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        <identifier>oai:www.ideals.illinois.edu:2142/24153</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_16278</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Woods, Jeffrey A.</dc:contributor>
          <dc:creator>Greene, Ryan M.</dc:creator>
          <dc:date>2011-05-25T14:52:07Z</dc:date>
          <dc:date>2011-05-25T14:52:07Z</dc:date>
          <dc:date>2011-05-25T14:52:07Z</dc:date>
          <dc:date>2011-05</dc:date>
          <dc:description>Previous research suggests that mild traumatic brain injury (mTBI) results in significant 
cognitive and behavioral learning deficit, as well as long-term depressive like behavior in mice.  
mTBI has been identified as a major initiating event in long-term depressive-like behavior and 
early fatality observed in soldiers returning from conflicts in Iraq and Afghanistan, as well as 
athletes in amateur and professional sport. Purpose- The purpose of the proposed study was to 
investigate brain tissue for the presence of proinflammatory cytokines as a potential mechanism 
to explain long-term depressive-like behavior seen in previous mTBI studies.  Methods- Male 
ICR mice (n=16) were randomly assigned to one of 2 treatment groups:  mTBI (n=8) and Sham 
(n=8).  Mice were anaesthetized and given mTBI by dropping a weight similar to previously 
measured body weight to an area located between the ear and the eye from a height of two feet.  
Baseline behavioral data was measured for both treatment groups for 8 days prior to treatment. Following mTBI, at the 48 and 72 hour time point, Roto-rod testing was conducted to ensure any 
differences in baseline behavioral deficit in either treatment group was not do to motor cortex 
impairment.  Mice were sacrificed 7 days following treatment and tissue was tested for presence 
of proinflammatory cytokines detected via RtPCR.  Results- There was only a significant 
treatment effect seen in the expression of proinflammatory cytokine TNF-α.  All other 
proinflammatory cytokine expression had a high degree of variability between both groups.  
Roto-rod data confirmed there was no motor cortex deficit involved in deficit in behavioral 
measurements gathered following treatment.  Conclusion- These circumstantial data suggest that 
proinflammatory cytokines may play a role in instigating long-term depressive like behavior by 
infiltrating neurological tissue in individuals afflicted with mTBI, but the weight drop model used to inflict mTBI was too mild to induce large scale significant changes in pro-inflammatory 
cytokines or long-term behavioral depression.</dc:description>
          <dc:description>Item withdrawn by Alexis Thompson (athmpsn1@illinois.edu) on 2011-04-20T14:43:21Z
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University of Illinois Theses &amp; Dissertations (ID: 1)
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          <dc:identifier>http://hdl.handle.net/2142/24153</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2011 Ryan M. Greene</dc:rights>
          <dc:subject>Mild Traumatic Brain Injury (mTBI)</dc:subject>
          <dc:subject>Brain</dc:subject>
          <dc:subject>Cytokines</dc:subject>
          <dc:title>The effect of mild traumatic brain injury on cytokine expression in brain tissue</dc:title>
          <degree>
            <department>Kinesiology &amp; Community Health</department>
            <departmentCode>1581</departmentCode>
            <discipline>Kinesiology</discipline>
            <disciplineCode>0351</disciplineCode>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Thesis</level>
            <name>M.S.</name>
            <program>MS:Kinesiology -UIUC</program>
            <programCode>10KS0351MS</programCode>
          </degree>
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