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Adolescent Δ9-THC Exposure Differentially Affects Mice Depending on Their Personality.

Dilorom Begmatova, Liudmila Vinnikova, Natalya Zemliana, Kenneth Blum, Panayotis K Thanos, Natalya M Kogan, Albert Pinhasov

Pharmaceuticals (Basel, Switzerland) June 29, 2026 DOI: 10.3390/ph19071009 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study Peer reviewed
Population Selectively bred Dominant and Submissive Sabra mice
Intervention Δ9-tetrahydrocannabinol (THC)
Duration Adolescent exposure, assessed in adulthood
Topics Cannabis
Keywords Adolescence Dominant-submissive relationship
Key findings Adolescent THC exposure produced opposite effects on anxiety-like behavior and NMDA receptor sensitivity in Dominant versus Submissive mice, indicating that stress-coping traits modulate long-term outcomes.

Abstract

Background: Adolescence is a sensitive period for brain maturation during which exposure to Δ9-tetrahydrocannabinol (THC) can induce long-lasting neurobehavioral alterations. Yet, preclinical and clinical studies report inconsistent long-term outcomes of adolescent THC exposure, ranging from clear impairments to apparently normalizing effects. We hypothesize that these discrepancies reflect stable individual differences in stress-coping abilities.

Methods: To test this, selectively bred Dominant (Dom; stress-resilient, risk-prone) and Submissive (Sub; stress-vulnerable, depressive-like) Sabra mice received THC or vehicle during adolescence and were assessed in adulthood.

Results: Anxiety-like and exploratory behavior, measured in the hole-board test, were differentially affected by THC as a function of stress vulnerability: in Sub mice, THC increased exploration and reduced anxiety-like behavior, whereas in Dom mice THC produced the opposite pattern. Recognition memory, evaluated by the novel object recognition test, showed modest, line-dependent alterations. Sensitivity to N-methyl-D-aspartate (NMDA) receptor hypofunction, a widely used index of vulnerability to schizophrenia-like symptoms, was examined using MK-801-induced locomotion. Adolescent THC potentiated MK-801-evoked hyperlocomotion in Dom mice but attenuated it in Sub mice.

Conclusions: In the context of increasing medical and recreational cannabis exposure, these in vivo findings suggest that stress-vulnerability-related traits may be an important variable to consider in future preclinical and translational studies of adolescent THC exposure.

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