Adolescent ketamine exposure impairs spike timing-dependent plasticity and GABAergic transmission in pyramidal neurons of the mouse prefrontal cortex.

Summary

Adolescent exposure to subanaesthetic ketamine leads to lasting deficits in GABAergic transmission and alters spike-timing-dependent plasticity (STDP) in the medial prefrontal cortex (mPFC) of adult mice. Specifically, ketamine-exposed mice showed reduced frequencies of inhibitory postsynaptic currents and a shift from synaptic depression to potentiation during STDP. These changes indicate that NMDA receptor hypofunction during adolescence disrupts the excitatory-inhibitory balance necessary for normal cognitive function.

Study at a glance

Abstract

The medial prefrontal cortex (mPFC) undergoes extensive GABAergic interneuron maturation during adolescence, a process that establishes excitatory-inhibitory balance and supports adult cognitive function. Disruptions during this critical developmental period contribute to neuropsychiatric disorders, yet the enduring consequences for adult synaptic plasticity remain poorly understood. Here we examine how adolescent NMDA receptor (NMDAR) hypofunction impacts adult mPFC transmission and plasticity. We exposed adolescent mice to subanaesthetic ketamine and performed whole-cell patch-clamp recordings in adulthood to examine excitatory and inhibitory synaptic currents and spike timing-dependent plasticity (STDP). Ketamine-exposed mice exhibited persistent GABAergic transmission deficits in pyramidal neurons (PyNs), as evidenced by reduced spontaneous and miniature IPSC frequencies and elevated paired-pulse ratios, consistent with impaired presynaptic GABA release and reduced functional output of parvalbumin-positive interneurons (PV-INs). PyN STDP was altered in ketamine-exposed mice, with spike pairings in the post-before-pre order inducing potentiation, in contrast to the synaptic depression observed in vehicle mice. Together, these results demonstrate that adolescent NMDAR hypofunction produces enduring impairments in PV-IN-mediated inhibitory transmission and disrupts the bidirectional expression of STDP in the adult mPFC. This shift in plasticity rules reflects a loss of inhibitory control over synaptic integration and indicates that developmental NMDAR disruption produces persistent alterations in cortical circuit function. Together, these findings provide mechanistic insight into how adolescent NMDAR hypofunction leads to enduring circuit dysfunction, with relevance to neurodevelopmental disorders emerging during adolescence. KEY POINTS: Adolescence is a critical period for GABAergic maturation in the medial prefrontal cortex (mPFC). Adolescent ketamine exposure reverses adult mPFC spike timing-dependent plasticity from depression to potentiation. Adolescent ketamine exposure impairs GABAergic transmission in adulthood. Adolescent ketamine exposure reduces the functional output of parvalbumin-positive interneurons. These findings demonstrate that adolescent NMDA receptor hypofunction disrupts adult prefrontal inhibitory balance and reverses plasticity polarity.

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