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. Author manuscript; available in PMC: 2022 Mar 2.
Published in final edited form as: Prog Neuropsychopharmacol Biol Psychiatry. 2020 Sep 6;106:110096. doi: 10.1016/j.pnpbp.2020.110096

Table 5.

Postmortem studies of endocannabinoid metabolism in psychotic disorders.

1Metabolic enzymes
Condition & brain region n (cases/controls) AEA/PEA/OEA 2-AG AEA 2-AG Reference
Dorsolateral prefrontal cortex
 Schizophrenia 42/42 - - - n.s. DAGL Volk et al., 2010
n.s. MAGL
 Schizophrenia 42/42 - - - n.s. ABHD6 Volk et al., 2013
  >15 years duration2 30/42 n.s.ABHD6
  <15 years duration2 12/42 ↑ABHD6
 Schizophrenia 19/19 n.s.AEA n.s.
FAAH,
↑FAAH activity
n.s. MAGL Muguruza et al., 2013;
Muguruza et al., 2019
n.s.PEA
n.s.OEA
Superior frontal gyrus (anterior)
 Schizophrenia 27/396 n.s.AEA - - (Yu et al., 2018)
Hippocampus
 Schizophrenia 19/19 ↓AEA - - (Muguruza et al., 2013)
n.s.PEA
n.s.OEA
Cerebellum
 Schizophrenia 19/19 ↓AEA n.s. - - (Muguruza et al., 2013)
↓PEA
n.s.OEA

↑: higher; ↓: lower; n.s: no significant difference from controls; -: no available data;

AEA: anandamide; PEA: N-palmitoylethanolamide; OEA: N-oleoylethanolamide; 2-AG: 2-arachidonoyglycerol; NAPE-PLD: N-acyl phosphatidylethanolamine phospholipase D; FAAH: fatty acid amide hydrolase; DAGL: diacylglycerol lipase; MAGL: monoacylglycerol lipase; ABHD6: α/β-hydrolase domain-containing 6;

1

Results reflect mRNA levels unless noted as enzyme activity.

2

This is a subgroup within Volk et al., 2013 study.