Inoue K, König L A
Abteilung für Experimentelle Anaesthesiologie, Universität Düsseldorf, Federal Republic of Germany.
Br J Anaesth. 1988 Oct;61(4):456-61. doi: 10.1093/bja/61.4.456.
The effects of methohexitone, ketamine, Althesin and droperidol on the peripheral vagal transmission to the heart were studied in decerebrate cats by evaluating the influences of the drugs on the heart rate responses to vagal electrostimulation and the injection of acetylcholine i.v. The sites of the peripheral vagal transmission (vagal ganglia and sino-atrial pacemaker cells) were reached by the application of the drugs to the pericardial space. The bradycardia in response to vagal electrostimulation was attenuated by Althesin (2.1 x 10(-4)-3.3 x 10(-3) mol litre-1; expressed as the concentration of alphaxalone), ketamine (2.9 x 10(-4)-4.6 x 10(-3) mol litre-1) and droperidol (2.6 x 10(-5)-6.6 x 10(-4) mol litre-1) in a concentration-dependent manner, but not influenced by methohexitone (2.8 x 10(-4)-4.4 x 10(-3) mol litre-1). The bradycardia-attenuating effects were probably caused by an atropine-like action since the heart rate responses to the injection of acetylcholine i.v. were also attenuated by the same three drugs.
在去大脑猫中,通过评估美索比妥、氯胺酮、阿耳忒辛和氟哌利多对迷走神经电刺激及静脉注射乙酰胆碱引起的心率反应的影响,研究了这些药物对心脏外周迷走神经传导的作用。将药物应用于心包腔,从而作用于外周迷走神经传导部位(迷走神经节和窦房结起搏细胞)。阿耳忒辛(2.1×10⁻⁴ - 3.3×10⁻³摩尔/升;以α-羟孕酮的浓度表示)、氯胺酮(2.9×10⁻⁴ - 4.6×10⁻³摩尔/升)和氟哌利多(2.6×10⁻⁵ - 6.6×10⁻⁴摩尔/升)可浓度依赖性地减弱迷走神经电刺激引起的心动过缓,但美索比妥(2.8×10⁻⁴ - 4.4×10⁻³摩尔/升)对此无影响。这些药物减弱心动过缓的作用可能是由类似阿托品的作用引起的,因为静脉注射乙酰胆碱引起的心率反应也被这三种药物减弱。