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Astrocytic Ensemble at vHip-NAc synapses Modulates Cognitive Impairments Induced by Chronic THC Exposure

Marta Navarrete, Cristina Martín-Monteagudo, Nagore Puente, Pedro Grandes, Giovanni Marsicano, Ana Covelo

preprint DOI: 10.21203/rs.3.rs-5999833/v1 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study in mice
Population Mice (wild-type and astrocyte-specific p38αMAPK knockout)
Interventions Tetrahydrocannabinol (THC) AstroLight tool
Duration Chronic THC exposure (duration not specified)
Measures fiber photometry (astrocytic calcium and glutamate dynamics), electrophysiological assessments, behavioral assessments (spatial learning)
Topics Cannabis
Key findings Chronic THC increased astrocytic calcium activity and glutamatergic tone in the nucleus accumbens via p38αMAPK signaling; astrocytic glutamate release in a ventral hippocampus-to-nucleus accumbens ensemble was required for THC-induced cognitive deficits, and attenuating THC-induced calcium activity in this ensemble prevented spatial learning and synaptic plasticity impairments.

Abstract

Abstract Cannabis is the most widely used illicit drug, particularly during adolescence, and its consumption disrupts glutamate homeostasis and synaptic plasticity in the nucleus accumbens (NAc). While astrocytic cannabinoid receptors (CB1Rs) are known to modulate synaptic plasticity and behavior, the extent to which specific astrocytic ensembles drive tetrahydrocannabinol (THC)-induced alterations remains unclear. Here, we identify a functionally distinct accumbal astrocytic ensemble, related to ventral hippocampus-NAc (vHip->NAc) circuit, that is critical for THC-induced synaptic and behavioral impairments. Using fiber photometry, we monitored astrocytic calcium and glutamate dynamics within the NAc of wild-type and p38αMAPK −/− (Astrop38α) mice following chronic THC exposure, complemented by electrophysiological and behavioral assessments. Additionally, we employed AstroLight tool to selectively manipulate this astrocytic ensemble. Our findings reveal that: (1) THC increases astrocytic calcium activity and glutamatergic tone within the NAc; (2) the THC-induced glutamatergic alterations are absent in Astrop38α mice, implicating p38αMAPK signaling in astrocyte-mediated plasticity; (3) astrocytic glutamate release within the vHip->NAc ensemble is required for THC-induced cognitive deficits; and (4) targeted attenuation of THC-induced calcium activity in this ensemble prevents both spatial learning and synaptic plasticity impairments. These results highlight a critical role for astrocytic ensembles in shaping behavior and emphasize their potential as therapeutic targets for mitigating the cognitive consequences of THC exposure.

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Study Year Design Participants
Cognitive Impairment Induced by Delta9-tetrahydrocannabinol Occurs through Heteromers between Cannabinoid CB1 and Serotonin 5-HT2A Receptors Mice 2015 Preclinical study
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Long-term hippocampal interneuronopathy drives sex-dimorphic spatial memory impairment induced by prenatal THC exposure Mice prenatally exposed to THC, including conditional CB1R knockout mice 2020 Animal experimental study
Chronic cannabis promotes pro-hallucinogenic signaling of 5-HT2A receptors through Akt/mTOR pathway Mice exposed to chronic THC early in life 2018 Animal experimental study
Effects of cannabinoid drugs on the deficit of prepulse inhibition of startle in an animal model of schizophrenia: the SHR strain Spontaneously hypertensive rats (SHRs) and Wistar rats 2014 Animal experimental study

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