<?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>2026-04-14T16:25:35Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/7121" metadataPrefix="edm">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/7121</identifier><datestamp>2025-03-03T10:19:18Z</datestamp><setSpec>com_10324_1134</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1213</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xsi:schemaLocation="http://www.w3.org/1999/02/22-rdf-syntax-ns# http://www.europeana.eu/schemas/edm/EDM.xsd">
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<dc:creator>González Martínez, Constancio</dc:creator>
<dc:creator>Agapito Serrano, María Teresa</dc:creator>
<dc:creator>Rocher Martín, María Asunción</dc:creator>
<dc:creator>Martín González, María del Carmen</dc:creator>
<dc:creator>Vega Agapito, María Victoria</dc:creator>
<dc:creator>Gómez Niño, María Ángeles</dc:creator>
<dc:creator>Rigual Bonastre, Ricardo Jaime</dc:creator>
<dc:creator>Castañeda, Francisco Javier</dc:creator>
<dc:creator>Obeso Cáceres, Ana María de la Luz</dc:creator>
<dc:date>2007</dc:date>
<dc:description>Producción Científica</dc:description>
<dc:description>Superoxide anion is the most important reactive oxygen species (ROS) primarily generated in cells. The main cellular constituents with capabilities&#xd;
to generate superoxide anion areNADPHoxidases and mitochondrial respiratory chain. The emphasis of our article is centered in critically examining&#xd;
hypotheses proposing that ROS generated by NADPH oxidase and mitochondria are key elements in O2-sensing and hypoxic responses generation&#xd;
in carotid body chemoreceptor cells. Available data indicate that chemoreceptor cells express a specific isoform of NADPH oxidase that is activated&#xd;
by hypoxia; generated ROS acting as negative modulators of the carotid body (CB) hypoxic responses. Literature is also consistent in supporting&#xd;
that poisoned respiratory chain can produce high amounts of ROS, making mitochondrial ROS potential triggers-modulators of the CB activation&#xd;
elicited by mitochondrial venoms. However, most data favour the notion that levels of hypoxia, capable of strongly activating chemoreceptor cells,&#xd;
would not increase the rate of ROS production in mitochondria, making mitochondrial ROS unlikely triggers of hypoxic responses in the CB.&#xd;
Finally, we review recent literature on heme oxygenases from two perspectives, as potential O2-sensors in chemoreceptor cells and as generators&#xd;
of bilirubin which is considered to be a ROS scavenger of major quantitative importance in mammalian cells.</dc:description>
<dc:format>application/pdf</dc:format>
<dc:identifier>http://uvadoc.uva.es/handle/10324/7121</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>Elsevier</dc:publisher>
<dc:subject>Respiración celular</dc:subject>
<dc:title>Chemoreception in the context of the general biology of ROS</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
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