Laboratory of Metabolism, Division of Endocrinology, Diabetology and Nutrition, Department of Internal Medicine, Faculty of Medicine, University of Geneva, 1211 Geneva 4, Switzerland.
Physiol Behav. 2011 Mar 28;102(5):481-4. doi: 10.1016/j.physbeh.2010.12.006. Epub 2010 Dec 14.
Ghrelin is one of the most potent orexigens known to date. Recent data suggested that ghrelin is involved in reward-mediated processes such as the rewarding value of food. Whereas the neuronal pathways by which ghrelin regulates energy balance are well described, those involved in ghrelin-induced reward are still confusing. Therefore, we attempted to delineate the involvement of physiological and pharmacological rises in plasma ghrelin in the modulation of food reward seeking behaviours, using the classical conditioned place preference (CPP) procedure in C57BL6J mice, as well as in mice lacking the ghrelin receptor (GHSR1a -/-). We also determined whether these effects on reward-related behaviours could be partly mediated by cholinergic pathways by pre-treating mice with mecamylamine.
Upon moderate caloric restriction, systemic ghrelin levels increased from 108 ± 21 to 148 ± 39 pg/ml in C57BL6J mice and from 111 ± 24 to 179 ± 41 pg/ml in GHSR1a-null mice. Short exposure to rewarding food elicited a strong CPP and stimulation of locomotor activity in GHSR1a wild-type and C57BL6J mice. Conversely, the GHSR1a -/- mice did not exhibit such a food CPP, despite a negative energy balance. Pharmacological rise in systemic ghrelin further increased the time spent in the food-paired side with a higher CPP score (+71%) and this effect was blunted after cholinergic blockade by mecamylamine.
The ghrelin receptor is obligatory to acquire a food-CPP. The level of plasma ghrelin during conditioning determines the strength of food-induced reward seeking behaviours. The cholinergic pathway partly mediates the further enhancement of food reward induced by pharmacological rises in plasma ghrelin, but not that induced by physiological increases in ghrelin.
胃饥饿素是迄今为止已知的最有效的食欲刺激素之一。最近的数据表明,胃饥饿素参与了奖励介导的过程,例如食物的奖励价值。虽然调节能量平衡的胃饥饿素神经元途径已经得到很好的描述,但参与胃饥饿素诱导的奖励的途径仍然令人困惑。因此,我们试图通过经典条件位置偏好(CPP)程序在 C57BL6J 小鼠中以及在缺乏胃饥饿素受体(GHSR1a -/-)的小鼠中阐明生理和药理学升高血浆胃饥饿素在调节食物奖励寻求行为中的作用。我们还确定了这些对奖励相关行为的影响是否可以部分通过烟碱型乙酰胆碱能受体途径来介导,方法是用美金刚胺预先治疗小鼠。
在适度的热量限制下,系统胃饥饿素水平从 C57BL6J 小鼠的 108 ± 21 pg/ml 增加到 148 ± 39 pg/ml,从 GHSR1a 缺失小鼠的 111 ± 24 pg/ml 增加到 179 ± 41 pg/ml。短暂接触奖励性食物会引起 GHSR1a 野生型和 C57BL6J 小鼠的强烈 CPP 和运动活动刺激。相反,尽管存在负能量平衡,GHSR1a -/- 小鼠也没有表现出这种食物 CPP。系统胃饥饿素的药理学升高进一步增加了与食物配对的一侧的时间,CPP 评分提高了 71%,并且这种作用在烟碱型乙酰胆碱能受体阻断后被削弱。
胃饥饿素受体是获得食物-CPP 的必要条件。调节期间的血浆胃饥饿素水平决定了食物诱导的奖励寻求行为的强度。胆碱能途径部分介导了药理学升高血浆胃饥饿素诱导的食物奖励的进一步增强,但不介导生理升高胃饥饿素诱导的食物奖励的增强。