Department of Cell Biology and Physiology, School of Medicine, University of Kansas Medical Center, Kansas City, Kansas, United States.
Kansas Intellectual and Developmental Disabilities Research Association, School of Medicine, University of Kansas Medical Center, Kansas City, Kansas, United States.
Am J Physiol Regul Integr Comp Physiol. 2023 Mar 1;324(3):R353-R367. doi: 10.1152/ajpregu.00216.2022. Epub 2023 Jan 24.
Exposure to stress early in life has been associated with adult-onset comorbidities such as chronic pain, metabolic dysregulation, obesity, and inactivity. We have established an early-life stress model using neonatal maternal separation (NMS) in mice, which displays evidence of increased body weight and adiposity, widespread mechanical allodynia, and hypothalamic-pituitary-adrenal axis dysregulation in male mice. Early-life stress and consumption of a Western-style diet contribute to the development of obesity; however, relatively few preclinical studies have been performed in female rodents, which are known to be protected against diet-induced obesity and metabolic dysfunction. In this study, we gave naïve and NMS female mice access to a high-fat/high-sucrose (HFS) diet beginning at 4 wk of age. Robust increases in body weight and fat were observed in HFS-fed NMS mice during the first 10 wk on the diet, driven partly by increased food intake. Female NMS mice on an HFS diet showed widespread mechanical hypersensitivity compared with either naïve mice on an HFS diet or NMS mice on a control diet. HFS diet-fed NMS mice also had impaired glucose tolerance and fasting hyperinsulinemia. Strikingly, female NMS mice on an HFS diet showed evidence of hepatic steatosis with increased triglyceride levels and altered glucocorticoid receptor levels and phosphorylation state. They also exhibited increased energy expenditure as observed via indirect calorimetry and expression of proinflammatory markers in perigonadal adipose. Altogether, our data suggest that early-life stress exposure increased the susceptibility of female mice to develop diet-induced metabolic dysfunction and pain-like behaviors.
生命早期接触压力与成年后出现的多种合并症有关,如慢性疼痛、代谢失调、肥胖和不活动。我们使用新生期母鼠分离(NMS)建立了一种早期生活应激模型,该模型显示雄性小鼠的体重和肥胖增加、广泛的机械性痛觉过敏以及下丘脑-垂体-肾上腺轴失调。早期生活应激和西式饮食的摄入导致肥胖的发生;然而,很少有针对雌性啮齿动物的临床前研究,因为已知雌性啮齿动物可以预防饮食引起的肥胖和代谢功能障碍。在这项研究中,我们让新生期和 NMS 雌性小鼠从 4 周龄开始摄入高脂肪/高蔗糖(HFS)饮食。在饮食的前 10 周,HFS 喂养的 NMS 小鼠体重和脂肪显著增加,部分原因是食物摄入量增加。与 HFS 饮食喂养的新生期 NMS 小鼠或 NMS 对照饮食喂养的小鼠相比,HFS 饮食喂养的 NMS 小鼠表现出广泛的机械性超敏反应。HFS 饮食喂养的 NMS 小鼠还表现出葡萄糖耐量受损和空腹高胰岛素血症。引人注目的是,HFS 饮食喂养的 NMS 雌性小鼠表现出肝脂肪变性的证据,表现为甘油三酯水平升高,糖皮质激素受体水平和磷酸化状态改变。它们还通过间接测热法和peri 性腺脂肪组织中促炎标志物的表达显示出能量消耗增加。总的来说,我们的数据表明,早期生活应激暴露增加了雌性小鼠易患饮食诱导的代谢功能障碍和类似疼痛行为的易感性。