Aguiar Lais Marinho, Moura Carolina Soares de, Ballard Cintia Reis, Roquetto Aline Rissetti, Silva Maia Juliana Kelly da, Duarte Gustavo H B, Costa Larissa Bastos Eloy da, Torsoni Adriana Souza, Amaya-Farfan Jaime, Maróstica Junior Mário R, Cazarin Cinthia Baú Betim
University of Campinas, School of Food Engineering, Department of Food Science and Nutrition, Rua Monteiro Lobato, 80, Cidade Universitária Zeferino Vaz, Campinas, SP, Brazil.
Federal University of Rio Grande Do Norte, Center for Health Sciences, Department of Nutrition, Av. Senador Salgado Filho 3000, Lagoa Nova, Natal, RN, Brazil.
Curr Res Physiol. 2022 Nov 23;5:436-444. doi: 10.1016/j.crphys.2022.11.001. eCollection 2022.
Researchers from different fields have studied the causes of obesity and associated comorbidities, proposing ways to prevent and treat this condition by using a common animal model of obesity to create a profound energy imbalance in young adult rodents. However, to confirm the harmful effects of consuming a high-fat and hypercaloric diet, it is common to include normolipidic and normocaloric control groups in the experimental protocols. This study compared the effect of three experimental diets described in the literature - namely, a high-fat diet, a high-fat and high-sucrose diet, and a high-fat and high-fructose diet - to induce obesity in C57BL/6 J mice with the standard AIN-93G diet as a control. We hypothesize that the AIN diet formulation is not a good control in this type of experiment because this diet promotes weight gain and metabolic dysfunctions similar to the hypercaloric diet. The metabolic data of animals fed the AIN-93G diet were similar to those of the high-calorie groups (development of steatosis and hyperlipidemia). However, it is important to emphasize that the group fed a high-fat diet had a higher percentage of total fat (p = 0.0002) and abdominal fat (p = 0.013) compared to the other groups. Also, the high-fat group responded poorly to glucose and insulin tolerance tests, showing a picture of insulin resistance. As expected, the intake of the AIN-93G diet promotes metabolic alterations in the animals like the high-fat formulations. Therefore, although this diet continues to be used as the gold standard for growth and maintenance, it warrants a reassessment of its composition to minimize the metabolic changes observed in this study, thus updating its fitness as a normocaloric model of a standard rodent diet.
来自不同领域的研究人员对肥胖及其相关合并症的病因进行了研究,他们提出通过使用一种常见的肥胖动物模型,在年轻成年啮齿动物中制造严重的能量失衡,来预防和治疗这种疾病。然而,为了证实食用高脂肪和高热量饮食的有害影响,实验方案中通常会设置正常脂质和正常热量的对照组。本研究比较了文献中描述的三种实验性饮食——即高脂肪饮食、高脂肪高蔗糖饮食和高脂肪高果糖饮食——与标准AIN-93G饮食作为对照,对C57BL/6 J小鼠诱导肥胖的效果。我们假设,在这类实验中AIN饮食配方并非一个良好的对照,因为这种饮食会促进体重增加和代谢功能障碍,与高热量饮食类似。喂食AIN-93G饮食的动物的代谢数据与高热量组相似(出现脂肪变性和高脂血症)。然而,需要强调的是,与其他组相比,喂食高脂肪饮食的组总脂肪百分比更高(p = 0.0002),腹部脂肪百分比更高(p = 0.013)。此外,高脂肪组对葡萄糖和胰岛素耐受性测试反应不佳,呈现出胰岛素抵抗的情况。正如预期的那样,AIN-93G饮食的摄入会像高脂肪配方饮食一样促进动物的代谢改变。因此,尽管这种饮食仍被用作生长和维持的金标准,但有必要重新评估其成分,以尽量减少本研究中观察到的代谢变化,从而更新其作为标准啮齿动物正常热量模型的适用性。