4.8 Article

Control of aversion by glycine-gated GluN1/GluN3A NMDA receptors in the adult medial habenula

期刊

SCIENCE
卷 366, 期 6462, 页码 250-+

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aax1522

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资金

  1. Emergence Sorbonne [S17JRSU003]
  2. CNRS [PICS 7415]
  3. European Research Council [693021]
  4. ERC-FRONTHAL [742595]
  5. National Institute of Drug Abuse [05010]
  6. National Institute on Alcohol Abuse and Alcoholism [16658]
  7. FRM grant [FDT20100919977]
  8. Paris School of Neuroscience Chair of Excellence award
  9. NARSAD Y.I. Award
  10. [(NKTH-)ANR-09-BLAN-0401]
  11. [ANR-17-CE16-0014]
  12. [FK124434]
  13. [2017-1.2.1-NKP-2017-00002]
  14. European Research Council (ERC) [693021, 742595] Funding Source: European Research Council (ERC)

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The unconventional N-methyl-D-aspartate (NMDA) receptor subunits GluN3A and GluN3B can, when associated with the other glycine-binding subunit GluN1, generate excitatory conductances purely activated by glycine. However, functional GluN1/GluN3 receptors have not been identified in native adult tissues. We discovered that GluN1/GluN3A receptors are operational in neurons of the mouse adult medial habenula (MHb), an epithalamic area controlling aversive physiological states. In the absence of glycinergic neuronal specializations in the MHb, glial cells tuned neuronal activity via GluN1/GluN3A receptors. Reducing GluN1/GluN3A receptor levels in the MHb prevented place-aversion conditioning. Our study extends the physiological and behavioral implications of glycine by demonstrating its control of negatively valued emotional associations via excitatory glycinergic NMDA receptors.

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