The endogenous endocannabinoid (eCB) system includes cannabinoid receptor 1 (CB1R), CB2R, and two endogenous ligands (N-arachidonoylethanolamine;? AEA and 2-arachidonoylglycerol, 2AG). Animal findings demonstrate that the eCB system undergoes dynamic changes during adolescence and suggest a significant role in neurodevelopment, especially in CB1R-dense prefrontal, parietal, striatal and limbic brain regions. Research in adults have found that eCB system signaling modulates executive functioning, reward response, and stress and affective processing. Thus, there is strong preclinical evidence that the eCB system plays a substantial role in neuronal activity and neurodevelopment and disruption of or reduced eCB signaling during adolescencemayresultinabnormalneurocognitivedevelopment,riskforpsychopathology,andincreasedrisk for substance use, especially cannabis (CAN) use. Despite this evidence, no study to date has examined the role of the eCB system on neurocognition, mood, or early onset cannabis use and early cannabis subjective effects ex vivo in human youth due to the inherent challenges in employing invasive techniques [i.e., PET studies or collecting CSF]. However, there is now an available bioassay to measure circulating AEA and 2AG in serum collected from blood, that can be measured ex vivo in humans. Serum AEA and 2AG levels reflect both peripheral system synthesis and overflow from the brainand animal evidence has shown that circulating and brain eCB concentrations are robustly and significantly correlated. Further, adult studies have found significant associations between circulating serum eCBs and executive functioning, stress response, reward signaling, affective processing, mood and anxiety symptoms and regular CAN use. Notably, studies relating serumeCBlevelsandneurocognitive,psychopathology,andCANuseoutcomeshavenotyetbeenconducted in youth- despite convincing preclinical evidence that the impact may be greater during these critical neurodevelopmentalyears.Thus,thisR21projectwillbethefirsttoestablishthelinkbetweencirculatingeCB levelsandneurocognitive,psychopathology,andearlyCANuseoutcomesinasubsetof2000youthaged11- 14 who are already enrolled in the longitudinal Adolescent Brain Cognitive Development (ABCD) Study (at 8 geographically-diverse research sites). We will also examine sex differences in these effects. Ultimately, this project will inform policy and health campaigns regarding the role of the eCB system in adolescent developmentandprovidemechanisticinformationregardingthelong-termimpactofCANexposureinyouth.

Public Health Relevance

Preclinicalanimalfindingshavedemonstratedthattheendogenousendocannabinoid(eCB)systemplaysan importantroleinneuronalsignalinganddevelopment,includingduringtheadolescentyears.Adultstudies havefoundalinkbetweeneCBlevelsandoutcomesrelatedtoneurocognition,mood,andmentalhealth, althoughthesestudieshaveneverbeenconductedinyouth.Thisstudyaddressesthisgapinknowledgeby examiningtheroleofeCBlevelsandneurocognitive,moodandmentalhealth,andearlycannabisuse outcomesinasubsetof2,000youthages11-14whoareenrolledinthelongitudinalAdolescentBrain CognitiveDevelopment(ABCD)Study.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21DA049109-02
Application #
10019508
Study Section
Neural Basis of Psychopathology, Addictions and Sleep Disorders Study Section (NPAS)
Program Officer
Pariyadath, Vani
Project Start
2019-09-30
Project End
2021-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Wisconsin Milwaukee
Department
Type
Graduate Schools
DUNS #
627906399
City
Milwaukee
State
WI
Country
United States
Zip Code
53201