Fig. 5From: Assessment of NSAIDs as potential inhibitors of the fatty acid amide hydrolase I (FAAH-1) using three different primary fatty acid amide substrates in vitroMode of inhibition of rat liver FAAH-1 hydrolysis of (a) oleamide and (b) arachidonamide by meclofenamic acid and indomethacin. Data are mean ± SEM (Standard Error of the Mean) of four separate preparations (n = 4) conducted in triplicateBack to article page