Modification of the Marmarou and Foda model of diffuse axonal injury (DAI) improves percentage survival of rats at 24 h and increases the amount of DAI identified
More than two decades ago, Marmarou published a valid model for producing diffuse axonal injury (DAI) in rats. Since then, both mild and severe injuries have been obtained by researchers using the original method and a weight of 450 g. However, the diffuse brain injuries produced in rats were only s...
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Veröffentlicht in: | Journal of forensic sciences 2023-07, Vol.68 (4), p.1228-1236 |
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creator | Fernández‐Liste, Alberto González‐Cantalapiedra, Antonio Cascallana, José L. García‐Caballero, Tomás Gallego, Rosalía |
description | More than two decades ago, Marmarou published a valid model for producing diffuse axonal injury (DAI) in rats. Since then, both mild and severe injuries have been obtained by researchers using the original method and a weight of 450 g. However, the diffuse brain injuries produced in rats were only similar to those seen in humans when the rats sustained severe brain injuries. In these cases, rat mortality in the original article was around 50%, and the cause of death was prolonged apnea post‐impact. Rat survival after impact is critical for studying the progression of DAI. In order to explain the cause of death in human victims with cranial trauma who do not show gross brain injury, testing for the presence of DAI is essential. Thus, in order to minimize local and cervical injuries to increase rat survival, attention should be paid to the following aspects: a wider head protector disc should be used, the head of the rat should be elevated at the time of impact, and the foam bed should be soft enough to allow the movement caused by acceleration. With our modified method, rat survival increased by 30% compared to the original model (80% versus 50%). Moreover, 85.7% of rats demonstrated DAI after 24 h of survival. With these modifications, injuries appear in the same locations as in humans; thus, the method is suitable for the study of traumatic DAI in humans. |
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Since then, both mild and severe injuries have been obtained by researchers using the original method and a weight of 450 g. However, the diffuse brain injuries produced in rats were only similar to those seen in humans when the rats sustained severe brain injuries. In these cases, rat mortality in the original article was around 50%, and the cause of death was prolonged apnea post‐impact. Rat survival after impact is critical for studying the progression of DAI. In order to explain the cause of death in human victims with cranial trauma who do not show gross brain injury, testing for the presence of DAI is essential. Thus, in order to minimize local and cervical injuries to increase rat survival, attention should be paid to the following aspects: a wider head protector disc should be used, the head of the rat should be elevated at the time of impact, and the foam bed should be soft enough to allow the movement caused by acceleration. With our modified method, rat survival increased by 30% compared to the original model (80% versus 50%). Moreover, 85.7% of rats demonstrated DAI after 24 h of survival. With these modifications, injuries appear in the same locations as in humans; thus, the method is suitable for the study of traumatic DAI in humans.</description><identifier>ISSN: 0022-1198</identifier><identifier>EISSN: 1556-4029</identifier><identifier>DOI: 10.1111/1556-4029.15276</identifier><identifier>PMID: 37171023</identifier><language>eng</language><publisher>United States</publisher><subject>diffuse axonal injury ; foam bed ; forensic pathology ; impact acceleration ; Marmarou model ; method modification ; neuropathology ; rat model ; traumatic brain injury</subject><ispartof>Journal of forensic sciences, 2023-07, Vol.68 (4), p.1228-1236</ispartof><rights>2023 American Academy of Forensic Sciences.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2976-75535343d5a9204db424605062bbc7255f6dde5da7404eb81e4ddb87e039d1393</cites><orcidid>0000-0003-4718-8461</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1556-4029.15276$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1556-4029.15276$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37171023$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fernández‐Liste, Alberto</creatorcontrib><creatorcontrib>González‐Cantalapiedra, Antonio</creatorcontrib><creatorcontrib>Cascallana, José L.</creatorcontrib><creatorcontrib>García‐Caballero, Tomás</creatorcontrib><creatorcontrib>Gallego, Rosalía</creatorcontrib><title>Modification of the Marmarou and Foda model of diffuse axonal injury (DAI) improves percentage survival of rats at 24 h and increases the amount of DAI identified</title><title>Journal of forensic sciences</title><addtitle>J Forensic Sci</addtitle><description>More than two decades ago, Marmarou published a valid model for producing diffuse axonal injury (DAI) in rats. Since then, both mild and severe injuries have been obtained by researchers using the original method and a weight of 450 g. However, the diffuse brain injuries produced in rats were only similar to those seen in humans when the rats sustained severe brain injuries. In these cases, rat mortality in the original article was around 50%, and the cause of death was prolonged apnea post‐impact. Rat survival after impact is critical for studying the progression of DAI. In order to explain the cause of death in human victims with cranial trauma who do not show gross brain injury, testing for the presence of DAI is essential. Thus, in order to minimize local and cervical injuries to increase rat survival, attention should be paid to the following aspects: a wider head protector disc should be used, the head of the rat should be elevated at the time of impact, and the foam bed should be soft enough to allow the movement caused by acceleration. With our modified method, rat survival increased by 30% compared to the original model (80% versus 50%). Moreover, 85.7% of rats demonstrated DAI after 24 h of survival. With these modifications, injuries appear in the same locations as in humans; thus, the method is suitable for the study of traumatic DAI in humans.</description><subject>diffuse axonal injury</subject><subject>foam bed</subject><subject>forensic pathology</subject><subject>impact acceleration</subject><subject>Marmarou model</subject><subject>method modification</subject><subject>neuropathology</subject><subject>rat model</subject><subject>traumatic brain injury</subject><issn>0022-1198</issn><issn>1556-4029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkT1P3DAch62qVbnSzmzIIwwBvzsZEfRaKhBLO1tO_E8xSuKrnRy9jZXvwSfjk-DcUdZ6sWQ_v8cvP4QOKDmheZxSKVUhCKtOqGRavUOLt5X3aEEIYwWlVbmHPqV0RwhRVNGPaI9rqilhfIGeroPzrW_s6MOAQ4vHW8DXNvY2hgnbweFlcBb3wUE3b2e4nRJg-zcMtsN-uJviBh9dnF0eY9-vYlhDwiuIDQyj_Q04TXHt13abjXZM2I6YieeHx9ut3A9NBJtyZj7X9mEaxhnNPuxdduS7gfuMPrS2S_Dldd5Hv5Zff55_L65uvl2en10VDau0KrSUXHLBnbQVI8LVgglFJFGsrhvNpGyVcyCd1YIIqEsKwrm61EB45Siv-D462nnzO_5MkEbT-9RA19kBwpQMKymXSlNaZvR0hzYxpBShNavo86dtDCVmrsbMRZi5CLOtJicOX-VT3YN74_91kQG5A-59B5v_-cyP5c1O_AKfuplm</recordid><startdate>202307</startdate><enddate>202307</enddate><creator>Fernández‐Liste, Alberto</creator><creator>González‐Cantalapiedra, Antonio</creator><creator>Cascallana, José L.</creator><creator>García‐Caballero, Tomás</creator><creator>Gallego, Rosalía</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4718-8461</orcidid></search><sort><creationdate>202307</creationdate><title>Modification of the Marmarou and Foda model of diffuse axonal injury (DAI) improves percentage survival of rats at 24 h and increases the amount of DAI identified</title><author>Fernández‐Liste, Alberto ; González‐Cantalapiedra, Antonio ; Cascallana, José L. ; García‐Caballero, Tomás ; Gallego, Rosalía</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2976-75535343d5a9204db424605062bbc7255f6dde5da7404eb81e4ddb87e039d1393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>diffuse axonal injury</topic><topic>foam bed</topic><topic>forensic pathology</topic><topic>impact acceleration</topic><topic>Marmarou model</topic><topic>method modification</topic><topic>neuropathology</topic><topic>rat model</topic><topic>traumatic brain injury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernández‐Liste, Alberto</creatorcontrib><creatorcontrib>González‐Cantalapiedra, Antonio</creatorcontrib><creatorcontrib>Cascallana, José L.</creatorcontrib><creatorcontrib>García‐Caballero, Tomás</creatorcontrib><creatorcontrib>Gallego, Rosalía</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of forensic sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernández‐Liste, Alberto</au><au>González‐Cantalapiedra, Antonio</au><au>Cascallana, José L.</au><au>García‐Caballero, Tomás</au><au>Gallego, Rosalía</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modification of the Marmarou and Foda model of diffuse axonal injury (DAI) improves percentage survival of rats at 24 h and increases the amount of DAI identified</atitle><jtitle>Journal of forensic sciences</jtitle><addtitle>J Forensic Sci</addtitle><date>2023-07</date><risdate>2023</risdate><volume>68</volume><issue>4</issue><spage>1228</spage><epage>1236</epage><pages>1228-1236</pages><issn>0022-1198</issn><eissn>1556-4029</eissn><abstract>More than two decades ago, Marmarou published a valid model for producing diffuse axonal injury (DAI) in rats. Since then, both mild and severe injuries have been obtained by researchers using the original method and a weight of 450 g. However, the diffuse brain injuries produced in rats were only similar to those seen in humans when the rats sustained severe brain injuries. In these cases, rat mortality in the original article was around 50%, and the cause of death was prolonged apnea post‐impact. Rat survival after impact is critical for studying the progression of DAI. In order to explain the cause of death in human victims with cranial trauma who do not show gross brain injury, testing for the presence of DAI is essential. Thus, in order to minimize local and cervical injuries to increase rat survival, attention should be paid to the following aspects: a wider head protector disc should be used, the head of the rat should be elevated at the time of impact, and the foam bed should be soft enough to allow the movement caused by acceleration. With our modified method, rat survival increased by 30% compared to the original model (80% versus 50%). Moreover, 85.7% of rats demonstrated DAI after 24 h of survival. With these modifications, injuries appear in the same locations as in humans; thus, the method is suitable for the study of traumatic DAI in humans.</abstract><cop>United States</cop><pmid>37171023</pmid><doi>10.1111/1556-4029.15276</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4718-8461</orcidid></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | diffuse axonal injury foam bed forensic pathology impact acceleration Marmarou model method modification neuropathology rat model traumatic brain injury |
title | Modification of the Marmarou and Foda model of diffuse axonal injury (DAI) improves percentage survival of rats at 24 h and increases the amount of DAI identified |
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