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Interleukin-18 mediates cardiac dysfunction induced by western diet independent of obesity and hyperglycemia in the mouse

机译:白细胞介素18介导由西方饮食诱发的心脏功能障碍,与肥胖和高血糖无关,小鼠

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Obesity and diabetes are independent risk factors for heart failure and are associated with the consumption of diet rich in saturated fat and sugar, Western diet (WD), known to induce cardiac dysfunction in the mouse through incompletely characterized inflammatory mechanisms. We hypothesized that the detrimental cardiac effects of WD are mediated by interleukin-18 (IL-18), pro-inflammatory cytokine linked to cardiac dysfunction. C57BL/6J wild-type male mice and IL-18 knockout male mice were fed high-saturated fat and high-sugar diet for 8 weeks. We measured food intake, body weight and fasting glycemia. We assessed left ventricular (LV) systolic and diastolic function by Doppler echocardiography and cardiac catheterization. In wild-type mice, WD induced a significant increase in isovolumetric relaxation time, myocardial performance index and left ventricular end-diastolic pressure, reflecting an impairment in diastolic function, paired with a mild reduction in LV ejection fraction. IL-18 KO mice had higher food intake and greater increase in body weight without significant differences in hyperglycemia. Despite displaying greater obesity, IL-18 knockout mice fed with WD for 8 weeks had preserved cardiac diastolic function and higher left ventricular ejection fraction. IL-18 mediates diet-induced cardiac dysfunction, independent of food intake and obesity, thus highlighting a disconnect between the metabolic and cardiac effects of IL-18.
机译:肥胖和糖尿病是心力衰竭的独立危险因素,与食用富含饱和脂肪和糖的饮食,西方饮食(WD)有关,众所周知,西方饮食通过不完全表征的炎症机制在小鼠中引起心脏功能障碍。我们假设WD的有害心脏作用是由与心脏功能障碍有关的促炎细胞因子白介素18(IL-18)介导的。给C57BL / 6J野生型雄性小鼠和IL-18敲除雄性小鼠喂食高饱和脂肪和高糖饮食8周。我们测量了食物摄入量,体重和空腹血糖。我们通过多普勒超声心动图和心脏导管检查评估了左心室(LV)的收缩和舒张功能。在野生型小鼠中,WD导致等容松弛时间,心肌性能指数和左心室舒张末期压力显着增加,反映出舒张功能受损,同时左室射血分数轻度降低。 IL-18 KO小鼠的食物摄入量更高,体重增加更大,而高血糖没有显着差异。尽管表现出更大的肥胖症,但以WD喂养8周的IL-18基因敲除小鼠保留了心脏舒张功能和较高的左心室射血分数。 IL-18介导饮食引起的心脏功能障碍,与食物摄入和肥胖无关,因此突出了IL-18的代谢和心脏作用之间的联系。

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