4.8 Article

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

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 116, 期 12, 页码 3229-3239

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI29867

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资金

  1. NIAAA NIH HHS [P50 AA015632] Funding Source: Medline
  2. NIA NIH HHS [AG022880, R01 AG022880] Funding Source: Medline
  3. NIDDK NIH HHS [P01 DK056863, R01 DK070723, R01 DK074386, R01 DK060711, DK060711, DK074386, DK070723, R01 DK069987, DK056863, DK069987] Funding Source: Medline
  4. NIMH NIH HHS [MH057483, R01 MH057483, R37 MH014092, MH014092, R01 MH014092] Funding Source: Medline
  5. NINDS NIH HHS [NS041725, R01 NS041725] Funding Source: Medline

向作者/读者索取更多资源

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.

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