Inhibitory Effect of Ethanol Extract of Piper longum L. on Rabbit Platelet Aggregation through Antagonizing Thromboxane A_2 Receptor(Pharmacology)
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概要
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Piper longum L. has been used as a crude drug for the treatment of disorders of poor peripheral blood circulation in Asia. However, the detailed mechanism of its action has not been clarified as yet. In the present study, we examined the effects of several extracts of Piper longum L. on rabbit platelet function. Thromboxane A_2 receptor agonist U46619 caused rabbit platelet aggregation, which was potently inhibited by the ethanol or butanol extract of Piper longum L. The ethanol extract inhibited U46619-induced platelet aggregation in a concentration-dependent manner, but only weakly inhibited that induced by thrombin. The maximum response to U46619 was reduced by 100% ethanol extract concentration dependency, suggesting that the inhibitory mode of U46619-induced platelet aggregation by the ethanol extract was non-competitive. The extract also inhibited U46619-induced phosphoinositide hydrolysis with a similar concentration dependency to the platelet aggregation. Furthermore, the extract inhibited binding of [^3H]SQ29548 to thromboxane A_2 receptor in intact platelets in a concentration-dependent manner. These results suggest that Piper longum L. contains a constituent(s) that inhibits platelet aggregation as a non-competitive thromboxane A_2 receptor antagonist.
- 2007-07-01
著者
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Nakahata Norimichi
Department of Cellular Signaling, Graduate School of Pharmaceutical Sciences, Tohoku University, Jap
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SAITO Masaki
Department of Biochemistry, Hyogo College of Medicine
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Yamaguchi Yasunaga
Research Center Maruzen Pharmaceuticals Co. Ltd.
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Nakahata N
Department Of Cellular Signaling Graduate School Of Pharmaceutical Sciences Tohoku University
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Nakahata Norimichi
Department Of Cellular Signaling And 21st Century Coe Program Graduate School Of Pharmaceutical Scie
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Nakahata Norimichi
Inst. For International Advanced Res. And Education Tohoku Univ. International Advanced Res. And Edu
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IWASHITA Masaya
Department of Cellular Signaling, Graduate School of Pharmaceutical Sciences, Tohoku University
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TAKAGAKI Ryoji
Research Center, Maruzen Pharmaceuticals Co., Ltd.
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Takagaki Ryoji
Research Center Maruzen Pharmaceuticals Co. Ltd.
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Saito Masaki
Department Of Biochemistry Hyogo College Of Medicine
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