<?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>2026-04-29T05:37:37Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/22750" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/22750</identifier><datestamp>2024-11-28T19:37:48Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16967</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Ribot, Joan</subfield>
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      <subfield code="a">Arreguin, Andrea</subfield>
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      <subfield code="a">Kuda, Ondrej</subfield>
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      <subfield code="a">Kopecky, Jan</subfield>
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      <subfield code="a">Palou, Andreu</subfield>
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      <subfield code="a">Luisa Bonet, Maria</subfield>
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      <subfield code="c">2019-08</subfield>
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      <subfield code="a">Treatment with all-trans retinoic acid (ATRA), the carboxylic form of vitamin A, lowers body weight in rodents by promoting oxidative metabolism in multiple tissues including white and brown adipose tissues. We aimed to identify novel markers of the metabolic impact of ATRA through targeted blood metabolomics analyses, with a focus on acylcarnitines and amino acids. Blood was obtained from mice treated with a high ATRA dose (50 mg/kg body weight/day, subcutaneous injection) or placebo (controls) during the 4 days preceding collection. LC-MS/MS analyses with a focus on acylcarnitines and amino acids were conducted on plasma and PBMC. Main results showed that, relative to controls, ATRA-treated mice had in plasma: increased levels of carnitine, acetylcarnitine, and longer acylcarnitine species; decreased levels of citrulline, and increased global arginine bioavailability ratio for nitric oxide synthesis; increased levels of creatine, taurine and docosahexaenoic acid; and a decreased n-6/n-3 polyunsaturated fatty acids ratio. While some of these features likely reflect the stimulation of lipid mobilization and oxidation promoted by ATRA treatment systemically, other may also play a causal role underlying ATRA actions. The results connect ATRA to specific nutrition-modulated biochemical pathways, and suggest novel mechanisms of action of vitamin A-derived retinoic acid on metabolic health.</subfield>
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      <subfield code="a">Ribot J, Arreguin A, Kuda O, Kopecky J, Palou Oliver A, Bonet ML. Novel Markers of the Metabolic Impact of Exogenous Retinoic Acid with A Focus on Acylcarnitines and Amino Acids. Int J Mol Sci. 2019 Aug;20(15):3640.</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/22750</subfield>
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      <subfield code="a">31349613</subfield>
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      <subfield code="a">10.3390/ijms20153640</subfield>
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      <subfield code="a">1422-0067</subfield>
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      <subfield code="a">International Journal of Molecular Sciences</subfield>
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      <subfield code="a">2-s2.0-85070686257</subfield>
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      <subfield code="a">Acylcarnitines</subfield>
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      <subfield code="a">Amino acids</subfield>
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      <subfield code="a">Targeted metabolomics</subfield>
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      <subfield code="a">Retinoic acid</subfield>
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      <subfield code="a">Vitamin A</subfield>
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      <subfield code="a">Novel Markers of the Metabolic Impact of Exogenous Retinoic Acid with A Focus on Acylcarnitines and Amino Acids</subfield>
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