Prostanoid Receptor-Mediated Calcium Signaling in Cultured Rat Astrocytes.
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- Kitanaka Junichi
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University
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- Takuma Kazuhiro
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University
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- Kondo Kaoru
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University
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- Baba Akemichi
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University
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We investigated prostanoid-induced intracellular Ca2+ mobilization in Ca2+-sensitive dye fura-2-loaded cultured astrocytes. The thromboxane (TX) A2 analog STA2 (9, 11-epithio-11, 12-methanoTXA2) and/or prostaglandin (PG) F2α (each used at 1 μM) stimulated intracellular Ca2+ mobilization in single cultured rat type 1 astrocytes. Three response patterns were observed: only STA2-sensitive, only PGF2α-sensitive, and both prostanoids-sensitive cells. The Ca2+ response was prostanoid-dose-dependent (0.1-1 μM) and showed a rapid spike-like Ca2+ rise that peaked within 30 sec after the stimulation by the ligand. These observations suggest that type 1 astrocytes are heterogeneous with respect to the expression of receptors for TXA2 and PGF2α, which are linked to Ca2+ mobilization.
収録刊行物
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- Jpn.J.Pharmacol.
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Jpn.J.Pharmacol. 71 (1), 85-87, 1996
公益社団法人 日本薬理学会
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詳細情報 詳細情報について
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- CRID
- 1390001204287887488
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- NII論文ID
- 10008188411
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- NII書誌ID
- AA00691188
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- COI
- 1:CAS:528:DyaK28XjtF2msbw%3D
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- ISSN
- 13473506
- 00215198
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- PubMed
- 8791175
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可