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. 2017 Feb 16;11(4):329–337. doi: 10.1080/17474124.2017.1292851

Table 1.

Differential expression of ECS components in human IBD compared to controls as described in the literature.

    IBD
 
ECS component UC CD References
Receptors CB1 No change, downregulation, or upregulation Upregulation [2628]
CB2 Upregulation   [27,30]
Upregulation (protein) or no change (mRNA, protein) [26,28]
Ligands AEA Upregulation   [10]
Downregulation [26]
2-AG No change [10,26]
Synthesizing enzymes NAPE-PLD Downregulation or reduced activity [26,27]
DAGL Upregulation   [27]
Degrading enzymes FAAH No change (epithelium) or upregulation (immune cells) or increased activity [26,27]
MGL Upregulation   [27]

CB1: cannabinoid receptor 1; CB2: cannabinoid receptor 2; AEA: anandamide; 2-AG: 2-arachidonoylglycerol; ECS: endocannabinoid system; IBD: inflammatory bowel disease; NAPE-PLD: N-acyl phosphatidylethanolamine phospholipase D; DAGL: diacylglycerol lipase; FAAH: fatty acid amide hydrolase; MGL: monoacylglycerol lipase.