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        <identifier>oai:www.ideals.illinois.edu:2142/77446</identifier>
        <datestamp>2023-07-11</datestamp>
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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:description>Embargo set by: Seth Robbins for item 78657
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>132 p.</dc:description>
          <dc:creator>Magrum, Linda Joyce</dc:creator>
          <dc:date>2015-05-13T15:44:18Z</dc:date>
          <dc:date>2015-05-13T15:44:18Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1983</dc:date>
          <dc:date>1983</dc:date>
          <dc:description>Prostaglandins, synthesized from arachidonic acid (20:4(omega)6) in high amounts by the macrophage, are known to regulate a number of activities important to the immune response. In view of the findings that (alpha)-linolenic acid (18:3(omega)3) inhibits the conversion of linoleic acid (18:2(omega)6) to 20:4(omega)6 and that 18:3(omega)3 and both 20:5(omega)3 and 22:6(omega)3, its elongated, desaturated products, inhibit the conversion of 20:4(omega)6 into prostaglandins (PGs), a study of the effect of nutritionally provided (omega)3 fatty acids on the fatty acid composition, PG synthesis, and function of the macrophage was undertaken.</dc:description>
          <dc:description>Male Sprague-Dawley weanling rats were fed purified diets containing 10% either corn oil or linseed oil, providing a low (1/32) or high (3.5/1) ratio of 18:3(omega)3 to 18:2(omega)6, respectively. Phospholipid fatty analysis of macrophages from animals fed the diets showed an appreciable increase in the percentage of (omega)3 fatty acids and a decrease in the (omega)6 fatty acids in macrophages from rats fed linseed oil. These changes were associated with a significant decrease in PG synthesis and shown not to involve increased PG degradation.</dc:description>
          <dc:description>These results were comparable to those found in macrophages cultured with 20:4(omega)6 or 20:5(omega)3. Differences in phospholipid content of 20:4(omega)6 in macrophages altered in vitro were more striking than those in macrophages altered in vivo; however, in both cases, choline phosphoglyceride exhibited the greatest disparity in 20:4(omega)6 content between the two nutritional treatments. Macrophages altered in vitro exhibited marked differences in their ability to synthesize PGE. Those cultured with 20:5(omega)3 synthesized approximately one-tenth the amount synthesized by macrophages cultured with 20:4(omega)6. Culturing with 20:4(omega)6 or 20:5(omega)3 also overcame dietarily induced changes in PG synthesis.</dc:description>
          <dc:description>Activities of the macrophage reported to be influenced by PGs were examined. Phagocytosis was not altered by the increase in dietary 18:3(omega)3. In agreement with previous reports, arginase activity was greater in macrophages showing greater PG synthesis. The synthesis of H(,2)O(,2) as measured by chemiluminescence was greater in macrophages cultured with 20:5(omega)3 than with 20:4(omega)6; however, since indomethacin, an inhibitor of PG synthesis, did not increase chemiluminescence in the 20:4(omega)6-cultured cells, it was concluded this effect was not mediated by PGs.</dc:description>
          <dc:description>Made available in DSpace on 2015-05-13T15:44:18Z (GMT). No. of bitstreams: 2
license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5)
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  Previous issue date: 1983</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1983.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/77446</dc:identifier>
          <dc:identifier>(UMI)AAI8409992</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:subject>Health Sciences, Nutrition</dc:subject>
          <dc:title>Modulation of Arachidonic Acid Metabolism in Rat Peritoneal Macrophages Through Nutritional Means</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Food Science</department>
            <discipline>Food Science</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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