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清醒训练犬对安定和溴西泮的心脏变时反应分析。

Analysis of cardiac chronotropic responses to diazepam and bromazepam in conscious trained dogs.

作者信息

Gerold M, Cavero I, Riggenbach H, Wall M, Haeusler G

出版信息

Eur J Pharmacol. 1976 Feb;35(2):361-8. doi: 10.1016/0014-2999(76)90239-9.

Abstract

In conscious trained dogs, administration of bromazepam (0.3 mg/kg p.o.) or diazepam (0.3 and 1.0 mg/kg p.o.) had no influence on heart rate. A higher dose (10 mg/kg p.o.) of two benzodiazepines elicited a positive chronotropic effect which was rapid in onset and of long duration. The beta-adrenoceptor blocking agent practolol (2.5 mg/kg i.v.) did not revert heart rate after the benzodiazepines to the same level as in controls, indicating that the tachycardia was not produced by an increase in sympathetic outflow to the heart. For diazepam, a sympathetic--parasympathetic interaction cannot be excluded. However, diazepam and bromazepam significantly reduced the tachycardia which is normally observed after administration of methylatropine (0.5 mg/kg i.v.) alone or in combination with practolol. In anaesthetized dogs, bromazepam failed to modify the heart rate responses to electrical stimulation of cardiac vagal or sympathetic nerves, excluding an action on this compound on ganglionic transmission and cardiac cholinoceptors and adrenoceptors. It is concluded that high doses of diazepam and bromazepam influence the heart rate of conscious dogs in a biphasic way. Firstly, they cause a central reduction of vagal tone to the heart resulting in tachycardia. Secondly, the two drugs decrease the cardiac pacemaker rate directly. Since the overall effect is tachycardia, the central action is more pronounced.

摘要

在经过训练的清醒犬中,口服溴西泮(0.3毫克/千克)或地西泮(0.3和1.0毫克/千克)对心率无影响。两种苯二氮䓬类药物的较高剂量(口服10毫克/千克)引起正性变时作用,起效迅速且持续时间长。β-肾上腺素能受体阻滞剂心得宁(静脉注射2.5毫克/千克)在给予苯二氮䓬类药物后未能使心率恢复到与对照组相同的水平,这表明心动过速并非由心脏交感神经传出增加所致。对于地西泮,不能排除交感-副交感神经相互作用。然而,地西泮和溴西泮显著降低了单独或与心得宁联合静脉注射甲基阿托品(0.5毫克/千克)后通常观察到的心动过速。在麻醉犬中,溴西泮未能改变对心脏迷走神经或交感神经电刺激的心率反应,排除了该化合物对神经节传递以及心脏胆碱能受体和肾上腺素能受体的作用。结论是高剂量的地西泮和溴西泮以双相方式影响清醒犬的心率。首先,它们导致心脏迷走神经张力中枢性降低,从而引起心动过速。其次,这两种药物直接降低心脏起搏器速率。由于总体效应是心动过速,中枢作用更为明显。

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