Mechanism-guided identification of antidepressant G protein-coupled receptor drug targets

  • Cell. 2026 Apr 30;189(9):2612-2632.e24. doi: 10.1016/j.cell.2026.04.006.
Hermany Munguba  1 ,  Anisul Arefin  2 ,  Ryota Hasegawa  3 ,  Luca Posa  2 ,  Giovanna R Romano  2 ,  Teja N Peddada  4 ,  Alexander Donatelle  1 ,  Ashna Singh  1 ,  Vanessa A Gutzeit  2 ,  Akshara Vijay  2 ,  Prerana Vaddi  2 ,  Melanie Kristt  2 ,  Daniel Shaver  3 ,  Shanjida Hoque  2 ,  Johannes Broichhagen  5 ,  Joseph M Stujenske  6 ,  Francis S Lee  3 ,  Evan O'Brien  7 ,  Joshua Levitz  8 ,  Conor Liston  9
Affiliations
  • 1. Department of Biochemistry and Biophysics, Weill Cornell Medicine, New York, NY, USA; Department of Psychiatry, Weill Cornell Medicine, New York, NY, USA.
  • 2. Department of Biochemistry and Biophysics, Weill Cornell Medicine, New York, NY, USA.
  • 3. Department of Psychiatry, Weill Cornell Medicine, New York, NY, USA.
  • 4. Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA.
  • 5. Department of Chemical Biology, Forschungsinstitut für Molekulare Pharmakologie, Berlin, Germany.
  • 6. Department of Psychiatry, Weill Cornell Medicine, New York, NY, USA; Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
  • 7. Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA; Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • 8. Department of Biochemistry and Biophysics, Weill Cornell Medicine, New York, NY, USA; Department of Psychiatry, Weill Cornell Medicine, New York, NY, USA. Electronic address: [email protected].
  • 9. Department of Psychiatry, Weill Cornell Medicine, New York, NY, USA. Electronic address: [email protected].
Abstract

Depression is driven by dysfunction in discrete neural circuits, but a deeper understanding of the underlying molecular and synaptic mechanisms is needed to guide the development of therapeutics. Here, we decipher the mechanisms of action of the fast-acting antidepressant ketamine to enable the identification of G protein-coupled receptor (GPCR) antidepressant targets. We find that the behavioral effects of ketamine rely on mu-opioid receptors (MORs), which are enriched in somatostatin-expressing interneurons (Sst+ INs) in the medial prefrontal cortex (mPFC). Chronic stress drives presynaptic hypertrophy of mPFC Sst+ INs and excessive inhibition of pyramidal neurons, which is rescued by ketamine. Motivated by these findings, we use RNA Sequencing to identify mPFC Sst+ IN-enriched GPCRs and validate the antidepressant potential of promising targets. Synergistic targeting of multiple GPCRs enables potent antidepressant-like responses with reduced side effects. Together, these findings reveal a general approach to identifying therapeutic GPCR targets for brain disorders.

Keywords
GPCR; antidepressant; ketamine; neuromodulation; opioid receptor; photopharmacology; prefrontal cortex; somatostatin interneuron; synaptic plasticity; two-photon imaging.
Products