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The scientists also created a synthetic analogue of conolidine, RTI-5152-12, which displays a fair higher activity to the receptor. These results, which were being posted on June 3rd in the Global journal Signal Transduction and Specific TherapyThe comments form on this website page may be used to report written content that isn't precise, up-to-da
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2015). These experiments, taken together, propose that, Though a direct activation of GPR55 or PPAR‐α happens, PEA can generate its anti‐inflammatory motion in the gut also by using oblique activation of CB1 and CB2 receptors, possibly because of the ability of the compound to potentiate the action of endocannabinoids at these receptors.The la
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