Inhibitory Mechanism of Monensin on High K〔+〕-Induced Contraction in Guniea-Pig Urinary Bladder
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- Kaneda Takeharu
- Division of Veterinary Pharmacology, Nippon Veterinary and Animal Science University, Japan
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- Takeuchi Mayumi
- Division of Veterinary Pharmacology, Nippon Veterinary and Animal Science University, Japan
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- Shimizu Kazumasa
- Division of Veterinary Pharmacology, Nippon Veterinary and Animal Science University, Japan
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- Urakawa Norimoto
- Division of Veterinary Pharmacology, Nippon Veterinary and Animal Science University, Japan
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- Nakajyo Shinjiro
- Division of Veterinary Pharmacology, Nippon Veterinary and Animal Science University, Japan
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- Mochizuki-Kobayashi Mariko
- Division of Veterinary Public Health, Nippon Veterinary and Animal Science University, Japan
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- Ueda Fukiko
- Division of Veterinary Public Health, Nippon Veterinary and Animal Science University, Japan
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- Hondo Ryo
- Division of Veterinary Public Health, Nippon Veterinary and Animal Science University, Japan
書誌事項
- タイトル別名
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- Inhibitory Mechanism of Monensin on High K+-Induced Contraction in Guniea-Pig Urinary Bladder
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抄録
In this study, we examined the inhibitory mechanism of monensin on high K+-induced contraction in guinea-pig urinary bladder. The relaxant effect of monensin (0.001 – 10 μM) was more potent than those of NaCN (100 μM – 1 mM) and forskolin (3 – 10 μM). Monensin (0.1 μM), NaCN (300 μM), or forskolin (10 μM) inhibited high K+-induced contraction without decreasing [Ca2+]i level. Monensin and NaCN remarkably decreased creatine phosphate and ATP contents. Monensin and NaCN inhibited high K+-induced increases in flavoprotein fluorescence, which is involved in mitochondrial respiration. Forskolin increased cAMP content but monensin did not. Monensin increased Na+ content at 10 μM but not at 0.1 μM that induced maximum relaxation. In the α-toxin-permeabilized muscle, forskolin significantly inhibited the Ca2+-induced contraction, but monensin did not affect it. These results suggest that the relaxation mechanism of monensin in smooth muscle of urinary bladder may be an inhibition of oxidative metabolism.<br>
収録刊行物
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- Journal of Pharmacological Sciences
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Journal of Pharmacological Sciences 100 (2), 133-141, 2006
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
- 1390001205177573504
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- NII論文ID
- 10018240726
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- NII書誌ID
- AA11806667
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- ISSN
- 13478648
- 13478613
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- NDL書誌ID
- 7821850
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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
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- 使用不可