Dose-dependent effect of acute THC on extinction memory recall and fear renewal: a randomized, double-blind, placebo-controlled study.
Zabik et al.·PsychopharmacologyImpact 2.8
MixedGRADEModerate8 citations
Samplen = 36 Pat.
Duration24 hours and one week follow-up
ControlPlacebo
EndpointfMRI activation
Blindingdoppelblind
DesignRCT
Cannabinoidthc
Max. dose10.0 mg
Routeoral
”Key finding
5 mg THC showed increased brain activation in ACC and PFC during early fear renewal after 24 h; 10 mg THC showed increased hippocampal activation during extinction recall and PFC activation during fear renewal after one week – dose-dependent effects on fear memory processes.
Summary
RCT, n=36 adults with PTSD, randomized to placebo (n=11), 5 mg THC (n=11) or 10 mg THC (n=14) before extinction learning. 24h after THC administration: 5 mg THC → increased ACC and PFC activation during early fear renewal. One week later: 10 mg THC → increased hippocampal activation during extinction recall and PFC activation during fear renewal. Dose- and timing-dependent effects on fear memory processes.
InterventionOral THC 5 mg or 10 mg, single dose before extinction learning
C
ControlPlacebo (oral)
O
Outcome5 mg THC: increased ACC and PFC activation during early fear renewal after 24 h; 10 mg THC: increased hippocampal activation during extinction recall and PFC activation during fear renewal after one week
Confidence in the evidence
Very lowLowModerateHigh
Moderate
The third of four GRADE levels, the effect estimate is probably reliable.
Downgraded for
Imprecision
Quality profile
Sample size★★★★★
BlindingDouble-blind
Effect sizeMixed
Citations / year★★★★★
Authors
Zabik NL, Iadipaolo A, Peters CA, Baglot SL, Hill MN, Rabinak CA
Rationale: Prior work from our lab and others demonstrates that the endocannabinoid system is a promising avenue for improving fear memory deficits in posttraumatic stress disorder (PTSD). Specifically, 7.5 mg of delta-9-tetrahydrocannabinol (THC) decreases fear responding in healthy adults and increases prefrontal cortex activation during extinction learning and fear renewal in adults with
Ptsd. Objectives: The present study will determine whether there is a dose-dependent effect of THC on short-term (24 h) and long-term (one week) fear learning and memory in adults with
Ptsd. Methods: Using a randomized, double-blind, placebo-controlled design, N = 36 adults with PTSD completed the study and were randomized to receive placebo (PBO, n = 11), 5 mg of THC (n = 11), or 10 mg of THC (n = 14) prior to fear extinction learning. Participants completed a Pavlovian conditioning paradigm with extinction recall and fear renewal occurring 24 h and one week later, where we measured concurrent functional imaging and behavioral responses.
Results: Twenty-four hours after drug administration, individuals with PTSD given 5 mg of THC exhibited greater anterior cingulate cortex and prefrontal cortex activation during early fear renewal. One week later, individuals given 10 mg of THC exhibited greater hippocampus activation during extinction recall and prefrontal cortex activation during fear renewal.
Conclusions: These data suggest that dosing and timing are critical for facilitating fear memory processes in PTSD, and that low-dose oral THC prior to extinction learning can affect brain indices of fear learning and memory both acutely and one week after administration.