Fiset C, Kargacin M E, Kondo C S, Lester W M, Duff H J
Cardiovascular Research Group, University of Calgary, Alberta, Canada.
J Am Coll Cardiol. 1996 Jun;27(7):1771-6. doi: 10.1016/0735-1097(96)00089-7.
We sought to compare the incidence of sudden death in rats treated with magnesium-deficient and control diets and to address the electrophysiologic characteristics associated with these end points.
Although magnesium deficiency is associated with an increased incidence of sudden cardiac death in patients, there has been no clear cause and effect relation because of a number of covariables, including diuretic use, hypokalemia, digitalis use and left ventricular dysfunction.
Hypomagnesemic rats and their paired control rats underwent in vivo electrophysiologic studies and measurements of the total calcium and magnesium content of their cardiac ventricles
Serum magnesium levels were 0.5 +/- 0.3 mEq/liter (mean +/- SD) in hypomagnesemic animals and 1.2 +/- 0.9 mEq/liter in control animals. A modest but significant prolongation of the repolarization time was seen at the apical epicardial site (83 +/- 8 ms in hypomagnesemic rats vs. 68 +/- 13 ms in control rats, p < 0.05), but not at the other sites studied. Bradyarrhythmias and tachyarrhythmias were observed in 82% of the hypomagnesemic rats during the in vivo electrophysiologic studies, compared with 0% in the control group. During these studies, sudden, unexpected asystolic deaths were observed in 4 of 11 hypomagnesemic rats and 0 of 8 control rats. Polymorphic nonsustained ventricular tachycardia was provoked by rapid pacing in 5 to 11 hypomagnesemic rats and 0 of 8 control rats. Three of six hypomagnesemic rats exposed to auditory stimuli developed seizures, followed immediately by sudden deaths-two due to asystole and one due to ventricular fibrillation-although no end points occurred in the control animals.
In this model, magnesium deficiency results in sudden cardiac death. The presence of startle induction of sudden death preceded by seizures suggests that sudden cardiac death results from a neurologic trigger.
我们试图比较食用缺镁饮食的大鼠和对照饮食大鼠的猝死发生率,并探讨与这些终点相关的电生理特征。
虽然镁缺乏与患者心脏性猝死发生率增加有关,但由于包括利尿剂使用、低钾血症、洋地黄使用和左心室功能障碍等多种协变量,尚未有明确的因果关系。
低镁血症大鼠及其配对的对照大鼠接受体内电生理研究,并测量其心室的总钙和镁含量。
低镁血症动物的血清镁水平为0.5±0.3 mEq/升(平均值±标准差),对照动物为1.2±0.9 mEq/升。在心尖心外膜部位观察到复极时间有适度但显著的延长(低镁血症大鼠为83±8毫秒,对照大鼠为68±13毫秒,p<0.05),但在其他研究部位未观察到。在体内电生理研究期间,82%的低镁血症大鼠出现缓慢性心律失常和快速性心律失常,而对照组为0%。在这些研究中,11只低镁血症大鼠中有4只出现突然、意外的心脏停搏死亡,8只对照大鼠中无死亡。快速起搏诱发5至11只低镁血症大鼠出现多形性非持续性室性心动过速,8只对照大鼠中无诱发。6只暴露于听觉刺激的低镁血症大鼠中有3只发生惊厥,随后立即出现猝死——2只因心脏停搏,1只因心室颤动——而对照动物未出现任何终点事件。
在该模型中,镁缺乏导致心脏性猝死。惊厥前惊吓诱导猝死的存在表明心脏性猝死是由神经触发因素引起的。