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        <identifier>oai:www.ideals.illinois.edu:2142/22459</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</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>Odle, Jack</dc:contributor>
          <dc:creator>Adams, Sean Harrison</dc:creator>
          <dc:date>2011-05-07T13:40:30Z</dc:date>
          <dc:date>2011-05-07T13:40:30Z</dc:date>
          <dc:date>1994</dc:date>
          <dc:description>Reports of low circulating ketone bodies ($\beta$-hydroxybutyrate, $\beta$-OHB &amp; acetoacetate) in suckling piglets and evidence of minimal hepatic ketone body production from fatty acids in vitro suggested that, unlike previously-studied neonates, enhanced ketogenesis does not characterize the metabolism of the newborn pig. This apparent idiosyncracy of piglet metabolism prompted a series of studies examining development and regulation of ketogenesis in piglets, and the physiological implications of low ketonemia in piglets. The extent of alternative pathways (non-ketogenic routes of carbon flux into Krebs cycle intermediates, e.g.) of fatty acid $\beta$-oxidation was also assessed. Low ketogenic capacity in piglets was confirmed by the small change in plasma ($\beta$-OHB) relative to (C8:0) (regression slope) following a dose of C8:0. This slope was 1-2 orders of magnitude lower vs. that of mature pigs and newborn or mature rabbits. Minimal fatty acid carboxyl-carbon accumulated in ketone bodies after incubations of piglet liver homogenates or hepatocytes with (1-$\sp{14}$C) -C7:0, -C8:0, or -C16:0 in vitro, consistent with the in vivo results. The observed low activity of the ketogenic enzyme mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase (HMG-CoA synthase) increased plasma (insulin) with suckling (patterns opposite that seen in ketotic neonatal rats, e.g.) may in part explain attenuated ketogenic capacity in piglets. Piglets accumulated fatty acid carboxyl-carbon in acetate to a high degree relative to ketone bodies in incubations of liver tissue with radiolabeled fatty acids, a phenomenon previously unreported for any animal. It is thus speculated that acetate plays a more important physiological role than the ketone bodies in newborn piglets, an idea supported by the small contribution of ketone bodies to the energy budget of piglets ($&lt;$3% of metabolic rate from ketone bodies at normal physiological plasma ($\beta$- OHB)), and the 10-fold higher plasma (acetate) relative to the (ketone bodies) in piglets.</dc:description>
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  Previous issue date: 1994</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:57:46Z
Item is restricted indefinitely.</dc:description>
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Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>Open Restriction set for Item 22594 on 2019-02-11T17:05:54Z with date null by fschaef2@illinois.edu.</dc:description>
          <dc:description>Open Restriction set for Item 22594 on 2019-02-11T17:05:56Z with date null by fschaef2@illinois.edu.</dc:description>
          <dc:description>Open</dc:description>
          <dc:identifier>AAI9512276</dc:identifier>
          <dc:identifier>(UMI)AAI9512276</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/22459</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:rights>Copyright 1994 Adams, Sean Harrison</dc:rights>
          <dc:subject>Biology, Animal Physiology</dc:subject>
          <dc:subject>Health Sciences, Nutrition</dc:subject>
          <dc:title>Hepatic acetogenesis and ketogenesis in neonatal swine</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Food Science and Human Nutrition</department>
            <discipline>Food Science and Human Nutrition</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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