Ghrelin modulates the activity and synaptic input organization of midbrain dopamine neurons while promoting appetite

被引:724
作者
Abizaid, Alfonso
Liu, Zhong-Wu
Andrews, Zane B.
Shanabrough, Marya
Borok, Erzsebet
Elsworth, John D.
Roth, Robert H.
Sleeman, Mark W.
Picciotto, Marina R.
Tschop, Matthias H.
Gao, Xiao-Bing
Horvath, Tamas L.
机构
[1] Yale Univ, Sch Med, Comparat Med Sect, New Haven, CT 06519 USA
[2] Yunyang Med Coll, Dept Neurobiol, Hubei, Peoples R China
[3] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[4] Regeneron Inc, Tarrytown, NY USA
[5] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT USA
[6] Univ Cincinnati, Dept Psychiat, Cincinnati, OH USA
[7] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT 06519 USA
关键词
D O I
10.1172/JCI29867
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The gut hormone ghrelin targets the brain to promote food intake and adiposity. The ghrelin receptor growth hormone secretagogue 1 receptor (GHSR) is present in hypothalamic centers controlling energy metabolism as well as in the ventral tegmental area (VTA), a region important for motivational aspects of multiple behaviors, including feeding. Here we show that in mice and rats, ghrelin bound to neurons of the VTA, where it triggered increased dopamine neuronal activity, synapse formation, and dopamine turnover in the nucleus accumbens in a GHSR-dependent manner. Direct VTA administration of ghrelin also triggered feeding, while intra-VTA delivery of a selective GHSR antagonist blocked the orexigenic effect of circulating ghrelin and blunted rebound feeding following fasting. In addition, ghrelin- and GHSR-deficient mice showed attenuated feeding responses to restricted feeding schedules. Taken together, these data suggest that the mesolimbic reward circuitry is targeted by peripheral ghrelin to influence physiological mechanisms related to feeding.
引用
收藏
页码:3229 / 3239
页数:11
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