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[17] Either of these actions by themselves has been shown to reduce pain, and are a possible mechanism for paracetamol, though it has been demonstrated that, after blocking cannabinoid receptors and hence making any action of cannabinoid reuptake irrelevant, paracetamol no longer has any analgesic effect, suggesting its pain-relieving action is indeed mediated by the endogenous cannabinoid system

Silica

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PGI2 inhibits platelet aggregation by activating platelet IP receptors, which couple to Gs proteins and increase intracellular cAMP