 10.1016/S0002-9149(99)80177-5 10.1016/S1474-4422(13)70049-8 10.1001/archneurol.2009.42 10.1016/j.jns.2010.09.031 10.1212/WNL.0b013e3182452928 10.1126/scitranslmed.3002761 10.1161/STROKEAHA.114.005786 10.1038/sj.jcbfm.9600155 10.1371/journal.pone.0026612 10.1016/j.critrevonc.2006.06.004 10.1212/WNL.54.12.2298 10.1371/journal.pone.0054203 10.1161/STROKEAHA.114.005787 10.1161/01.STR.0000231842.32153.74 10.1038/jcbfm.2011.22 |
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Copyright | COPYRIGHT 2019 Public Library of Science 2019 Chan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2019 Chan et al 2019 Chan et al |
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SubjectTerms | Age Age Factors Aging Aging - physiology Analgesics Animals Anticoagulants Arterioles Arterioles - drug effects Arterioles - pathology Arterioles - surgery Aspirin Aspirin - administration & dosage Aspirin - adverse effects Biology and Life Sciences Biomedical engineering Bleeding Blood Blood cells Blood plasma Blood platelets Brain Brain damage Cerebral Cortex - blood supply Cerebral Cortex - pathology Cerebral Hemorrhage - etiology Cerebral Hemorrhage - pathology Cerebral Hemorrhage - physiopathology Cognitive ability Coronary artery Cortex Disease Models, Animal Drinking water Engineering Engineering and Technology Erythrocytes Female Hematoma Hematoma, Subdural, Intracranial - diagnosis Hematoma, Subdural, Intracranial - etiology Hematoma, Subdural, Intracranial - pathology Hemorrhage Hemostasis - drug effects Heparin Humans Intravenous administration Laboratory animals Laser ablation Lasers Male Medicine and Health Sciences Metabolism Mice Mice, Inbred C57BL Neurodegenerative diseases Neurological diseases Neurology Occlusion Patient outcomes Physiology Platelet Aggregation Inhibitors - administration & dosage Platelet Aggregation Inhibitors - adverse effects Prevention Rupturing Severity of Illness Index Stroke Surgery Tissues |
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Title | Aspirin treatment does not increase microhemorrhage size in young or aged mice |
URI | https://www.ncbi.nlm.nih.gov/pubmed/30608925 https://www.proquest.com/docview/2163344839 https://search.proquest.com/docview/2164102192 https://pubmed.ncbi.nlm.nih.gov/PMC6319729 https://doaj.org/article/e5b50800f75c476aa296b4b814d5b17f http://dx.doi.org/10.1371/journal.pone.0204295 |
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