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Central administration of palmitoylethanolamide minimizes hyperalgesia in mice by means of inhibition of NF??B nuclear signalling in dorsal root ganglia. Eur J PharmacolThe exogenous administration of PEA could in this sort of circumstances provide to replenish levels of endogenous PEA, restoring its protective, anti-inflammatory and analgesic outc

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2015). These scientific tests, taken jointly, suggest that, Though a immediate activation of GPR55 or PPAR?? happens, PEA can produce its anti?inflammatory motion in the intestine also by way of indirect activation of CB1 and CB2 receptors, likely as a consequence of the flexibility of this compound to potentiate the motion of endocannabinoids at t

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