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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. 1. 査読済論文(医学・保健)

Intracellular calcium level is an important factor influencing ion channel modulations by PLC-coupled metabotropic receptors in hippocampal neurons

http://hdl.handle.net/2297/35107
http://hdl.handle.net/2297/35107
f37178d8-6b04-404a-b5da-45d4a7869484
名前 / ファイル ライセンス アクション
ME-PR-SHOSAKU-T-9.pdf ME-PR-SHOSAKU-T-9.pdf (331.4 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 Intracellular calcium level is an important factor influencing ion channel modulations by PLC-coupled metabotropic receptors in hippocampal 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 Sugawara, Yuto

× Sugawara, Yuto

WEKO 23703

Sugawara, Yuto

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Echigo, Ryousuke

× Echigo, Ryousuke

WEKO 23704

Echigo, Ryousuke

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Kashima, Kousuke

× Kashima, Kousuke

WEKO 23705

Kashima, Kousuke

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Minami, Hanae

× Minami, Hanae

WEKO 23706

Minami, Hanae

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Watanabe, Megumi

× Watanabe, Megumi

WEKO 23707

Watanabe, Megumi

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Nishikawa, Yuiko

× Nishikawa, Yuiko

WEKO 23708

Nishikawa, Yuiko

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Muranishi, Miho

× Muranishi, Miho

WEKO 23709

Muranishi, Miho

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Yoneda, Mitsugu

× Yoneda, Mitsugu

WEKO 465
e-Rad 70334787
金沢大学研究者情報 70334787
研究者番号 70334787

Yoneda, Mitsugu

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Ohno-Shosaku, Takako

× Ohno-Shosaku, Takako

WEKO 21890
金沢大学研究者情報 60179025
研究者番号 60179025

Ohno-Shosaku, Takako

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書誌情報 Brain Research

巻 1512, p. 9-21, 発行日 2013-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0006-8993
NCID
収録物識別子タイプ NCID
収録物識別子 AA1152177X
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1016/j.brainres.2013.03.040
出版者
出版者 Elsevier B. V.
抄録
内容記述タイプ Abstract
内容記述 Signaling pathways involving phospholipase C (PLC) are involved in various neural functions. Understanding how these pathways are regulated will lead to a better understanding of their roles in neural functions. Previous studies demonstrated that receptor-driven PLCβ activation depends on intracellular Ca2+ concentration ([Ca2+]i), suggesting the possibility that PLCβ-dependent cellular responses are basically Ca 2+ dependent. To test this possibility, we examined whether modulations of ion channels driven by PLC-coupled metabotropic receptors are sensitive to [Ca2+]i using cultured hippocampal neurons. Muscarinic activation triggered an inward current at -100 mV (the equilibrium potential for K+) in a subpopulation of neurons. This current response was suppressed by pirenzepine (an M1-preferring antagonist), PLC inhibitor, non-selective cation channel blocker, and lowering [Ca 2+]i. Using the neurons showing no response at -100 mV, effects of muscarinic activation on K+ channels were examined at -40 mV. Muscarinic activation induced a transient decrease of the holding outward current. This current response was mimicked and occluded by XE991, an M-current K+ channel blocker, suppressed by pirenzepine, PLC inhibitor and lowering [Ca2+]i, and enhanced by elevating [Ca 2+]i. Similar results were obtained when group I metabotropic glutamate receptors were activated instead of muscarinic receptors. These results clearly show that ion channel modulations driven by PLC-coupled metabotropic receptors are dependent on [Ca2+]i, supporting the hypothesis that cellular responses induced by receptor-driven PLCβ activation are basically Ca2+ dependent. © 2013 Elsevier B.V.
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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