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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 2.査読済論文(薬)

Activator protein-1 responsive to the group II metabotropic glutamate receptor subtype in association with intracellular calcium in cultured rat cortical neurons

http://hdl.handle.net/2297/7392
http://hdl.handle.net/2297/7392
2809d9e0-2d15-4755-9bfc-a5995d829445
名前 / ファイル ライセンス アクション
PH-PR-NAKAMICHI-N-467.pdf PH-PR-NAKAMICHI-N-467.pdf (361.4 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Activator protein-1 responsive to the group II metabotropic glutamate receptor subtype in association with intracellular calcium in cultured rat cortical neurons
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Sugiyama, Chie

× Sugiyama, Chie

WEKO 26376

Sugiyama, Chie

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Nakamichi, Noritaka

× Nakamichi, Noritaka

WEKO 293
e-Rad 10401895
金沢大学研究者情報 10401895
研究者番号 10401895

Nakamichi, Noritaka

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Ogura, Masato

× Ogura, Masato

WEKO 26377

Ogura, Masato

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Honda, Eriko

× Honda, Eriko

WEKO 26378

Honda, Eriko

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Maeda, Sayaka

× Maeda, Sayaka

WEKO 26379

Maeda, Sayaka

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Taniura, Hideo

× Taniura, Hideo

WEKO 26380
研究者番号 80263325

Taniura, Hideo

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Yoneda, Yukio

× Yoneda, Yukio

WEKO 20157
e-Rad 50094454
研究者番号 50094454

Yoneda, Yukio

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提供者所属
内容記述タイプ Other
内容記述 金沢大学大学院自然科学研究科分子作用学
書誌情報 Neurochemistry International

巻 51, 号 8, p. 467-475, 発行日 2007-12-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0197-0186
NCID
収録物識別子タイプ NCID
収録物識別子 AA0032399X
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1016/j.neuint.2007.04.025
出版者
出版者 Elsevier
抄録
内容記述タイプ Abstract
内容記述 Activation of ionotropic glutamate (Glu) receptors, such as N-methyl-d-aspartate receptors, is shown to modulate the gene transcription mediated by the transcription factor activator protein-1 (AP1) composed of Fos and Jun family proteins in the brain, while little attention has been paid to the modulation of AP1 expression by metabotropic Glu receptors (mGluRs). In cultured rat cortical neurons, where constitutive expression was seen with all groups I, II and III mGluR subtypes, a significant and selective increase was seen in the DNA binding activity of AP1 120 min after the brief exposure to the group II mGluR agonist (2S,2′R,3′R)-2-(2′,3′-dicarboxycyclopropyl)glycine (DCG-IV) for 5 min. In cultured rat cortical astrocytes, by contrast, a significant increase was induced by a group I mGluR agonist, but not by either a group II or III mGluR agonist. The increase by DCG-IV was significantly prevented by a group II mGluR antagonist as well as by either an intracellular Ca2+ chelator or a voltage-sensitive Ca2+ channel blocker, but not by an intracellular Ca2+ store inhibitor. Moreover, DCG-IV significantly prevented the increase of cAMP formation by forskolin in cultured neurons. Western blot analysis revealed differential expression profiles of Fos family members in neurons briefly exposed to DCG-IV and NMDA. Prior or simultaneous exposure to DCG-IV led to significant protection against neuronal cell death by NMDA. These results suggest that activation of the group II mGluR subtype would modulate the gene expression mediated by AP1 through increased intracellular Ca2+ levels in cultured rat cortical neurons. © 2007.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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