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Ghrelin modulates the activity and synaptic input organization of midbrain dopamine neurons while promoting appetite
Alfonso Abizaid, … , Xiao-Bing Gao, Tamas L. Horvath
Alfonso Abizaid, … , Xiao-Bing Gao, Tamas L. Horvath
Published December 1, 2006
Citation Information: J Clin Invest. 2006;116(12):3229-3239. https://doi.org/10.1172/JCI29867.
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Research Article Metabolism

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

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Abstract

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.

Authors

Alfonso Abizaid, Zhong-Wu Liu, Zane B. Andrews, Marya Shanabrough, Erzsebet Borok, John D. Elsworth, Robert H. Roth, Mark W. Sleeman, Marina R. Picciotto, Matthias H. Tschöp, Xiao-Bing Gao, Tamas L. Horvath

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Figure 4

Ghrelin alters inhibitory and excitatory inputs of VTA DA cells.

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Ghrelin alters inhibitory and excitatory inputs of VTA DA cells.
(A and ...
(A and B) Appositions between vGlut2-immunoreactive (red) and TH-immunopositive (green) VTA perikarya were significantly greater in ghrelin-treated animals compared with saline-treated controls. In contrast, appositions between GAD-67–immunolabeled boutons and TH-immunoreactive VTA perikarya were significantly lower in ghrelin-treated animals compared with saline-treated controls. Scale bars: 10 μm. (C) Corresponding to the observed changes in the number of synapses by light and electron microscopy, ghrelin treatment induced a significant elevation in the frequency of mEPSCs compared with saline controls. (D) Conversely, ghrelin administration triggered a significant decrease in the frequency of mIPSCs that was also in line with the light and electron microscopy results. †P < 0.05 versus respective saline-treated controls.

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