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Table 1 Summary of endocannabinoid (EC) molecules identified in circulation and tissues of endometriosis (EMS) patients. Most prominent ECs in circulation such as N-arachidonoylethanolamine (AEA), 2-arachidonoylglycerol (2-AG), palmitoylethanolamide (PEA), and oleoylethanolamide (OEA) were found to be altered in circulation. PEA, fatty acid amide hydrolase (FAAH), and N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD) were also found to be altered in the EMS lesions, along with cannabinoid receptors 1 (CB1) and (CB2) 2 and transient receptor potential cation channel subfamily V member 1 (TRPV1)

From: Role of the endocannabinoid system in the pathophysiology of endometriosis and therapeutic implications

Area

Endocannabinoid system component

Levels

Significance

Systemic

AEA/2-AG (Sanchez et al. 2016)

Elevated

Correlates with pain levels

PEA/OEA (Sanchez et al. 2016)

Elevated

 

Peritoneal fluid

AEA/2-AGa (Andrieu et al. 2022)

Elevated/reduced

Inflammation

Follicular fluid

AEA (Fonseca et al. 2021)

Elevated

Inflammation

Eutopic endometrium

CB1 receptor (Resuehr et al. 2012)

Decreased

Regardless of the cycle phase

CB1 receptor/CB2 receptor (Shen et al. 2019a)

Decreased

 

TRPV1 (Bohonyi et al. 2017)

Increased

Impact on pain

Ectopic lesion

PEA (Lingegowda et al. 2021a)

Increased

Anti-inflammatory

CB1 receptor/CB2 receptor (Lingegowda et al. 2021a; Bilgic et al. 2017; Shen et al. 2019a)

Decreased

Inflammation

FAAH/NAPE-PLD (Bilgic et al. 2017)

Decreased

Higher AEA levels

TRPV1/TRPA1 (Bohonyi et al. 2017)

Increased

Increased pain

Myometrium

CB1 receptor/CB2 receptor (Shen et al. 2019b)

Increased

Correlates with pain levels

  1. aDuring the proliferative phase of the menstrual cycle only