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在小鼠模型中,急性高脂饮食的摄入会激活中脑边缘回路,且需要食欲素信号传导。

Acute high fat diet consumption activates the mesolimbic circuit and requires orexin signaling in a mouse model.

作者信息

Valdivia Spring, Patrone Anabela, Reynaldo Mirta, Perello Mario

机构信息

Laboratory of Neurophysiology; Multidisciplinary Institute of Cell Biology (CONICET/CICPBA), La Plata, Argentina.

出版信息

PLoS One. 2014 Jan 23;9(1):e87478. doi: 10.1371/journal.pone.0087478. eCollection 2014.

Abstract

Overconsumption of palatable energy-dense foods has negative health implications and it is associated with obesity and several eating disorders. Currently, little is known about the neuronal circuitries activated by the acute ingestion of a rewarding stimulus. Here, we used a combination of immunohistochemistry, pharmacology and neuronal tracing analyses to examine the role of the mesolimbic system in general, and the orexin neurons in particular, in a simple experimental test in which naïve mice are allowed to spontaneously eat a pellet of a high fat diet (HFD) for 2 h. We found that acute HFD activates c-Fos expression in several reward-related brain areas, including the ventral tegmental area (VTA), nucleus accumbens, central amygdala and lateral hypothalamic area. We also found that: i- HFD-mediated orosensory stimulation was required for the mesolimbic pathway activation, ii- acute HFD differentially activates dopamine neurons of the paranigral, parabrachial pigmented and interfascicular sub-regions of the VTA, and iii- orexin neurons of the lateral hypothalamic area are responsive to acute HFD. Moreover, orexin signaling blockade, with the orexin 1 receptor antagonist SB-334867, reduces acute HFD consumption and c-Fos induction in the VTA but not in the other mesolimbic nuclei under study. Finally, we found that most orexin neurons responsive to acute HFD innervate the VTA. Our results show that acute HFD consumption recruits the mesolimbic system and that the full manifestation of this eating behavior requires the activation of orexin signaling.

摘要

过量食用美味的高能量食物会对健康产生负面影响,且与肥胖及多种饮食失调有关。目前,对于由急性摄入奖励性刺激所激活的神经回路知之甚少。在此,我们运用免疫组织化学、药理学及神经追踪分析等方法,在一项简单的实验测试中,研究中脑边缘系统尤其是食欲素神经元的作用,该实验让未经训练的小鼠自发食用高脂肪饮食(HFD)颗粒2小时。我们发现,急性HFD会激活包括腹侧被盖区(VTA)、伏隔核、中央杏仁核和下丘脑外侧区在内的多个与奖励相关脑区的c-Fos表达。我们还发现:i-HFD介导的口腔感觉刺激是中脑边缘通路激活所必需的;ii-急性HFD对VTA的旁黑质、臂旁色素沉着和束间亚区域的多巴胺神经元有不同程度的激活作用;iii-下丘脑外侧区的食欲素神经元对急性HFD有反应。此外,使用食欲素1受体拮抗剂SB-334867阻断食欲素信号传导,可减少急性HFD的摄入量,并降低VTA中c-Fos的诱导,但不影响所研究的其他中脑边缘核团。最后,我们发现,大多数对急性HFD有反应的食欲素神经元支配VTA。我们的研究结果表明,急性HFD的摄入会激活中脑边缘系统,且这种进食行为的充分表现需要食欲素信号的激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c5/3900715/d3d1c8d81a44/pone.0087478.g001.jpg

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