Department of Psychology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Biol Psychiatry. 2013 May 1;73(9):915-23. doi: 10.1016/j.biopsych.2012.07.002. Epub 2012 Aug 11.
The stomach-derived hormone ghrelin drives higher-order feeding processes related to food reward and food seeking via central nervous system signaling at its receptor (GHSR1A). The specific nuclei mediating these effects are only partially understood. Here, we use a rat model to examine whether ghrelin signaling in the ventral subregion of the hippocampus (VHPC), a brain substrate of recent interest in energy balance control, affects learned and motivational aspects of feeding behavior.
The effects of VHPC ghrelin administration were examined on feeding-relevant behavioral paradigms, including meal pattern analysis, operant lever pressing for sucrose, and conditioned stimulus-induced feeding. The intracellular signaling and downstream neuronal pathways stimulated by VHPC GHSR1A activation were assessed with immunoblot analysis and behavioral pharmacology.
Ghrelin delivery to the VHPC but not the dorsal hippocampus increased food intake primarily by increasing meal frequency. Intra-VHPC ghrelin delivery also increased willingness to work for sucrose and increased spontaneous meal initiation in nondeprived rats after the presentation of a conditioned stimulus that previously signaled meal access when the rats were food-restricted. The food intake enhancing effects of VHPC ghrelin were blocked by co-administration of a phosphoinositide 3-kinase (PI3K) inhibitor (LY294002). Immunoblot analyses provided complementary support for ghrelin activated PI3K-Akt signaling in the VHPC and revealed that this activation is blunted with high-fat diet consumption. Other immunoblot results show that VHPC GHSR1A signaling activates downstream dopaminergic activity in the nucleus accumbens.
These findings illuminate novel neuronal and behavioral mechanisms mediating ghrelinergic control of cognitive aspects of feeding control.
胃来源的激素 ghrelin 通过其受体 (GHSR1A) 在中枢神经系统信号传导中驱动与食物奖励和食物寻求相关的更高阶进食过程。介导这些效应的特定核仅部分被理解。在这里,我们使用大鼠模型来研究海马腹侧 subregion(VHPC)中的 ghrelin 信号是否影响能量平衡控制中最近感兴趣的大脑底物的进食行为的学习和动机方面。
检查 VHPC ghrelin 给药对与进食相关的行为范式的影响,包括进食模式分析、蔗糖操作杆按压和条件刺激诱导的进食。通过免疫印迹分析和行为药理学评估 VHPC GHSR1A 激活刺激的细胞内信号和下游神经元途径。
ghrelin 递送至 VHPC 但不是背侧海马增加了食物摄入量,主要是通过增加进食频率。内源性 VHPC ghrelin 给药还增加了蔗糖的工作意愿,并在非饥饿大鼠中增加了条件刺激后自发进食的起始,该条件刺激在大鼠处于食物限制时曾经表示进食进入。VHPC ghrelin 的摄食增强作用被 PI3K 抑制剂 (LY294002) 的共同给药阻断。免疫印迹分析为 ghrelin 在 VHPC 中激活 PI3K-Akt 信号提供了补充支持,并表明这种激活在高脂肪饮食消耗时减弱。其他免疫印迹结果表明,VHPC GHSR1A 信号在伏隔核中激活下游多巴胺能活性。
这些发现阐明了介导 ghrelin 对进食控制的认知方面的控制的新型神经元和行为机制。