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氨氯吡咪对豚鼠和大鼠左心房收缩的影响:受刺激频率和[Ca2+]0-[Na+]0比值的影响及Na+/Ca2+交换的作用

Effects of amiloride in guinea-pig and rat left atrial contraction as affected by frequency of stimulation and [Ca2+]0-[Na+]0 ratio: role of Na+/Ca2+ exchange.

作者信息

Cargnelli G, Bova S, Luciani S

机构信息

Department of Pharmacology, University of Padova, Italy.

出版信息

Br J Pharmacol. 1989 Jun;97(2):533-41. doi: 10.1111/j.1476-5381.1989.tb11982.x.

Abstract
  1. The effect of amiloride (0.5 mM) on guinea-pig and rat left atria driven at various rates of stimulation and different [Ca2+]0-[Na+]0 ratios has been studied. 2. Amiloride elicited a positive inotropic response in guinea-pig left atria driven at 0.1 Hz, 0.5 Hz and 1 Hz when [Ca2+]0 was 3.6 mM, 1.8 mM and 0.9 mM respectively but not when [Ca2+]0 was 2.7 mM at 0.1 Hz, 0.9 mM at 0.5 Hz and 0.45 mM at 1 Hz. 3. A positive inotropic response was obtained in guinea-pig left atria driven at 0.1 Hz and 1 Hz when [Ca2+]0-[Na+]0(2) was increased respectively from 8 x 10(-5) to 16 x 10(-5) and from 2 x 10(-5) to 8 x 10(-5). The positive inotropic effect was evident only when the ratio was increased by increasing [Ca2+]0 and not by decreasing [Na+]0. 4. In the presence of amiloride, the force of contraction of guinea-pig left atria decreased instead of increasing, when the rate of stimulation was lowered from 1 Hz to 0.01 Hz. Amiloride inhibited the post-rest potentiation. 5. In rat left atria amiloride was devoid of any effect in all the above-mentioned experimental conditions. 6. It is suggested that the pattern of cardiac actions of amiloride can be explained by the inhibition of the Na+/Ca2+ exchange system.
摘要
  1. 研究了氨氯吡脒(0.5 mM)对不同刺激频率及不同[Ca2+]0-[Na+]0比值驱动的豚鼠和大鼠左心房的作用。2. 当[Ca2+]0分别为3.6 mM、1.8 mM和0.9 mM时,氨氯吡脒在0.1 Hz、0.5 Hz和1 Hz驱动的豚鼠左心房中引发正性肌力反应,但当[Ca2+]0在0.1 Hz时为2.7 mM、0.5 Hz时为0.9 mM、1 Hz时为0.45 mM时则无此反应。3. 当[Ca2+]0-[Na+]0(2)分别从8×10(-5)增加到16×10(-5)以及从2×10(-5)增加到8×10(-5)时,在0.1 Hz和1 Hz驱动的豚鼠左心房中获得了正性肌力反应。正性肌力作用仅在通过增加[Ca2+]0而非降低[Na+]0来提高该比值时才明显。4. 在氨氯吡脒存在的情况下,当刺激频率从1 Hz降至0.01 Hz时,豚鼠左心房的收缩力下降而非增加。氨氯吡脒抑制了静息后增强作用。5. 在上述所有实验条件下,氨氯吡脒对大鼠左心房均无任何作用。6. 提示氨氯吡脒的心脏作用模式可通过抑制Na+/Ca2+交换系统来解释。

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