ATP Suppresses the K+ Current Responses to FSH and Adenosine in the Follicular Cells of Xenopus Oocyte.
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- Fujita Reiko
- Department of Chemistry, School of Liberal Arts and Sciences, Iwate Medical University
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The application of either follicle-stimulating hormone (FSH) or adenosine (Ade) induces a K+-current response in the follicular cells surrounding a Xenopus oocyte under a voltage clamp. These K+-current responses are reported to be produced by an increase in intracellular cAMP. A previous application of ATP to the same cells markedly depressed the K+-current responses to FSH and Ade. Furthermore, a 2 min application of phorbol 12,13-dibutyrate (PDBu), an activator of protein kinase C (PKC), significantly depressed the K+-current responses to FSH and Ade, but it had no significant effect on the Cl−-current response to ATP. An application of either ATP or PDBu also depressed the K+-current response induced by intracellularly applied cAMP. In contrast to the effect of PDBu, the application of 1-octanol, an inhibitor of gap junction channel, significantly depressed both the Ade- and ATP-induced responses, indicating that the acting site of 1-octanol is different from that of PKC. The results suggest that the depressing effect of ATP on the FSH- and Ade-induced K+-current responses might be mediated by PKC activation and that the site of PKC action might be downstream of the cAMP production involved in the K+ channel opening.<br>
収録刊行物
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- The Japanese Journal of Physiology
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The Japanese Journal of Physiology 51 (4), 491-500, 2001
一般社団法人 日本生理学会
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詳細情報 詳細情報について
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- CRID
- 1390001205040930560
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- NII論文ID
- 130004435781
- 10008294481
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- NII書誌ID
- AA00691224
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- COI
- 1:CAS:528:DC%2BD3MXntlahsbk%3D
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- ISSN
- 18811396
- 0021521X
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- NDL書誌ID
- 5907219
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- PubMed
- 11564286
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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
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 使用不可