4.8 Article

AgRP neurons control feeding behaviour at cortical synapses via peripherally derived lysophospholipids

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NATURE METABOLISM
卷 4, 期 6, 页码 683-+

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NATURE PORTFOLIO
DOI: 10.1038/s42255-022-00589-7

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资金

  1. Deutsche Forschungsgemeinschaft [FB 1039, 1193, 1451, 1080]
  2. Germany's Excellence Strategy [EXC 2030, 390661388]
  3. European Research Council
  4. Boehringer-Ingelheim Foundation
  5. Stiftung Rheinland-Pfalz
  6. InfectControl [03ZZ0826, 03ZZ0835]
  7. German Research Foundation [FOR2107, DA1151/5-1, DA1151/5-2, SFB-TRR58, C09, Z02]
  8. Interdisciplinary Center for Clinical Research of the Medical Faculty of Munster [Dan3/012/17]
  9. Federal Ministry of Education and Research [01ZZ9603, 01ZZ0103, 01ZZ0403, 03ZIK012]
  10. Ministry of Cultural Affairs
  11. Social Ministry of the Federal State of Mecklenburg-West Pomerania
  12. Siemens Healthineers
  13. Erlangen
  14. European Union
  15. European Social Fund grant [EFOP-3.6.216-2017-0008]
  16. NKFIH [KKP126998]
  17. NIH [AG052005, AG067329, DK126447]
  18. Klarman Family Foundation

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Hypothalamic AgRP neurons control cortical excitability, hyperphagia, and body weight gain by regulating peripheral and central levels of lysophospholipids in association with food deprivation. Changes in peripheral metabolism affect brain lipid levels and cortical excitability. Lysophosphatidic acid (LPA) species are elevated after fasting and contribute to higher cortical excitability. This effect is mediated by hypothalamic AgRP neurons and plays a role in fasting-induced hyperphagia.
Hypothalamic AgRP neurons are shown to control peripheral and central levels of lysophospholipids in association with food deprivation, which leads to cortical excitability, hyperphagia and body weight gain. Phospholipid levels are influenced by peripheral metabolism. Within the central nervous system, synaptic phospholipids regulate glutamatergic transmission and cortical excitability. Whether changes in peripheral metabolism affect brain lipid levels and cortical excitability remains unknown. Here, we show that levels of lysophosphatidic acid (LPA) species in the blood and cerebrospinal fluid are elevated after overnight fasting and lead to higher cortical excitability. LPA-related cortical excitability increases fasting-induced hyperphagia, and is decreased following inhibition of LPA synthesis. Mice expressing a human mutation (Prg-1(R346T)) leading to higher synaptic lipid-mediated cortical excitability display increased fasting-induced hyperphagia. Accordingly, human subjects with this mutation have higher body mass index and prevalence of type 2 diabetes. We further show that the effects of LPA following fasting are under the control of hypothalamic agouti-related peptide (AgRP) neurons. Depletion of AgRP-expressing cells in adult mice decreases fasting-induced elevation of circulating LPAs, as well as cortical excitability, while blunting hyperphagia. These findings reveal a direct influence of circulating LPAs under the control of hypothalamic AgRP neurons on cortical excitability, unmasking an alternative non-neuronal route by which the hypothalamus can exert a robust impact on the cortex and thereby affect food intake.

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