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双嘧达莫对大鼠心房率的百日咳毒素敏感效应。

Pertussis toxin sensitive effects of dipyridamole on rat atrial rate.

作者信息

Filinger E J, Adler-Graschinsky E

机构信息

Instituto de Investigaciones Farmacológicas, CONICET, Buenos Aires, Argentina.

出版信息

J Auton Pharmacol. 1993 Aug;13(4):267-73. doi: 10.1111/j.1474-8673.1993.tb00274.x.

Abstract
  1. In the spontaneously beating rat isolated atria the effects of dipyridamole (0.01, 0.1, 1 and 10 microM) and of adenosine (10 microM) on the chronotropic responses to exogenous noradrenaline (NA) were compared. 2. Dipyridamole (0.01 microM) reduced the chronotropic responses to NA throughout the entire concentration-response curve. A decrease in the maximal response to the agonist was also observed. 3. Neither the spontaneous outflow of [3H]-NA nor its metabolic distribution were altered by dipyridamole (0.01 microM). 4. As observed with dipyridamole, the concentration-response curve to NA was shifted to the right by 10 microM adenosine. 8-Phenyltheophylline (8-PT), 10 microM prevented the decrease in the chronotropic response to NA produced by both 10 microM adenosine and 0.01 microM dipyridamole. 5. The preincubation of rat atria with 1 micrograms ml-1 pertussis toxin prevented the diminution in the chronotropic responses to NA produced by 0.01 microM dipyridamole. 6. The present results suggest that the decrease caused by dipyridamole in rat atrial chronotropic responses involves the participation of adenosine, probably through the interaction with type A1 adenosine receptors.
摘要
  1. 在自发搏动的大鼠离体心房中,比较了双嘧达莫(0.01、0.1、1和10微摩尔)和腺苷(10微摩尔)对外源性去甲肾上腺素(NA)变时反应的影响。2. 双嘧达莫(0.01微摩尔)在整个浓度-反应曲线中均降低了对NA的变时反应。还观察到对激动剂最大反应的降低。3. 双嘧达莫(0.01微摩尔)既未改变[3H]-NA的自发释放,也未改变其代谢分布。4. 如双嘧达莫观察到的那样,10微摩尔腺苷使对NA的浓度-反应曲线右移。10微摩尔8-苯基茶碱(8-PT)可防止10微摩尔腺苷和0.01微摩尔双嘧达莫引起的对NA变时反应的降低。5. 用1微克/毫升百日咳毒素预孵育大鼠心房可防止0.01微摩尔双嘧达莫引起的对NA变时反应的减弱。6. 目前的结果表明,双嘧达莫引起的大鼠心房变时反应降低涉及腺苷的参与,可能是通过与A1型腺苷受体相互作用。

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