Reno Candace M, VanderWeele Jennifer, Bayles Justin, Litvin Marina, Skinner Allie, Jordan Andrew, Daphna-Iken Dorit, Fisher Simon J
Division of Endocrinology, Metabolism, and Diabetes, Department of Internal Medicine, University of Utah, Salt Lake City, UT.
Division of Endocrinology, Metabolism, and Lipid Research, Department of Medicine, Washington University in St. Louis, St. Louis, MO.
Diabetes. 2017 Dec;66(12):3091-3097. doi: 10.2337/db17-0306. Epub 2017 Sep 8.
We previously demonstrated that insulin-mediated severe hypoglycemia induces lethal cardiac arrhythmias. However, whether chronic diabetes and insulin deficiency exacerbates, and whether recurrent antecedent hypoglycemia ameliorates, susceptibility to arrhythmias remains unknown. Thus, adult Sprague-Dawley rats were randomized into four groups: ) nondiabetic (NONDIAB), ) streptozotocin-induced insulin deficiency (STZ), ) STZ with antecedent recurrent (3 days) hypoglycemia (∼40-45 mg/dL, 90 min) (STZ+RH), and ) insulin-treated STZ (STZ+Ins). Following treatment protocols, all rats underwent hyperinsulinemic (0.2 units ⋅ kg ⋅ min), severe hypoglycemic (10-15 mg/dL) clamps for 3 h with continuous electrocardiographic recordings. During matched nadirs of severe hypoglycemia, rats in the STZ+RH group required a 1.7-fold higher glucose infusion rate than those in the STZ group, consistent with the blunted epinephrine response. Second-degree heart block was increased 12- and 6.8-fold in the STZ and STZ+Ins groups, respectively, compared with the NONDIAB group, yet this decreased 5.4-fold in the STZ+RH group compared with the STZ group. Incidence of third-degree heart block in the STZ+RH group was 5.6%, 7.8-fold less than the incidence in the STZ group (44%). Mortality due to severe hypoglycemia was 5% in the STZ+RH group, 6.2-fold less than that in the STZ group (31%). In summary, severe hypoglycemia-induced cardiac arrhythmias were increased by insulin deficiency and diabetes and reduced by antecedent recurrent hypoglycemia. In this model, recurrent moderate hypoglycemia reduced fatal severe hypoglycemia-induced cardiac arrhythmias.
我们之前证明,胰岛素介导的严重低血糖会诱发致命性心律失常。然而,慢性糖尿病和胰岛素缺乏是否会加剧心律失常易感性,以及既往反复发生的低血糖是否会改善心律失常易感性,目前仍不清楚。因此,将成年Sprague-Dawley大鼠随机分为四组:)非糖尿病组(NONDIAB),)链脲佐菌素诱导的胰岛素缺乏组(STZ),)有既往反复(3天)低血糖(~40-45mg/dL,90分钟)的STZ组(STZ+RH),以及)胰岛素治疗的STZ组(STZ+Ins)。按照治疗方案,所有大鼠均接受高胰岛素血症(0.2单位·kg·min)、严重低血糖(10-15mg/dL)钳夹3小时,并持续进行心电图记录。在严重低血糖的匹配最低点期间,STZ+RH组大鼠的葡萄糖输注速率比STZ组大鼠高1.7倍,这与肾上腺素反应减弱一致。与NONDIAB组相比,STZ组和STZ+Ins组的二度心脏传导阻滞分别增加了12倍和6.8倍,但与STZ组相比,STZ+RH组的二度心脏传导阻滞减少了5.4倍。STZ+RH组三度心脏传导阻滞的发生率为5.6%,比STZ组(44%)的发生率低7.8倍。STZ+RH组因严重低血糖导致的死亡率为5%,比STZ组(31%)低6.2倍。总之,严重低血糖诱发的心律失常因胰岛素缺乏和糖尿病而增加,因既往反复低血糖而减少。在该模型中,反复发生的中度低血糖减少了致命性严重低血糖诱发的心律失常。