Of Notice is the fact, because of PEA’s high lipophilicity, micronized or extremely-micronized formulations are considered to be extra easily absorbable, with additional favorable pharmacokinetics and greater efficacy. Though there is some proof supporting this idea, there remains no proof with the superiority of micronized PEA [sixteen].All 3 ex
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2015). These research, taken alongside one another, suggest that, Whilst a immediate activation of GPR55 or PPAR‐α occurs, PEA can produce its anti‐inflammatory action from the gut also via oblique activation of CB1 and CB2 receptors, almost certainly as a result of the flexibility of this compound to potentiate the action of endocannabinoids
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