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        <identifier>oai:kdu.repo.nii.ac.jp:00000950</identifier>
        <datestamp>2026-02-17T07:08:13Z</datestamp>
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        <jpcoar:jpcoar xmlns:datacite="https://schema.datacite.org/meta/kernel-4/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcndl="http://ndl.go.jp/dcndl/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:jpcoar="https://github.com/JPCOAR/schema/blob/master/2.0/" xmlns:oaire="http://namespace.openaire.eu/schema/oaire/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:rioxxterms="http://www.rioxx.net/schema/v2.0/rioxxterms/" xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns="https://github.com/JPCOAR/schema/blob/master/2.0/" xsi:schemaLocation="https://github.com/JPCOAR/schema/blob/master/2.0/jpcoar_scm.xsd">
          <dc:title xml:lang="en">Orexin-B antagonized respiratory depression induced by sevoflurane, propofol, and remifentanil in isolated brainstem-spinal cords of neonatal rats</dc:title>
          <dcterms:alternative xml:lang="ja">新生ラットの単離脳幹脊髄標本を用いたセボフルラン、プロポフォール、レミフェンタニルによる呼吸抑制に対するオレキシンＢによる拮抗作用について</dcterms:alternative>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="ja">梅澤, 伸夫</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">ウメザワ, ノブオ</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Umezawa, Nobuo</jpcoar:creatorName>
          </jpcoar:creator>
          <dcterms:accessRights rdf:resource="http://purl.org/coar/access_right/c_abf2">open access</dcterms:accessRights>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Anesthetics</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Animals</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Animals, Newborn</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Brain Stem</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Disease Models, Animal</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Intracellular Signaling Peptides and Proteins</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Methyl Ethers</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Neuropeptides</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Orexins</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Piperidines</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Propofol</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Rats</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Rats, Wistar</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Respiratory Insufficiency</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">Spinal Cord</jpcoar:subject>
          <datacite:description descriptionType="Other">2015</datacite:description>
          <datacite:description descriptionType="Other">application/pdf</datacite:description>
          <datacite:description descriptionType="Abstract">Orexins (hypocretins) play a crucial role in arousal, feeding, and endocrine function. We previously reported that orexin-B activated respiratory neurons in the isolated brainstem-spinal cords of neonatal rats. We herein determined whether orexin-B antagonized respiratory depression induced by sevoflurane, propofol, or remifentanil. We recorded C4 nerve bursts as an index of inspiratory activity in a brainstem-spinal cord preparation. The preparation was superfused with a solution equilibrated with 3% sevoflurane alone for 10 min and the superfusate was then switched to a solution containing sevoflurane plus orexin-B. Sevoflurane decreased the C4 burst rate and the integrated C4 amplitude. The C4 burst rate and amplitude were reversed by 0.5 μM orexin-B, but not by 0.1 μM orexin-B. The decrease induced in the C4 burst rate by 10 μM propofol or 0.01 μM remifentanil was significantly antagonized by 0.1 μM orexin-B. Respiratory depression induced by a higher concentration (0.1 μM) of remifentanil was not restored by 0.1 μM orexin-B. These results demonstrated that orexin-B antagonized respiratory depression induced by sevoflurane, propofol, or remifentanil.</datacite:description>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_db06">doctoral thesis</dc:type>
          <oaire:version rdf:resource="http://purl.org/coar/version/c_970fb48d4fbd8a85">VoR</oaire:version>
          <jpcoar:identifier identifierType="URI">https://kdu.repo.nii.ac.jp/records/950</jpcoar:identifier>
          <jpcoar:relation>
            <jpcoar:relatedTitle>Respiratory Physiology &amp; Neurobiology, 205:61-65, 2015. doi: 10.1016/j.resp.2014.10.013</jpcoar:relatedTitle>
          </jpcoar:relation>
          <jpcoar:relation>
            <jpcoar:relatedIdentifier identifierType="DOI">https://doi.org/10.1016/j.resp.2014.10.013</jpcoar:relatedIdentifier>
            <jpcoar:relatedTitle>Elsevier</jpcoar:relatedTitle>
          </jpcoar:relation>
          <dcndl:dissertationNumber>甲第484号</dcndl:dissertationNumber>
          <dcndl:degreeName>博士（歯学）</dcndl:degreeName>
          <dcndl:dateGranted>2016-03-17</dcndl:dateGranted>
          <jpcoar:degreeGrantor>
            <jpcoar:nameIdentifier nameIdentifierScheme="kakenhi">32703</jpcoar:nameIdentifier>
            <jpcoar:degreeGrantorName>神奈川歯科大学</jpcoar:degreeGrantorName>
          </jpcoar:degreeGrantor>
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            <jpcoar:URI label="Full Text（全文）" objectType="fulltext">https://kdu.repo.nii.ac.jp/record/950/files/kou484_fulltext.pdf</jpcoar:URI>
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            <datacite:date dateType="Available">2021-03-26</datacite:date>
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            <jpcoar:URI label="論文内容要旨">https://kdu.repo.nii.ac.jp/record/950/files/kou484_summary.pdf</jpcoar:URI>
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            <datacite:date dateType="Available">2016-07-06</datacite:date>
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            <datacite:date dateType="Available">2016-07-06</datacite:date>
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