氯化物通道%心肌再灌注损伤%心律失常,心性
氯化物通道%心肌再灌註損傷%心律失常,心性
록화물통도%심기재관주손상%심률실상,심성
Chloride channels%Myocardial reperfusion injury%Arrhythmias,cardiac
目的 探索氯离子通道及其阻滞剂DIDS、SITS和NPPB对心肌缺血再灌注所致心律失常的影响.方法 40只家兔分为对照组、缺血再灌注组、DIDS低剂量组、DIDS高剂量组、SITS低剂量组、SITS高剂量组、NPPB低剂量组和NPPB高剂量组,每组各5只,通过结扎后松扎冠状动脉前降支建立心肌缺血再灌注模型,实验过程中持续监测家兔标准肢体Ⅱ导联心电图,比较各组间家兔心率、心电图P波、R波、T波、ST段变化和心律失常评分.结果 缺血30 min时,与对照组比较,各组家兔均出现心率减慢[(199.8±4.0) ~ (253.6 ±2.1)比(267.0±3.4),均P<0.01],心电图出现P波[(0.216 ±0.019) ~ (0.356 ±0.024)比(0.186 ±0.019),均P<0.01]、R波[(0.564±0.017) ~(1.138±0.048)比(0.506 ±0.018),均P<0.01]和T波[(0.542 ±0.013)~(0.856 ±0.045)比(0.278±0.015),均P<0.01]增高及ST段[(0.326±0.027) ~ (0.668±0.054)比(0.024±0.023),均P<0.01]抬高,各组心律失常评分[(1.4±0.5) ~(4.6±0.5)比(0.4±0.5),均P<0.01]均显著增高;与缺血再灌注组比较,各干预组上述指标均显著改善[心率(214.8±3.4) ~ (246.8±4.0)比(199.8 ±4.0),均P<0.01;P波(0.216 ±0.019)~(0.316 ±0.011)比(0.356 ±0.024),均P<0.01;R波(0.564±0.017)~(0.980±0.035)比(1.138 ±0.048),均P<0.01;T波(0.542±0.013) ~(0.792±0.026)比(0.856 ±0.045),均P<0.01;ST段(0.326±0.027)~(0.596±0.018)比(0.668 ±0.054),均P<0.01;心律失常评分(1.4±0.5)~(3.8±0.4)比(4.6±0.5),均P<0.01],以DIDS组最优,其次为SITS组,再次为NPPB组,且高剂量亚组效果均优于低剂量亚组.再灌注60 min时,各组家兔心率均显著回升,心电图增高的P波、R波和T波及抬高的ST段逐渐回落,以DIDS组变化幅度最大,其次为SITS组,再次为NPPB组,且高剂量亚组效果均优于低剂量亚组,再灌注期心律失常评分比较亦有同样的趋势.结论 氯离子通道参与了心肌缺血再灌注心律失常的发生,在心肌缺血再灌注早期静脉予以氯离子通道阻滞剂DIDS、SITS和NPPB能够改善家兔心肌缺血及再灌注时的心电图表现并能够减轻再灌注心律失常的程度,其中以DIDS效果最好,其次为SITS,NPPB效果略差,且均以高剂量的效果较好.
目的 探索氯離子通道及其阻滯劑DIDS、SITS和NPPB對心肌缺血再灌註所緻心律失常的影響.方法 40隻傢兔分為對照組、缺血再灌註組、DIDS低劑量組、DIDS高劑量組、SITS低劑量組、SITS高劑量組、NPPB低劑量組和NPPB高劑量組,每組各5隻,通過結扎後鬆扎冠狀動脈前降支建立心肌缺血再灌註模型,實驗過程中持續鑑測傢兔標準肢體Ⅱ導聯心電圖,比較各組間傢兔心率、心電圖P波、R波、T波、ST段變化和心律失常評分.結果 缺血30 min時,與對照組比較,各組傢兔均齣現心率減慢[(199.8±4.0) ~ (253.6 ±2.1)比(267.0±3.4),均P<0.01],心電圖齣現P波[(0.216 ±0.019) ~ (0.356 ±0.024)比(0.186 ±0.019),均P<0.01]、R波[(0.564±0.017) ~(1.138±0.048)比(0.506 ±0.018),均P<0.01]和T波[(0.542 ±0.013)~(0.856 ±0.045)比(0.278±0.015),均P<0.01]增高及ST段[(0.326±0.027) ~ (0.668±0.054)比(0.024±0.023),均P<0.01]抬高,各組心律失常評分[(1.4±0.5) ~(4.6±0.5)比(0.4±0.5),均P<0.01]均顯著增高;與缺血再灌註組比較,各榦預組上述指標均顯著改善[心率(214.8±3.4) ~ (246.8±4.0)比(199.8 ±4.0),均P<0.01;P波(0.216 ±0.019)~(0.316 ±0.011)比(0.356 ±0.024),均P<0.01;R波(0.564±0.017)~(0.980±0.035)比(1.138 ±0.048),均P<0.01;T波(0.542±0.013) ~(0.792±0.026)比(0.856 ±0.045),均P<0.01;ST段(0.326±0.027)~(0.596±0.018)比(0.668 ±0.054),均P<0.01;心律失常評分(1.4±0.5)~(3.8±0.4)比(4.6±0.5),均P<0.01],以DIDS組最優,其次為SITS組,再次為NPPB組,且高劑量亞組效果均優于低劑量亞組.再灌註60 min時,各組傢兔心率均顯著迴升,心電圖增高的P波、R波和T波及抬高的ST段逐漸迴落,以DIDS組變化幅度最大,其次為SITS組,再次為NPPB組,且高劑量亞組效果均優于低劑量亞組,再灌註期心律失常評分比較亦有同樣的趨勢.結論 氯離子通道參與瞭心肌缺血再灌註心律失常的髮生,在心肌缺血再灌註早期靜脈予以氯離子通道阻滯劑DIDS、SITS和NPPB能夠改善傢兔心肌缺血及再灌註時的心電圖錶現併能夠減輕再灌註心律失常的程度,其中以DIDS效果最好,其次為SITS,NPPB效果略差,且均以高劑量的效果較好.
목적 탐색록리자통도급기조체제DIDS、SITS화NPPB대심기결혈재관주소치심률실상적영향.방법 40지가토분위대조조、결혈재관주조、DIDS저제량조、DIDS고제량조、SITS저제량조、SITS고제량조、NPPB저제량조화NPPB고제량조,매조각5지,통과결찰후송찰관상동맥전강지건립심기결혈재관주모형,실험과정중지속감측가토표준지체Ⅱ도련심전도,비교각조간가토심솔、심전도P파、R파、T파、ST단변화화심률실상평분.결과 결혈30 min시,여대조조비교,각조가토균출현심솔감만[(199.8±4.0) ~ (253.6 ±2.1)비(267.0±3.4),균P<0.01],심전도출현P파[(0.216 ±0.019) ~ (0.356 ±0.024)비(0.186 ±0.019),균P<0.01]、R파[(0.564±0.017) ~(1.138±0.048)비(0.506 ±0.018),균P<0.01]화T파[(0.542 ±0.013)~(0.856 ±0.045)비(0.278±0.015),균P<0.01]증고급ST단[(0.326±0.027) ~ (0.668±0.054)비(0.024±0.023),균P<0.01]태고,각조심률실상평분[(1.4±0.5) ~(4.6±0.5)비(0.4±0.5),균P<0.01]균현저증고;여결혈재관주조비교,각간예조상술지표균현저개선[심솔(214.8±3.4) ~ (246.8±4.0)비(199.8 ±4.0),균P<0.01;P파(0.216 ±0.019)~(0.316 ±0.011)비(0.356 ±0.024),균P<0.01;R파(0.564±0.017)~(0.980±0.035)비(1.138 ±0.048),균P<0.01;T파(0.542±0.013) ~(0.792±0.026)비(0.856 ±0.045),균P<0.01;ST단(0.326±0.027)~(0.596±0.018)비(0.668 ±0.054),균P<0.01;심률실상평분(1.4±0.5)~(3.8±0.4)비(4.6±0.5),균P<0.01],이DIDS조최우,기차위SITS조,재차위NPPB조,차고제량아조효과균우우저제량아조.재관주60 min시,각조가토심솔균현저회승,심전도증고적P파、R파화T파급태고적ST단축점회락,이DIDS조변화폭도최대,기차위SITS조,재차위NPPB조,차고제량아조효과균우우저제량아조,재관주기심률실상평분비교역유동양적추세.결론 록리자통도삼여료심기결혈재관주심률실상적발생,재심기결혈재관주조기정맥여이록리자통도조체제DIDS、SITS화NPPB능구개선가토심기결혈급재관주시적심전도표현병능구감경재관주심률실상적정도,기중이DIDS효과최호,기차위SITS,NPPB효과략차,차균이고제량적효과교호.
Objective To explore the impact of chloride ion channel and its blockers 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS),cyanato-stilbene-2,2'-disulfonic acid (SITS) and 5-nitro-2-(3-phenyl-propylamino) benzoic acid (NPPB) on arrhythmias caused by myocardial ischemia reperfusion.Methods A total of 40 rabbits were divided into control,ischemia reperfusion,DIDS lowdose,DIDS high-dose,SITS low-dose,SITS high-dose,NPPB low-dose and NPPB high-dose groups.Myocardial ischemia reperfusion model was established by ligation of anterior descending coronary artery.And standard limb lead Ⅱ of electrocardiogram (ECG) was continuously monitored during the experimental process.Then comparisons of heart rate,ECG P wave,R wave,T wave,ST segment changes and arrhythmias score were made between the above groups.Results During 30-minute ischemia,compared with the control group,all other groups showed significantly decreased heart rate ((199.8 ±4.0)-(253.6 ± 2.1) vs (267.0 ±3.4),all P <0.0l),elevated ECG P wave ((0.216 ±0.019)-(0.356 ±0.024) vs (0.186±0.019),all P<0.01),Rwave ((0.564±0.017)-(1.138 ±0.048) vs (0.506±0.018),all P<0.01),T wave ((0.542 ±0.013)-(0.856 ±0.045) vs (0.278 ±0.015),all P <0.01) and ST segment ((0.326 ± 0.027)-(0.668 ± 0.054) vs (0.024 ± 0.023),all P < 0.01) and increased arrhythmia score ((1.4 ± 0.5)-(4.6 ± 0.5) vs (0.4 ± 0.5),all P < 0.01).Compared with the ischemia reperfusion group,the above indices significantly improved in the intervention groups (heart rate:(214.8 ± 3.4)-(246.8±4.0) vs (199.8±4.0),allP<0.01; Pwave:(0.216±0.019)-(0.316±0.011) vs (0.356 ±0.024),all P<0.01; R wave:(0.564 ±0.017)-(0.980 ±0.035) vs (1.138 ±0.048),all P < 0.01 ; T wave:(0.542 ± 0.013)-(0.792 ± 0.026) vs (0.856 ± 0.045),all P < 0.01 ; ST segment:(0.326 ±0.027)-(0.596 ±0.018) vs (0.668 ±0.054),all P <0.01 ; arrhythmia score:(1.4 ±0.5)-(3.8 ±0.4) vs (4.6 ±0.5),all P <0.01).Among which,the DIDS group was the best,followed by the SITS group and then the NPPB group.And the high-dose subgroups were better than those of the low-dose subgroups.During 60-minute reperfusion,the decreased heart rate upswung significantly in each group and the elevated P wave,R wave,T wave and ST segment fell back gradually.The DIDS group showed the most obvious amplitude change,followed by the SITS group and then the NPPB group.And the high-dose subgroups were better than those of the low-dose subgroups.The arrhythmia score during reperfusion showed the same trend.Conclusion Chloride ion channel is involved in the generation of myocardial ischemia reperfusion arrhythmia.Early application of chloride ion channel blockers DIDS,SITS and NPPB may improve the ECG manifestations and reduce the degree of reperfusion arrhythmia.