Vieira A K G, Soares V M, Bernardo A F, Neves F A, Mattos A B M, Guedes R M, Cortez E, Andrade D C, Lacerda-Miranda G, Garcia-Souza E P, Moura A S
Laboratory of Physiology of Nutrition and Development, Department of Physiological Sciences, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Laboratory of Cell Culture, Department of Histology and Embryology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Nutr Metab Cardiovasc Dis. 2015 Nov;25(11):1062-9. doi: 10.1016/j.numecd.2015.07.009. Epub 2015 Jul 29.
In this study, the effects of postnatal overfeeding on heart energy homoeostasis and cardiac haemodynamics in adult male Swiss mice were examined.
During the suckling period, the mice were divided into four groups of control or overfed pups in combination with baseline or ischaemia/reperfusion treatments (control group baseline, CGBL; overfed group baseline, OGBL; control group ischaemia/reperfusion, CGIR; and overfed group ischaemia/reperfusion, OGIR). End diastolic pressure (EDP), heart contraction speed (Max dP/dt), relaxation speed (Min dP/dt), isovolumetric relaxation time (Tau) and frequency by beats per minute (BPM) were measured. During baseline and ischaemia/reperfusion, key proteins such as AKT1, AKT2, AKT3, pAKT, adenosine monophosphate-activated protein kinase (AMPK), pAMPK, insulin receptor beta (IRβ), protein tyrosine phosphatase 1B (PTP1B), insulin receptor substrate 1 (IRS1), fatty acid binding protein (FABP), CD36, phosphoinositide 3-kinase (PI3K) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α) were studied. The expression of atrial natriuretic peptide (ANP), B-type natriuretic peptide (BNP), carnitine palmitoyltransferase 1 (CPT1) and uncoupling protein 3 (UCP3) was studied as a marker of cardiac hypertrophy and energetic metabolism. Cardiac fibrosis was analyzed by quantifying collagen deposition, which is increased in the OGBL and OGIR groups compared with the control groups.
The OGBL group showed reduced EDP compared with the CGBL group and high Max dP/dt compared with the OGBL group. Ischaemia/reperfusion increased EDP and Min dP/dt in the intragroup comparison. By contrast, Tau and frequency were not significantly different among groups. The OGIR mice showed significant alterations in heart metabolism proteins, including AKT2, pAKT/AKT1, pAKT/AKT2, AMPK, pAMPK/AMPK, PTP1B, IRS1, FABP and CD36. Furthermore, alterations in ANP, BNP, CPT1 and UCP3 messenger RNA (mRNA) expression indicated hypertrophy and reduction in their efficiency, such that exclusive overnutrition in childhood induces a long-term effect on haemodynamics, metabolism and heart remodelling.
本研究检测了出生后过度喂养对成年雄性瑞士小鼠心脏能量稳态和心脏血流动力学的影响。
在哺乳期,将小鼠分为四组,即对照组或过度喂养组,并分别结合基线或缺血/再灌注处理(对照组基线,CGBL;过度喂养组基线,OGBL;对照组缺血/再灌注,CGIR;过度喂养组缺血/再灌注,OGIR)。测量舒张末期压力(EDP)、心脏收缩速度(最大dP/dt)、舒张速度(最小dP/dt)、等容舒张时间(Tau)和每分钟心跳频率(BPM)。在基线和缺血/再灌注期间,研究关键蛋白,如AKT1、AKT2、AKT3、pAKT、腺苷单磷酸激活蛋白激酶(AMPK)、pAMPK、胰岛素受体β(IRβ)、蛋白酪氨酸磷酸酶1B(PTP1B)、胰岛素受体底物1(IRS1)、脂肪酸结合蛋白(FABP)、CD36、磷酸肌醇3激酶(PI3K)和过氧化物酶体增殖物激活受体γ共激活因子1α(PGC1α)。研究心房利钠肽(ANP)、B型利钠肽(BNP)、肉碱棕榈酰转移酶1(CPT1)和解偶联蛋白3(UCP3)的表达,作为心脏肥大和能量代谢的标志物。通过量化胶原沉积分析心脏纤维化,与对照组相比,OGBL组和OGIR组的胶原沉积增加。
与CGBL组相比,OGBL组的EDP降低;与OGBL组相比,则具有较高的最大dP/dt。在组内比较中,缺血/再灌注增加了EDP和最小dP/dt。相比之下,Tau和频率在各组之间无显著差异。OGIR小鼠的心脏代谢蛋白出现显著改变,包括AKT2、pAKT/AKT1、pAKT/AKT2、AMPK、pAMPK/AMPK、PTP1B、IRS1、FABP和CD36。此外,ANP、BNP、CPT1和UCP3信使核糖核酸(mRNA)表达的改变表明心脏肥大及其效率降低,因此儿童期单纯的营养过剩会对血流动力学、代谢和心脏重塑产生长期影响。