Visker J R, Ferguson D P
Department of Kinesiology,Michigan State University,East Lansing,MI,USA.
J Dev Orig Health Dis. 2018 Aug;9(4):417-424. doi: 10.1017/S2040174418000156. Epub 2018 Apr 12.
Growth restriction caused by postnatal undernutrition increases risk for cardiovascular disease in adulthood with the potential to induce arrhythmogenesis. Thus, the purpose was to determine if undernutrition during development produced arrhythmias at rest and when stressed with dobutamine in adulthood. Mouse dams were fed (CON: 20% protein), or low-protein (LP: 8%) diet before mating. A cross-fostering model was used where pups nursed by dams fed LP diet in early [EUN; postnatal day (PN) 1-10], late (LUN; PN11-21) and whole (PUN; 1-21) phases of postnatal life. Weaned pups were switched to CON diets for the remainder of the study (PN80). At PN80, body composition (magnetic resonance imaging), and quantitative electrocardiogram (ECG) measurements were obtained under 1% isoflurane anesthesia. After baseline ECG, an IP injection (1.5 µg/g body weight) of dobutamine was administered and ECG repeated. Undernutrition significantly (P<0.05) reduced body weight in LUN (22.68±0.88 g) and PUN (19.96±0.32 g) but not in CON (25.05±0.96 g) and EUN (25.28±0.9207 g). Fat mass decreased in all groups compared with controls (CON: 8.00±1.2 g, EUN: 6.32±0.65 g, LUN: 5.11±1.1 g, PUN: 3.90±0.25 g). Lean mass was only significantly reduced in PUN (CON: 17.99±0.26 g, EUN: 17.78±0.39 g, LUN: 17.34±0.33 g, PUN: 15.85±0.28 g). Absolute heart weights were significantly less from CON, with PUN having the smallest. ECG showed LUN had occurrences of atrial fibrillation; EUN had increases of 1st degree atrioventricular block upon stimulation, and PUN had increased risk for ventricular depolarization arrhythmias. CON did not display arrhythmias. Undernutrition in early life resulted in ventricular arrhythmias under stressed conditions, but undernutrition occurring in later postnatal life there is an increased incidence of atrial arrhythmias.
出生后营养不足导致的生长受限会增加成年后患心血管疾病的风险,并有可能诱发心律失常。因此,本研究的目的是确定发育期间的营养不足是否会在成年期静息状态以及多巴酚丁胺应激状态下诱发心律失常。在交配前,给母鼠喂食正常蛋白质含量(CON:20%蛋白质)或低蛋白质(LP:8%)的饮食。采用交叉寄养模型,幼崽在出生后早期[EUN;出生后第(PN)1 - 10天]、晚期(LUN;PN11 - 21天)和整个(PUN;1 - 21天)阶段由喂食LP饮食的母鼠哺乳。断奶后的幼崽在研究剩余时间(PN80)切换至正常饮食。在PN80时,在1%异氟烷麻醉下测量身体成分(磁共振成像)和定量心电图(ECG)。在基线心电图测量后,静脉注射(1.5μg/g体重)多巴酚丁胺,并再次进行心电图测量。营养不足显著(P<0.05)降低了LUN组(22.68±0.88g)和PUN组(19.96±0.32g)的体重,但CON组(25.05±0.96g)和EUN组(25.28±0.9207g)体重未降低。与对照组相比,所有组的脂肪量均减少(CON组:8.00±1.2g,EUN组:6.32±0.65g,LUN组:5.11±1.1g,PUN组:3.90±0.25g)。仅PUN组的瘦体重显著降低(CON组:17.99±0.26g,EUN组:17.78±0.39g,LUN组:17.34±0.33g,PUN组:15.85±0.28g)。CON组的绝对心脏重量显著高于其他组,PUN组的心脏重量最小。心电图显示LUN组出现房颤;EUN组在刺激后一度房室传导阻滞增加,PUN组发生心室去极化心律失常的风险增加。CON组未出现心律失常。生命早期的营养不足在应激条件下会导致室性心律失常,但出生后后期发生的营养不足会增加房性心律失常的发生率。