Table 1.
Sex differences in PAG ECS proteome
Accession | Max fold change over other sex | Anova (p) | |
---|---|---|---|
Detected greater in female | ABHD6_MOUSE* | 1.51 | 0.03 |
MGLL_MOUSE* | 1.44 | 0.01 | |
NAPEP_MOUSE | 1.34 | 0.93 | |
PLD3A_MOUSE | 1.11 | 0.46 | |
PLD2_MOUSE | 1.18 | 0.56 | |
DGLB_MOUSE | 1.05 | 0.56 | |
DGLA_RAT;DGLA_MOUSE | 1.01 | 0.85 | |
Detected greater in male | PHLD_MOUSE | 1.52 | 0.15 |
PLD1_RAT;PLD1_MOUSE | 1.18 | 0.30 | |
PLD3_MOUSE | 1.07 | 0.40 | |
PLD6_MOUSE | 1.15 | 0.84 | |
CNR1_RAT | 2.49 | 0.13 | |
CNRP1_MOUSE;CNRP1_RAT | 1.02 | 0.82 | |
ABD12_MOUSE | 1.02 | 0.79 |
Summary of endocannabinoid system (ECS) enzymes detected in greater quantity in either female or male PAG samples, as measured by quantitative proteomics. The 2-AG hydrolyzing enzymes MAGL and ABHD6 (bold) were detected at significantly higher fold-detection for females vs males (*ABHD6 female vs. male p = 0.03, MAGL female vs. male p = 0.01). Italics indicate study via IHC. CNR2 and FAAH were below the level of detection in this study.
Protein gene abbreviations: ABHD6 alpha/beta-hydrolase domain containing 6; MGLL monoacylglycerol lipase; NAPEP N-acyl-phosphatidylethanolamine-specific phospholipase D; PLD3A phospholipase D3A; PLD2 phospholipase D2; DGLB diacylglycerol lipase beta; DGLA diacylglycerol lipase alpha; PHLD phosphatidylinositol-glycan-specific phospholipase D; PLD1 phospholipase D1; PLD3 phospholipase D3; PLD6 phospholipase D6; CNR1 cannabinoid receptor 1; CNRP1 cannabinoid receptor interacting protein 1; ABD12 alpha/beta-hydrolase domain containing 12