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L-精氨酸对兔右冠状动脉缺血再灌注时窦房结功能及房室结传导有效不应期的干预作用

Effect of L-arginine on rabbit sinoatrial node functions and atrioventricular nodal effective refractory period during ischemia-reperfusion of the right coronary artery
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摘要 目的观察L-精氨酸(L-Arg)对兔右冠状动脉缺血再灌注(IR)窦房结(SAN)传导时间(SACT)和恢复时间(SNRT)及房室结(AVN)传导有效不应期(AVERP)的影响。方法在体成年兔右冠状动脉缺血再灌注模型分4组正常对照组,IR(缺血90min,再灌注90min)+生理盐水组,IR+L-Arg组和IR+左型精氨酸甲酯(L-NAME)组。在不同时相分别测定各组心房快速起搏或程序电刺激后的SACT、SNRT和AVERP。结果IR+L-Arg组缺血期及再灌注早期3项指标均有不同程度的下降,而再灌注后期升高;IR+L-NAME组结果却基本相反(P<0.01)。3组组内比,IR+L-Arg组和L-NAME组于缺血期与再灌早期3项指标均升高;再灌注后期,IR+L-Arg组无治疗意义甚至加重SAN和AVN损伤,而IR+L-NAME组3项指标下降。结论随着缺血时间延长SAN功能损伤加重;早期再灌注损伤敏感;组织内适当补充L-Arg,于缺血期和再灌早期对SAN电生理功能和AVERP恢复是有益的,于再灌注后期可能加重损伤。 Objective To study the effect of L-arginine (L-Arg) on sinoatrial conduction time (SACT) and sinus node recovery time (SNRT) and atrioventricular nodal effective refractory period (AVERP) in the course of ischemia- reperfusion (IR) of the right coronary artery in rabbits. Methods Thirty-two rabbit models of ischemia-reperfusion of the right coronary artery were randomly divided into control group, IR+saline group, IR+L-Arg group and IR+ L-arginine-methyl ester (IR+L-NAME group, 8 rabits in each group. At different time points after ligation or loosening of the artery , SACT, SNRT and AVERP were measured respectively by fast pacing of the right atrium and programmed electrical stimulations. Results Compared with the control group, SACT, SNRT and AVERP of the other groups were all prolonged significantly(P<0.01). In comparison with IR+NS group, at each time point , SACT, SNRT and AVERP of IR+L-Arg group were decreased during ischemia and in the early phases of reperfusion, followed by elevation during the latter stages of the reperfusion, as were contrary to the changes in IR+L-NAME group. Conclusions The longer duration of ischemia persists, the severer are the functional damages of the sinoatrial node. Adequate supply of L-Arg to the tissues during ischemia and the early stages of the reperfusion may alleviate the damages, but its administration in the latter stages of reperfusion might contribute to the contrary result.
出处 《第一军医大学学报》 CSCD 北大核心 2004年第8期897-899,共3页 Journal of First Military Medical University
基金 河南省科技攻关计划资助(424410122)~~
关键词 缺血再灌注 一氧化氮 右冠状动脉 窦房结功能 房室有效不应期 ischemia-reperfusion nitric oxide right coronary artery functions, sinus node atrioventricular nodal effective refractory period
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  • 1Berges A, Van Nassauw L, Bosmans J, et al. Role of nitric oxide and oxidative stress in ischemic myocardial injury and preconditioning[J]. Heart Fail Rev, 2003, 8(2): 127-41.
  • 2Araki M, Tanaka M, Hasegawa K, et al. Nitric oxide inhibition improved myocardial metabolism independent of tissue perfusion during ischemia but not during repeffusion [J]. J Mol Cell Cardiol,2000, 32(3): 375-84.
  • 3Baker CS, Kumar S, Rimoldi OE. Effects of brief ischemia and reperfusion on the myocardium and the role of nitric oxide [J].Heart Fail Rev, 2003, 8(2): 127-41.
  • 4宋治远,李永华,姚青,仝识非.兔右冠状动脉急性闭塞与再灌注时心律失常的发生与演变[J].中国心脏起搏与心电生理杂志,2003,17(1):48-51. 被引量:12
  • 5Hogan N, Casadei B, Paterson D J. Nitric oxide donors can increase heart rate independent of autonomic activation [J]. J Appl Physiol,1999, 87(1): 97-103.
  • 6张炎,凌凤东.窦房结应用基础研究进展[J].解剖科学进展,1998,4(2):104-110. 被引量:9
  • 7Herring N, Rigg L, Terrar DA, et al. NO-cGMP pathway increases the hyperpolarisation-activated current, I(f), and heart rate during adrenergic stimulation[ J ]. Cardiovasc Res, 2001, 52(3): 446-53.
  • 8Zhang C, Reiter C, Eiserich JP, et al. L-arginine chlorination products inhibit endothelial nitric oxide production[J]. J Biol Chem, 2001,276(29): 27159-65.
  • 9周忠江,叶海燕,吴赛珠,孟素荣.NO前体—左旋精氨酸相关肽对大鼠血小板聚集、血栓形成及血浆NO、cGMP、PGI_2的影响[J].第一军医大学学报,1999,19(6):540-542. 被引量:10
  • 10Widhirt S M, Weismuller S, Schulze C, et al. Inducible nitric oxide synthase activation after ischemia/reperfusion contributes to myocardial dysfunction and extent of infract size in rabbits:evidence for a late phase of nitric oxide-mediated perfusion injury[J]. Cardiovasc Res, 1999, 43(3): 698-711.

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