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雌性大鼠高脂饮食机会受限会改变内源性大麻素水平。

Limited Access to a High Fat Diet Alters Endocannabinoid Tone in Female Rats.

作者信息

Satta Valentina, Scherma Maria, Piscitelli Fabiana, Usai Paolo, Castelli M Paola, Bisogno Tiziana, Fratta Walter, Fadda Paola

机构信息

Division of Neuroscience and Clinical Pharmacology, Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy.

Endocannabinoid Research Group, Institute of Biomolecular Chemistry, National Research Council, Pozzuoli, Italy.

出版信息

Front Neurosci. 2018 Feb 2;12:40. doi: 10.3389/fnins.2018.00040. eCollection 2018.

Abstract

Emerging evidence suggest an impaired endocannabinoid activity in the pathophysiology of binge eating disorder (BED). Herein, we investigated whether endocannabinoid tone could be modified as a consequence of dietary-induced binge eating in female rats. For this purpose, brain levels of the endocannabinoids anandamide (AEA) and 2-arachidonoyl glycerol (2-AG), as well as two endocannabinoid-like lipids, oleoylethanolamide (OEA) and palmitoylethanolamide (PEA), were assessed in different brain areas involved in the hedonic feeding (i.e., prefrontal cortex, nucleus accumbens, amygdala, hippocampus, and hypothalamus). The brain density of cannabinoid type-1 receptors (CB) was also evaluated. Furthermore, we determined plasma levels of leptin, ghrelin, and corticosterone hormones, which are well-known to control the levels of endocannabioids and/or CB1 receptors in the brain. To induce binge eating behavior, rats were subject to an intermittent and limited access to a high fat diet (HFD) (margarine). Three experimental groups were used, all with access to chow: control (CTRL), with no access to margarine; low restriction (LR), with 2 h margarine access 7 days/week; high restriction (HR), with 2 h margarine access 3 days/week. Bingeing was established when margarine intake in the HR group exceeded that of the LR group. Our results show that, compared to CTRL, AEA significantly decreased in the caudate putamen, amygdala, and hippocampus of HR group. In contrast, 2-AG significantly increased in the hippocampus while OEA decreased in the hypothalamus. Similar to the HR group, AEA and OEA decreased respectively in the amygdala and hypothalamus and 2-AG increased in the hippocampus of LR group. Moreover, LR group also had AEA decreased in the prefrontal cortex and increased in the nucleus accumbens. In both groups we found the same reduction of CB receptor density in the prefrontal cortex compared to CTRL. Also, LR and HR groups showed alterations in both ghrelin and corticosterone levels, while leptin remained unaltered. In conclusion, our findings show a modified endocannabinoid tone due to margarine exposure, in several brain areas that are known to influence the hedonic aspect of food. Even if not uniquely specific to binge eating, margarine-induced changes in endocannabinoid tone could contributes to the development and maintenance of this behavior.

摘要

新出现的证据表明,内源性大麻素活性在暴饮暴食症(BED)的病理生理学中受损。在此,我们研究了雌性大鼠因饮食诱导的暴饮暴食是否会导致内源性大麻素水平的改变。为此,我们评估了参与享乐性进食的不同脑区(即前额叶皮层、伏隔核、杏仁核、海马体和下丘脑)中内源性大麻素花生四烯乙醇胺(AEA)和2-花生四烯酸甘油酯(2-AG),以及两种类内源性大麻素脂质油酰乙醇胺(OEA)和棕榈酰乙醇胺(PEA)的脑内水平。还评估了1型大麻素受体(CB)的脑密度。此外,我们测定了瘦素、胃饥饿素和皮质酮激素的血浆水平,众所周知,这些激素可控制脑内内源性大麻素和/或CB1受体的水平。为了诱导暴饮暴食行为,让大鼠间歇性且有限地获取高脂饮食(HFD)(人造黄油)。使用了三个实验组,所有组都可获取普通食物:对照组(CTRL),无法获取人造黄油;低限制组(LR),每周7天有2小时可获取人造黄油;高限制组(HR),每周3天有2小时可获取人造黄油。当HR组的人造黄油摄入量超过LR组时,即确定出现了暴饮暴食。我们的结果表明,与CTRL组相比,HR组尾状壳核、杏仁核和海马体中的AEA显著降低。相反,海马体中的2-AG显著增加,而下丘脑中的OEA降低。与HR组相似,LR组杏仁核和下丘脑中的AEA和OEA分别降低,海马体中的2-AG增加。此外,LR组前额叶皮层中的AEA也降低,伏隔核中的AEA增加。在两组中,与CTRL组相比,我们发现前额叶皮层中CB受体密度均降低。此外,LR组和HR组的胃饥饿素和皮质酮水平均发生了改变,而瘦素水平保持不变。总之,我们的研究结果表明,由于接触人造黄油,在几个已知会影响食物享乐方面的脑区中,内源性大麻素水平发生了改变。即使并非暴饮暴食所特有,人造黄油引起的内源性大麻素水平变化也可能有助于这种行为的发展和维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e579/5801427/ab619e9f80c9/fnins-12-00040-g0001.jpg

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