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首页> 外文期刊>Japanese Journal of Pharmacology >Inhibitory Effects of KW-3902, a Selective Adenosine A1-Receptor Antagonist, on the Adenosine-Induced Shortening o f Action Potential Duration in Guinea Pig Atrial Muscles
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Inhibitory Effects of KW-3902, a Selective Adenosine A1-Receptor Antagonist, on the Adenosine-Induced Shortening o f Action Potential Duration in Guinea Pig Atrial Muscles

机译:选择性腺苷A1受体拮抗剂KW-3902对腺苷诱导的豚鼠心房肌动作电位持续时间的抑制作用

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References(13) We investigated the effects of KW-3902 (8-(noradamantan-3-yl)-1, 3-dipropylxanthine), a newly-synthesized selective adenosine A1-receptor antagonist, on the shortening of action potential duration (APD) in guinea pig atria exposed to adenosine. The APD shortening by adenosine was inhibited by KW-3902 at higher than 10-8 M, but not by 10-5 M of KF17837, an adenosine A2-receptor antagonist. These results support the notion that the APD shortening by adenosine in atria is mediated via adenosine A1-receptors. The potency of KW-3902 in antagonizing the APD-shortening were similar to those in antagonizing the negative inotropic and chronotropic action of adenosine in the isolated right atria, suggesting that these responses to adenosine are mediated via the receptors of the same type.
机译:参考文献(13)我们研究了新合成的选择性腺苷A1受体拮抗剂KW-3902(8-(noradamantan-3-yl)-1,3-dipropylxanthine)对缩短动作电位持续时间(APD)的影响)在豚鼠心房中暴露于腺苷。 KW-3902在高于10-8 M的条件下抑制了腺苷对APD的缩短,但对腺苷A2受体拮抗剂KF17837的抑制作用则为10-5M。这些结果支持这样的观点,即心房中腺苷在APD上的缩短是通过腺苷A1受体介导的。 KW-3902拮抗APD缩短的功效类似于拮抗腺苷在离体右心房的负性变力和变时作用,这表明这些对腺苷的反应是通过相同类型的受体介导的。

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