| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2792838 | Cell Metabolism | 2011 | 8 Pages |
SummarySerotonin (5-HT) and leptin play important roles in the modulation of energy balance. Here we investigated mechanisms by which leptin might interact with CNS 5-HT pathways to influence appetite. Although some leptin receptor (LepRb) neurons lie close to 5-HT neurons in the dorsal raphe (DR), 5-HT neurons do not express LepRb. Indeed, while leptin hyperpolarizes some non-5-HT DR neurons, leptin does not alter the activity of DR 5-HT neurons. Furthermore, 5-HT depletion does not impair the anorectic effects of leptin. The serotonin transporter-cre allele (Sertcre) is expressed in 5-HT (and developmentally in some non-5-HT) neurons. While Sertcre promotes LepRb excision in a few LepRb neurons in the hypothalamus, it is not active in DR LepRb neurons, and neuron-specific Sertcre-mediated LepRb inactivation in mice does not alter body weight or adiposity. Thus, leptin does not directly influence 5-HT neurons and does not meaningfully modulate important appetite-related determinants via 5-HT neuron function.
► 5-HT neurons do not express leptin receptors and are not directly leptin responsive ► 5-HT depletion does not impair anorectic leptin action ► Sertcre-mediated neuronal LepRb deletion does not affect DR leptin action, body weight, or adiposity ► Thus, leptin does not meaningfully influence appetite or body weight via brain 5-HT
