蝎毒纯化因子Ⅱ对大鼠神经肌肉兴奋性的影响  被引量:1

Effects of AFSVC-Ⅱon neuromuscular excitability

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作  者:王成裕[1] 雷留根[1] 韩雪飞[1] 王永奎[1] 陈秋菊[1] 齐艳 孔天翰[1] 

机构地区:[1]河南医科大学医学实验中心生物毒素研究室,河南医科大学第一附属医院

出  处:《河南医科大学学报》1996年第3期19-22,共4页Journal of Henan Medical University

基  金:河南省科技攻关基金

摘  要:雄性大鼠21只(体重200~250g),随机分为A、B、C三组,氨基甲酸乙酯(1g/kg)腹腔麻醉,双针记录电极置于右侧股二头肌以记录肌电,双侧腋窝皮下埋藏板状电极以引导心电信号。肌电信号及心电信号,经生物信号处理系统(SMUP-PC)Z自动记录心电幅值、频率及屈肌反射阈值、潜伏期,并进行定量分析处理。尾静脉注射蝎毒纯化因子Ⅱ(AFSVC-Ⅱ)的剂量,A组为43μg/kg,B组为65μg/kg,C组为130μg/kg,注入容量均为0.3ml。AFSVCⅡ注射前及注射后(每隔10min测定1次,80min停止观察)分别对上述各项生理指标进行测定。结果:AFSVC-Ⅱ尾静脉注射43~65μg/kg对心电幅值没有显著影响,但注射130μg/kg10~30min,可明显减低心电幅值;AFSVC-Ⅱ尾静脉注射43~65μg/kg对屈肌反射没有显著影响,但注射130μg/kg10~30min,可明显减低神经肌肉的兴奋性及减慢神经传导的速度。提示:蝎毒可通过抑制Na+通道,从而明显降低神经肌肉的兴奋性。rats were divided at random into 3(A. b.c) groups, and given abdominal anesthesia by injecting urethan(1 g/kg).Dual-needle electrode was located in the biceps femora to record myoeletricity; plate electrode was located subcutaneously in axillary fossa to record myocardioelectricity; the amplitude and frequency of myocardioelectricity,the threshold and latency of flexion reflex were recorded automatically through the biological signal translating system (SMUPPC);quantitative analysis was performed.43 μg/kg AFSVC-Ⅱ were injected through the tail vein in Group A;65 μg/kg in Group B; 130 μg/kg in Group C;the contents of injection were0.3ml. Before and after AFSVC-Ⅱ was injected, the above physiological standards were measured separately (the measuring interval was 10 min,observation was stopt in 80 min).The results demonstrated that 43~65 μg/kg AFSVC-Ⅱ injected via tail vein had no eminent effects on the amplitude of myocardioelectricity, while 130 μg/kg AFSVC-Ⅱ could markedly decrease it during 10 to 30 min; 43~65 μg/kg AFSVC-Ⅱ had no eminent effects on the flexion reflex,whereas 130 μg/kg AFSVC-Ⅱ could markedly depress the neuromuscular excitability and prolong the nerve conducting speed. The experiment provided new theoretical proof of scorpion venom binding sodium channel.

关 键 词:蝎毒 屈肌反射 神经肌肉兴奋性 

分 类 号:R971[医药卫生—药品] R977[医药卫生—药学]

 

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