Possible Involvement of Calcium-Calmodulin Pathways in the Positive Chronotropic Response to Angiotensin 2 on the Canine Cardiac Sympathetic Ganglia
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- Tokunaga Ryoko
- Department of Pharmacology, School of Medicine, Fukuoka University
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- Kushiku Kazushi
- Department of Pharmacology, School of Medicine, Fukuoka University
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- Yamada Katsuhiro
- Department of Pharmacology, School of Medicine, Fukuoka University
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- Yamada Hiromi
- Department of Pharmacology, School of Medicine, Fukuoka University
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- Furukawa Tatsuo
- Department of Pharmacology, School of Medicine, Fukuoka University
書誌事項
- タイトル別名
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- Possible Involvement of Calcium-Calmodulin Pathways in the Positive Chronotropic Response to Angiotensin II on the Canine Cardiac Sympathetic Ganglia.
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説明
We investigated the ganglionic effects of angiotensin II (Ang II) and the signal transduction involved in the cardiac sympathetic ganglia by the direct administration of agents to the ganglia through the right subclavian artery and monitoring the heart rate as an indicator of the ganglionic function in pithed dogs. Ang II given i.a. caused increases in the heart rate, which was inhibited by the treatment with the AT1-receptor antagonist forasartan, but not by the AT2-receptor antagonist PD-123319. The stimulation by Ang II, but not by acetylcholine, was inhibited after treatment with an inhibitor of phospholipase C, U-73122; a cell-permeant modulator of the Ins(1,4,5)P3 receptors, 2-aminoethoxydiphenyl borate; an intracellular calcium and calcium-associated protein kinase inhibitor, HA-1077; calmodulin (CaM) inhibitor, W-7; Ca2+/CaM-dependent protein kinase II inhibitor, KN-93; a selective protein kinase C inhibitor, calphostin C; and Na+-H+ exchange inhibitor, dimethylamiloride. These results suggest that Ang II stimulates the ganglionic transmission at postsynaptic sites via the activation of AT1 receptor coupled to either activation of phospholipase C, phosphoinositide hydrolysis and subsequent increase in intracellular Ca2+ and activation of protein kinase C and Ca2+/CaM kinase II, although this ganglionic stimulation seems to involve, at least in part, the protein kinases-dependent increase of amiloride-sensitive Na+ inflow.
収録刊行物
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- Jpn.J.Pharmacol.
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Jpn.J.Pharmacol. 86 (4), 381-389, 2001
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
- 1390282679264479360
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- NII論文ID
- 10007123128
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- NII書誌ID
- AA00691188
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- COI
- 1:CAS:528:DC%2BD3MXmtlCgsrw%3D
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- ISSN
- 13473506
- 00215198
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- NDL書誌ID
- 5885808
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- PubMed
- 11569611
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- Web Site
- http://id.ndl.go.jp/bib/5885808
- https://ndlsearch.ndl.go.jp/books/R000000004-I5885808
- https://api.elsevier.com/content/article/PII:S0021519819303233?httpAccept=text/xml
- https://api.elsevier.com/content/article/PII:S0021519819303233?httpAccept=text/plain
- https://search.jamas.or.jp/link/ui/2002070670
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- 本文言語コード
- en
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- 資料種別
- journal article
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