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        <identifier>oai:miyazaki-u.repo.nii.ac.jp:00003868</identifier>
        <datestamp>2024-02-09T07:57:19Z</datestamp>
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          <dc:title xml:lang="en">Adrenomedullin Does Not Contribute toward the Development of Abdominal Aortic Aneurysm in Mice</dc:title>
          <dc:title xml:lang="ja">腹部大動脈瘤形成におけるアドレノメデュリンの役割</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="ja">坂元, 紀陽</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">サカモト, スミハル</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="en">Sakamoto, Sumiharu</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="ja">坂元</jpcoar:familyName>
            <jpcoar:familyName xml:lang="ja-Kana">サカモト</jpcoar:familyName>
            <jpcoar:familyName xml:lang="en">Sakamoto</jpcoar:familyName>
            <jpcoar:givenName xml:lang="ja">紀陽</jpcoar:givenName>
            <jpcoar:givenName xml:lang="ja-Kana">スミハル</jpcoar:givenName>
            <jpcoar:givenName xml:lang="en">Sumiharu</jpcoar:givenName>
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          <jpcoar:subject xml:lang="en" subjectScheme="Other">Aneurysm, Angiotensin II, Aortic Rupture</jpcoar:subject>
          <datacite:description xml:lang="ja" descriptionType="Other">2014年度</datacite:description>
          <datacite:description xml:lang="en" descriptionType="Abstract">Abdominal aortic aneurysm (AAA) develops based on advanced atherosclerosis; however, the underlying pathogenesis remains unknown. Adrenomedullin (AM) is widely expressed in various human and rodent tissues, and has been reported to protect blood vessels. We have previously reported that AM is produced in mast cells of human AAA and that AM exhibited the antifibrotic activity of mast cell-derived AM on fibroblasts. In the present study, we investigated the role of AM in the development of AAA in 12-week-old male apolipoprotein (apo)E﹣/﹣ mice bred with AM heterozygous, or its role when recombinant human (rh) AM was administrated to the apoE﹣/﹣ male mice, which was infused with 1000 ng/kg/min of angiotensin II (Ang II) for 28 days. The incidence of the development of AAA in Ang II-infused apoE﹣/﹣ AM﹢/﹣ mice did not change compared with that in apoE﹣/﹣ mice (33.3% vs. 47.4%, p = 0.2333). In addition, rhAM administration had little effect on the incidence of the development of AAA formation (AM: 0 ng/kg/hr 47.4%; 300 ng/kg/hr 36.4%; 3000 ng/kg/hr 27.3%; p = 0.2595). In conclusion, this study suggests that AM does not contribute toward the development of AAA.</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="HDL">http://hdl.handle.net/10458/4934</jpcoar:identifier>
          <jpcoar:identifier identifierType="URI">https://miyazaki-u.repo.nii.ac.jp/records/3868</jpcoar:identifier>
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            <jpcoar:relatedTitle>http://hdl.handle.net/10458/4935</jpcoar:relatedTitle>
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          <dcndl:dissertationNumber>医博甲第421号</dcndl:dissertationNumber>
          <dcndl:degreeName xml:lang="ja">博士(医学)</dcndl:degreeName>
          <dcndl:dateGranted>2014-06-24</dcndl:dateGranted>
          <jpcoar:degreeGrantor>
            <jpcoar:nameIdentifier nameIdentifierScheme="kakenhi">17601</jpcoar:nameIdentifier>
            <jpcoar:degreeGrantorName xml:lang="ja">宮崎大学</jpcoar:degreeGrantorName>
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            <datacite:date dateType="Available">2020-06-21</datacite:date>
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            <jpcoar:URI label="学位論文審査結果の要旨" objectType="other">https://miyazaki-u.repo.nii.ac.jp/record/3868/files/A421Yshinsa.pdf</jpcoar:URI>
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            <datacite:date dateType="Available">2020-06-21</datacite:date>
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