4.8 Article

MC4R-expressing glutamatergic neurons in the paraventricular hypothalamus regulate feeding and are synaptically connected to the parabrachial nucleus

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.1407843111

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Funding

  1. National Institutes of Health (NIH) [R01 DK096010, R01 DK089044, R01 DK071051, R01 DK075632, R37 DK053477]
  2. Boston Nutrition Obesity Research Center Transgenic Core [P30 DK046200]
  3. Boston Area Diabetes Endocrinology Research Center Transgenic Core [P30 DK57521]
  4. NIH [R01 DK088423, RL1 DK081185, P01 DK088761, R37 DK053301, F32 DK078478, K08 DK071561, F32 DK089710]
  5. American Diabetes Association Mentor-Based Fellowship

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Activation of melanocortin-4 receptors (MC4Rs) restrains feeding and prevents obesity; however, the identity, location, and axonal projections of the neurons bearing MC4Rs that control feeding remain unknown. Reexpression of MC4Rs on single-minded 1 (SIM1)(+) neurons in mice otherwise lacking MC4Rs is sufficient to abolish hyperphagia. Thus, MC4Rs on SIM1(+) neurons, possibly in the paraventricular hypothalamus (PVH) and/or amygdala, regulate food intake. It is unknown, however, whether they are also necessary, a distinction required for excluding redundant sites of action. Hence, the location and nature of obesity-preventing MC4R-expressing neurons are unknown. Here, by deleting and reexpressing MC4Rs from cre-expressing neurons, establishing both necessity and sufficiency, we demonstrate that the MC4R-expressing neurons regulating feeding are SIM1(+), located in the PVH, glutamatergic and not GABAergic, and do not express oxytocin, corticotropin-releasing hormone, vasopressin, or prodynorphin. Importantly, these excitatory MC4R-expressing PVH neurons are synaptically connected to neurons in the parabrachial nucleus, which relays visceral information to the forebrain. This suggests a basis for the feeding-regulating effects of MC4Rs.

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