Food for Health Ireland, University College Cork, Cork, Ireland.
Neuroscience. 2011 Sep 29;192:351-60. doi: 10.1016/j.neuroscience.2011.06.072. Epub 2011 Jul 1.
Obesity and stress-related psychiatric disorders are frequently comorbid. However, our understanding of the relationship between diet, everyday life stress and psychiatric disorders is limited. Although the ability of stress to increase the likelihood to develop obesity and its comorbidities in a feed-forward loop has been studied there is a dearth of studies especially at the behavioural level investigating the feedback hypothesis, that is, the consequences of high-fat diet consumption on chronic stress-induced alterations. The effects of unpredictable chronic psychosocial stress on anxiety-like behaviour in the light-dark box, depressive-like behaviour in the forced swim test, hedonic behaviour in the female urine sniffing test and social avoidance in the social interaction test were investigated in a mouse model of diet-induced obesity. Changes in plasma levels of leptin, insulin and corticosterone were also assessed. A clear dissociation in behaviours was observed in mice subjected to diet-induced obesity coupled with chronic stress, with anxiety- and depressive-like behaviour observed in mice on a low- but not on a high-fat diet exposed to chronic social stress. On the other hand, social avoidance and anhedonic behaviour was present following stress independent of diet. Moreover, the effect of chronic stress in lowering leptin levels was most apparent in mice on a high-fat diet. Plasma insulin levels however where only decreased in mice on high- but not low-fat diet. In conclusion, long-term exposure to high-fat diet selectively and robustly protects against some of the behavioural sequelae of chronic unpredictable social stressors. These data show that there is a clear discrimination in the nature of stress-induced behavioural effects sensitive to protection by high-fat diet. Moreover, these results illustrate the strong influence of dietary components on stress-induced psychological factors and thereby emphasize the importance of the brain-gut-axis as a point of future therapeutic intervention.
肥胖症和与压力相关的精神障碍常常并发。然而,我们对饮食、日常生活压力与精神障碍之间关系的理解是有限的。尽管压力增加肥胖及其合并症发生的可能性的前馈回路已经得到研究,但特别是在行为水平上,缺乏研究来调查反馈假说,即高脂肪饮食对慢性应激诱导的改变的后果。在肥胖症的小鼠模型中,研究了不可预测的慢性心理社会应激对明暗箱中的焦虑样行为、强迫游泳试验中的抑郁样行为、女性尿液嗅探试验中的享乐行为以及社会互动试验中的社会回避的影响。还评估了血浆中瘦素、胰岛素和皮质酮水平的变化。在饮食诱导肥胖的小鼠中观察到行为明显分离,在接受慢性社会应激的低脂饮食而非高脂肪饮食的小鼠中观察到焦虑和抑郁样行为。另一方面,独立于饮食的压力会导致社会回避和快感缺失行为。此外,慢性应激降低瘦素水平的作用在高脂肪饮食的小鼠中最为明显。然而,血浆胰岛素水平仅在高脂肪饮食的小鼠中降低。总之,长期暴露于高脂肪饮食选择性且强烈地保护免受一些慢性不可预测的社会应激源的行为后果。这些数据表明,压力诱导的行为效应具有明显的差异性,对高脂肪饮食有保护作用。此外,这些结果说明了饮食成分对压力引起的心理因素的强烈影响,从而强调了脑-肠轴作为未来治疗干预的一个重点。