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Zebrafish behavioural profiling identifies GABA and serotonin receptor ligands related to sedation and paradoxical excitation

Author

Listed:
  • Matthew N. McCarroll

    (University of California)

  • Leo Gendelev

    (University of California)

  • Reid Kinser

    (University of California)

  • Jack Taylor

    (University of California)

  • Giancarlo Bruni

    (Massachusetts General Hospital, Harvard Medical School
    Harvard Medical School)

  • Douglas Myers-Turnbull

    (University of California)

  • Cole Helsell

    (University of California)

  • Amanda Carbajal

    (San Francisco State University)

  • Capria Rinaldi

    (University of California)

  • Hye Jin Kang

    (University of North Carolina Chapel Hill Medical School)

  • Jung Ho Gong

    (Brown University)

  • Jason K. Sello

    (Brown University)

  • Susumu Tomita

    (Yale University School of Medicine)

  • Randall T. Peterson

    (Massachusetts General Hospital, Harvard Medical School
    University of Utah)

  • Michael J. Keiser

    (University of California
    University of California)

  • David Kokel

    (University of California
    University of California)

Abstract

Anesthetics are generally associated with sedation, but some anesthetics can also increase brain and motor activity—a phenomenon known as paradoxical excitation. Previous studies have identified GABAA receptors as the primary targets of most anesthetic drugs, but how these compounds produce paradoxical excitation is poorly understood. To identify and understand such compounds, we applied a behavior-based drug profiling approach. Here, we show that a subset of central nervous system depressants cause paradoxical excitation in zebrafish. Using this behavior as a readout, we screened thousands of compounds and identified dozens of hits that caused paradoxical excitation. Many hit compounds modulated human GABAA receptors, while others appeared to modulate different neuronal targets, including the human serotonin-6 receptor. Ligands at these receptors generally decreased neuronal activity, but paradoxically increased activity in the caudal hindbrain. Together, these studies identify ligands, targets, and neurons affecting sedation and paradoxical excitation in vivo in zebrafish.

Suggested Citation

  • Matthew N. McCarroll & Leo Gendelev & Reid Kinser & Jack Taylor & Giancarlo Bruni & Douglas Myers-Turnbull & Cole Helsell & Amanda Carbajal & Capria Rinaldi & Hye Jin Kang & Jung Ho Gong & Jason K. Se, 2019. "Zebrafish behavioural profiling identifies GABA and serotonin receptor ligands related to sedation and paradoxical excitation," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11936-w
    DOI: 10.1038/s41467-019-11936-w
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