<?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>2026-04-13T00:56:34Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10459.1/57176" metadataPrefix="mets">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10459.1/57176</identifier><datestamp>2024-12-05T22:36:29Z</datestamp><setSpec>com_2072_3622</setSpec><setSpec>col_2072_479130</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_10459.1-57176" 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:10459.1/57176">
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Parisi Capdevila, Eva</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Bozic, Milica</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>Ibarz Escuer, Mercedes</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Panizo García, Sara</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Valcheva, Petya</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Coll, Blai</mods:namePart>
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               <mods:name>
                  <mods:role>
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                  <mods:namePart>Fernández i Giráldez, Elvira</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Valdivielso Revilla, José Manuel</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-12-05T22:36:29Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2016-06-09T08:29:39Z2025-01-012010</mods:dateIssued>
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               <mods:identifier type="none"/>
               <mods:identifier type="uri">http://hdl.handle.net/10459.1/57176</mods:identifier>
               <mods:abstract>N-methyl-D-aspartate&#xd;
(NMDA) receptors (NMDAR) are tetrameric amino acid receptors&#xd;
that act as membrane calcium channels. The presence of the receptor&#xd;
has been detected in the principal organs responsible for calcium&#xd;
homeostasis (kidney, bone, and parathyroid gland), pointing to a&#xd;
possible role in mineral metabolism. The aim of this study was to test&#xd;
the effect of NMDAR activation in the kidney and on 1,25(OH)2D3&#xd;
synthesis. We determined the presence of NMDAR subunits in HK-2&#xd;
(human kidney cells) cells and proved its functionality. NMDA&#xd;
treatment for 4 days induced a decrease in 1 -hydroxylase levels and&#xd;
1,25(OH)2D3 synthesis through the activation of the MAPK/ERK&#xd;
pathway in HK-2 cells. In vivo administration of NMDA for 4 days&#xd;
also caused a decrease in blood 1,25(OH)2D3 levels in healthy animals&#xd;
and an increase in blood PTH levels. This increase in PTH induced a&#xd;
decrease in the urinary excretion of calcium and an increase in urinary&#xd;
excretion of phosphorous and sodium as well as in diuresis. Bone&#xd;
turnover markers also increased. Animals with 5/6 nephrectomy&#xd;
showed low levels of renal 1 -hydroxylase as well as high levels of&#xd;
renal glutamate compared with healthy animals. In conclusion,&#xd;
NMDAR activation in the kidney causes a decrease in 1,25(OH)2D3&#xd;
synthesis, which induces an increase on PTH synthesis and release. In&#xd;
animals with chronic kidney disease, high renal levels of glutamate&#xd;
could be involved in the downregulation of 1 -hydroxylase expression.This work was supported by FIS PI09/0299, FIS PI07/0427, and REDINREN&#xd;
(16/06).</mods:abstract>
               <mods:language>
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               </mods:language>
               <mods:accessCondition type="useAndReproduction">(c) American Physiological Society, 2010 info:eu-repo/semantics/restrictedAccess</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Paratyroid hormone</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Mitogen- activated protein kinase</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Hyerparatyroidism</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Sustained activation of renal N-methyl-D-aspartate receptors decreases vitamin D synthesis: a possible role for glutamate on the onset of secondary HPT</mods:title>
               </mods:titleInfo>
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