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新型促智药BY - 1949增强豚鼠离体结肠带和主动脉腺苷诱导的舒张反应:与双嘧达莫比较

Enhancement of adenosine-induced relaxant responses of the guinea-pig isolated taenia coli and aortae by a novel nootropic agent BY-1949: comparison with dipyridamole.

作者信息

Tanabe S, Ikeda Y, Shiraki Y, Sakai K

机构信息

Department of Pharmacology, Chugai Pharmaceutical Co., Ltd., Shizuoka, Japan.

出版信息

J Pharm Pharmacol. 1988 Aug;40(8):582-4. doi: 10.1111/j.2042-7158.1988.tb05310.x.

Abstract

In muscle strips of guinea-pig taenia coli and aortae, the effects of 3-methoxy-11-methyldibenz[b,f][1,4]oxazepine-8-carboxylate (BY-1949) on the relaxant response to adenosine have been compared with those of dipyridamole. BY-1949 (3 x 10(-5)-10(-4) M) as well as dipyridamole (3 x 10(-7)-10(-5) M) resulted in a significant potentiation of relaxant responses to a cumulative administration of adenosine (10(-6)-10(-3) M), but the drugs did not affect the response to noradrenaline and acetylcholine. The results indicate that BY-1949 exerts a selective potentiating effect on reactivity to exogenous adenosine.

摘要

在豚鼠结肠带和主动脉的肌条中,比较了3-甲氧基-11-甲基二苯并[b,f][1,4]恶唑嗪-8-羧酸酯(BY-1949)与双嘧达莫对腺苷舒张反应的影响。BY-1949(3×10⁻⁵ - 10⁻⁴ M)以及双嘧达莫(3×10⁻⁷ - 10⁻⁵ M)均可使对累积给予腺苷(10⁻⁶ - 10⁻³ M)的舒张反应显著增强,但这两种药物对去甲肾上腺素和乙酰胆碱的反应没有影响。结果表明,BY-1949对外源性腺苷的反应具有选择性增强作用。

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