Dyba Stefan, Tychowska Ingeborga, Klukowska Lidia, Nadulska Anna
Department of Human Physiology, Medical University of Lublin.
Ann Univ Mariae Curie Sklodowska Med. 2002;57(1):67-73.
The purpose of our investigations was to investigate the effect of baclofen upon the reflex fall of arterial blood pressure and heart rate evoked by stimulation of bilateral vagus nerves. The experiments were carried out on 30 rabbits of both sexes and mixed breed weighing 3000-4500 g under urethane anaesthesia (1.5 g/kg). Mean arterial pressure and heart rate were measured in the ear middle artery by the electromanometer and registered by PC computer. Parameters of stimulation were: frequency 5c/s., duration-20 s., width of single rectangular pulse-1 msec., intensity of stimulation--multiplicity of threshold excitation (T). The intervals between stimulations were not shorter than 5 min. Baclofen was administrated intravenously (1.0 mg/kg). In the control group the facilitation of circulatory reaction was observed only at the smallest intensity of stimulation (1.0T-1.5T). When greater intensity of stimulations was applied the sum of unilateral effects was greater than the effect of simultaneous bilateral vagus nerve stimulation. This occlusion effect increased up to the stimulus value of 4-5T. After baclofen administration the facilitation of circulatory responses disappeared and only occlusion was observed. Baclofen increased the size of the area of active overlapping of the afferent innervation of the vagus nerve. Administration of baclofen produced an increase in mean arterial blood pressure (15 +/- 6 mm Hg) and heart rate (16 +/- 5 beats per minute) and decrease in the vagal reflex fall of mean arterial pressure and heart rate. Stimulating of the GABAB receptors markedly attenuates the baroreceptor reflex resulting in increase in mean arterial blood pressure and heart rate. These results support the hypothesis that GABA acts tonically on GABAB receptors to attenuate the baroreceptor reflex, thereby contributing to the regulation of circulatory parameters.
我们研究的目的是探究巴氯芬对刺激双侧迷走神经所诱发的动脉血压和心率反射性下降的影响。实验在30只体重3000 - 4500克的不同性别和品种的兔子身上进行,采用氨基甲酸乙酯麻醉(1.5克/千克)。通过电子血压计在耳中动脉测量平均动脉压和心率,并由个人电脑记录。刺激参数为:频率5次/秒,持续时间20秒,单个矩形脉冲宽度1毫秒,刺激强度为阈刺激(T)的倍数。刺激间隔不短于5分钟。巴氯芬通过静脉注射(1.0毫克/千克)。在对照组中,仅在最小刺激强度(1.0T - 1.5T)时观察到循环反应的易化作用。当施加更大强度的刺激时,单侧效应的总和大于双侧迷走神经同时刺激的效应。这种总和效应增加至刺激值4 - 5T。给予巴氯芬后,循环反应的易化作用消失,仅观察到总和效应。巴氯芬增加了迷走神经传入神经支配的有效重叠区域的大小。给予巴氯芬导致平均动脉血压升高(15±6毫米汞柱)和心率加快(每分钟16±5次),并降低了平均动脉压和心率的迷走反射性下降。刺激GABAB受体明显减弱压力感受器反射,导致平均动脉血压和心率升高。这些结果支持以下假设:γ-氨基丁酸(GABA)持续作用于GABAB受体以减弱压力感受器反射,从而有助于循环参数的调节。