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          <dc:title>大うつ病におけるアリピプラゾールによる増強療法の分子機序</dc:title>
          <dc:title xml:lang="en">Molecular mechanisms underlying augmentation therapy with aripiprazole for major depression</dc:title>
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            <jpcoar:creatorName>小杉, 桜子</jpcoar:creatorName>
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          <datacite:description descriptionType="Abstract">①慢性ストレス負荷後の動物に、生食、SSRI あるいはアリピプラゾールを慢性投与した後、側坐核の興奮性シナプス関連タンパク質に対する影響について検討したところ、２つの薬剤は全く異なる作用を有することが確認された。②対照動物のドパミン依存性行動の個体差を知る目的にて、意欲ならびにコスト/利益バランスに応じた意思決定の個体差に基づく亜群分けを試みたところ、大きく４つの亜群に分けられた。さらに慢性ストレス負荷後にそれぞれの亜群が異なるストレス誘導性の表現型を示した。従って、ストレス負荷後のうつ病様表現型の発現は、病前の個体差に大きく依存し、そこからストレス負荷後の反応も予測できることが示唆された。</datacite:description>
          <datacite:description descriptionType="Abstract">We found that SSRI and dopamine partial agonist aripiprazole have distinct effects on the regulations of synaptic proteins in the rat nucleus accumbens after chronic stress. To investigate if we could predict the responses to chronic unpredictable stress of each individual based on the pre-stress individual differences, we next aimed to classify several subgroups from naive rats based on their performance of food-instrumental training with progressive ratio schedule. We succeeded to classify 4 from a group of original naive into 4 subgroups that represent distinctive response in motivation or reactions in cost/benefit decision-making. In addition, each 4 subgroups demonstrated distinct phenotypes after 3-weeks chronic unpredictable stress. These data implicate that the phenotypes induced after chronic stress in rats largely depend on individual differences that exist at pre-stress stages, and it would be possible to predict the responses to stress of each  by taking advantage of it.</datacite:description>
          <datacite:description descriptionType="Other">研究課題/領域番号:24791208, 研究期間(年度):2012-04-01 – 2014-03-31</datacite:description>
          <datacite:description descriptionType="Other">出典：「大うつ病におけるアリピプラゾールによる増強療法の分子機序」研究成果報告書　課題番号24791208
（KAKEN：科学研究費助成事業データベース（国立情報学研究所））
（https://kaken.nii.ac.jp/ja/report/KAKENHI-PROJECT-24791208/24791208seika/)を加工して作成</datacite:description>
          <datacite:description descriptionType="Other">金沢大学医薬保健研究域医学系</datacite:description>
          <datacite:date dateType="Issued">2014-05-20</datacite:date>
          <dc:language>jpn</dc:language>
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          <jpcoar:identifier identifierType="DOI">https://doi.org/10.24517/00059699</jpcoar:identifier>
          <jpcoar:identifier identifierType="HDL">http://hdl.handle.net/2297/00059699</jpcoar:identifier>
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            <jpcoar:relatedTitle>https://kaken.nii.ac.jp/ja/grant/KAKENHI-PROJECT-24791208</jpcoar:relatedTitle>
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            <jpcoar:relatedTitle>https://kaken.nii.ac.jp/ja/report/KAKENHI-PROJECT-24791208/24791208seika/</jpcoar:relatedTitle>
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          <jpcoar:sourceTitle>平成25(2013)年度 科学研究費補助金 若手研究(B) 研究成果報告書</jpcoar:sourceTitle>
          <jpcoar:sourceTitle xml:lang="en">2013 Fiscal Year Final Research Report</jpcoar:sourceTitle>
          <jpcoar:pageStart>5p.</jpcoar:pageStart>
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            <datacite:date dateType="Available">2020-10-16</datacite:date>
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