<?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>2026-07-21T14:05:54Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18074" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18074</identifier><datestamp>2024-09-21T23:44:10Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</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">Navarro, Juan A</subfield>
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      <subfield code="a">Decara, Juan</subfield>
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      <subfield code="a">Medina-Vera, Dina</subfield>
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      <subfield code="a">Suarez, Juan|Pavón, Francisco-Javier</subfield>
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      <subfield code="a">Serrano, Antonia</subfield>
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      <subfield code="a">Vida, Margarita</subfield>
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      <subfield code="a">Gutierrez-Adan, Alfonso</subfield>
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      <subfield code="a">Sanjuan, Carlos</subfield>
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      <subfield code="a">Baixeras, Elena</subfield>
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      <subfield code="a">Fonseca, Fernando Rodríguez de</subfield>
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      <subfield code="c">2020-07-08</subfield>
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      <subfield code="a">To characterize the metabolic actions of D-Pinitol, a dietary inositol, in male Wistar rats, we analyzed its oral pharmacokinetics and its effects on (a) the secretion of hormones regulating metabolism (insulin, glucagon, IGF-1, ghrelin, leptin and adiponectin), (b) insulin signaling in the liver and (c) the expression of glycolytic and neoglucogenesis enzymes. Oral D-Pinitol administration (100 or 500 mg/Kg) resulted in its rapid absorption and distribution to plasma and liver compartments. Its administration reduced insulinemia and HOMA-IR, while maintaining glycaemia thanks to increased glucagon activity. In the liver, D-Pinitol reduced the key glycolytic enzyme pyruvate kinase and decreased the phosphorylation of the enzymes AKT and GSK-3. These observations were associated with an increase in ghrelin concentrations, a known inhibitor of insulin secretion. The profile of D-Pinitol suggests its potential use as a pancreatic protector decreasing insulin secretion through ghrelin upregulation, while sustaining glycaemia through the liver-based mechanisms of glycolysis control.</subfield>
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      <subfield code="a">10.3390/nu12072030</subfield>
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      <subfield code="a">2072-6643</subfield>
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      <subfield code="a">http://hdl.handle.net/10668/15920</subfield>
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      <subfield code="a">32650579</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/18074</subfield>
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      <subfield code="a">AKT</subfield>
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      <subfield code="a">D-Pinitol</subfield>
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      <subfield code="a">Ghrelin</subfield>
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      <subfield code="a">Insulin</subfield>
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      <subfield code="a">Insulin resistance</subfield>
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      <subfield code="a">D-Pinitol from Ceratonia siliqua Is an Orally Active Natural Inositol That Reduces Pancreas Insulin Secretion and Increases Circulating Ghrelin Levels in Wistar Rats.</subfield>
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