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Mu opioid receptors in the medial habenula contribute to naloxone aversion

Neuropsychopharmacology (2019) | Download Citation


The medial habenula (MHb) is considered a brain center regulating aversive states. The mu opioid receptor (MOR) has been traditionally studied at the level of nociceptive and mesolimbic circuits, for key roles in pain relief and reward processing. MOR is also densely expressed in MHb, however, MOR function at this brain site is virtually unknown. Here we tested the hypothesis that MOR in the MHb (MHb-MOR) also regulates aversion processing. We used chnrb4-Cre driver mice to delete the Oprm1 gene in chnrb4-neurons, predominantly expressed in the MHb. Conditional mutant (B4MOR) mice showed habenula-specific reduction of MOR expression, restricted to chnrb4-neurons (50% MHb-MORs). We tested B4MOR mice in behavioral assays to evaluate effects of MOR activation by morphine, and MOR blockade by naloxone. Locomotor, analgesic, rewarding, and motivational effects of morphine were preserved in conditional mutants. In contrast, conditioned place aversion (CPA) elicited by naloxone was reduced in both naïve (high dose) and morphine-dependent (low dose) B4MOR mice. Further, physical signs of withdrawal precipitated by either MOR (naloxone) or nicotinic receptor (mecamylamine) blockade were attenuated. These data suggest that MORs expressed in MHb B4-neurons contribute to aversive effects of naloxone, including negative effect and aversive effects of opioid withdrawal. MORs are inhibitory receptors, therefore we propose that endogenous MOR signaling normally inhibits chnrb4-neurons of the MHb and moderates their known aversive activity, which is unmasked upon receptor blockade. Thus, in addition to facilitating reward at several brain sites, tonic MOR activity may also limit aversion within the MHb circuitry.

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We thank the staff at the animal facility of the Neurophenotyping Center Douglas Research Center (Montréal, Canada), as well as Aude Villemain, Eujin Kim, Annie Salesse, Karine Lachapelle, Aimee Lee Luco, and DaWoon Park for animal care and genotyping. We thank the National Institute of Drug Abuse (NIDA) Drug Supply Program for providing us Morphine and the Molecular and Cellular Microscopy Platform (MCMP) of the Douglas Research center.

Author information


  1. McGill University, Faculty of Medicine, Douglas Research Centre, Montreal, Canada

    • L. J. Boulos
    • , S. Ben Hamida
    • , J. Bailly
    • , M. Maitra
    • , A. T. Ehrlich
    • , E. Darcq
    •  & B. L. Kieffer
  2. Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch-Graffenstaden, Strasbourg, France

    • L. J. Boulos
    • , S. Ben Hamida
    • , A. T. Ehrlich
    • , C. Gavériaux-Ruff
    •  & B. L. Kieffer
  3. Université de Strasbourg, Illkirch, France

    • L. J. Boulos
    • , S. Ben Hamida
    • , A. T. Ehrlich
    • , C. Gavériaux-Ruff
    •  & B. L. Kieffer
  4. Centre National de la Recherche Scientifique, UMR7104, Illkirch, France

    • L. J. Boulos
    • , S. Ben Hamida
    • , A. T. Ehrlich
    • , C. Gavériaux-Ruff
    •  & B. L. Kieffer
  5. Institut National de la Santé et de la Recherche Médicale, U 1258, Illkirch, France

    • L. J. Boulos
    • , S. Ben Hamida
    • , A. T. Ehrlich
    • , C. Gavériaux-Ruff
    •  & B. L. Kieffer


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Correspondence to B. L. Kieffer.

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