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高热量高脂肪饮食对啮齿动物产生的不良代谢影响先于体重的可见变化。

Adverse metabolic effects of a hypercaloric, high-fat diet in rodents precede observable changes in body weight.

机构信息

Division of Maternal-Fetal Medicine, Departments of Obstetrics & Gynecology, Diagnostic Imaging, and Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Canada.

出版信息

Nutr Res. 2011 Sep;31(9):707-14. doi: 10.1016/j.nutres.2011.08.009.

Abstract

Although a high-fat diet (HFD) is recognized as an important contributor to obesity, human research is limited by confounders such as income, whereas animal research has typically examined diet during specific developmental periods rather than throughout the lifespan. We hypothesized that the use of an HFD in short-term studies as has been commonly done in animals does not adequately reflect the lifelong dietary patterns seen frequently in humans with consequent metabolic disturbances. We examined the impact of HFD from weaning until 39 weeks (middle age) on the metabolism of male rats. At 7, 26, and 39 weeks, glucose tolerance tests were performed, a subset of animals was euthanized, and serum and tissues were collected. After 4 weeks, preceding increased body weight, HFD animals had increased intra-abdominal fat, triglycerides, and hyperglycemia. Hyperinsulinemia was insufficient to maintain normoglycemia, and beta cell mass and glucagon-like peptide 1 decreased over time in HFD and control animals. Despite lacking significant lipid abnormalities, nonalcoholic fatty liver disease was evident by 39 weeks. Our HFD model demonstrated that significant metabolic abnormalities may go undetected by current standard screening such as weighing and biochemistry.

摘要

尽管高脂肪饮食(HFD)被认为是肥胖的一个重要诱因,但人类研究受到收入等混杂因素的限制,而动物研究通常只在特定的发育阶段研究饮食,而不是在整个生命周期内研究。我们假设,像动物研究中常见的那样,在短期研究中使用 HFD 并不能充分反映人类常见的终生饮食模式,从而导致代谢紊乱。我们研究了从断奶到 39 周(中年)期间 HFD 对雄性大鼠代谢的影响。在 7、26 和 39 周时,进行了葡萄糖耐量试验,部分动物被安乐死,收集了血清和组织。在体重增加之前的 4 周内,HFD 动物的内脏脂肪、甘油三酯和高血糖增加。高胰岛素血症不足以维持血糖正常,HFD 和对照组动物的β细胞质量和胰高血糖素样肽 1 随时间减少。尽管没有明显的脂质异常,但非酒精性脂肪性肝病在 39 周时已经明显。我们的 HFD 模型表明,目前的标准筛查(如称重和生物化学)可能无法检测到显著的代谢异常。

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