<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T03:13:59Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.12327/79" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:20.500.12327/79</identifier><datestamp>2025-10-22T11:03:04Z</datestamp><setSpec>com_2072_4428</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_487898</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Ballester, Maria</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Amills, Marcel</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">González-Rodríguez, Olga</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Cardoso, Tainã F.</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Pascual, Mariam</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">González-Prendes, Rayner</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Panella-Riera, Núria</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Díaz, Isabel</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Tibau, Joan</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Quintanilla, Raquel</subfield>
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      <subfield code="c">2018-09-17</subfield>
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      <subfield code="a">Background: The molecular basis of compensatory growth in monogastric animals has not yet been fully explored.&#xd;
Herewith, in this study we aim to determine changes in the pig skeletal muscle transcriptome profile during&#xd;
compensatory growth following a feed restriction period. A RNA-Seq experiment was performed with a total of 24&#xd;
females belonging to a Duroc commercial line. Half of the animals received either a restricted (RE) or ad libitum&#xd;
(AL) diet during the first fattening period (60–125 d of age). After that, all gilts were fed ad libitum for a further ~30&#xd;
d until the age of ~155 d, when animals were slaughtered and samples of gluteus medius muscle were harvested to&#xd;
perform RNA-Seq analyses and intramuscular fat content determination.&#xd;
Results: During the period following food restriction, RE animals re-fed ad libitum displayed compensatory growth,&#xd;
showed better feed conversion rate and tended to deposit more subcutaneous fat than AL fed animals. Animals&#xd;
were slaughtered in the phase of accelerated growth, when RE animals had not completely compensated the&#xd;
performance of AL group, showing lower live and carcass weights. At intramuscular level, RE gilts showed a higher&#xd;
content of polyunsaturated fatty acids during the compensatory growth phase. The comparison of RE and AL&#xd;
expression profiles allowed the identification of 86 (ǀlog2Fold-Changeǀ > 1, padj &lt; 0.05) differentially expressed (DE)&#xd;
genes. A functional categorization of these DE genes identified AMPK Signaling as the most significantly enriched&#xd;
canonical pathway. This kinase plays a key role in the maintenance of energy homeostasis as well as in the&#xd;
activation of autophagy. Among the DE genes identified as components of AMPK Signaling pathway, five out of six&#xd;
genes were downregulated in RE pigs.&#xd;
Conclusions: Animals re-fed after a restriction period exhibited a less oxidative metabolic profile and catabolic&#xd;
processes in muscle than animals fed ad libitum. The downregulation of autophagy observed in the skeletal muscle&#xd;
of pigs undergoing compensatory growth may constitute a mechanism to increase muscle mass thus ensuring an&#xd;
accelerated growth rate. These results reveal that the downregulation of AMPK Signaling plays an important role in&#xd;
compensatory growth in pigs.</subfield>
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      <subfield code="a">Ballester, M., Amills, M., González-Rodríguez, O., Cardoso, T., Pascual, M., &amp; González-Prendes, R. et al. (2018). Role of AMPK signalling pathway during compensatory growth in pigs. BMC Genomics, 19(1). doi:10.1186/s12864-018-5071-5</subfield>
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      <subfield code="a">1471-2164</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12327/79</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://doi.org/10.1186/s12864-018-5071-5</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Role of AMPK signalling pathway during compensatory growth in pigs</subfield>
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