目的探究apelin-13对离体Wistar大鼠心脏缺血再灌注后的作用效果及机制。方法55只大鼠随机分为五组:正常组(N组)、apelin-13+正常组(A组)、缺血再灌注组(I-R组)、apelin-13+缺血再灌注组(A/I.R组)及经典后处理组(I.Post组)。N组持续正常液灌流150min;apelin组给予含apelin-13(500nmol/L)正常液持续灌注150min;I-R组正常液稳定灌流30mill后,结扎前降支30-rain,继以正常液再灌注90min;A/I.R组给予含apelin-13(500nmol/L)正常液再灌注20min,继而以正常液灌流70min;I-Post组再灌注前行经典后处理(30S再通30S缺血,共3次循环)。记录分析左心室发展压(LvI)P)、再灌注心律失常(RA)、心肌梗死面积、各组L型钙通道蛋白ctlc亚单位及钠通道蛋白Vet亚单位的表达水平。结果(1)与N组相比,给予apelin后(即A组)LVDP明显增高(P〈O.05),而进行缺血再灌注处理后LVDP均持续下降,但apelin.13及后处理均可减缓其降低,二者对LVDP的影响差异无统计学意义。(2)对RA的影响:A/I-R组较I-R组RA评分降低(P〈O.05),A/I-R组与I-Post组间RA评分差异无统计学意义(P〉0.05)。(3)对心肌梗死面积的影响:A/I-R组心肌梗死面积较I-R组减小(P〈O.05),A/I-R组与I-Post组间心肌梗死面积差异无统计学意义(P〉O.05)。(4)组间心肌钠、钙通道蛋白表达无差异。结论在心肌缺血再灌注时apelin-13可减少再灌注损伤,改善缺血再灌注后心脏泵功能,减少再灌注性心律失常的发生,缩小梗死面积。apelin-13再灌注具有与经典后处理相似作用,但其作用机制并不是通过改变心肌钠、钙通道蛋白的表达来实现的。
Objective To observe the effects and mechanism of apelin-13 to ischernia reperfusion through establishing Langendorff rats model. Methods Wistar male rats were randomly divided into 5 groups: normal group (N), apelin-13 group (A), ischemla reperfusion group (I-R), apelin-13+I-R group (A/I-R) and classical ischemia post conditioning group (I-post C). N group: continued perfusion for 150 win with KH liquid. A group: continued perfusion for 150 min with KH liquid containing Apelin-13 (500 nmol/L). I-R group: stable perfusion for 30 rain followed by ligating LAD 30 rain, then reperfusion for 90 rain. A/I-R group: reperfusion with apelin-13 (500 nmol/L) for 20 rain. Then perfused with KH liquid for 70 rain. I-post C group: I-Post C (reperfusion for 30 s, ligation for 30 s, and 3 cycles in all) before reperfusion. Recorded and observed R.A, LVDP by 16 physiological recorder and calculated myocardial infarct size. Observed the expression of myocardial Na+ channel protein and voltage-gated Ca2+ channel protein with Western blot. Results About the LVDP: compared with N group, LVDP was significantly increased in apelin-13 administration group (A group)(P〈O.05), but a steady decline was arisen in groups which treated with I-R. The depression was attenuated by apelin- 13 and I-Post C. A/I-R and I-Post C group had no significant difference in LVDP at the same time (P〉0.05). About RA score: RA score in A/I-R group was lower than I-R group (P〈0.05), A/I-R and I-Post C group had no significant difference in RA score (P〉0.05). About myocardial infarct size: myocardial infarct size in A/I-R was smaller than I-R group (37.45±3.53 vs. 54.27+3.88, P〈0.05), A/I-R and I-Post C group had no significant difference in myocardial infarct area (P〉0.05). The expression of myocardial Na^2+ channel protein and voltage-gated Ca^2+ channel protein had no significant difference (P〉0.05). Conclusions Apelin-13 has the positive inotropic eff