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Effects of Cannabinoid Exposure during Neurodevelopment on Future Effects of Drugs of Abuse: A Preclinical Perspective

Aaron Mark Farrelly, Styliani Vlachou

International Journal of Molecular Sciences September 15, 2021 DOI: 10.3390/ijms22189989 (opens in new tab)

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AI-extracted from the abstract
Characteristics Systematic review Peer reviewed
Population Rodents (preclinical studies)
Interventions Δ9-THC cannabinoid agonists
Citations 10
Key findings In rodents, perinatal Δ9-THC exposure affected later opiate and amphetamine reward-related behaviors mainly in males but not cocaine or alcohol effects; adolescent cannabinoid agonist exposure consistently affected opioid responses across sex but not amphetamines or cocaine, with adolescent studies mostly male. The authors conclude that perinatal research is sparse and future work should address sex-specific effects and use more clinically relevant cannabinoid treatments.

Abstract

The endocannabinoid system plays a central role in the earliest stages of embryonic, postnatal and adolescent neurodevelopment. Aberrant activity of this system at key developmental phases has been shown to affect neural development. The aim of this review is to synthesise and analyse preclinical insights within rodent populations, focusing on the effects that perinatal (embryonic, gestational and early postnatal developmental stages) and adolescent (postnatal day 21–60) cannabinoid exposure impose across time on the subsequent activity of various drugs of abuse. Results in rodents show that exposure to cannabinoids during the perinatal and adolescent period can lead to multifaceted behavioural and molecular changes. In the perinatal period, significant effects of Δ9-THC exposure on subsequent opiate and amphetamine reward-related behaviours were observed primarily in male rodents. These effects were not extended to include cocaine or alcohol. In adolescence, various cannabinoid agonists were used experimentally. This array of cannabinoids demonstrated consistent effects on opioids across sex. In contrast, no significant effects were observed regarding the future activity of amphetamines and cocaine. However, these studies focused primarily on male rodents. In conclusion, numerous gaps and limitations are apparent in the current body of research. The sparsity of studies analysing the perinatal period must be addressed. Future research within both periods must also focus on delineating sex-specific effects, moving away from a male-centric focus. Studies should also aim to utilise more clinically relevant cannabinoid treatments.

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