Ruiz-Hurtado Gema, García-Prieto Concha F, Pulido-Olmo Helena, Velasco-Martín Juan P, Villa-Valverde Palmira, Fernández-Valle María E, Boscá Lisardo, Fernández-Velasco María, Regadera Javier, Somoza Beatriz, Fernández-Alfonso María S
Unidad de Hipertensión, Instituto de Investigación Imas12, Hospital Universitario 12 de OctubreMadrid, Spain; Facultad de Farmacia, Instituto Pluridisciplinar, Universidad Complutense de MadridMadrid, Spain.
Departamento de Ciencias Farmacéuticas y de la Salud, Facultad de Farmacia, Universidad CEU-San Pablo Madrid, Spain.
Front Physiol. 2017 Feb 1;8:42. doi: 10.3389/fphys.2017.00042. eCollection 2017.
Caloric restriction (CR) ameliorates cardiac dysfunction associated with obesity. However, most of the studies have been performed under severe CR (30-65% caloric intake decrease) for several months or even years in aged animals. Here, we investigated whether mild (20% food intake reduction) and short-term (2-weeks) CR prevented the obese cardiomyopathy phenotype and improved the metabolic profile of young (14 weeks of age) genetically obese Zucker rats. Heart weight (HW) and HW/tibia length ratio was significantly lower in rats after 2 weeks of CR than in counterparts fed . Invasive pressure measurements showed that systolic blood pressure, maximal rate of positive left ventricle (LV) pressure, LV systolic pressure and LV end-diastolic pressure were all significantly higher in obese rats than in counterparts, which were prevented by CR. Magnetic resonance imaging revealed that the increase in LV end-systolic volume, stroke volume and LV wall thickness observed in rats was significantly lower in animals on CR diet. Histological analysis also revealed that CR blocked the significant increase in cardiomyocyte diameter in obese rats. High resolution magic angle spinning magnetic resonance spectroscopy analysis of the LV revealed a global decrease in metabolites such as taurine, creatine and phosphocreatine, glutamate, glutamine and glutathione, in obese rats, whereas lactate concentration was increased. By contrast, fatty acid concentrations in LV tissue were significantly elevated in obese rats. CR failed to restore the LV metabolomic profile of obese rats. In conclusion, mild and short-term CR prevented an obesity-induced cardiomyopathy phenotype in young obese rats independently of the cardiac metabolic profile.
热量限制(CR)可改善与肥胖相关的心脏功能障碍。然而,大多数研究是在老年动物中进行的,采用严重热量限制(热量摄入减少30 - 65%),持续数月甚至数年。在此,我们研究了轻度(食物摄入量减少20%)和短期(2周)热量限制是否能预防年轻(14周龄)遗传性肥胖Zucker大鼠的肥胖性心肌病表型,并改善其代谢状况。热量限制2周后的大鼠心脏重量(HW)和HW/胫骨长度比值显著低于喂食对照的大鼠。有创压力测量显示,肥胖大鼠的收缩压、左心室(LV)压力最大上升速率、LV收缩压和LV舒张末期压力均显著高于对照大鼠,而热量限制可预防这些情况。磁共振成像显示,肥胖大鼠中观察到的LV收缩末期容积、每搏输出量和LV壁厚度的增加在热量限制饮食的动物中显著降低。组织学分析还显示,热量限制可阻止肥胖大鼠心肌细胞直径的显著增加。对LV进行的高分辨率魔角旋转磁共振波谱分析显示,肥胖大鼠中牛磺酸、肌酸和磷酸肌酸、谷氨酸、谷氨酰胺和谷胱甘肽等代谢物整体减少,而乳酸浓度增加。相比之下,肥胖大鼠LV组织中的脂肪酸浓度显著升高。热量限制未能恢复肥胖大鼠的LV代谢组学特征。总之,轻度和短期热量限制可预防年轻肥胖大鼠的肥胖诱导性心肌病表型,且与心脏代谢状况无关。