<?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>2026-07-23T19:37:08Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18806" metadataPrefix="mets">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18806</identifier><datestamp>2024-09-21T18:43:15Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_20.500.12105-18806" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:20.500.12105/18806">
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               <mods:name>
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                  <mods:namePart>Silvério, Renata</mods:namePart>
               </mods:name>
               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Barth, Robson</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Heimann, Andrea S</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Reckziegel, Patrícia</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Dos Santos, Gustavo J</mods:namePart>
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                  <mods:namePart>Romero-Zerbo, Silvana Y</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Bermúdez-Silva, Francisco J</mods:namePart>
               </mods:name>
               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Rafacho, Alex</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Ferro, Emer S</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-27T15:16:24Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2022-04-07</mods:dateIssued>
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               <mods:identifier type="doi">10.3390/ijms23084082</mods:identifier>
               <mods:identifier type="e-issn">1422-0067</mods:identifier>
               <mods:identifier type="journal">International journal of molecular sciences</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/10668/21149</mods:identifier>
               <mods:identifier type="pubmedID">35456900</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/18806</mods:identifier>
               <mods:abstract>Peptide DIIADDEPLT (Pep19) has been previously suggested to improve metabolic parameters, without adverse central nervous system effects, in a murine model of diet-induced obesity. Here, we aimed to further evaluate whether Pep19 oral administration has anti-obesogenic effects, in a well-established high-fat diet-induced obesity model. Male Swiss mice, fed either a standard diet (SD) or high-fat diet (HFD), were orally administrated for 30 consecutive days, once a day, with saline vehicle or Pep19 (1 mg/kg). Next, several metabolic, morphological, and behavioral parameters were evaluated. Oral administration of Pep19 attenuated HFD body-weight gain, reduced in approximately 40% the absolute mass of the endocrine pancreas, and improved the relationship between circulating insulin and peripheral insulin sensitivity. Pep19 treatment of HFD-fed mice attenuated liver inflammation, hepatic fat distribution and accumulation, and lowered plasma alanine aminotransferase activity. The inguinal fat depot from the SD group treated with Pep19 showed multilocular brown-fat-like cells and increased mRNA expression of uncoupling protein 1 (UCP1), suggesting browning on inguinal white adipose cells. Morphological analysis of brown adipose tissue (BAT) from HFD mice showed the presence of larger white-like unilocular cells, compared to BAT from SD, Pep19-treated SD or HFD mice. Pep19 treatment produced no alterations in mice behavior. Oral administration of Pep19 ameliorates some metabolic traits altered by diet-induced obesity in a Swiss mice model.</mods:abstract>
               <mods:language>
                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:accessCondition type="useAndReproduction"/>
               <mods:subject>
                  <mods:topic>bioactive peptides</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>intracellular peptides</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>metabolism</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>obesity</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>orally active peptides</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>overweight</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Pep19 Has a Positive Effect on Insulin Sensitivity and Ameliorates Both Hepatic and Adipose Tissue Phenotype of Diet-Induced Obese Mice.</mods:title>
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