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Sex dependence of opioid-mediated responses to subanesthetic ketamine in rats

Tommaso Di Ianni, Sedona N. Ewbank, Marjorie R. Levinstein, Matine M. Azadian, Reece C Budinich, Michael Michaelides, Raag D. Airan

Nature Communications January 30, 2024 DOI: 10.1038/s41467-024-45157-7 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study Peer reviewed
Population Rats
Intervention Subanesthetic ketamine
Measures pharmacological functional ultrasound imaging, postsynaptic density, behavioral sensitization, opioid receptor density
Topics Addiction Esketamine Ketamine
Key findings Blocking opioid receptors suppressed neurophysiologic changes evoked by subanesthetic ketamine, but not by a more selective NMDA receptor antagonist, in limbic regions. This opioid-dependent response was evident in males but not females and was reversed by surgical removal of the male gonads. Similar sex-dependent opioid effects were observed for ketamine-evoked postsynaptic density, behavioral sensitization, and opioid receptor density.

Abstract

Subanesthetic ketamine is increasingly used for the treatment of varied psychiatric conditions, both on- and off-label. While it is commonly classified as an N -methyl D-aspartate receptor (NMDAR) antagonist, our picture of ketamine’s mechanistic underpinnings is incomplete. Recent clinical evidence has indicated, controversially, that a component of the efficacy of subanesthetic ketamine may be opioid dependent. Using pharmacological functional ultrasound imaging in rats, we found that blocking opioid receptors suppressed neurophysiologic changes evoked by ketamine, but not by a more selective NMDAR antagonist, in limbic regions implicated in the pathophysiology of depression and in reward processing. Importantly, this opioid-dependent response was strongly sex-dependent, as it was not evident in female subjects and was fully reversed by surgical removal of the male gonads. We observed similar sex-dependent effects of opioid blockade affecting ketamine-evoked postsynaptic density and behavioral sensitization, as well as in opioid blockade-induced changes in opioid receptor density. Together, these results underscore the potential for ketamine to induce its affective responses via opioid signaling, and indicate that this opioid dependence may be strongly influenced by subject sex. These factors should be more directly assessed in future clinical trials. In rats, functional ultrasound imaging reveals that blocking opioid receptors modulates the effects of subanesthetic ketamine on neural activity in males but not in females, with parallel changes in ketamine’s effects on brain structure and behavior.