Once introduced into your extracellular Area by a putative endocannabinoid transporter, messengers are prone to glial mobile inactivation. Endocannabinoids are taken up by a transporter on the glial cell and degraded by fatty acid amide hydrolase (FAAH), which cleaves anandamide into arachidonic acid and ethanolamine or monoacylglycerol lipase (MAG
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