医药导报
醫藥導報
의약도보
HERALD OF MEDICINE
2015年
4期
448-451
,共4页
封郭生%罗攀%陈江伟%朱莉%甘露
封郭生%囉攀%陳江偉%硃莉%甘露
봉곽생%라반%진강위%주리%감로
注射用华蟾素%心率%心律失常%心电图
註射用華蟾素%心率%心律失常%心電圖
주사용화섬소%심솔%심률실상%심전도
Cinobufotalin freeze-dry powder%Heart rate%Cavdiac rhythm%Electrocardiogram
目的:观察注射用华蟾素对大鼠心率及心电图的影响,为该药在临床应用时监控心脏的不良反应提供实验依据。方法大鼠经颈外静脉插管后恒速蠕动泵给药,标准肢体Ⅱ导联监测大鼠的心率及心电图;比较给药前后心率及心电图的变化。结果静脉注射华蟾素注射液与注射用华蟾素中、大剂量30 min后均可使大鼠心率加快,分别为:(469±40),(466±29)和(484±40)次·min-1,与空白对照组[(411±17)次·min-1]比较,差异有统计学意义(P<0.05),但随后恢复正常。少数大鼠可偶致心律失常(期前收缩、传导阻滞等),且相比于空白对照组[P-R 间期:(46.90±3.90) ms,Q-T间期:(61.29±9.46) ms],给药后能明显缩短心电图的P-R间期[华蟾素注射液组(39.70±2.54) ms,注射用华蟾素中剂量组(37.70±3.77) ms,注射用华蟾素大剂量组(39.30±7.12) ms]和Q-T间期[注射用华蟾素中剂量组(55.13±4.67) ms,注射用华蟾素大剂量组(51.75±11.53) ms](P<0.05),而对QRS与S-T段无明显改变。结论注射用华蟾素对大鼠心脏有一定的毒副作用,可引起心率加快,偶发心律失常。
目的:觀察註射用華蟾素對大鼠心率及心電圖的影響,為該藥在臨床應用時鑑控心髒的不良反應提供實驗依據。方法大鼠經頸外靜脈插管後恆速蠕動泵給藥,標準肢體Ⅱ導聯鑑測大鼠的心率及心電圖;比較給藥前後心率及心電圖的變化。結果靜脈註射華蟾素註射液與註射用華蟾素中、大劑量30 min後均可使大鼠心率加快,分彆為:(469±40),(466±29)和(484±40)次·min-1,與空白對照組[(411±17)次·min-1]比較,差異有統計學意義(P<0.05),但隨後恢複正常。少數大鼠可偶緻心律失常(期前收縮、傳導阻滯等),且相比于空白對照組[P-R 間期:(46.90±3.90) ms,Q-T間期:(61.29±9.46) ms],給藥後能明顯縮短心電圖的P-R間期[華蟾素註射液組(39.70±2.54) ms,註射用華蟾素中劑量組(37.70±3.77) ms,註射用華蟾素大劑量組(39.30±7.12) ms]和Q-T間期[註射用華蟾素中劑量組(55.13±4.67) ms,註射用華蟾素大劑量組(51.75±11.53) ms](P<0.05),而對QRS與S-T段無明顯改變。結論註射用華蟾素對大鼠心髒有一定的毒副作用,可引起心率加快,偶髮心律失常。
목적:관찰주사용화섬소대대서심솔급심전도적영향,위해약재림상응용시감공심장적불량반응제공실험의거。방법대서경경외정맥삽관후항속연동빙급약,표준지체Ⅱ도련감측대서적심솔급심전도;비교급약전후심솔급심전도적변화。결과정맥주사화섬소주사액여주사용화섬소중、대제량30 min후균가사대서심솔가쾌,분별위:(469±40),(466±29)화(484±40)차·min-1,여공백대조조[(411±17)차·min-1]비교,차이유통계학의의(P<0.05),단수후회복정상。소수대서가우치심률실상(기전수축、전도조체등),차상비우공백대조조[P-R 간기:(46.90±3.90) ms,Q-T간기:(61.29±9.46) ms],급약후능명현축단심전도적P-R간기[화섬소주사액조(39.70±2.54) ms,주사용화섬소중제량조(37.70±3.77) ms,주사용화섬소대제량조(39.30±7.12) ms]화Q-T간기[주사용화섬소중제량조(55.13±4.67) ms,주사용화섬소대제량조(51.75±11.53) ms](P<0.05),이대QRS여S-T단무명현개변。결론주사용화섬소대대서심장유일정적독부작용,가인기심솔가쾌,우발심률실상。
Objective To observe the effect of cinobufotalin freeze-dry powder on heart rate ( HR ) and electrocardiogram ( ECG) of SD rats and to provide experimental basis for monitoring its adverse effect on heart in clinical application. Methods The drug was administered into external jugular vein at constant speed throughout the whole experiment;standard-Ⅱ limb lead monitored the HR and ECG, and then the changes in HR and ECG before and after administration of cinobufotalin were compared. Results Thirty minutes after administration of cinobufotalin injection and cinobufotalin freeze-dry powder at middle dose and high dose, HR of the rats was significantly increased as compared with blank control group[(469±40) bpm, (466±29) bpm and (484±40) bpm vs. (411±17) bpm] (P<0. 05), but soon afterwards, it returned to normal. A small number of rats also developed arrhythmia. In addition, administration of cinobufotalin significantly shortened the P-R interval[blank control group: (46. 90±3. 90) ms, cinobufotalin injection administration group: (39. 70± 2. 54) ms;middle dose of cnobufotalin freeze-dry powder administration group: (37. 70±3. 77) ms; high dose of cinobufotalin freeze-dry powder administration group:(39. 30±7. 12) ms] and Q-T interval[blank control group:(61. 29±9. 46) ms;middle dose of cinobufotalin freeze-dry powder administration group: (55. 13±4. 67) ms; high dose of cinobufotalin freeze-dry powder administration group:(51.75±11. 53) ms] (P<0. 05), but QRS and S-T were unchanged (P>0. 05). Conclusion Cinobufotalin freeze-dry powder has some side effects on rat heart and can increase HR, even lead to arrhythmia.