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        <identifier>oai:www.ideals.illinois.edu:2142/44463</identifier>
        <datestamp>2023-07-11</datestamp>
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          <dc:contributor>Freund, Gregory G.</dc:contributor>
          <dc:creator>Joesting, Jennifer J.</dc:creator>
          <dc:date>2013-05-24T22:16:56Z</dc:date>
          <dc:date>2013-05-24T22:16:56Z</dc:date>
          <dc:date>2015-05-24T10:00:53Z</dc:date>
          <dc:date>2013-05</dc:date>
          <dc:date>2013-05-24T22:16:56Z</dc:date>
          <dc:date>2013-05</dc:date>
          <dc:description>Dietary regimens involving fasting have long been linked to beneficial health outcomes including; reduction in heart disease, diabetes, improved mood and cognition, and resistance to sickness behaviors such as anorexia and fever.  The mechanisms underlying fasting-induced health benefits and alterations in immunity and sickness behavior continues to remain debated despite over 20 years of interest.  This research project confirms that acute dietary restriction (24 h water-only fast) is able to attenuate IL-1β-induced anorexia, in addition to other sickness behaviors at early stages of the acute phase response. We previously reported that fasting was able to reduce gene expression of inflammatory IL-1α in the brain, here we looked at liver and adipose in addition to brain and uncovered a major up-regulation of IL-1 endogenous inhibitors, IL-1RA and IL-1R2 in peripheral tissues. These findings imply that attenuation in sickness behaviors observed may be due to counter-regulation of IL-1 via up-regulation of IL-1R2 and/or IL-1RA shown in metabolically active organs, which is capable of blunting the centrally-mediated effects of induced peripheral challenge. Our results further demonstrate that the mechanisms involved in IL-1R2 and IL-1RA up-regulation are independent of IL-1, TLR-4, IL-4 and glucocordicoid signaling. Here we also demonstrate that free fatty acids (FFA) are increased in the plasma as a consequence of fasting. Using palmitic acid injection to mimic fastings FFA increase, we elucidated a novel mechanism by which IL-1R2 is up-regulated. This method showed increased IL-1R2 gene transcripts in the liver of mice. FFA signaling, which produces an immune response, is shown here to be TLR-4-independent, implicating free fatty acid receptor 1 (FFAR1) as the key signaling receptor initiating the anti-inflammatory result of fasting documented in this study.</dc:description>
          <dc:description>Item withdrawn by Alexis Thompson (athmpsn1@illinois.edu) on 2013-04-18T14:16:43Z
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          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Seth Robbins (srobbins@illinois.edu) on 2013-05-24T22:19:11Z
Item is restricted until 2015-05-24T22:18:31Z</dc:description>
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Original Data
Group with Access UIUC Users [automated]
Release Date: 2015-05-24 17:18:31 UTC
Reason: Author requested U of Illinois access only (OA after 2yrs) in Vireo ETD system</dc:description>
          <dc:description>U of I Only Restriction Lifted for Item 44436 on 2015-05-24T10:00:53Z.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/44463</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2013 Jennifer J. Joesting</dc:rights>
          <dc:subject>Fasting</dc:subject>
          <dc:subject>Dietary Restriction</dc:subject>
          <dc:subject>Anti-inflammation</dc:subject>
          <dc:subject>Interleukin 1 Receptor Type 2 (IL-1R2)</dc:subject>
          <dc:subject>Interleukin 1 Receptor Antagonist (IL-1RA)</dc:subject>
          <dc:subject>sickness behavior</dc:subject>
          <dc:subject>IL-1 decoy receptor</dc:subject>
          <dc:subject>Free Fatty Acids (FFA)</dc:subject>
          <dc:subject>Non-Esterified Fatty Acids (NEFA)</dc:subject>
          <dc:title>The effect of fasting on anti-inflammatory mediators, IL-1RA and IL-1R2, and their role in resistance to sickness behaviors in mice</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Animal Sciences</department>
            <departmentCode>1538</departmentCode>
            <discipline>Animal Sciences</discipline>
            <disciplineCode>0002</disciplineCode>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Thesis</level>
            <name>M.S.</name>
            <program>MS:Animal Sciences -UIUC</program>
            <programCode>10KS0002MS</programCode>
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